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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Endocrinol.</journal-id>
<journal-title>Frontiers in Endocrinology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Endocrinol.</abbrev-journal-title>
<issn pub-type="epub">1664-2392</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fendo.2025.1534852</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Endocrinology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Factors associated with hypertension among patients with type 2 diabetes: evidence from a resource-limited setting&#x2014;Southern Ethiopia</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Yakob</surname>
<given-names>Begidu</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
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<contrib contrib-type="author">
<name>
<surname>Israel</surname>
<given-names>Eskinder</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
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<contrib contrib-type="author">
<name>
<surname>Jaldo</surname>
<given-names>Mesfin Menza</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
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<contrib contrib-type="author">
<name>
<surname>Abraham</surname>
<given-names>Awoke</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
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<contrib contrib-type="author">
<name>
<surname>Yakob</surname>
<given-names>Tagese</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
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<aff id="aff1">
<sup>1</sup>
<institution>Montioring and Evaluation, Wolaita Zone Health Department</institution>, <addr-line>Wolaita Sodo</addr-line>,&#xa0;<country>Ethiopia</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>School of Public Health, College of Health Science and Medicine, Wolaita Sodo University</institution>, <addr-line>Wolaita Sodo</addr-line>,&#xa0;<country>Ethiopia</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>School of Public Health, College of Medicine and Health Sciences, Wachemo University</institution>, <addr-line>Hossana</addr-line>,&#xa0;<country>Ethiopia</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>School of Public Health, Walailak University</institution>, <addr-line>Nakhon Si Thammarat</addr-line>,&#xa0;<country>Thailand</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Alexander Akhmedov, University of Zurich, Switzerland</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Maria Guadalupe Moreno Trevi&#xf1;o, University of Monterrey, Mexico</p>
<p>Srividya Velagapudi, University of Zurich, Switzerland</p>
<p>Jamol Uzokov, Ministry of Health of the Republic Uzbekistan, Uzbekistan</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Begidu Yakob, <email xlink:href="mailto:yakobegidu@gmail.com">yakobegidu@gmail.com</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>01</day>
<month>08</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>16</volume>
<elocation-id>1534852</elocation-id>
<history>
<date date-type="received">
<day>26</day>
<month>11</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>08</day>
<month>07</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Yakob, Israel, Jaldo, Abraham and Yakob.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Yakob, Israel, Jaldo, Abraham and Yakob</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec>
<title>Background</title>
<p>Globally, non-communicable diseases contribute to about three-quarters of all deaths. Developing nations face particular difficulties with the concurrent presence of diabetes and high blood pressure, problems intensified by poor nutrition habits, lack of physical exercise, and continuing high rates of illnesses like HIV/AIDS and malaria. A significant data gap in primary healthcare (PHC) data has been determined and prioritized by governments seeking to assess and enhance the prevention and management of chronic disease.</p>
</sec>
<sec>
<title>Objective</title>
<p>The main aim of the current study is to determine factors related to hypertension among patients with type 2 diabetes in public PHC facilities in Southern Ethiopia.</p>
</sec>
<sec>
<title>Methods</title>
<p>A facility-based cross-sectional study was conducted from 6 March 2023 to 5 April 2023 among 409 patients with diabetes. A systematic random sampling technique was employed to select the study participants. The data were cleaned, coded, and entered into Epi-data version 4.6.0.2 and exported to STATA version 14 for analysis. For descriptive statistics, both bivariate and multivariable logistic regression analyses were employed. Variables with a <italic>p</italic>-value &lt;0.05 in the multivariable logistic regression analysis were declared as significantly associated with outcome variables.</p>
</sec>
<sec>
<title>Results</title>
<p>A total of 407 patients with type 2 diabetes mellitus (T2DM) were included in the current study with a response rate of 99.5%, and the mean age of the study participants was 57.1 years (SD &#xb1;9.91). The prevalence of hypertension among patients with T2DM was 66.1% with a 95% confidence interval (CI) of 59.9&#x2013;70.3. The age group of &gt;60 years [adjusted odds ratio (AOR) = 2.09, 95% CI (1.02&#x2013;4.28)], patients with &#x2265;10 years&#x2019; duration of T2DM [AOR = 1.79, 95% CI (1.05&#x2013;3.03)], body mass index &#x2265;25 kg/m<sup>2</sup> [AOR = 4.19, 95% CI (2.10&#x2013;8.33)], and patients who have a family history of hypertension [AOR = 11.73, 95% CI (5.82&#x2013;23.66)] were significantly associated with hypertension among patients with type 2 diabetes.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>The prevalence of hypertension is high and the majority has poor blood pressure control. Hence, DM care providers and other health sector stakeholders have to work in collaboration to prevent it by designing appropriate strategies especially for those at higher risk of developing hypertension.</p>
</sec>
</abstract>
<kwd-group>
<kwd>hypertension</kwd>
<kwd>type 2 diabetes mellitus</kwd>
<kwd>primary healthcare</kwd>
<kwd>Ethiopia</kwd>
<kwd>resource limited setting</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="64"/>
<page-count count="11"/>
<word-count count="5151"/>
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<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Cardiovascular Endocrinology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<title>Introduction</title>
<p>High blood pressure stands as the third-leading cause of health burden measured in disability-adjusted life years (DALYs). While impacting 972 million adults globally in 2000, projections indicate this may rise to 1.56 billion cases by 2025 (<xref ref-type="bibr" rid="B1">1</xref>). Low- and middle-income countries (LMICs) bear 60% of the total impact, reflecting system healthcare and preventive care challenges (<xref ref-type="bibr" rid="B1">1</xref>). In sub-Saharan Africa (SSA), the burden reaches up to 38% in some communities, with an estimated 10&#x2013;20 million hypertensive individuals among 650 million people in SSA (<xref ref-type="bibr" rid="B2">2</xref>&#x2013;<xref ref-type="bibr" rid="B4">4</xref>). In Addis Ababa, Ethiopia, hypertension (HTN) burden ranges from 155 to 305, indicating significant regional variability and underdiagnosis (<xref ref-type="bibr" rid="B5">5</xref>).</p>
<p>Diabetes mellitus (DM), a chronic condition marked by hyperglycemia, affected 460 million individuals globally in 2019 and categorized as the world&#x2019;s eighth-leading disability-adjusted fatal disease and ranking as the eighth-leading cause of disability-related mortality (<xref ref-type="bibr" rid="B6">6</xref>). By 2021, the International Diabetes Federation (IDF) reported 537 million cases, with health expenditures nearing $966 billion. Undiagnosed cases are rampant, particularly in LMICs (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B8">8</xref>). In 2022, approximately 54 million adults aged above 18 years in the WHO Africa region had diabetes, with &gt;50% undiagnosed (34 million untreated), exacerbating complications like renal failure and amputation (<xref ref-type="bibr" rid="B9">9</xref>). National prevalence was 3.2% in Ethiopia in 2015 by the WHO survey (<xref ref-type="bibr" rid="B10">10</xref>).</p>
<p>DM and HTN are worldwide public health issues (<xref ref-type="bibr" rid="B11">11</xref>). These have been shown to be two of the main risk factors for cardiocerebrovascular illnesses, which are the top causes of adult mortality and disability (<xref ref-type="bibr" rid="B12">12</xref>). DM and HTN are additional problems facing the healthcare system in LMICs (<xref ref-type="bibr" rid="B13">13</xref>), attributable to shifts in dietary patterns and physical inactivity (<xref ref-type="bibr" rid="B14">14</xref>, <xref ref-type="bibr" rid="B15">15</xref>), and with malaria and HIV on the rise, this region faces a growing dual burden, resulting in significant public health consequences (<xref ref-type="bibr" rid="B16">16</xref>). This disease is disproportionately more common in countries with limited resources and underdeveloped healthcare systems (<xref ref-type="bibr" rid="B17">17</xref>). In underdeveloped nations, the death rate is increased by 7.2 times when diabetes and HTN coexist. According to epidemiological research, DM increases the risk of HTN (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>). An American research, for example, found that up to three-fourths of adults with diabetes also had HTN (<xref ref-type="bibr" rid="B20">20</xref>), and in China, approximately 15 million people have both conditions (<xref ref-type="bibr" rid="B21">21</xref>).</p>
<p>Type 2 diabetes mellitus (T2DM) and HTN together are especially deadly and greatly increase a person&#x2019;s cardiovascular risk. High BP and T2DM also raise the risk of acquiring additional diabetes-related conditions, such as renal disease and retinopathy, which can result in blindness (<xref ref-type="bibr" rid="B22">22</xref>). Furthermore, the formation of resistant HTN is linked to their cohabitation (<xref ref-type="bibr" rid="B23">23</xref>, <xref ref-type="bibr" rid="B24">24</xref>). To reduce the risk of diabetic complications, early identification of HTN and related cardiovascular risk factors is necessary (<xref ref-type="bibr" rid="B25">25</xref>). The treatment of HTN&#x2019;s side effects, such as dialysis, cardiac bypass surgery, and stroke prevention, is an expensive intervention that depletes both private and public funds (<xref ref-type="bibr" rid="B26">26</xref>). Early identification and effective management of HTN are associated with significant health and financial benefits (<xref ref-type="bibr" rid="B27">27</xref>).</p>
<p>Approximately 4 out of 10 (41%) patients had at least one of the following seven chronic conditions: diabetes, asthma, HTN, and others (<xref ref-type="bibr" rid="B28">28</xref>). Effectively managing patients with many chronic diseases in primary care is crucial, as the prevalence of multimorbidity rises with age (<xref ref-type="bibr" rid="B29">29</xref>). A significant data gap in primary healthcare (PHC) data has been determined and prioritized by governments seeking to assess and enhance the prevention and care of chronic diseases (<xref ref-type="bibr" rid="B5">5</xref>, <xref ref-type="bibr" rid="B30">30</xref>). To effectively prevent and control HTN, PHC settings need to collect comparable and aggregated data on the disease burden from the condition. This study aims to determine factors associated with HTN among patients with T2DM in Southern Ethiopia.</p>
</sec>
<sec id="s2" sec-type="materials|methods">
<title>Materials and methods</title>
<sec id="s2_1">
<title>Research framework, duration, and location</title>
<p>This cross-sectional study enrolled 409 patients with diabetes attending primary hospitals in the Wolaita zone between 6 March and 5 April 2023. The Wolaita zone is located in the southern region of Ethiopia, which is 380 km away from Ethiopia&#x2019;s capital, Addis Ababa. In the study area, there exist eight primary hospitals providing services to all zonal districts&#x2019; population and other population groups near the Wolaita zone.</p>
</sec>
<sec id="s2_2">
<title>Population</title>
<p>The study included adult patients with DM aged &#x2265;18 years who were under follow-up at selected public PHC chronic outpatient departments and met the inclusion criteria. Eligible participants had a documented history of at least three consecutive follow-up visits at the study facility. Critically ill patients and pregnant women with DM were excluded during the data collection period.</p>
</sec>
<sec id="s2_3">
<title>Sample size determination and sampling procedure</title>
<p>The sample size (<italic>n</italic>) was calculated using the single population proportion formula, assuming an HTN prevalence of 59.5% among patients with T2DM of another study conducted at DMGH (<xref ref-type="bibr" rid="B31">31</xref>) with 95% confidence interval (CI) and 5% margin of error, and 10% of the population size was added to adjust the non-response rate of&#xa0;study participants and to estimate our study sample size. Thus, <inline-formula>
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<mml:mtext>&#x2009;</mml:mtext>
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</inline-formula>, and after adding 10% of the non-response rate, the sample used for final study was <italic>n</italic>&#xa0;= 407.</p>
<p>The study was conducted at seven randomly selected primary hospitals (Tebela, Bele awassa, Bodit, Bedesa, Gesuba, Bitana, and Bomb primary hospital) across the study setting. An SRS method was used to identify the study subjects and 81 adult patients with DM who were followed at Tebela primary hospital, 85 at Bele awassa primary hospital, 92 at Bodit primary hospital, 69 at Gesuba primary hospital, 48 at Bitana primary hospital, 41 at Bedesa primary hospital, and 65 at Bomb primary hospital. The patient&#x2019;s medical registration number from each primary hospital HTN registration log book was first used to establish a sampling frame. Following that, each hospital received a proportionate share of the computed sample size. Next, a computer-generated specialized random sampling procedure was used to choose research participants from each of the chosen hospitals.</p>
</sec>
<sec id="s2_4">
<title>Operational definition</title>
<p>HTN: Participants were classified as hypertensive if they met either of the following criteria: (1) average systolic blood pressure (SBP) &#x2265;140 mmHg and/or diastolic blood pressure (DBP) &#x2265;90 mmHg, or (2) current use of antihypertensive medication (<xref ref-type="bibr" rid="B32">32</xref>). HTN staging followed standard classifications: prehypertension (120&#x2013;139/80&#x2013;89 mmHg), stage 1 (140&#x2013;159/90&#x2013;99 mmHg), stage 2 (160&#x2013;179/100&#x2013;109 mmHg), and hypertensive crisis (&#x2265;180/110 mmHg) (<xref ref-type="bibr" rid="B33">33</xref>). Current smokers were defined as individuals who reported cigarette use at least once during the month preceding the study (<xref ref-type="bibr" rid="B34">34</xref>). Poor glycemic control was operationally defined as having a hemoglobin A1c (HbA1c) level exceeding 7% (<xref ref-type="bibr" rid="B35">35</xref>).</p>
<p>Patients with diabetes were identified through medical records as individuals with an established diagnosis who were actively engaged in follow-up care at the participating healthcare facilities, as evidenced by possession of a medical record number.</p>
</sec>
<sec id="s2_5">
<title>Data collection instrument and procedure</title>
<p>Data were collected using a pretested interviewer-administered questionnaire adapted from relevant literature (<xref ref-type="bibr" rid="B31">31</xref>, <xref ref-type="bibr" rid="B36">36</xref>). The study employed a mixed-method approach involving face-to-face interviews, physical examinations, and medical record reviews. Behavioral risk factors were evaluated using the WHO STEPwise surveillance methodology for chronic disease risk factors. Anthropometric measurements included weight, measured to the nearest 0.1 kg using a calibrated scale, and height, measured in meters using a stadiometer with participants standing erect on a level surface. Body mass index (BMI) was subsequently calculated as weight in kilograms divided by height in squared meters.</p>
<p>Blood pressure measurements were obtained using a manual mercury sphygmomanometer, with the left arm positioned at heart level. Participants rested for at least 10 min before measurement (extended to 30 min for those who consumed hot beverages like coffee). Three consecutive readings were taken, and the average of these measurements was used for analysis.</p>
<p>To ensure data quality, the questionnaire was pretested on 5% of the total sample size at a non-selected primary hospital, with reliability assessed using Cronbach&#x2019;s alpha. Data collection was conducted by four nurses holding bachelor&#x2019;s degrees, who received 1 day of training on fundamental data collection principles. Supervisors underwent additional training focused on ensuring data completeness, cross-checking entries, and error correction.</p>
</sec>
<sec id="s2_6">
<title>Data analysis</title>
<p>The collected data were cleaned using Epi-Data software version 4.6.0.2 before being exported to SPSS version 26 for statistical analysis. Initial analysis involved computation of descriptive statistics, with results presented as frequencies and percentages. Associations between explanatory and outcome variables were examined using bivariate and multivariable logistic regression with a stepwise approach. Statistical significance was determined by an adjusted odds ratio (AOR) with a 95% CI and a <italic>p</italic>-value of less than 0.05.</p>
<p>Data normality was assessed through visual inspection of Q-Q plots and histograms, with the Q-Q plot approximating the diagonal line and the histogram showing no skewness, confirming normal distribution. Multicollinearity among predictor variables was evaluated using tolerance values greater than 0.1 and variance inflation factors (VIFs) less than 10, indicating no significant collinearity. Model fitness was assessed using the Hosmer&#x2013;Lemeshow goodness-of-fit test, which yielded a <italic>p</italic>-value of 0.501 (&#x3c7;&#xb2; = 1.44), confirming that the model was well-fitted to the data.</p>
</sec>
<sec id="s2_7">
<title>Ethics statement</title>
<p>The Ethical Review Committee (ERC) of the College of Health Science, School of Public Health, Wachemo University performed a review and allowed the study to proceed (ref. no. wcu/000981/15). In addition, formal letters of permission were obtained from the Tebela town administrative health office, the Bele awassa town administrative health office, the Bodit town administrative health office, the Bedesa district health office, the Gesuba town administrative health office, the Bitana district health office, and the Bomb district health office. The letters of permission written from district/town health offices were submitted to the respective hospitals. The study&#x2019;s objectives and methods were explained to each participant. Additionally, prior to participation, all study participants provided written informed permission. The study&#x2019;s goal, the thorough review of their medical records, and the potential benefits of the research were also explained to the participants. The data gathered were used for the study&#x2019;s objectives. All of the information gathered throughout the study was kept private, available only to the research team and utilized only for that reason. The participants&#x2019; medical record numbers were utilized instead of personal identifiers for the purpose of gathering data. The study was carried out in compliance with the applicable rules, laws, and Helsinki Declaration principles.</p>
</sec>
<sec id="s2_8">
<title>Patient and public involvement</title>
<p>No patients or public groups were involved in the design, analysis, or interpretation of this study, and they were also not involved in the dissemination of the results.</p>
</sec>
</sec>
<sec id="s3" sec-type="results">
<title>Results</title>
<sec id="s3_1">
<title>Socio-demographic characteristics of study participants</title>
<p>The study included 407 out of 409 eligible patients with T2DM, yielding a response rate of 99.5%. The mean age of the participants was 57.1 years (&#xb1; 9.91 SD), with the largest age group (35.6%, <italic>n</italic> = 145) being 51&#x2013;60 years old. The cohort consisted of predominantly male (52.1%, <italic>n</italic> = 212) and urban-dwelling (85.7%, <italic>n</italic> = 349) individuals. Educationally, 41.0% (<italic>n</italic> = 167) had attained education beyond a college diploma, while 73.0% (<italic>n</italic> = 297) were married. Government employees constituted 39.6% (<italic>n</italic> = 161) of participants, and over half (52.8%, <italic>n</italic> = 215) reported a monthly income exceeding 5,000 Ethiopian birr (ETB). These characteristics collectively describe an urban-predominant, middle-aged population with relatively high educational attainment and income levels compared to national averages (<xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>).</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Socio-demographic characteristics of patients with type 2 diabetes mellitus: evidence from a resource-limited setting&#x2014;Southern Ethiopia.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" rowspan="2" align="left">Variables</th>
<th valign="top" rowspan="2" align="left">Response category</th>
<th valign="top" colspan="2" align="left">Hypertension</th>
<th valign="top" rowspan="2" align="left">Total (N)</th>
</tr>
<tr>
<th valign="top" align="left">Yes (%)</th>
<th valign="top" align="left">No (%)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" rowspan="3" align="left">Age of mother (in years)</td>
<td valign="top" align="left">&lt;50</td>
<td valign="top" align="left">70 (26.0)</td>
<td valign="top" align="left">49 (35.5)</td>
<td valign="top" align="left">119 (29.2)</td>
</tr>
<tr>
<td valign="top" align="left">51&#x2013;60</td>
<td valign="top" align="left">87 (32.3)</td>
<td valign="top" align="left">58 (42.0)</td>
<td valign="top" align="left">145 (35.6)</td>
</tr>
<tr>
<td valign="top" align="left">&gt;60</td>
<td valign="top" align="left">112 (41.6)</td>
<td valign="top" align="left">31 (22.6)</td>
<td valign="top" align="left">143 (35.1)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Sex</td>
<td valign="top" align="left">Male</td>
<td valign="top" align="left">140 (52.1)</td>
<td valign="top" align="left">72 (52.2)</td>
<td valign="top" align="left">212 (52.1)</td>
</tr>
<tr>
<td valign="top" align="left">Female</td>
<td valign="top" align="left">129 (47.9)</td>
<td valign="top" align="left">66 (47.8)</td>
<td valign="top" align="left">195 (47.9)</td>
</tr>
<tr>
<td valign="top" rowspan="3" align="left">Marital status</td>
<td valign="top" align="left">Single</td>
<td valign="top" align="left">18 (6.9)</td>
<td valign="top" align="left">12 (8.6)</td>
<td valign="top" align="left">10 (1.1)</td>
</tr>
<tr>
<td valign="top" align="left">Married</td>
<td valign="top" align="left">186 (69.1)</td>
<td valign="top" align="left">111 (80.4)</td>
<td valign="top" align="left">364 (95.4)</td>
</tr>
<tr>
<td valign="top" align="left">Others*</td>
<td valign="top" align="left">65 (24.2)</td>
<td valign="top" align="left">15 (10.8)</td>
<td valign="top" align="left">32(3.5)</td>
</tr>
<tr>
<td valign="top" rowspan="5" align="left">Educational status</td>
<td valign="top" align="left">Illiterate</td>
<td valign="top" align="left">23 (8.6)</td>
<td valign="top" align="left">13 (8.8)</td>
<td valign="top" align="left">36 (8.8)</td>
</tr>
<tr>
<td valign="top" align="left">Literate</td>
<td valign="top" align="left">12 (4.5)</td>
<td valign="top" align="left">19 (12.8)</td>
<td valign="top" align="left">31 (7.6)</td>
</tr>
<tr>
<td valign="top" align="left">Primary</td>
<td valign="top" align="left">45 (16.7)</td>
<td valign="top" align="left">21 (14.2)</td>
<td valign="top" align="left">66 (16.2)</td>
</tr>
<tr>
<td valign="top" align="left">Secondary</td>
<td valign="top" align="left">64 (23.8)</td>
<td valign="top" align="left">43 (29.1)</td>
<td valign="top" align="left">107 (26.3)</td>
</tr>
<tr>
<td valign="top" align="left">College/university diploma or above</td>
<td valign="top" align="left">125 (46.5)</td>
<td valign="top" align="left">52 (35.1)</td>
<td valign="top" align="left">167 (41.0)</td>
</tr>
<tr>
<td valign="top" rowspan="5" align="left">Occupation status</td>
<td valign="top" align="left">Merchant</td>
<td valign="top" align="left">27 (10.0)</td>
<td valign="top" align="left">13 (8.5)</td>
<td valign="top" align="left">35 (8.6)</td>
</tr>
<tr>
<td valign="top" align="left">Government employee</td>
<td valign="top" align="left">98 (36.4)</td>
<td valign="top" align="left">73 (47.8)</td>
<td valign="top" align="left">161 (39.6)</td>
</tr>
<tr>
<td valign="top" align="left">Housewife</td>
<td valign="top" align="left">73 (27.1)</td>
<td valign="top" align="left">29 (18.9)</td>
<td valign="top" align="left">102 (25.1)</td>
</tr>
<tr>
<td valign="top" align="left">Farmer</td>
<td valign="top" align="left">29 (10.8)</td>
<td valign="top" align="left">15 (9.8)</td>
<td valign="top" align="left">44 (10.8)</td>
</tr>
<tr>
<td valign="top" align="left">Others**</td>
<td valign="top" align="left">42 (15.6)</td>
<td valign="top" align="left">23 (15.0)</td>
<td valign="top" align="left">65 (16.0)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Residents</td>
<td valign="top" align="left">Urban</td>
<td valign="top" align="left">232 (86.3)</td>
<td valign="top" align="left">117 (59.1)</td>
<td valign="top" align="left">349 (85.7)</td>
</tr>
<tr>
<td valign="top" align="left">Rural</td>
<td valign="top" align="left">37 (13.7)</td>
<td valign="top" align="left">21 (40.9)</td>
<td valign="top" align="left">58 (14.3)</td>
</tr>
<tr>
<td valign="top" rowspan="4" align="left">Monthly income (ETB)</td>
<td valign="top" align="left">&lt;1,599</td>
<td valign="top" align="left">14 (5.2)</td>
<td valign="top" align="left">42 (30.2)</td>
<td valign="top" align="left">55 (13.5)</td>
</tr>
<tr>
<td valign="top" align="left">1,600&#x2013;3,599</td>
<td valign="top" align="left">19 (7.1)</td>
<td valign="top" align="left">9 (6.5)</td>
<td valign="top" align="left">28 (6.9)</td>
</tr>
<tr>
<td valign="top" align="left">3,600&#x2013;4,999</td>
<td valign="top" align="left">65 (24.2)</td>
<td valign="top" align="left">44 (31.7)</td>
<td valign="top" align="left">109 (26.8)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;5,000</td>
<td valign="top" align="left">171 (63.5)</td>
<td valign="top" align="left">44 (31.7)</td>
<td valign="top" align="left">215 (52.8)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>*Divorced and widowed. **Driver, security, and self-employee. ETB, Ethiopian birr.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3_2">
<title>Clinical characteristics of participants</title>
<p>The study population had an average diabetes duration of 10.8 years (&#xb1; 3.68 SD), ranging from 3 to 25 years. Glycemic control measurements showed a mean HbA1c of 8.2% (&#xb1; 2.37 SD), with 54.1% (<italic>n</italic> = 220) of participants exhibiting poor glycemic control (HbA1c &gt;7%). The average fasting blood glucose level was 152.2 mg/dL (&#xb1; 45.8 SD), while mean blood pressure readings were 131.4/82.5 mmHg (&#xb1; 16.7/9.0 SD) for systolic and diastolic pressures, respectively. Treatment patterns revealed that 39.8% (<italic>n</italic> = 162) of patients were on oral hypoglycemic monotherapy, while 37.6% (<italic>n</italic> = 153) received dual therapy for diabetes management. Anthropometric data indicated that 66.1% (<italic>n</italic> = 269) of participants fell within the normal BMI range (18.5&#x2013;24.9 kg/m&#xb2;). These metabolic parameters collectively demonstrate the clinical characteristics and management profile of the studied diabetic population. Approximately 281 (69.05%) study participants had no history of HTN in the family. Majority of study participants, 403 (99.0%), had no history of chronic kidney disease (CKD), 375 (92.1%) had no history of cardiac heart disease (CHD), 376 (92.4%) had no history of alcohol drinking, and 395 (97.1%) had no history of smoking. Greater than half, 219 (53.8%), of study participants had physical activity of less 3 days per week. Greater than two-thirds, 274 (67.3%), of participants had a history of diabetes for more than 10 years&#x2019; duration and 293 (72.0%) participants had a self-glucometer at home. Majority of respondents, 405 (99.5%), had a history of attending health education on DM at a health facility (<xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref>).</p>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption>
<p>Clinical characteristics of patients with type 2 diabetes mellitus: evidence from a resource-limited setting&#x2014;Southern Ethiopia.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" rowspan="2" align="left">Variables</th>
<th valign="top" rowspan="2" align="left">Response category</th>
<th valign="top" colspan="2" align="left">Hypertension</th>
<th valign="top" rowspan="2" align="left">Total (<italic>N</italic>)</th>
</tr>
<tr>
<th valign="top" align="left">Yes</th>
<th valign="top" align="left">No</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" rowspan="2" align="left">Hypertensive history with anti-hypertensive therapy</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">146 (54.3)</td>
<td valign="top" align="left">55 (39.9)</td>
<td valign="top" align="left">201 (49.4)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">123 (45.7)</td>
<td valign="top" align="left">83 (60.1)</td>
<td valign="top" align="left">206 (50.6)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">If yes, how long (<italic>n</italic> = 201)</td>
<td valign="top" align="left">&lt;10 years</td>
<td valign="top" align="left">108 (77.1)</td>
<td valign="top" align="left">55 (87.3)</td>
<td valign="top" align="left">163 (40.0)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;10 years</td>
<td valign="top" align="left">32 (22.9)</td>
<td valign="top" align="left">6 (12.7)</td>
<td valign="top" align="left">38 (9.3)</td>
</tr>
<tr>
<td valign="top" rowspan="5" align="left">Current SBP in mmHg</td>
<td valign="top" align="left">90&#x2013;119</td>
<td valign="top" align="left">32 (11.9)</td>
<td valign="top" align="left">33 (23.9)</td>
<td valign="top" align="left">65 (16.0)</td>
</tr>
<tr>
<td valign="top" align="left">120&#x2013;139</td>
<td valign="top" align="left">110 (40.8)</td>
<td valign="top" align="left">67 (48.6)</td>
<td valign="top" align="left">177 (43.5)</td>
</tr>
<tr>
<td valign="top" align="left">140&#x2013;159</td>
<td valign="top" align="left">112 (41.6)</td>
<td valign="top" align="left">26 (18.8)</td>
<td valign="top" align="left">138 (33.9)</td>
</tr>
<tr>
<td valign="top" align="left">160&#x2013;179</td>
<td valign="top" align="left">13 (4.8)</td>
<td valign="top" align="left">10 (7.2)</td>
<td valign="top" align="left">23 (5.7)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;180</td>
<td valign="top" align="left">2 (0.7)</td>
<td valign="top" align="left">2 (1.4)</td>
<td valign="top" align="left">4 (1.0)</td>
</tr>
<tr>
<td valign="top" rowspan="4" align="left">Current DBP in mmHg</td>
<td valign="top" align="left">60&#x2013;79</td>
<td valign="top" align="left">37 (13.8)</td>
<td valign="top" align="left">60 (44.5)</td>
<td valign="top" align="left">97 (23.8)</td>
</tr>
<tr>
<td valign="top" align="left">80&#x2013;89</td>
<td valign="top" align="left">108 (40.1)</td>
<td valign="top" align="left">33 (24.5)</td>
<td valign="top" align="left">141 (34.6)</td>
</tr>
<tr>
<td valign="top" align="left">90&#x2013;99</td>
<td valign="top" align="left">123 (45.7)</td>
<td valign="top" align="left">43 (31.9)</td>
<td valign="top" align="left">166 (40.8)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;100</td>
<td valign="top" align="left">1 (0.4)</td>
<td valign="top" align="left">2 (1.5)</td>
<td valign="top" align="left">3 (0.7)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Hypertensive history in the family</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">114 (42.4)</td>
<td valign="top" align="left">12 (8.7)</td>
<td valign="top" align="left">126 (31.0)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">155 (57.6)</td>
<td valign="top" align="left">126 (91.3)</td>
<td valign="top" align="left">281 (69.0)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">History of CKD</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">3 (0.01)</td>
<td valign="top" align="left">1 (0.7)</td>
<td valign="top" align="left">4 (1.0)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">266 (99.9)</td>
<td valign="top" align="left">137 (99.3)</td>
<td valign="top" align="left">403 (99.0)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">History of CHD</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">30 (7.9)</td>
<td valign="top" align="left">2 (1.4)</td>
<td valign="top" align="left">32 (7.9)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">239 (92.1)</td>
<td valign="top" align="left">136 (98.6)</td>
<td valign="top" align="left">375 (92.1)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Smoking history</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">7 (0.8)</td>
<td valign="top" align="left">5 (3.6)</td>
<td valign="top" align="left">12 (2.9)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">262 (97.2)</td>
<td valign="top" align="left">133 (96.4)</td>
<td valign="top" align="left">395 (97.1)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Alcohol intake</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">15 (5.6)</td>
<td valign="top" align="left">16 (11.5)</td>
<td valign="top" align="left">31 (7.6)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">254 (94.4)</td>
<td valign="top" align="left">122 (88.5)</td>
<td valign="top" align="left">376 (92.4)</td>
</tr>
<tr>
<td valign="top" rowspan="3" align="left">Physical activity status/week</td>
<td valign="top" align="left">&lt;3 days</td>
<td valign="top" align="left">114 (42.4)</td>
<td valign="top" align="left">60 (43.5)</td>
<td valign="top" align="left">219 (53.8)</td>
</tr>
<tr>
<td valign="top" align="left">3&#x2013;5 days</td>
<td valign="top" align="left">155 (57.6)</td>
<td valign="top" align="left">58 (42.0)</td>
<td valign="top" align="left">138 (33.9)</td>
</tr>
<tr>
<td valign="top" align="left">&gt;5 days</td>
<td valign="top" align="left">114 (42.4)</td>
<td valign="top" align="left">20 (14.5)</td>
<td valign="top" align="left">50 (12.3)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">BMI (kg/m<sup>2</sup>)</td>
<td valign="top" align="left">&lt;25</td>
<td valign="top" align="left">147 (54.6)</td>
<td valign="top" align="left">122 (88.4)</td>
<td valign="top" align="left">269 (66.1)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;25</td>
<td valign="top" align="left">122 (45.3)</td>
<td valign="top" align="left">16 (11.6)</td>
<td valign="top" align="left">138 (33.9)</td>
</tr>
<tr>
<td valign="top" rowspan="3" align="left">Anti-diabetic drug use</td>
<td valign="top" align="left">OHA</td>
<td valign="top" align="left">99 (36.8)</td>
<td valign="top" align="left">63 (45.6)</td>
<td valign="top" align="left">162 (39.8)</td>
</tr>
<tr>
<td valign="top" align="left">Insulin</td>
<td valign="top" align="left">59 (21.9)</td>
<td valign="top" align="left">33 (23.9)</td>
<td valign="top" align="left">92 (22.6)</td>
</tr>
<tr>
<td valign="top" align="left">OHA + insulin</td>
<td valign="top" align="left">111 (41.2)</td>
<td valign="top" align="left">42 (30.4)</td>
<td valign="top" align="left">153 (37.6)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Glycemic control</td>
<td valign="top" align="left">Good</td>
<td valign="top" align="left">105 (39.0)</td>
<td valign="top" align="left">82 (59.4)</td>
<td valign="top" align="left">187 (45.9)</td>
</tr>
<tr>
<td valign="top" align="left">Poor</td>
<td valign="top" align="left">164 (60.9)</td>
<td valign="top" align="left">56 (40.6)</td>
<td valign="top" align="left">220 (54.1)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Fasting glucose level</td>
<td valign="top" align="left">&lt;126 mg/dL</td>
<td valign="top" align="left">112 (41.6)</td>
<td valign="top" align="left">37 (26.8)</td>
<td valign="top" align="left">149 (36.6)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;126 mg/dL</td>
<td valign="top" align="left">157 (58.4)</td>
<td valign="top" align="left">101 (73.2)</td>
<td valign="top" align="left">258 (64.4)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Duration of T2DM</td>
<td valign="top" align="left">&lt;10 years</td>
<td valign="top" align="left">70 (26.1)</td>
<td valign="top" align="left">63 (45.6)</td>
<td valign="top" align="left">133 (32.7)</td>
</tr>
<tr>
<td valign="top" align="left">&#x2265;10 years</td>
<td valign="top" align="left">199 (73.9)</td>
<td valign="top" align="left">75 (54.4)</td>
<td valign="top" align="left">274 (67.3)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Have glucometer at home</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">76 (28.3)</td>
<td valign="top" align="left">38 (27.5)</td>
<td valign="top" align="left">114 (28.0)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">193 (71.7)</td>
<td valign="top" align="left">100 (72.5)</td>
<td valign="top" align="left">293 (72.0)</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">Attending health education on DM</td>
<td valign="top" align="left">Yes</td>
<td valign="top" align="left">267 (99.2)</td>
<td valign="top" align="left">138 (100.0)</td>
<td valign="top" align="left">405 (99.5)</td>
</tr>
<tr>
<td valign="top" align="left">No</td>
<td valign="top" align="left">2 (0.8)</td>
<td valign="top" align="left">0 (0.0)</td>
<td valign="top" align="left">2 (0.5)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>*CKD: chronic kidney disease, CHD: cardiac heart disease, DM: diabetic mellitus, BMI: body mass index.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3_3">
<title>Prevalence and patterns of hypertension among patients with T2DM</title>
<p>HTN was identified in 66.1% (95% CI: 59.9&#x2013;70.3) of the participants with type 2 diabetes. From these, 68 (25.2%) were newly diagnosed at the time of data collection. The majority, 177 (43.5%), of patients with type 2 diabetes were prehypertensive, followed by stage 1 hypertensive, 138 (33.9%); 23 (5.7%) study participants were stage 2 hypertensive and 4 (1%) were in the hypertensive crisis category.</p>
</sec>
<sec id="s3_4">
<title>Statistical analysis of hypertension risk factors</title>
<p>The association between potential predictors and HTN was examined through binary logistic regression analysis. Initial candidate variables considered for the model included age, marital status, family history of HTN, physical activity level, duration of T2DM, BMI, use of anti-diabetic medications, glycemic control status, and fasting blood glucose levels. In the final multivariate analysis, four factors emerged as statistically significant predictors of HTN: age, duration of T2DM, BMI, and family history of HTN.</p>
<p>Advanced age showed a significant association with HTN risk. After adjusting for all other variables in the model, participants aged over 60 years demonstrated 2.09 times greater odds of developing HTN compared to those younger than 50 years (AOR = 2.09; 95% CI: 1.02&#x2013;4.28; <italic>p</italic> = 0.044). Elevated BMI also proved to be an important risk factor, with overweight or obese participants (BMI &#x2265; 25 kg/m&#xb2;) having 4.19 times higher odds of HTN than those with normal BMI (AOR = 4.19; 95% CI: 2.10&#x2013;8.33; <italic>p</italic> = 0.001).</p>
<p>The duration of diabetes showed a significant relationship with HTN risk. Patients with a T2DM duration of 10 years or more had 1.8 times greater odds of developing HTN compared to those with a shorter disease duration (AOR = 1.8; 95% CI: 1.05&#x2013;3.03; <italic>p</italic> = 0.03). Most strikingly, family history of HTN emerged as the strongest predictor, with affected participants showing 11.7 times higher odds of developing HTN compared to those without such history (AOR = 11.73; 95% CI: 5.82&#x2013;23.66; <italic>p</italic> = 0.001). The notably wide CI for family history may reflect limited precision due to the relatively small subgroup size (<italic>n</italic> = 126). This finding was further validated using Firth&#x2019;s penalized regression analysis, which addresses small-sample bias, confirming the strong association (AOR = 10.41; 95% CI: 5.12&#x2013;21.14) (<xref ref-type="table" rid="T3">
<bold>Table&#xa0;3</bold>
</xref>).</p>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption>
<p>Multivariable logistic regression analysis of factors associated with hypertension among patients with type 2 diabetes mellitus: evidence from a resource-limited setting&#x2014;Southern Ethiopia.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" rowspan="2" align="left">Variable</th>
<th valign="top" align="left">Hypertension</th>
<th valign="top" colspan="3" align="left">Odds ratio (95% CI)</th>
<th valign="top" align="left">Firth&#x2019;s penalized</th>
</tr>
<tr>
<th valign="top" align="left">Yes (%)</th>
<th valign="top" align="left">No (%)</th>
<th valign="top" align="left">COR with 95% CI</th>
<th valign="top" align="left">AOR with 95% CI</th>
<th valign="top" align="left">AOR (95% CI)*</th>
</tr>
</thead>
<tbody>
<tr>
<th valign="top" colspan="8" align="left">Age (years)</th>
</tr>
<tr>
<td valign="top" align="center">&#x2264;50</td>
<td valign="top" align="left">70 (26.0)</td>
<td valign="top" align="left">49 (35.5)</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">51&#x2013;60</td>
<td valign="top" align="left">87 (32.3)</td>
<td valign="top" align="left">58 (42.0)</td>
<td valign="top" align="left">1.05 (0.64&#x2013;1.72)</td>
<td valign="top" align="left">094 (0.50&#x2013;1.77)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">&#x2265;60</td>
<td valign="top" align="left">112 (41.6)</td>
<td valign="top" align="left">31 (22.6)</td>
<td valign="top" align="left">2.53 (1.47&#x2013;4.34)</td>
<td valign="top" align="left">2.09(1.02&#x2013;4.28)*</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Marital status</th>
</tr>
<tr>
<td valign="top" align="center">Single</td>
<td valign="top" align="left">18 (6.9)</td>
<td valign="top" align="left">12 (8.6)</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">Married</td>
<td valign="top" align="left">186 (69.1)</td>
<td valign="top" align="left">111 (80.4)</td>
<td valign="top" align="left">1.12 (0.52&#x2013;0.41)</td>
<td valign="top" align="left">0.77 (0.29&#x2013;1.99)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">Others***</td>
<td valign="top" align="left">65 (24.2)</td>
<td valign="top" align="left">15 (10.8)</td>
<td valign="top" align="left">2.89 (1.15&#x2013;7.26)</td>
<td valign="top" align="left">1.16 (0.35&#x2013;3.79)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Family history of hypertension</th>
</tr>
<tr>
<td valign="top" align="center">Yes</td>
<td valign="top" align="left">114 (42.4)</td>
<td valign="top" align="left">12 (8.7)</td>
<td valign="top" align="left">7.72 (4.07&#x2013;14.6)</td>
<td valign="top" align="left">
<bold>11.7 (5.8&#x2013;23.6)*</bold>
</td>
<td valign="top" align="left">10.41 (5.12&#x2013;21.14)*</td>
</tr>
<tr>
<td valign="top" align="center">No</td>
<td valign="top" align="left">155 (57.6)</td>
<td valign="top" align="left">126 (91.3)</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="center">1.00</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Physical activity (days per week)</th>
</tr>
<tr>
<td valign="top" align="center">&#x2264;3</td>
<td valign="top" align="left">114 (42.4)</td>
<td valign="top" align="left">60 (43.5)</td>
<td valign="top" align="left">1.76 (0.93&#x2013;3.35)</td>
<td valign="top" align="left">1.23 (0.55&#x2013;2.76)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">3&#x2013;5</td>
<td valign="top" align="left">155 (57.6)</td>
<td valign="top" align="left">58 (42.0)</td>
<td valign="top" align="left">0.92 (0.47&#x2013;1.77)</td>
<td valign="top" align="left">0.65 (0.29&#x2013;1.44)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">&gt;5</td>
<td valign="top" align="left">114 (42.4)</td>
<td valign="top" align="left">20 (14.5)</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Body mass index (BMI)</th>
</tr>
<tr>
<td valign="top" align="center">&lt;25 kg/m<sup>2</sup>
</td>
<td valign="top" align="left">147 (54.6)</td>
<td valign="top" align="left">122 (88.4)</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="left">1.00</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">&#x2265;25 kg/m<sup>2</sup>
</td>
<td valign="top" align="left">122 (45.3)</td>
<td valign="top" align="left">16 (11.6)</td>
<td valign="top" align="left">6.32 (3.56&#x2013;11.2)</td>
<td valign="top" align="left">4.19 (2.11&#x2013;8.33)*</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Anti-diabetic drug</th>
</tr>
<tr>
<td valign="top" align="center">OHA</td>
<td valign="top" align="left">99 (36.8)</td>
<td valign="top" align="left">63 (45.6)</td>
<td valign="top" align="left">1:00</td>
<td valign="top" align="left">1:00</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">Insulin</td>
<td valign="top" align="left">59 (21.9)</td>
<td valign="top" align="left">33 (23.9)</td>
<td valign="top" align="left">1.14 (0.66&#x2013;1.93)</td>
<td valign="top" align="left">0.94 (0.48&#x2013;1.80)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">Both OHA and insulin</td>
<td valign="top" align="left">111 (41.2)</td>
<td valign="top" align="left">42 (30.4)</td>
<td valign="top" align="left">1.68 (1.04&#x2013;2.70)</td>
<td valign="top" align="left">1.14 (0.64&#x2013;2.0)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Glycemic control</th>
</tr>
<tr>
<td valign="top" align="center">Good</td>
<td valign="top" align="left">105 (39.0)</td>
<td valign="top" align="left">82 (59.4)</td>
<td valign="top" align="left">1:00</td>
<td valign="top" align="left">1:00</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">Poor</td>
<td valign="top" align="left">164 (60.9)</td>
<td valign="top" align="left">56 (40.6)</td>
<td valign="top" align="left">2.28 (1.50&#x2013;3.47)</td>
<td valign="top" align="left">0.69 (0.41&#x2013;1.18)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<th valign="top" colspan="8" align="left">Duration of T2DM</th>
</tr>
<tr>
<td valign="top" align="center">&lt;10 years</td>
<td valign="top" align="left">70 (26.0)</td>
<td valign="top" align="left">63 (45.6)</td>
<td valign="top" align="left">1 (reference)</td>
<td valign="top" align="left">1 (reference)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="center">&#x2265;10 years</td>
<td valign="top" align="left">199 (73.9)</td>
<td valign="top" align="left">75 (54.4)</td>
<td valign="top" align="left">2.38 (1.55&#x2013;3.67)</td>
<td valign="top" align="left">1.79 (1.06&#x2013;3.03)*</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>COR, crude odds ratio; T2DM, type 2 diabetic mellitus. *Statistically significant at <italic>p</italic> &lt; 0.05. ***Divorced and widowed.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec id="s4" sec-type="discussion">
<title>Discussion</title>
<p>This study showed the prevalence of HTN and associated factors among patients with T2DM in public PHC facilities in Southern Ethiopia. The prevalence of HTN in this study was 66.1% with a 95% CI of 59.9&#x2013;70.3. The current findings are in line with studies in Botswana (63.1%) (<xref ref-type="bibr" rid="B32">32</xref>) and in Israel (60.2%) (<xref ref-type="bibr" rid="B5">5</xref>). However, the current findings are higher than the prevalence reported in Nigeria (54.2%) (<xref ref-type="bibr" rid="B33">33</xref>), Jimma (46.5%) (<xref ref-type="bibr" rid="B18">18</xref>), Hosanna (55%) (<xref ref-type="bibr" rid="B37">37</xref>), Debor Tabour, Ethiopia (59.5%) (<xref ref-type="bibr" rid="B31">31</xref>), Adama, Ethiopia (56.3%) (<xref ref-type="bibr" rid="B38">38</xref>), a national diabetes center in Greece (55.6%) (<xref ref-type="bibr" rid="B39">39</xref>), and the United States (49.8%) (<xref ref-type="bibr" rid="B40">40</xref>). The observed HTN prevalence (66.1%) was lower than that reported in Jordan (72.4%) (<xref ref-type="bibr" rid="B41">41</xref>). The substantial differences in HTN prevalence across studies may be attributed to several factors, including variations in diagnostic criteria and distinct population characteristics. Notably, a prospective cohort study conducted in Iraq from August 2008 to April 2011 involving 5,578 patients with T2DM reported an HTN prevalence of 89.6%, with 45.3% of cases being newly identified during the study period (<xref ref-type="bibr" rid="B42">42</xref>). The observed discrepancies may stem from variations in diagnostic thresholds (e.g., &gt;130/80 mmHg versus higher cutoffs), differences in study populations&#x2019; sociodemographic profiles, and methodological factors including study design, healthcare access patterns, and lifestyle variations among participants. These elements collectively contribute to prevalence rate differences across studies while highlighting the importance of standardized diagnostic criteria and population-specific considerations in HTN research. Such variations underscore the need for careful interpretation of findings relative to each study&#x2019;s unique context and methodology.</p>
<p>The prevalence of newly diagnosed HTN was 25.2% with a 95% CI of 21.7&#x2013;29.0. The current findings were in line with studies conducted in Dire Dawa city, eastern Ethiopia (24.43%) (<xref ref-type="bibr" rid="B43">43</xref>) and in Gimbi Town, western Ethiopia (24.8%) (<xref ref-type="bibr" rid="B44">44</xref>). However, the HTN prevalence identified in our study substantially exceeds the 15.8% rate documented in Ethiopia&#x2019;s national NCD STEPS survey of the general adult population (<xref ref-type="bibr" rid="B45">45</xref>), in Debre-Markos, northwest Ethiopia (12.7%) (<xref ref-type="bibr" rid="B31">31</xref>), and Durame town, southern Ethiopia (14%) (<xref ref-type="bibr" rid="B46">46</xref>). However, the current findings were lower than those in community-based studies in Addis Ababa, central Ethiopia (newly diagnosed HTN prevalence, 29.2%) (<xref ref-type="bibr" rid="B47">47</xref>) and a multicenter facility-based study in Addis Ababa, central Ethiopia (newly diagnosed HTN prevalence, 32.3%) (<xref ref-type="bibr" rid="B48">48</xref>). This discrepancy may occur because individuals at risk of HTN are more likely to seek screening at urban tertiary care centers than at PHC facilities. The increased access to specialized services in major urban areas could lead to higher case detection rates compared to peripheral health institutions.</p>
<p>The study demonstrated a significant age-dependent association with HTN, where participants aged &gt;60 years had 2.09 times higher odds of developing HTN (AOR = 2.09; 95% CI: 1.02&#x2013;4.28) compared to those &lt;50 years. These findings align with previous epidemiological studies conducted in Israel (<xref ref-type="bibr" rid="B49">49</xref>), Iraq (<xref ref-type="bibr" rid="B42">42</xref>), and Botswana (<xref ref-type="bibr" rid="B50">50</xref>), confirming the well-established relationship between advancing age and increased HTN prevalence. The observed association can be attributed to age-related physiological and structural changes in the cardiovascular system. With progressive aging, the vascular system undergoes significant remodeling characterized by endothelial dysfunction, reduced arterial elasticity, and increased vascular stiffness. These changes result from complex pathophysiological alterations affecting all three layers of the arterial wall&#x2014;the intima, media, and adventitia. Key mechanisms include diminished nitric oxide bioavailability, increased collagen deposition, elastin fragmentation, and medial calcification (<xref ref-type="bibr" rid="B51">51</xref>).</p>
<p>This study further demonstrated that individuals with a BMI of &#x2265;25 kg/m&#xb2; had a significantly elevated risk of developing HTN compared to those with normal BMI. These findings align with previous research conducted in various settings, including Jimma, Gondar, Jijiga, Bayisa State, Nigeria, Kenya, and urban Varanasi (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B52">52</xref>&#x2013;<xref ref-type="bibr" rid="B57">57</xref>). The pathophysiological basis for this association involves multiple interrelated mechanisms. Excess adiposity contributes to increased cardiovascular risk through endothelial dysfunction, chronic low-grade inflammation, and hemodynamic alterations that collectively promote atherosclerosis (<xref ref-type="bibr" rid="B58">58</xref>). Furthermore, overweight and obesity induce insulin resistance and dyslipidemia, characterized by elevated low-density lipoprotein cholesterol deposition in vascular walls. These metabolic disturbances lead to progressive arterial stiffening and luminal narrowing, ultimately resulting in HTN development (<xref ref-type="bibr" rid="B32">32</xref>).</p>
<p>The study demonstrated a significant duration-dependent relationship between T2DM and HTN, with longer diabetes duration correlating with increased HTN prevalence. This finding is consistent with prior research indicating that prolonged T2DM exacerbates metabolic and vascular dysfunction, thereby elevating HTN risk (<xref ref-type="bibr" rid="B16">16</xref>, <xref ref-type="bibr" rid="B30">30</xref>, <xref ref-type="bibr" rid="B31">31</xref>). The underlying mechanisms involve progressive metabolic and hemodynamic disturbances associated with chronic hyperglycemia. Extended exposure to insulin resistance, dyslipidemia, and sustained hyperglycemia leads to cumulative microvascular damage, endothelial dysfunction, and sympathetic nervous system overactivation. Additionally, prolonged diabetes duration enhances renin&#x2013;angiotensin&#x2013;aldosterone system (RAAS) activity while reducing insulin-mediated vasodilation, further contributing to elevated blood pressure (<xref ref-type="bibr" rid="B34">34</xref>).</p>
<p>The study demonstrated a robust association between familial HTN history and HTN development in patients with T2DM. Individuals with a family history of HTN exhibited a 10.4-fold increased likelihood of developing HTN compared to those without such history (AOR = 10.4, 95% CI: 5.12&#x2013;21.14). These findings align with epidemiological evidence from Sri Lanka (<xref ref-type="bibr" rid="B58">58</xref>), Northern India (<xref ref-type="bibr" rid="B59">59</xref>), and multiple international studies (<xref ref-type="bibr" rid="B60">60</xref>&#x2013;<xref ref-type="bibr" rid="B64">64</xref>). The observed familial aggregation likely reflects both shared genetic susceptibility and common environmental exposures. From a genetic perspective, multiple polygenic variants affecting renal sodium handling, vascular&#xa0;tone regulation, and RAAS system function may contribute to this&#xa0;predisposition (<xref ref-type="bibr" rid="B26">26</xref>). Additionally, familial clustering of modifiable risk factors&#x2014;including dietary patterns (particularly sodium and potassium intake), physical activity levels, and stress coping mechanisms&#x2014;may synergistically interact with genetic predisposition to elevate HTN risk within families.</p>
<sec id="s4_1">
<title>Limitation of the study</title>
<p>While this study identified four significant predictors of HTN (age, family history, BMI, and diabetes duration), several potential confounding variables remain unaccounted for in our analysis. These include medication adherence patterns, specific dietary factors (such as sodium intake or DASH diet compliance), and objective measures of physical activity. Such unmeasured variables may represent important modifiers of HTN risk that could influence the observed associations. Future research incorporating these additional parameters would provide a more comprehensive understanding of HTN risk factors in diabetic populations.</p>
</sec>
</sec>
<sec id="s5" sec-type="conclusion">
<title>Conclusion</title>
<p>This study revealed that over 50% of participants with T2DM also had HTN. Our analysis identified significant associations between HTN and four key factors: advanced age, family history of HTN, elevated BMI, and longer duration of T2DM.</p>
<p>Understanding the global prevalence of HTN in diabetic populations is crucial for formulating effective public health strategies. Such epidemiological data inform both national and international healthcare policies aimed at managing this dual disease burden. HTN and diabetes are well-established, independent risk factors for atherosclerotic cardiovascular diseases, including coronary artery disease and cerebrovascular accidents. When these conditions coexist, they synergistically amplify the risk of serious complications, creating a greater combined effect than either condition alone. Medical practitioners ought to recommend regular blood pressure checks for patients&#x2019; relatives and promote preventative measures including dietary improvements and increased physical activity. The Ministry of Health and other concerned policymaker bodies should enhance care through workforce training and support interdisciplinary teams of primary care providers, fund community-based screening approaches, integrate HbA1c testing into routine primary care, develop guidelines prioritizing intensive lifestyle program for patients with overweight and family history of the disease, and continue health advocacies and promote lifestyle modification. Furthermore, future studies should highlight the need for more comprehensive longitudinal studies with detailed risk factor assessment.</p>
</sec>
</body>
<back>
<sec id="s6" sec-type="data-availability">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec id="s7" sec-type="ethics-statement">
<title>Ethics statement</title>
<p>The studies involving humans were approved by The Ethical Review Committee (ERC) of College of Health Science, School of Public Health, Wachemo University. Also, formal letters of permission were obtained from Tebela town administrative health office, Beleawassa town administrative health office, Bodit town administrative health office, Bedesa district health office, Gesuba town administrative health office, Bitana district health office and Bomb district health office. The formal letter of permission was written to the respective hospitals. The study&#x2019;s objectives and methods were explained to each participant. Additionally, prior to participation, all study participants provided written informed permission. The study&#x2019;s goal, the thorough review of their medical records, and the potential benefits of the research were also explained to the participants. The data gathered was used for the study&#x2019;s objectives. All of the information gathered throughout the study was kept private, available only to the research team, and utilized only for that reason. Their medical record numbers were utilized instead of personal identifiers for the purpose of gathering data. The study was carried out in compliance with the applicable rules, laws, and Helsinki Declaration principles. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants&#x2019; legal guardians/next of kin in accordance with the national legislation and institutional requirements.</p>
</sec>
<sec id="s8" sec-type="author-contributions">
<title>Author contributions</title>
<p>BY: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. EI: Conceptualization, Methodology, Project administration, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. MM: Investigation, Software, Validation, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. AA: Funding acquisition, Methodology, Visualization, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. TY: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing.</p>
</sec>
<sec id="s9" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare that no financial support was received for the research and/or publication of this article.</p>
</sec>
<sec id="s10" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s11" sec-type="ai-statement">
<title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was used in the creation of this manuscript.</p>
</sec>
<sec id="s12" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors&#xa0;and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<ref-list>
<title>References</title>
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