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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Neurol.</journal-id>
<journal-title>Frontiers in Neurology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurol.</abbrev-journal-title>
<issn pub-type="epub">1664-2295</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fneur.2025.1628976</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neurology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Risk of mortality in the elderly with different degree of sensorineural hearing loss in Taiwan</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Chen</surname>
<given-names>Jin-Cherng</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn0003"><sup>&#x2020;</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/validation/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Hsieh</surname>
<given-names>Pei-Shan</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="author-notes" rid="fn0003"><sup>&#x2020;</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/validation/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Hwang</surname>
<given-names>Juen-Haur</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/3067827/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
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</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Department of Neurosurgery, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation</institution>, <addr-line>Chiayi</addr-line>, <country>Taiwan</country></aff>
<aff id="aff2"><sup>2</sup><institution>School of Medicine, Tzu Chi University</institution>, <addr-line>Hualien</addr-line>, <country>Taiwan</country></aff>
<aff id="aff3"><sup>3</sup><institution>Department of Medical Research, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation</institution>, <addr-line>Chiayi</addr-line>, <country>Taiwan</country></aff>
<aff id="aff4"><sup>4</sup><institution>Deparments of Otolaryngology-Head and Neck Surgery, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation</institution>, <addr-line>Chiayi</addr-line>, <country>Taiwan</country></aff>
<aff id="aff5"><sup>5</sup><institution>Deparments of Otolaryngology-Head and Neck Surgery, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation</institution>, <addr-line>Taichung</addr-line>, <country>Taiwan</country></aff>
<aff id="aff6"><sup>6</sup><institution>Department of Medical Research, China Medical University Hospital, China Medical University</institution>, <addr-line>Taichung</addr-line>, <country>Taiwan</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/186429/overview">Jose Antonio Lopez-Escamez</ext-link>, University of Sydney, Australia</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2134164/overview">Mar&#x00ED;a Del Carmen Mole&#x00F3;n Gonz&#x00E1;lez</ext-link>, Junta de Andaluc&#x00ED;a de Gen&#x00F3;mica e Investigaci&#x00F3;n Oncol&#x00F3;gica (GENYO), Spain</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2925922/overview">Khuznita Dasa Novita</ext-link>, University of Brawijaya, Indonesia</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Juen-Haur Hwang, <email>g120796@tzuchi.com.tw</email></corresp>
<fn fn-type="equal" id="fn0003"><p><sup>&#x2020;</sup>These authors have contributed equally to this work</p></fn>
</author-notes>
<pub-date pub-type="epub">
<day>05</day>
<month>11</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>16</volume>
<elocation-id>1628976</elocation-id>
<history>
<date date-type="received">
<day>19</day>
<month>05</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>10</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Chen, Hsieh and Hwang.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Chen, Hsieh and Hwang</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 id="sec1">
<title>Introduction</title>
<p>Sensorineural hearing loss (SNHL) may lead to disability in many aspects. This study aims to investigate the risk of mortality in the elderly with sensorineural hearing loss (SNHL) in Taiwan.</p>
</sec>
<sec id="sec2">
<title>Methods</title>
<p>Three hundred and eighteen subjects with SNHL of age between 51 and 88&#x202F;years old were included between August 2000 and December 2002. Averaged pure tone threshold of all tested six frequencies (250&#x202F;Hz, 500&#x202F;Hz, 1,000&#x202F;Hz, 2000&#x202F;Hz, 4,000&#x202F;Hz, and 8,000&#x202F;Hz) of both ears with all audiogram shapes was divided into three cohorts: normal hearing group [0&#x2013;24 decibel hearing level (dBHL)]; mild SNHL group (25&#x2013;39 dBHL); moderate and severe SNHL group (40&#x2013;89 dBHL). The incidence rates of mortality were compared using the Kaplan&#x2013;Meier method with the log-rank test. Association of SNHL and mortality was examined by a Cox proportional hazard model with adjustment for all covariates.</p>
</sec>
<sec id="sec3">
<title>Results</title>
<p>Compared to the normal hearing group, the crude hazard ratio (HR) and adjusted hazard ratio (aHR) for mortality in mild SNHL group was 1.51 (95% CI&#x202F;=&#x202F;0.44&#x2013;5.14, <italic>p</italic>&#x202F;=&#x202F;0.5143) and 2.14 (95% CI&#x202F;=&#x202F;0.45&#x2013;10.23, <italic>p</italic>&#x202F;=&#x202F;0.3396), respectively. And, the crude HR and aHR for mortality in moderate and severe SNHL group was 4.82 (95% CI&#x202F;=&#x202F;1.65&#x2013;14.07, <italic>p</italic>&#x202F;=&#x202F;0.0041) and 6.96 (95% CI&#x202F;=&#x202F;1.60&#x2013;30.23, <italic>p</italic>&#x202F;=&#x202F;0.0096), respectively.</p>
</sec>
<sec id="sec4">
<title>Conclusion</title>
<p>The risk of mortality was significantly higher in the elderly with moderate and severe SNHL.</p>
</sec>
</abstract>
<kwd-group>
<kwd>mortality</kwd>
<kwd>age-related hearing impairment</kwd>
<kwd>elderly</kwd>
<kwd>sensorineural hearing loss</kwd>
<kwd>hearing level</kwd>
</kwd-group>
<counts>
<fig-count count="1"/>
<table-count count="1"/>
<equation-count count="0"/>
<ref-count count="21"/>
<page-count count="5"/>
<word-count count="3362"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Neuro-Otology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec5">
<label>1</label>
<title>Introduction</title>
<p>Sensorineural hearing loss (SNHL) may lead to disability in many aspects. Till now, only limited studies had discussed the relationship between SNHL and mortality in adults. Compared to normal-hearing control, subjects with severe [adjusted hazard ratio (aHR)&#x202F;=&#x202F;4.07] or profound hearing loss (aHR&#x202F;=&#x202F;4.22) were associated with a significant increase in mortality in Korean population who were older than 40&#x202F;years old after adjusting for age, sex, region of residence, income, and past histories (<xref ref-type="bibr" rid="ref1">1</xref>). They found that, compared with control group, the severe and profound hearing loss groups had higher mortality due to infection, metabolic, mental, circulatory, respiratory and digestive diseases, neoplasm, and trauma (<xref ref-type="bibr" rid="ref1">1</xref>).</p>
<p>Compared with normal hearing group, subjects with hearing impairment were related with increased risks for total mortality and mortality from heart disease in American adults (<xref ref-type="bibr" rid="ref2">2</xref>). The HRs for total mortality were 1.16, 1.54, and 1.85 for mild, moderate, and severe speech-frequency hearing loss, respectively. In addition, moderate SNHL (HR&#x202F;=&#x202F;1.90) and severe SNHL (HR&#x202F;=&#x202F;3.50) were significantly related with elevated risk of heart disease mortality, respectively (<xref ref-type="bibr" rid="ref2">2</xref>). Compared with normal hearing group, those who had hearing problems (a little trouble-HR: 1.17; a lot of trouble-HR: 1.45; deaf-HR: 1.54, respectively) were at an increased risk of mortality from all causes and cancers in American adults (<xref ref-type="bibr" rid="ref3">3</xref>). However, Zhang et al. (<xref ref-type="bibr" rid="ref4">4</xref>) reported that hearing impairment was not significantly associated with all-cause mortality risk in elderly Chinese subjects, adjusting for living area, life style, and medical conditions.</p>
<p>Although some studies had suggested that SNHL might be associated with increased mortality in older adults, but their relationship was still inconsistent. The weak point or inconsistency between previous studies might be caused by different study population, imperfect classification of hearing impairment, and/or statistical strategy. In fact, SNHL is a disease which was caused by many genetic and environmental variations (<xref ref-type="bibr" rid="ref5">5</xref>, <xref ref-type="bibr" rid="ref6">6</xref>). For example, obesity, hypertension, diabetes, dyslipidemia, coronary artery diseases, obstructive sleep apnea syndrome, transient ischemic attack might lead to SNHL (<xref ref-type="bibr" rid="ref6 ref7 ref8 ref9 ref10">6&#x2013;10</xref>). Thus, SNHL could be an intermediate indicator between many major diseases and mortality. Furthermore, SNHL itself might increase disability and the risks for cognition impairment, accident, depression, or stroke in the elderly (<xref ref-type="bibr" rid="ref11 ref12 ref13">11&#x2013;13</xref>). So, we supposed that SNHL could also increase the risk of mortality in the elderly independently.</p>
<p>Based on above introduction and criticism, we knew that the relationship between SHNL and mortality might be variable by ethnic groups and/or genetic background, and statistical strategy. Fortunately, compared to other nations, genetic heterogeneity was relatively low in Taiwan (<xref ref-type="bibr" rid="ref5">5</xref>, <xref ref-type="bibr" rid="ref6">6</xref>), which could reduce the violation the clinical revelence of SNHL on all-cause mortality no matter how it contributed dependently or independently. In this study, we aimed to clarify this question by a cohort study using real world data of the elderly in Taiwan and a new statistical strategy in this study.</p>
</sec>
<sec sec-type="materials|methods" id="sec6">
<label>2</label>
<title>Materials and methods</title>
<p>To investigate whether SNHL might increase the risk of mortality in the elderly. We identified 318 subjects with symmetric SNHL of age between 51 and 88 years at the outpatient department between August 2000 and December 2002. The date of having the first result of audiometry with all audiogram shapes was considered the index date (<xref ref-type="bibr" rid="ref14">14</xref>).</p>
<p>Averaged pure tone threshold of all tested six frequencies (250&#x202F;Hz, 500&#x202F;Hz, 1,000&#x202F;Hz, 2000&#x202F;Hz, 4,000&#x202F;Hz and 800&#x202F;Hz) of both ears was divided into three cohorts: normal hearing group [0&#x2013;24 decibel hearing level (dBHL)]; mild hearing-impaired group (25&#x2013;39 dBHL); moderate and severe hearing-impaired group (40&#x2013;89 dBHL) (<xref ref-type="bibr" rid="ref15">15</xref>). In addition, age, gender, body mass index (BMI), hypertension, diabetes mellitus (DM), dysplipidemia, coronary artery disease (CAD), acute myocardial infarction (AMI), chronic kidney disease (CKD), hepatitis, cirrhosis, Parkinson&#x2019;s disease, Alzheimer&#x2019;s disease, stroke, cancers, and trauma were recorded and will be adjusted during statistical analysis.</p>
<p>Patients who had conductive hearing impairment (averaged air-bone gap of hearing threshold greater than 10&#x202F;dB HL), mixed type hearing impairment, and asymmetric SNHL (averaged pure tone threshold greater than 15&#x202F;dB HL between both ears) before the index date were excluded.</p>
<sec id="sec7">
<label>2.1</label>
<title>Measurement of main outcome</title>
<p>Three cohorts were ended until the occurrence of death, or the July of 2011. That is, all cohorts were followed up to 10&#x202F;years. All causes of death were recorded and included.</p>
</sec>
<sec id="sec8">
<label>2.2</label>
<title>Ethical considerations</title>
<p>The institutional review board of Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation in Taiwan has approved this study. The informed consent of all patients was waived due to de-identified data during analysis (No. B10202021).</p>
</sec>
<sec id="sec9">
<label>2.3</label>
<title>Statistical analyses</title>
<p>Categorical and continuous variables were compared by Pearson&#x2019;s chi-squared test and one-way ANOVA test, respectively. The incidence rates (per 10<sup>2</sup> person-years) with 95% confidence intervals (CIs) of all-cause mortality were calculated by Kaplan&#x2013;Meier method and the log-rank test.</p>
<p>The association of SNHL and mortality was checked by a Cox proportional hazard model with adjustment for all covariates. As we introduced, SNHL could be an intermediate indicator between many major diseases and mortality. Also, SNHL itself might increase disability and the risks for cognition impairment, accident, depression, or stroke in the elderly (<xref ref-type="bibr" rid="ref11 ref12 ref13">11&#x2013;13</xref>). So, we treated SNHL as an independent variable during analysis with adjustment of other confounding factors for this study. By doing this, we could see whether SNHL could increase the risk of all-cause mortality independently or not.</p>
<p>All above analysis were performed in SAS (version 9.4; SAS Institute, Inc., Cary, NC, USA) and SPSS (version 20.0; IBM Corp., New York, NY, USA). The <italic>p</italic>&#x202F;&#x003C;&#x202F;0.05 was considered as having statistically significance.</p>
</sec>
</sec>
<sec sec-type="results" id="sec10">
<label>3</label>
<title>Results</title>
<p><xref ref-type="table" rid="tab1">Table 1</xref> showed the mean age was 62.6&#x202F;years [standard deviation (SD)&#x202F;=&#x202F;5.9] in normal hearing group, 66.6&#x202F;years (SD&#x202F;=&#x202F;7.0) in mild SNHL group, and 71.5 (SD&#x202F;=&#x202F;7.3) in moderate and severe SNHL group. The prevalence of age (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.0001), gender (<italic>p</italic>&#x202F;=&#x202F;0.0320), CAD (<italic>p</italic>&#x202F;=&#x202F;0.0424), but not other clinical variables, were significantly different between three cohorts.</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Basic characteristics for three groups.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Mean (SD) or <italic>N</italic> (%)</th>
<th align="center" valign="top">Normal group (<italic>n</italic> =&#x202F;94)</th>
<th align="center" valign="top">Mild hearing-impaired group (<italic>n</italic> =&#x202F;111)</th>
<th align="center" valign="top">Moderate to severe hearing-impaired group (<italic>n</italic> =&#x202F;113)</th>
<th align="center" valign="top"><italic>p</italic> value<sup>&#x002A;</sup></th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Age, years</td>
<td align="center" valign="top">62.6 (5.9)</td>
<td align="center" valign="top">66.6 (7.0)</td>
<td align="center" valign="top">71.5 (7.3)</td>
<td align="center" valign="top">&#x003C;0.0001</td>
</tr>
<tr>
<td align="left" valign="top">Female/male, %</td>
<td align="center" valign="top">68.1/31.9</td>
<td align="center" valign="top">55.0/45.1</td>
<td align="center" valign="top">50.4/49.6</td>
<td align="center" valign="top">0.0320</td>
</tr>
<tr>
<td align="left" valign="top">BMI, kg/m<sup>2</sup></td>
<td align="center" valign="top">24.4 (3.5)</td>
<td align="center" valign="top">24.7 (3.6)</td>
<td align="center" valign="top">24.2 (3.9)</td>
<td align="center" valign="top">0.5329</td>
</tr>
<tr>
<td align="left" valign="top">Hypertension, %</td>
<td align="center" valign="top">25.5</td>
<td align="center" valign="top">32.4</td>
<td align="center" valign="top">36.3</td>
<td align="center" valign="top">0.2501</td>
</tr>
<tr>
<td align="left" valign="top">Diabetes mellitus, %</td>
<td align="center" valign="top">12.8</td>
<td align="center" valign="top">15.3</td>
<td align="center" valign="top">15.9</td>
<td align="center" valign="top">0.7999</td>
</tr>
<tr>
<td align="left" valign="top">Dyslipidemia, %</td>
<td align="center" valign="top">5.3</td>
<td align="center" valign="top">6.3</td>
<td align="center" valign="top">9.7</td>
<td align="center" valign="top">0.4255</td>
</tr>
<tr>
<td align="left" valign="top">CAD, %</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0.9</td>
<td align="center" valign="top">4.4</td>
<td align="center" valign="top">0.0424</td>
</tr>
<tr>
<td align="left" valign="top">AMI, %</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">&#x2013;</td>
</tr>
<tr>
<td align="left" valign="top">CKD, %</td>
<td align="center" valign="top">6.4</td>
<td align="center" valign="top">4.5</td>
<td align="center" valign="top">3.5</td>
<td align="center" valign="top">0.6250</td>
</tr>
<tr>
<td align="left" valign="top">Hepatitis, %</td>
<td align="center" valign="top">11.7</td>
<td align="center" valign="top">12.6</td>
<td align="center" valign="top">7.1</td>
<td align="center" valign="top">0.3508</td>
</tr>
<tr>
<td align="left" valign="top">Cirrhosis, %</td>
<td align="center" valign="top">2.1</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">2.7</td>
<td align="center" valign="top">0.2446</td>
</tr>
<tr>
<td align="left" valign="top">Stroke, %</td>
<td align="center" valign="top">2.1</td>
<td align="center" valign="top">3.6</td>
<td align="center" valign="top">2.7</td>
<td align="center" valign="top">0.8095</td>
</tr>
<tr>
<td align="left" valign="top">Alzheimer&#x2019;s disease, %</td>
<td align="center" valign="top">1.1</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0.3026</td>
</tr>
<tr>
<td align="left" valign="top">Parkinson&#x2019;s disease, %</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">&#x2013;</td>
</tr>
<tr>
<td align="left" valign="top">Trauma, %</td>
<td align="center" valign="top">2.1</td>
<td align="center" valign="top">2.7</td>
<td align="center" valign="top">3.5</td>
<td align="center" valign="top">0.8261</td>
</tr>
<tr>
<td align="left" valign="top">Cancers, %</td>
<td align="center" valign="top">5.3</td>
<td align="center" valign="top">3.6</td>
<td align="center" valign="top">4.4</td>
<td align="center" valign="top">0.8369</td>
</tr>
<tr>
<td align="left" valign="top">Death, %</td>
<td align="center" valign="top">4.3</td>
<td align="center" valign="top">6.3</td>
<td align="center" valign="top">18.6</td>
<td align="center" valign="top">&#x003C;0.0001</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>AMI, acute myocardial infarction; BMI, body mass index; CAD, coronary artery disease; CKD, chronic kidney disease; SD, standard deviation.</p>
<p><sup>&#x002A;</sup><italic>p</italic> values were acquired by Pearson&#x2019;s chi-squared test or one-way ANOVA test for categorical or continuous variables, respectively.</p>
</table-wrap-foot>
</table-wrap>
<p>The mean duration of follow-up was 8.54&#x202F;years for normal hearing group, 8.33&#x202F;years for mild SNHL group, and 8.25&#x202F;years for moderate and severe SNHL group (<italic>p</italic>&#x202F;=&#x202F;0.214). The incidence rates of mortality were 0.04 per 10<sup>2</sup> person-years of follow-up in normal hearing group, 0.06 per 10<sup>2</sup> person-years of follow-up in mild SNHL group, and 0.19 per 10<sup>2</sup> person-years of follow-up in moderate and severe SNHL group, respectively (<italic>p</italic>&#x202F;=&#x202F;0.0008).</p>
<p><xref ref-type="fig" rid="fig1">Figure 1</xref> showed the survival rates in three groups. The survival rate in moderate and severe SNHL group, but not in mild SNHL group, was significantly lower than that in normal hearing group (log rank, <italic>p</italic>&#x202F;=&#x202F;0.0006). In other words, the elderly with moderate and severe SNHL have a significantly higher mortality rate than those with normal hearing.</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>The survival rates in three groups. The survival rate in moderate and severe SNHL group, but not in mild SNHL group, was significantly lower than that in normal hearing group (log rank, <italic>p</italic>&#x202F;=&#x202F;0.0006).</p>
</caption>
<graphic xlink:href="fneur-16-1628976-g001.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Kaplan-Meier plot showing survival rate percentages over ten years for three groups. Blue line for hearing levels 0 to less than 25 dBHL, green line for hearing levels 25 to less than 40 dBHL, and red line for hearing levels 40 dBHL and above. The survival rate decreases most sharply in the red line. Logrank test p-value is 0.0006.</alt-text>
</graphic>
</fig>
<p>Compared to the normal hearing group, the crude HR and aHR for mortality in mild SNHL group was 1.51 (95% CI&#x202F;=&#x202F;0.44&#x2013;5.14, <italic>p</italic>&#x202F;=&#x202F;0.5143) and 2.14 (95% CI&#x202F;=&#x202F;0.45&#x2013;10.23, <italic>p</italic>&#x202F;=&#x202F;0.3396), respectively. And, the crude HR and aHR for mortality in moderate and severe SNHL group was 4.82 (95% CI&#x202F;=&#x202F;1.65&#x2013;14.07, <italic>p</italic>&#x202F;=&#x202F;0.0041) and 6.96 (95% CI&#x202F;=&#x202F;1.60&#x2013;30.23, <italic>p</italic>&#x202F;=&#x202F;0.0096), respectively.</p>
</sec>
<sec sec-type="discussion" id="sec11">
<label>4</label>
<title>Discussion</title>
<p>In this cohort study based on detailed audiometry and clinical data, we have considered many clinical variables which might be associated with increased mortality during statistical analysis. The main finding was that the elderly with moderate and severe SNHL of age between 51 and 88 years are at greater risk of mortality than those with normal hearing significantly and independently in Taiwan with relatively low genetic heterogeneity (<xref ref-type="bibr" rid="ref5">5</xref>, <xref ref-type="bibr" rid="ref6">6</xref>).</p>
<p>Comparison with previous literatures, our results were slightly different to previous studies. In our study, moderate and severe SNHL was significantly associated with mortality. In Kim&#x2019;s study (2020), severe and profound SNHL was significantly associated with mortality in Korean older adults (<xref ref-type="bibr" rid="ref1">1</xref>). In Fang et al.&#x2019;s (<xref ref-type="bibr" rid="ref2">2</xref>) and Cui and Yan&#x2019;s (<xref ref-type="bibr" rid="ref3">3</xref>) studies, all degrees of SNHL were associated with mortality in adult Americans (<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref3">3</xref>). However, there was no association between SNHL and mortality in Zhang et al.&#x2019;s (<xref ref-type="bibr" rid="ref4">4</xref>) study in Chinese older people. These inconsistency between previous studies might be caused by different study population, imperfect classification of hearing impairment, and/or statistical strategy.</p>
<p>In addition, the SNHL-related mortality risk could be interacted by family status and visual acuity. Divorced status raised the adjusted SNHL-related mortality risk in subjects below 75&#x202F;years old in Norway (<xref ref-type="bibr" rid="ref16">16</xref>). Comparing with subjects without visual and hearing impairment, those with both of visual and hearing impairment have a higher risk for mortality (aHR&#x202F;=&#x202F;1.21). Those with visual impairment only have a slightly elevated risk for mortality (aHR&#x202F;=&#x202F;1.10), but those with hearing impairment only were not significantly associated with increased mortality in subjects aged 80 and older, adjusting for socio-demographic status, life style, and common diseases (<xref ref-type="bibr" rid="ref4">4</xref>).</p>
<p>In the aspect of biological plausibility, we believed that oxidative stress and neural inflammation are the most important mechanisms for SNHL in older adults (<xref ref-type="bibr" rid="ref17 ref18 ref19 ref20 ref21">17&#x2013;21</xref>). So, we suggested that SNHL was not only as an intermediate indicator between many major diseases and increased mortality, but also played an independent role on the mortality in older adults.</p>
<p>However, this study has several limitations. First, severity, duration and treatment compliance of major common diseases were not measured. Second, habits, exercise, socioeconomic status, geographic region, or urbanization level were unmeasured, too. However, we supposed that these confounder factors might affect three cohorts equally. So, these biases would not violate the results significantly.</p>
</sec>
<sec sec-type="conclusions" id="sec12">
<label>5</label>
<title>Conclusion</title>
<p>Taken together with the findings of previous studies and ours, we suggested that SNHL, especially of moderate to severe or profound severity, was associated with increased risks of mortality in the elderly independently in Taiwan. Therefore, we clinicians should pay more attention to SNHL. To treat its underlying risk factors and/or comorbidity. Also, we should encourage our hearing-impaired patients to use hearing aids more aggressively. By doing so, we could reduce the mortality rate in the elderly.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec13">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding authors.</p>
</sec>
<sec sec-type="ethics-statement" id="sec14">
<title>Ethics statement</title>
<p>The studies involving humans were approved by The institutional review board of Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation in Taiwan. 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 because The informed consent of all patients was waived due to de-identified data during analysis (No. B10202021).</p>
</sec>
<sec sec-type="author-contributions" id="sec15">
<title>Author contributions</title>
<p>J-CC: Formal analysis, Investigation, Validation, Writing &#x2013; review &#x0026; editing. P-SH: Data curation, Formal analysis, Investigation, Validation, Writing &#x2013; review &#x0026; editing. J-HH: Conceptualization, Methodology, Supervision, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing.</p>
</sec>
<sec sec-type="funding-information" id="sec16">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. The work was supported by Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation [TCMF-A 106-01-19].</p>
</sec>
<sec sec-type="COI-statement" id="sec17">
<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 sec-type="ai-statement" id="sec18">
<title>Generative AI statement</title>
<p>The authors declare that no Gen AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="sec19">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors 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>
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