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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Aging</journal-id>
<journal-title>Frontiers in Aging</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Aging</abbrev-journal-title>
<issn pub-type="epub">2673-6217</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1524186</article-id>
<article-id pub-id-type="doi">10.3389/fragi.2025.1524186</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Aging</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>The relationship between hearing loss and frailty in older adults at risk of cognitive decline: a cross-sectional study</article-title>
<alt-title alt-title-type="left-running-head">Tian et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fragi.2025.1524186">10.3389/fragi.2025.1524186</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Tian</surname>
<given-names>Rong</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2884471/overview"/>
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<role content-type="https://credit.niso.org/contributor-roles/Writing \x{2013} original draft/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Almeida</surname>
<given-names>Osvaldo P.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Ford</surname>
<given-names>Andrew H.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Flicker</surname>
<given-names>Leon</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1365913/overview"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Lautenschlager</surname>
<given-names>Nicola T.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/211737/overview"/>
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<contrib contrib-type="author">
<name>
<surname>Robinson</surname>
<given-names>Suzanne</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Makate</surname>
<given-names>Marshall</given-names>
</name>
<xref ref-type="aff" rid="aff7">
<sup>7</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1021765/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
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<contrib contrib-type="author">
<name>
<surname>Pettigrew</surname>
<given-names>Simone</given-names>
</name>
<xref ref-type="aff" rid="aff8">
<sup>8</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/494030/overview"/>
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<contrib contrib-type="author">
<name>
<surname>Lee</surname>
<given-names>Sin Huey</given-names>
</name>
<xref ref-type="aff" rid="aff9">
<sup>9</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Dorsheimer</surname>
<given-names>Ina</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/2971471/overview"/>
<xref ref-type="aff" rid="aff10">
<sup>10</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/Project administration"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Yiannos</surname>
<given-names>Jessica M.</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/1055884/overview"/>
<xref ref-type="aff" rid="aff9">
<sup>9</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Crawford</surname>
<given-names>Libby</given-names>
</name>
<xref ref-type="aff" rid="aff9">
<sup>9</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jayakody</surname>
<given-names>Dona M. P.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff9">
<sup>9</sup>
</xref>
<xref ref-type="aff" rid="aff11">
<sup>11</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/414734/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
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</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Medical School</institution>, <institution>University of Western Australia</institution>, <addr-line>Perth</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>WA Centre for Health and Ageing</institution>, <addr-line>Medical School</addr-line>, <institution>University of Western Australia</institution>, <addr-line>Perth</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Psychiatry, Faculty of Medicine, Dentistry and Health Sciences</institution>, <institution>The University of Melbourne</institution>, <addr-line>Melbourne</addr-line>, <addr-line>VIC</addr-line>, <country>Australia</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Older Adult Mental Health Program</institution>, <institution>Royal Melbourne Hospital Mental Health Service</institution>, <addr-line>Parkville</addr-line>, <addr-line>VIC</addr-line>, <country>Australia</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Deakin Health Economics</institution>, <institution>Institute for Health Transformation</institution>, <institution>Deakin University</institution>, <addr-line>Melbourne</addr-line>, <addr-line>VIC</addr-line>, <country>Australia</country>
</aff>
<aff id="aff6">
<sup>6</sup>
<institution>enAble Institute</institution>, <institution>Curtin University</institution>, <addr-line>Perth</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<aff id="aff7">
<sup>7</sup>
<institution>Department of Health Economics and Data Analytics</institution>, <institution>Curtin University</institution>, <addr-line>Perth</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<aff id="aff8">
<sup>8</sup>
<institution>The George Institute for Global Health</institution>, <institution>University of New South Wales</institution>, <addr-line>Sydney</addr-line>, <addr-line>NSW</addr-line>, <country>Australia</country>
</aff>
<aff id="aff9">
<sup>9</sup>
<institution>Ear Science Institute Australia</institution>, <addr-line>Subiaco</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<aff id="aff10">
<sup>10</sup>
<institution>Murdoch University</institution>, <addr-line>Perth</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<aff id="aff11">
<sup>11</sup>
<institution>Ear Sciences Centre</institution>, <institution>Faculty of Health and Medical Sciences</institution>, <institution>University of Western Australia</institution>, <addr-line>Perth</addr-line>, <addr-line>WA</addr-line>, <country>Australia</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1724782/overview">Kieran Reid</ext-link>, Brigham and Women&#x2019;s Hospital, United States</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1002613/overview">Lakshmi Kannan</ext-link>, Northeastern University, United States</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2158544/overview">Shannon Hernon</ext-link>, Brigham and Women&#x2019;s Hospital, United States</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2266755/overview">Nicole Bajdek</ext-link>, Brigham and Women&#x2019;s Hospital, United States</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Rong Tian, <email>rong.tian@research.uwa.edu.au</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>24</day>
<month>03</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>6</volume>
<elocation-id>1524186</elocation-id>
<history>
<date date-type="received">
<day>07</day>
<month>11</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>06</day>
<month>03</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Tian, Almeida, Ford, Flicker, Lautenschlager, Robinson, Makate, Pettigrew, Lee, Dorsheimer, Yiannos, Crawford and Jayakody.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Tian, Almeida, Ford, Flicker, Lautenschlager, Robinson, Makate, Pettigrew, Lee, Dorsheimer, Yiannos, Crawford and Jayakody</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>Objectives</title>
<p>To investigate the association between hearing loss and frailty among a group of older community volunteers with mild cognitive impairment.</p>
</sec>
<sec>
<title>Design</title>
<p>This study recruited 162 older community volunteers who have mild cognitive impairment and symmetric age-related hearing loss. Participants&#x2019; hearing ability (including peripheral hearing, hearing handicap and central auditory processing) and frailty status were assessed and analysed. An independent t-test was conducted to compare hearing performance between frail and non-frail groups.</p>
</sec>
<sec>
<title>Results</title>
<p>There were statistically significant differences between frail and non-frail groups for speech frequency hearing threshold, overall central auditory processing score and hearing handicap score, but not for high frequency hearing threshold.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>Frail individuals exhibit poorer performance in peripheral and central hearing assessments, as well as in self-reported hearing handicap. Future randomised controlled trials are necessary to find out if the correction of hearing loss decreases the proportion of people affected by frailty in later life.</p>
</sec>
</abstract>
<kwd-group>
<kwd>hearing loss</kwd>
<kwd>frailty</kwd>
<kwd>hearing handicap</kwd>
<kwd>central auditory processing</kwd>
<kwd>aging</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Musculoskeletal Aging</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Frailty is a common clinical syndrome among older adults, reportedly affecting 3.5%&#x2013;27% community-dwelling older adults in the Asia-pacific region, and over 50% in the socioeconomically disadvantaged and indigenous communities (<xref ref-type="bibr" rid="B8">Dent et al., 2017</xref>). This high variability can be attributed to different definitions of frailty and variations in sampling from the population (<xref ref-type="bibr" rid="B8">Dent et al., 2017</xref>). Currently, there are three major conceptual models of frailty: 1) the physical phenotype, developed by Fried et al., which describes frailty as a series of syndromes involving slowing, weakness, low energy and low activity (<xref ref-type="bibr" rid="B12">Fried et al., 2001</xref>); 2) the deficits accumulation model, developed by Rockwood and Mitnitsk, which conceptualises frailty as a multidimensional syndrome resulting from the accumulation of deficits across various domains of health and functioning (<xref ref-type="bibr" rid="B26">Mitnitski et al., 2001</xref>); and 3) mixed physical and psychosocial frailty models, which have gained more interest in recent years and several definitions have been established. Numerous tools have been developed based on these three models to measure frailty (<xref ref-type="bibr" rid="B9">de Vries et al., 2011</xref>). Each tool has its advantages and disadvantages and was developed to best fulfil the aim of measurement in clinical practice or research studies. In this present study, we focused solely on physical frailty only. Two widely used assessment tools, the Fried frailty phenotype and the FRAIL scale, were used. The Fried Frailty Phenotype is based on the physical phenotype model, while the FRAIL Scale is a simple, highly validated screening tool that combines elements of both the physical phenotype model and the deficits accumulation model.</p>
<p>While consensus on the best definition of frailty is lacking, there is agreement on the value of screening for it (<xref ref-type="bibr" rid="B8">Dent et al., 2017</xref>; <xref ref-type="bibr" rid="B35">Rodriguez-Manas et al., 2013</xref>). Frail individuals are more vulnerable to the deleterious effects of stressors and have an increased risk of dependency and mortality (<xref ref-type="bibr" rid="B8">Dent et al., 2017</xref>). In addition to negatively impacting the quality of life of older adults, healthcare expenses for frail individuals are about four times higher than those for their non-frail counterparts, imposing a significant burden on healthcare systems (<xref ref-type="bibr" rid="B8">Dent et al., 2017</xref>).</p>
<p>Several factors have been associated with frailty, including age-related physiological degeneration, multimorbidity, inflammation, sarcopenia, polypharmacy, endocrine disorders, protein energy malnutrition, social isolation, and poverty (<xref ref-type="bibr" rid="B8">Dent et al., 2017</xref>). Effective management of frailty risk factors, for example, through exercise, protein-calorie and vitamin D supplementation, and reduction of polypharmacy, holds potential for preventing or treating frailty effectively (<xref ref-type="bibr" rid="B29">Morley et al., 2013</xref>). Another emerging factor linked to increased risk of frailty is hearing loss, which ranks as the third leading cause of disability in the world (<xref ref-type="bibr" rid="B43">World Health Organization, 2021</xref>). Hearing loss has been reported to be linked to many frailty-related factors, including falls (<xref ref-type="bibr" rid="B19">Kamil et al., 2016</xref>), poor physical (<xref ref-type="bibr" rid="B39">Tareque et al., 2019</xref>) and psychosocial health (<xref ref-type="bibr" rid="B2">Almeida et al., 2019</xref>), dementia (<xref ref-type="bibr" rid="B10">Ford et al., 2018</xref>), and impaired activities of daily living (<xref ref-type="bibr" rid="B39">Tareque et al., 2019</xref>). Given its association with various frailty-related factors, hearing loss is likely associated with frailty. Studies investigating the association between hearing loss and frailty have emerged in recent years, however the available evidence remains inconclusive. That is, whilst reported findings mostly support the relationship between frailty and hearing loss, inconsistent results have been reported (<xref ref-type="bibr" rid="B40">Tian et al., 2021</xref>; <xref ref-type="bibr" rid="B38">Tan et al., 2020</xref>). It would be valuable to add further evidence to support this association. If hearing loss is indeed a risk factor of frailty, addressing such impairment could potentially reduce the risk or severity of frailty.</p>
<p>In a previous systematic review, the pooled results indicated that hearing loss was associated with an 87% increase in the risk of frailty among cross-sectional studies and 56% among longitudinal studies. However, the included studies varied significantly in study design, particularly in the measures used for hearing loss and frailty (<xref ref-type="bibr" rid="B40">Tian et al., 2021</xref>). The information regarding hearing loss in the available literature on this topic is not comprehensive. Many studies published to date have relied on self-reported hearing loss as the relevant exposure for frailty, and have predominantly focused on the role of peripheral hearing loss, which along with central auditory processing (CAP) constitute the two main components of the auditory system (<xref ref-type="bibr" rid="B40">Tian et al., 2021</xref>). Peripheral hearing ability refers to sound detection, whereas CAP is involved in speech comprehension, especially in the presence of background noise or competitive speech (<xref ref-type="bibr" rid="B37">Sardone et al., 2021</xref>). Given that both peripheral and central auditory abilities decline with age, the investigation of hearing loss and frailty should include the assessment of both components (<xref ref-type="bibr" rid="B31">Nuesse et al., 2021</xref>). Furthermore, hearing handicap, which describes the impact of hearing loss on an individual&#x2019;s daily life, should also be considered, as it is influenced by various physical, mental, and social factors (<xref ref-type="bibr" rid="B31">Nuesse et al., 2021</xref>).</p>
<p>The existing evidence regarding the relationship between hearing loss and frailty is neither conclusive nor comprehensive. Therefore, the aim of the present study is to investigate the association between hearing loss and frailty in older adults using audiological measures of peripheral hearing and CAP, as well as subjective self-reported hearing handicap. By examining multiple components of hearing loss and their association with frailty, we aim to enhance our understanding of their relationship.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>2 Materials and methods</title>
<sec id="s2-1">
<title>2.1 Study design and setting</title>
<p>This study employed a cross-sectional design and involved a sample of older community volunteers residing in Perth, Western Australia. Participants were recruited for the HearCog trial, and this study reports data derived from the baseline assessment. Further details about the study design and procedures have been published (<xref ref-type="bibr" rid="B17">Jayakody et al., 2020a</xref>). Hearing assessments were performed by qualified audiologists. Other assessments were conducted by trained research staff at the research centre. Questionnaires were predominantly self-administered and completed by participants during research appointments with guidance from study staff, and assistance was provided when necessary. Frailty status was calculated after all data collection were completed, therefore, audiologists and researchers were blinded to participants&#x2019; frailty status at the time of assessments. The Human Research Ethics Committee of the University of Western Australia approved the research protocol and related activities, and written consent was obtained from all participants.</p>
</sec>
<sec id="s2-2">
<title>2.2 Participants</title>
<p>The study included older adults aged 70&#xa0;years and older who were recruited through Ear Science Institute of Australia and Lions Hearing Clinics, as well as retirement villages, radio, newspaper, and social media advertisements. Participants were required to have symmetric age-related hearing loss, defined as better ear average hearing loss greater than 23.3&#xa0;dB HL at 0.5, 1, and 2&#xa0;kHz, or high-frequency average hearing loss of 40&#xa0;dB HL or greater at 2, 3, and 4&#xa0;kHz, in accordance with the Australian Hearing Services Program Guideline (<xref ref-type="bibr" rid="B3">Australian Government Department of Health and Aged Care, 2022</xref>), and have no prior exposure to the use of hearing aids. This study is a secondary analysis of the HearCog trial, which investigated the efficacy of hearing aids on cognitive function, therefore, participants originally recruited for the trial were required to have mild cognitive impairment (MCI) (scored greater than 18 and less than 26 on the Montreal Cognitive Assessment for the Hearing Impaired, HI-MoCA (<xref ref-type="bibr" rid="B24">Lin et al., 2017</xref>)).</p>
</sec>
<sec id="s2-3">
<title>2.3 Study measures</title>
<sec id="s2-3-1">
<title>2.3.1 Assessment of hearing</title>
<p>Peripheral hearing was assessed using pure-tone audiometry (PTA) with a clinical audiometer (MIDIMATE 602 Audiometer, GN Otometrics Ltd., Sydney) and supra-aural earphone. Qualified audiologists conducted bilateral air-conduction thresholds measurements at 0.25, 0.5, 1, 2, 4, 6, and 8&#xa0;kHz in a soundproof booth at the Ear Science Institute Australia. In cases where baseline PTA data were unavailable (n &#x3d; 15), data from the KUDUwave (KUDUwave&#x2122; 5,000 Plus, GeoAxon Global Ltd., South Africa) were used instead. KUDUwave is a portable diagnostic and screening audiometer that has been clinically validated. For the statistical analysis of the study, the average air conduction thresholds of the better ear across 0.5&#x2013;4&#xa0;kHz were considered speech-frequency hearing thresholds, while the average air conduction thresholds of the better ear at 4, 6, and 8&#xa0;kHz were considered as high-frequency hearing thresholds.</p>
<p>Self-reported hearing handicap was assessed by the Hearing Handicap Inventory of the Elderly (HHIE) (<xref ref-type="bibr" rid="B42">Ventry and Weinstein, 1982</xref>). The HHIE is a 10 items questionnaire assessing emotional and social impact of one&#x2019;s perceived hearing difficulties. Scores on this inventory range from 0 (no handicap) to 40 (maximum handicap).</p>
<p>The assessment of CAP included three tests. To simplify the analysis and reduce the risk of multiple comparisons, an overall CAP score was calculated using principal component analysis based on the results of these tests. The Dichotic Digits Test (DDT) evaluated the binaural integration (<xref ref-type="bibr" rid="B30">Musiek et al., 1991</xref>). Participants were presented with two digits in each ear simultaneously and asked to repeat all four digits to the best of their ability. The Synthetic Sentence Identification with Ipsilateral Competing Message (SSI-ICM) assessed participants&#x2019; ability to identify 10 short nonsense sentences against a background competing signal (<xref ref-type="bibr" rid="B32">Orchik and Burgess, 1977</xref>). Scores were based on the proportion of correct identification of sentences (0%&#x2013;100%). The scores of the better ear at message-competition ratio of 0&#xa0;dB were used for the analysis. Finally, the Quick Speech in Noise (Quick-SIN) measured participants&#x2019; ability to hear in a context of background noise (<xref ref-type="bibr" rid="B21">Killion et al., 2004</xref>). Participants were presented with two practice sentences and two sets of six test sentences for each ear. These sentences were presented with multi-talker babble noise, with signal-to-noise ratios of 25, 20, 15, 10, 5 and 0&#xa0;dB. Each sentence contained five keywords, and participants scored one point for each correctly repeated word. The total score was subtracted from 25.5 to calculate the signal-to-noise ratio loss. A higher score indicates poorer speech understanding ability with background noise.</p>
</sec>
<sec id="s2-3-2">
<title>2.3.2 Assessment of frailty</title>
<p>We used two validated measurement tools of frailty: the FRAIL scale and Fried frailty phenotype. Participants were classified as frail if they met the frailty criteria in either of these two measures; otherwise, they were classified as non-frail.</p>
<p>The FRAIL scale (<xref ref-type="bibr" rid="B1">Abellan van Kan et al., 2008</xref>; <xref ref-type="bibr" rid="B27">Morley et al., 2012a</xref>) assessed five relevant domains: fatigue, resistance, ambulation, illness, and loss of weight. Participants who scored positive in one or two domains of the FRAIL scale were considered pre-frail, and those score more than two were considered frail. Fatigue was determined by participants&#x2019; response to the question, &#x201c;how much of the time during the past 4&#xa0;weeks have you felt tired or worn out?&#x201d; Possible answers ranged from &#x201c;all or most of the time&#x201d; (positive) to &#x201c;a little or none of the time&#x201d; (negative). To assess resistance, ambulation, and loss of weight, participants answered &#x201c;yes&#x201d; or &#x201c;no&#x201d; to questions about difficulty walking up to 10 steps without resting in the past 4&#xa0;weeks, difficulty walking 200&#xa0;m or one block without aids in the past 4&#xa0;weeks, and weight loss of more than 5&#xa0;kg or 5% of body weight in the past year, respectively. The presence of illness was rated as present if participants reported having five or more of the following conditions: hypertension, diabetes, cancer (other than minor skin cancer), chronic lung disease (chronic bronchitis or emphysema), heart attack, congestive heart failure, angina, asthma, arthritis, stroke, and kidney disease (<xref ref-type="bibr" rid="B28">Morley et al., 2012b</xref>).</p>
<p>The Fried frailty phenotype had five components: unintentional weight loss, weakness, exhaustion, slow walking speed, and low physical activity (<xref ref-type="bibr" rid="B11">Fried et al., 2004</xref>). Participants who exhibited one or two components were defined as pre-frail, and those with three or more were considered to be frail. Unintentional weight loss and exhaustion was assessed using the same questions for weight loss and fatigue as the FRAIL scale. Weakness was defined as grip strength less than 26&#xa0;kg for men or less than 18&#xa0;kg for women (<xref ref-type="bibr" rid="B13">Gu et al., 2019</xref>), which was measured using a Jamar Smart Hand Dynamometer. Walking speed was self-reported, with participants selecting one of the following options to describe their usual unaided walking speed: &#x201c;fast or fairly brisk&#x201d;, &#x201c;normal speed for my age&#x201d;, &#x201c;slightly slow&#x201d;, &#x201c;very slow&#x201d;, or &#x201c;unable to walk independently&#x201d;. The walking speed of participants was deemed impaired if they responded &#x201c;slightly slow, very slow, or unable to walk independently&#x201d;. Physical activity was assessed using two self-reported questions: &#x201c;In a usual week, do you do any non-vigorous exercise for recreation or health and fitness?&#x201d; and &#x201c;In a usual week, do you do any non-vigorous exercise for recreation or health and fitness?&#x201d; Participants who reported no exercise (non-vigorous or vigorous) in a usual week were classified as having low physically activity.</p>
</sec>
<sec id="s2-3-3">
<title>2.3.3 Other measurements</title>
<p>Demographic and lifestyle information was collected using a questionnaire (summarised in <xref ref-type="table" rid="T1">Table 1</xref>). We calculated the age of participants (in years) by subtracting the date of birth from the date of the assessment and then dividing the result by 365.25. Participants were categorized according to whether they had completed a least 12 years of education. Smoking status was classified as never, former, or current. Risky drinking was defined by the consumption of four or more standard alcoholic drinks on any given day or 10 or more drinks in a usual week (<xref ref-type="bibr" rid="B3">Australian Institute of Health and Welfare, 2021</xref>). The Patient Health Questionnaire (PHQ-9) was administered to assess depressive symptoms, with a total score of 10 or greater indicating the presence of clinically significant symptoms of depression (<xref ref-type="bibr" rid="B22">Kroenke et al., 2001</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Sociodemographic and clinical characteristics of non-frail and frail participants. Group differences were assessed using t-tests for continuous variables and Chi-squared (&#x3c7;<sup>2</sup>) tests for categorical variables. The associated p-values are presented.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th colspan="2" align="left">Characteristics</th>
<th align="left">Non-frail<break/>N &#x3d; 151 n (%) or mean &#xb1; SD</th>
<th align="left">Frail<break/>N &#x3d; 11 n (%) or mean &#xb1; SD</th>
<th align="left">&#x3c7;2/t</th>
<th align="left">p-Value</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td rowspan="4" align="left">Age (years)</td>
<td align="left">70&#x2013;75</td>
<td align="left">64 (42.4)</td>
<td align="left">2 (18.2)</td>
<td rowspan="4" align="left">3.30</td>
<td rowspan="4" align="left">0.347</td>
</tr>
<tr>
<td align="left">75&#x2013;80</td>
<td align="left">48 (31.8)</td>
<td align="left">5 (45.5)</td>
</tr>
<tr>
<td align="left">80&#x2013;85</td>
<td align="left">27 (17.9)</td>
<td align="left">2 (18.2)</td>
</tr>
<tr>
<td align="left">&#x3e;85</td>
<td align="left">12 (8.0)</td>
<td align="left">2 (18.2)</td>
</tr>
<tr>
<td rowspan="2" align="left">Gender</td>
<td align="left">Female</td>
<td align="left">54 (35.8)</td>
<td align="left">7 (63.6)</td>
<td rowspan="2" align="left">3.39</td>
<td rowspan="2" align="left">0.065</td>
</tr>
<tr>
<td align="left">Male</td>
<td align="left">97 (64.2)</td>
<td align="left">4 (36.4)</td>
</tr>
<tr>
<td rowspan="2" align="left">Minimum of 12 years of education</td>
<td align="left">Yes</td>
<td align="left">51 (33.8)</td>
<td align="left">1 (9.1)</td>
<td rowspan="2" align="left">2.87</td>
<td rowspan="2" align="left">0.090</td>
</tr>
<tr>
<td align="left">No</td>
<td align="left">100 (66.2)</td>
<td align="left">10 (90.9)</td>
</tr>
<tr>
<td rowspan="3" align="left">Marital status</td>
<td align="left">Never married</td>
<td align="left">2 (1.3)</td>
<td align="left">1 (9.1)</td>
<td rowspan="3" align="left">19.28</td>
<td rowspan="3" align="left">&#x3c;0.000</td>
</tr>
<tr>
<td align="left">Married/Defacto</td>
<td align="left">117 (77.5)</td>
<td align="left">2 (18.2)</td>
</tr>
<tr>
<td align="left">Separated/Divorced/Widowed</td>
<td align="left">32 (21.2)</td>
<td align="left">8 (72.7)</td>
</tr>
<tr>
<td rowspan="3" align="left">Smoking Status</td>
<td align="left">Never</td>
<td align="left">81 (53.6)</td>
<td align="left">6 (54.6)</td>
<td rowspan="3" align="left">1.03</td>
<td rowspan="3" align="left">0.596</td>
</tr>
<tr>
<td align="left">Former</td>
<td align="left">65 (43.1)</td>
<td align="left">4 (36.4)</td>
</tr>
<tr>
<td align="left">Current</td>
<td align="left">5 (3.3)</td>
<td align="left">1 (9.1)</td>
</tr>
<tr>
<td rowspan="2" align="left">Risky alcohol use</td>
<td align="left">No</td>
<td align="left">134 (88.7)</td>
<td align="left">11 (100.0)</td>
<td rowspan="2" align="left">1.38</td>
<td rowspan="2" align="left">0.239</td>
</tr>
<tr>
<td align="left">Yes</td>
<td align="left">17 (11.3)</td>
<td align="left">0 (0.0)</td>
</tr>
<tr>
<td rowspan="2" align="left">Depression</td>
<td align="left">No</td>
<td align="left">146 (96.7)</td>
<td align="left">9 (81.8)</td>
<td rowspan="2" align="left">5.48</td>
<td rowspan="2" align="left">0.019</td>
</tr>
<tr>
<td align="left">Yes</td>
<td align="left">5 (3.3)</td>
<td align="left">2 (18.2)</td>
</tr>
<tr>
<td align="left">MoCA</td>
<td align="left"/>
<td align="left">22.5 &#xb1; 2.03</td>
<td align="left">21.1 &#xb1; 2.06</td>
<td align="left">2.29</td>
<td align="left">0.023</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="Tfn1">
<label>
<sup>a</sup>
</label>
<p>Abbreviations: SD: standard deviation; MoCA: the Montreal Cognitive Assessment.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec id="s2-4">
<title>2.4 Statistical analyses</title>
<p>An initial exploratory analysis was conducted to compare hearing performance between frailty groups. The methods and results of this analysis were described in the <xref ref-type="sec" rid="s12">Supplementary Material</xref>.</p>
<p>The data analysis was conducted using the statistical software Stata 16.0 (StataCorp LLC, 2019). Descriptive statistics were used to summarise continuous data using mean, standard deviation (SD), and range, while categorical variables were presented as counts and percentages (%). To calculate the overall CAP score for each participant, a factor analysis with principal component extraction was performed using the test scores of DDT, SSI-ICM, and Quick-SIN. An eigenvalue threshold greater than one was used in the factor analysis, and the resulting loading scores were used as an overall summary measure of CAP. Pearson chi-squared tests were used to investigate relationships between sociodemographic and lifestyle characteristics of non-frail and frail participants. An independent t-test was conducted to compare hearing measures between groups.</p>
<p>We completed a series of <italic>post hoc</italic> analyses using independent t-tests. We examined the association between each of three CAP tests score and frailty. In addition, to assess whether the association between hearing loss and frailty is influenced by the severity of frailty, we introduced a new pre-frail/frail group by combining participants who were pre-frail according to either the FRAIL scale or the Fried frailty phenotype with those who were frail. This new classification is different from that in the primary analysis, where both pre-frail and normal participants were categorised as non-frail. Hearing measures of this pre-frail/frail group were compared with normal group using t-tests. Alpha was set at 5% and all probability tests reported are two-tailed.</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>3 Results</title>
<p>We recruited 162 participants, with a mean age of 77.2 years (SD 5.2, range 69.8&#x2013;92.7). Sociodemographic and clinical characteristics according to frailty status are presented in <xref ref-type="table" rid="T1">Table 1</xref>. In total, 11 (6.8%) participants were frail according to either the FRAIL scale or Fried frailty phenotype. Fried frailty phenotype identified more frail participants (n &#x3d; 11, 6.8%) than the FRAIL scale (n &#x3d; 3, 1.9%).</p>
<p>Individuals in the frail groups exhibited poorer performance in all three measures of hearing compared to the non-frail group (<xref ref-type="table" rid="T2">Table 2</xref>). Independent t-tests showed statistically significant difference between frail and non-frail groups for speech frequency hearing threshold [t (160) &#x3d; &#x2212;3.40 p &#x3d; 0.001], overall CAP score [t (160) &#x3d; 2.64 p &#x3d; 0.009], and HHIE score [t (160) &#x3d; &#x2212;2.16 p &#x3d; 0.032], but not for high frequency hearing threshold (<xref ref-type="table" rid="T2">Table 2</xref>).</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Relationship between hearing measures and frailty status. Independent t-test results and p-values are presented.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th rowspan="2" align="left"/>
<th colspan="2" align="left">Non-frail<break/>N &#x3d; 151</th>
<th colspan="2" align="left">Frail<break/>N &#x3d; 11</th>
<th rowspan="2" align="left">t-test</th>
<th rowspan="2" align="left">p-Values</th>
</tr>
<tr>
<th align="left">Mean</th>
<th align="left">SD</th>
<th align="left">Mean</th>
<th align="left">SD</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Speech frequency hearing threshold</td>
<td align="left">36.17</td>
<td align="left">7.10</td>
<td align="left">43.98</td>
<td align="left">10.40</td>
<td align="left">&#x2212;3.40</td>
<td align="left">0.001</td>
</tr>
<tr>
<td align="left">High frequency hearing threshold</td>
<td align="left">60.83</td>
<td align="left">12.19</td>
<td align="left">68.03</td>
<td align="left">13.78</td>
<td align="left">&#x2212;1.87</td>
<td align="left">0.063</td>
</tr>
<tr>
<td align="left">Overall CAP score</td>
<td align="left">0.05</td>
<td align="left">0.85</td>
<td align="left">&#x2212;0.65</td>
<td align="left">0.87</td>
<td align="left">2.64</td>
<td align="left">0.009</td>
</tr>
<tr>
<td align="left">HHIE score</td>
<td align="left">18.03</td>
<td align="left">8.06</td>
<td align="left">23.45</td>
<td align="left">7.90</td>
<td align="left">&#x2212;2.16</td>
<td align="left">0.032</td>
</tr>
<tr>
<td align="left">DDT score</td>
<td align="left">84.42</td>
<td align="left">12.50</td>
<td align="left">75.09</td>
<td align="left">17.38</td>
<td align="left">2.32</td>
<td align="left">0.021</td>
</tr>
<tr>
<td align="left">Quick-SIN score</td>
<td align="left">10.65</td>
<td align="left">5.00</td>
<td align="left">13.45</td>
<td align="left">4.79</td>
<td align="left">&#x2212;1.80</td>
<td align="left">0.074</td>
</tr>
<tr>
<td align="left">SSI-ICM score</td>
<td align="left">73.91</td>
<td align="left">26.28</td>
<td align="left">48.18</td>
<td align="left">25.62</td>
<td align="left">3.14</td>
<td align="left">0.002</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="Tfn2">
<label>
<sup>a</sup>
</label>
<p>Abbreviations: SD: standard deviation; CAP: central auditory processing; HHIE: hearing handicap inventory of the elderly; DDT: dichotic digits test; Quick-SIN: quick speech in noise; SSI-ICM: synthetic sentence identification with ipsilateral competing message.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<sec id="s3-1">
<title>3.1 Post-hoc analyses</title>
<p>Further <italic>post hoc</italic> analyses investigating the association between each individual CAP measures and frailty status showed a statistically significant difference between frailty groups for the SSI-ICM [t (160) &#x3d; 3.14, P &#x3d; 0.002] and DDT [t (160) &#x3d; 2.32, P &#x3d; 0.021], but not QuickSIN [t (160) &#x3d; &#x2212;1.80, P &#x3d; 0.074] (<xref ref-type="table" rid="T2">Table 2</xref>).</p>
<p>When combining the pre-frail and frail participants, 76 (46.9%) were pre-frail/frail. We found no significant difference in any hearing measures between the pre-frail/frail and normal groups (<xref ref-type="table" rid="T3">Table 3</xref>).</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Hearing measures of normal and pre-frail/frail participants. Independent t-test results and p-values are presented.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th rowspan="2" align="left"/>
<th colspan="2" align="left">Normal<break/>N &#x3d; 86</th>
<th colspan="2" align="left">Pre-frail/frail<break/>N &#x3d; 76</th>
<th rowspan="2" align="left">t-test</th>
<th rowspan="2" align="left">p-Values</th>
</tr>
<tr>
<th align="left">Mean</th>
<th align="left">SD</th>
<th align="left">Mean</th>
<th align="left">SD</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Speech frequency hearing threshold</td>
<td align="left">36.18</td>
<td align="left">0.82</td>
<td align="left">37.29</td>
<td align="left">0.86</td>
<td align="left">&#x2212;0.93</td>
<td align="left">0.355</td>
</tr>
<tr>
<td align="left">High frequency hearing threshold</td>
<td align="left">60.71</td>
<td align="left">1.32</td>
<td align="left">62.02</td>
<td align="left">1.44</td>
<td align="left">&#x2212;0.67</td>
<td align="left">0.504</td>
</tr>
<tr>
<td align="left">Overall CAP score</td>
<td align="left">0.07</td>
<td align="left">0.09</td>
<td align="left">&#x2212;0.08</td>
<td align="left">0.11</td>
<td align="left">1.08</td>
<td align="left">0.281</td>
</tr>
<tr>
<td align="left">HHIE score</td>
<td align="left">18.21</td>
<td align="left">0.87</td>
<td align="left">18.61</td>
<td align="left">0.95</td>
<td align="left">&#x2212;0.31</td>
<td align="left">0.758</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="Tfn3">
<label>
<sup>a</sup>
</label>
<p>Abbreviations: SD: standard deviation; CAP: central auditory processing; HHIE: hearing handicap inventory of the elderly.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>4 Discussion</title>
<p>Our study examined the relationship between frailty and relevant measures of hearing in a sample of older adults with mild cognitive impairment. We found that frail participants had worse hearing compared with their non-frail peers. Specifically, a statistically significant difference was observed between groups on speech-frequency hearing thresholds, overall CAP, and self-reported hearing handicap.</p>
<p>We acknowledge that our sample size was modest and may have been subject to bias. The study included older adults from Perth, Western Australia, who volunteered to join the study. It is unclear how well they represent the population of older adults living in the community, particularly because they all had mild cognitive impairment and some level of hearing loss. Hence, the generalisability of our findings is uncertain. Mild cognitive impairment is the term given to patients with cognitive impairment that is detectable by clinical criteria but does not produce impairment in daily functioning (<xref ref-type="bibr" rid="B34">Petersen, 2004</xref>). The mean MoCA score of participants was 22.3 (range 18&#x2013;25). Participants scored within this range were classified as having MCI but expected to maintain normal daily functioning ability. While there is a risk that the accuracy of self-reported questionnaires could be affected by the MCI, we do not anticipate it significantly impact the quality of results. Similarly, the frail group (mean &#x3d; 21.1, SD &#x3d; 2.06) scored slightly lower on the MoCA compared to the non-frail group (mean &#x3d; 22.5, SD &#x3d; 2.03), although the imbalance between the groups could potentially introduce bias into our results, we do not expect significant impact as the difference is relatively small, and MCI should not substantially affect participants&#x27; performance. In addition, our investigation had a cross-sectional design, making it difficult to determine with confidence the direction of the association between hearing loss and frailty.</p>
<p>We utilised validated tools to measure both frailty and hearing loss. Our measures of frailty are well-validated and widely used. To increase the sensitivity of our measurements, we classified frailty as identified by either the FRAIL scale or Fried frailty phenotype. The 6.8% prevalence of frailty reported in this study is lower than that in other studies, which reported a pooled prevalence of 9.9% for physical frailty among community-dwelling adults aged 65 and older (<xref ref-type="bibr" rid="B7">Collard et al., 2012</xref>). Several other studies using the FRAIL scale (<xref ref-type="bibr" rid="B41">Tian et al., 2022</xref>) or Fried frailty phenotype (<xref ref-type="bibr" rid="B5">Castellana et al., 2021</xref>; <xref ref-type="bibr" rid="B14">Herr et al., 2018</xref>) also reported an association between hearing loss and frailty, giving some face-validity to our findings, although contrasting findings (<xref ref-type="bibr" rid="B13">Gu et al., 2019</xref>) also exist.</p>
<p>A strength of our study was the detailed assessment of hearing loss, which included a comprehensive evaluation of both peripheral and central hearing, and the subjective impact of hearing loss. We used PTA to examine peripheral hearing. PTA is considered a &#x201c;gold&#x201d; standard for hearing thresholds assessment, as it can provide diagnosis and detailed information regarding the degree and spectrum of hearing loss. We analysed both speech-frequency and high-frequency hearing thresholds, although the results for speech-frequency hearing thresholds had a narrow distribution, which limited the inferences that could be drawn from the data. Furthermore, most participants had mild hearing loss, and such a level of impairment may not have been sufficiently severe to demonstrate unequivocally its association with frailty, an issue that has also been discussed by others (<xref ref-type="bibr" rid="B19">Kamil et al., 2016</xref>; <xref ref-type="bibr" rid="B5">Castellana et al., 2021</xref>). Of note, the association between CAP and physical frailty has rarely been studied, and the use of principal component analysis to generate an overall CAP score contributed to circumvent the issue of multiple comparisons. Additionally, both frailty and CAP are associated with cognitive function (<xref ref-type="bibr" rid="B33">Panza et al., 2015</xref>), and the presence of MCI in our sample may have attenuated the observed association between CAP and frailty. Cognitive impairment is associated with frailty and incorporated in certain frailty measures. As all participants had MCI, there is a possibility that they were already predisposed to frailty. If MCI serves as one of the pathways linking CAP and frailty, the comparison between groups may fail to capture the effect of CAP through this pathway, but rather the effect of other pathways. Nonetheless, we found that frail participants exhibited poorer overall CAP performance than their non-frail peers. Another strength of our study was the inclusion of a measure of self-reported hearing handicap, particularly because people with the same severity of hearing loss may experience different degrees of hearing disability (<xref ref-type="bibr" rid="B6">Chen, 1994</xref>). Finally, we acknowledge that residual error and confounding by unmeasured factors could potentially account for some of the observed associations, and the modest overall sample size and the imbalance between frail and non-frail groups may limit the statistical power of our analyses.</p>
<p>Our <italic>post hoc</italic> analyses revealed that there was no significant difference in any hearing measures between pre-frail/frail group and normal group, whereas we found frail group exhibited poorer performance in speech frequency hearing thresholds, HHIE scores, and CAP scores compared to the rest. This indicates that the association between hearing loss and frailty may be more pronounced among individuals with higher severity of frailty.</p>
<p>We analysed three aspects of hearing. Firstly, for peripheral hearing, we assessed speech-frequency and high-frequency hearing thresholds, and only found a statistically significant difference in speech-frequency hearing threshold between the frail and non-frail/groups. Similarly, <xref ref-type="bibr" rid="B44">Yevenes-Briones et al. (2021)</xref> only found an association with speech-frequency but not with high-frequency hearing loss. <xref ref-type="bibr" rid="B25">Liu et al. (2022)</xref> investigated both speech and high frequency hearing loss and reported that both were associated with frailty, while <xref ref-type="bibr" rid="B37">Sardone et al. (2021)</xref> reported no significant association between peripheral hearing loss (both low-middle and high frequency hearing thresholds) and frailty, although they did find a higher prevalence of peripheral hearing loss in the frail than the non-frail group. Hura and colleagues also reported a linear association between PTA results (both low and high frequency hearing thresholds) and the Frailty Index (<xref ref-type="bibr" rid="B16">Hura et al., 2022</xref>). Taken together, our results and those of others indicate that speech-frequency hearing thresholds are the hearing measures most consistently associated with frailty. While both speech and high frequency hearing ability are important, speech frequencies are critical for audibility, with high frequencies contributing towards speech clarity. Extended high frequency hearing loss has also gained interest in recent years, and its association with frailty may be an area for future research. It is believed to be a very early sign of age-related hearing loss and may play important role in speech perception and localisation (<xref ref-type="bibr" rid="B15">Hunter et al., 2020</xref>). Extended high-frequency hearing thresholds were not assessed in this study, as they are not part of routine clinical testing and established norms are lacking. Secondly, we examined the association between self-reported hearing handicap and frailty, an area that has received limited attention in previous studies. Two studies have reported an association between hearing handicap and frailty (<xref ref-type="bibr" rid="B31">Nuesse et al., 2021</xref>; <xref ref-type="bibr" rid="B4">Campos et al., 2022</xref>), with our results suggesting a non-compelling association. Thirdly, in the present study, we found a difference in the overall CAP score between frail and non-frail groups. When examining the three CAP tests separately, we found significant differences in SSI-ICM scores (p &#x3d; 0.002). This discrepancy might be attributed to the SSI-ICM test&#x2019;s higher sensitivity in assessing CAP in individuals with MCI (<xref ref-type="bibr" rid="B18">Jayakody et al., 2020b</xref>). In line with this, Sardone and colleagues reported no association between the SSI-ICM test results and physical frailty, but an association was found when a frailty model including both physical and cognitive components was utilised (<xref ref-type="bibr" rid="B37">Sardone et al., 2021</xref>). A difference was also found in DDT, but not in QuickSIN scores.</p>
<p>Several proposed pathways have been suggested to link hearing loss and frailty: shared underlying pathological process, such as inflammation markers and vascular factors (<xref ref-type="bibr" rid="B19">Kamil et al., 2016</xref>; <xref ref-type="bibr" rid="B37">Sardone et al., 2021</xref>; <xref ref-type="bibr" rid="B5">Castellana et al., 2021</xref>; <xref ref-type="bibr" rid="B44">Yevenes-Briones et al., 2021</xref>; <xref ref-type="bibr" rid="B25">Liu et al., 2022</xref>; <xref ref-type="bibr" rid="B16">Hura et al., 2022</xref>), communication limitations leading to social limitations and restrictions in daily living (<xref ref-type="bibr" rid="B20">Kamil et al., 2014</xref>; <xref ref-type="bibr" rid="B23">Liljas et al., 2017</xref>), and concurrent cognitive decline (<xref ref-type="bibr" rid="B33">Panza et al., 2015</xref>). Current evidence is insufficient to determine the mechanisms linking hearing loss and frailty, and there is no compelling evidence showing that the remediation of hearing loss decreases frailty.</p>
<p>We believe future research on the relationship between hearing loss and frailty would be valuable. Hearing loss is highly prevalent among older adults, affecting over 65% of adults aged 60 years and above (<xref ref-type="bibr" rid="B43">World Health Organization, 2021</xref>). If hearing loss is an early marker of frailty, regular screening for hearing loss should be established in geriatric settings to detect early signs of frailty. Furthermore, if hearing loss is a modifiable risk factor of frailty and future evidence supports that hearing remediation can manage frailty, then hearing loss management should be recommended to individuals at risk of or with frailty. Hearing aids are the most common treatment for hearing loss. Given the high prevalence of hearing loss and the cost-effectiveness and safety of treatment with hearing aids, the appropriate management of hearing loss could represent a valuable intervention to decrease the prevalence of frailty or alleviate its symptoms.</p>
<p>In summary, our study revealed that frail individuals exhibited poorer performance in assessments evaluating both peripheral and central hearing, as well as in self-reported hearing handicap. We identified statistically significant differences between frail and non-frail participants in speech-frequency hearing thresholds, overall CAP scores, and hearing handicap scores. However, the modest sample size may restrict the statistical power and limit the robustness of our findings. Future studies with larger sample sizes, or conducted in populations with higher frailty prevalence would be beneficial. Additionally, randomised controlled trials investigating whether correcting hearing loss reduces the proportion of people affected by frailty in later life would also be of interest.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s5">
<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 sec-type="ethics-statement" id="s6">
<title>Ethics statement</title>
<p>The studies involving humans were approved by The Human Research Ethics Committee of the University of Western Australia. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec sec-type="author-contributions" id="s7">
<title>Author contributions</title>
<p>RT: Conceptualization, Investigation, Formal Analysis, Writing&#x2013;original draft. OA: Conceptualization, Funding acquisition, Methodology, Project administration, Supervision, Writing&#x2013;review and editing. AF: Conceptualization, Funding acquisition, Methodology, Project administration, Supervision, Writing&#x2013;review and editing. LF: Conceptualization, Funding acquisition, Writing&#x2013;review and editing. NL: Conceptualization, Funding acquisition, Writing&#x2013;review and editing. SR: Conceptualization, Funding acquisition, Writing&#x2013;review and editing. MM: Conceptualization, Funding acquisition, Writing&#x2013;review and editing. SP: Conceptualization, Funding acquisition, Writing&#x2013;review and editing. SL: Data curation, Investigation, Project administration, Writing&#x2013;review and editing. ID: Project administration, Investigation, Writing&#x2013;review and editing. JY: Investigation, Writing&#x2013;review and editing. LC: Investigation, Writing&#x2013;review and editing. DJ: Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Supervision, Writing&#x2013;review and editing.</p>
</sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. The HearCog study received funding from Ron and Peggy Bell Legacy Trust, WA Department of Health Research Translation Project Grant, RPH Research Foundation, and Rebecca L Cooper Foundation. Oticon A/S, Denmark, provided hearing aids for the study. None of the funding bodies have provided any intellectual input into the study design, data collection, analyses, and interpretation of data and in writing of the manuscript.</p>
</sec>
<ack>
<p>We especially thank all the people who participated in the HearCog trial. Thanks to all research assistants and audiologists who contributed to the trial. We would like to express our gratitude to Holly Menegola for her invaluable advice and assistance in participants&#x2019; hearing assessment and hearing aids fitting. We also thank the Ear Science Institute Australia and the Lions Hearing Clinic for their support.</p>
</ack>
<sec sec-type="COI-statement" id="s9">
<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="s10">
<title>Generative AI statement</title>
<p>The authors declare that no Generative AI was used in the creation of this manuscript.</p>
</sec>
<sec sec-type="disclaimer" id="s11">
<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>
<sec id="s12">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fragi.2025.1524186/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fragi.2025.1524186/full&#x23;supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="DataSheet1.PDF" id="SM1" mimetype="application/PDF" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
<sec id="s13">
<title>Abbreviations</title>
<p>CAP, central auditory processing; MCI, mild cognitive impairment; PTA, pure-tone audiometry; HHIE, the Hearing Handicap Inventory of the Elderly; SSI-ICM, the Synthetic Sentence Identification with Ipsilateral Competing Message; Quick-SIN, the Quick Speech in Noise; DDT, the Dichotic Digits Test; MoCA, the Montreal Cognitive Assessment.</p>
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