<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Armstrong NM</submitter><funding>Intramural NIH HHS</funding><funding>NIA NIH HHS</funding><funding>National Institute of Nursing Research</funding><funding>NINR NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Institute on Aging</funding><pagination>114-122</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10696594</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>317</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>We explored the associations of dual sensory impairment (DSI) with long-term depressive and anxiety symptoms as well as low perceived social support (LPSS) as a modifier of these associations.&lt;h4>Methods&lt;/h4>Multinomial logistic regression models were used to examine the associations of DSI and single sensory impairment (hearing [pure-tone average > 25 dB] and vision [impaired visual acuity and/or contrast sensitivity]) with long-term depressive symptom (≥8 on the 10-item Center for Epidemiologic Studies-Depression Scale) and anxiety symptom (present on the Hopkins Symptom Checklist) latent classes from group-based trajectory models (rare/never; mild/moderate increasing; chronically high) among 2102 Health, Aging and Body Composition Study participants (mean age:74.0 ± 2.8 years; 51.9 % female) over 10 years. Models were adjusted by demographic characteristics and cardiovascular risk factors, and LPSS. An additional model evaluated the two-way interaction between DSI and LPSS.&lt;h4>Results&lt;/h4&gt;DSI was associated with increased risk of being chronically depressed (Risk Ratio, RR = 1.99, 95 % Confidence Interval, CI: 1.25, 3.17), not mild/moderate increasingly depressed (RR = 1.25, 95 % CI: 0.91, 1.71). DSI had increased risk of being mild/moderate increasingly anxious (RR = 1.60, 95 % CI: 1.16, 2.19) and chronically anxious (RR = 1.86, 95 % CI: 1.05, 3.27) groups, as compared to no impairments. Hearing impairment was associated with being mild/moderate increasingly anxious (RR = 1.34, 95 % CI: 1.01, 1.79). No other associations were found for single sensory impairments. LPSS did not modify associations.&lt;h4>Limitations&lt;/h4>Sensory measures were time-fixed, and LPSS, depression and anxiety measures were self-reported.&lt;h4>Conclusions&lt;/h4>Future research is warranted to determine if DSI therapies may lessen long-term chronically high depressive and anxiety symptoms.</pubmed_abstract><journal>Journal of affective disorders</journal><pubmed_title>Associations of dual sensory impairment with long-term depressive and anxiety symptoms in the United States.</pubmed_title><pmcid>PMC10696594</pmcid><funding_grant_id>K01AG054693</funding_grant_id><funding_grant_id>K01AG062722</funding_grant_id><funding_grant_id>R01 AG028050</funding_grant_id><funding_grant_id>K01 AG054693</funding_grant_id><funding_grant_id>N01-AG-6-2106</funding_grant_id><funding_grant_id>R01 NR012459</funding_grant_id><funding_grant_id>K01 AG062722</funding_grant_id><funding_grant_id>R01-AG028050</funding_grant_id><funding_grant_id>N01-AG-6-2101</funding_grant_id><funding_grant_id>Z99 AG999999</funding_grant_id><funding_grant_id>R01-NR012459</funding_grant_id><funding_grant_id>R01-AG-6-2103</funding_grant_id><pubmed_authors>Swenor B</pubmed_authors><pubmed_authors>Lin FR</pubmed_authors><pubmed_authors>Deal JA</pubmed_authors><pubmed_authors>Simonsick EM</pubmed_authors><pubmed_authors>Powell DS</pubmed_authors><pubmed_authors>Jones RN</pubmed_authors><pubmed_authors>Armstrong NM</pubmed_authors><pubmed_authors>Brenowitz WD</pubmed_authors><pubmed_authors>Vieira Ligo Teixeira C</pubmed_authors><pubmed_authors>Gendron C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Associations of dual sensory impairment with long-term depressive and anxiety symptoms in the United States.</name><description>&lt;h4>Objective&lt;/h4>We explored the associations of dual sensory impairment (DSI) with long-term depressive and anxiety symptoms as well as low perceived social support (LPSS) as a modifier of these associations.&lt;h4>Methods&lt;/h4>Multinomial logistic regression models were used to examine the associations of DSI and single sensory impairment (hearing [pure-tone average > 25 dB] and vision [impaired visual acuity and/or contrast sensitivity]) with long-term depressive symptom (≥8 on the 10-item Center for Epidemiologic Studies-Depression Scale) and anxiety symptom (present on the Hopkins Symptom Checklist) latent classes from group-based trajectory models (rare/never; mild/moderate increasing; chronically high) among 2102 Health, Aging and Body Composition Study participants (mean age:74.0 ± 2.8 years; 51.9 % female) over 10 years. Models were adjusted by demographic characteristics and cardiovascular risk factors, and LPSS. An additional model evaluated the two-way interaction between DSI and LPSS.&lt;h4>Results&lt;/h4&gt;DSI was associated with increased risk of being chronically depressed (Risk Ratio, RR = 1.99, 95 % Confidence Interval, CI: 1.25, 3.17), not mild/moderate increasingly depressed (RR = 1.25, 95 % CI: 0.91, 1.71). DSI had increased risk of being mild/moderate increasingly anxious (RR = 1.60, 95 % CI: 1.16, 2.19) and chronically anxious (RR = 1.86, 95 % CI: 1.05, 3.27) groups, as compared to no impairments. Hearing impairment was associated with being mild/moderate increasingly anxious (RR = 1.34, 95 % CI: 1.01, 1.79). No other associations were found for single sensory impairments. LPSS did not modify associations.&lt;h4>Limitations&lt;/h4>Sensory measures were time-fixed, and LPSS, depression and anxiety measures were self-reported.&lt;h4>Conclusions&lt;/h4>Future research is warranted to determine if DSI therapies may lessen long-term chronically high depressive and anxiety symptoms.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-22T07:59:11.211Z</modification><creation>2025-04-05T22:25:08.407Z</creation></dates><accession>S-EPMC10696594</accession><cross_references><pubmed>35932940</pubmed><doi>10.1016/j.jad.2022.07.067</doi></cross_references></HashMap>