Association of Loneliness With Change in Physical and Emotional Health of Older Adults During the COVID-19 Shutdown.


Journal

The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry
ISSN: 1545-7214
Titre abrégé: Am J Geriatr Psychiatry
Pays: England
ID NLM: 9309609

Informations de publication

Date de publication:
12 2023
Historique:
received: 21 03 2023
revised: 21 07 2023
accepted: 24 07 2023
medline: 10 11 2023
pubmed: 9 11 2023
entrez: 8 11 2023
Statut: ppublish

Résumé

To examine factors influencing loneliness and the effect of loneliness on physical and emotional health, in the context of the COVID-19 pandemic. Prospective, observational cohort. Community-dwelling participants. Older adults (n = 238) enrolled in a longitudinal study. Interviews were completed July-December 2020. Loneliness was measured with the UCLA 3-item loneliness scale. Data including age, marriage, education, cognitive functioning, functional impairment, vision or hearing impairment, depression, anxiety, medical comorbidity, social network size, technology use, and activity engagement were collected. Health outcomes included self-rated health, and physical and mental composites from the 12-item Short Form Survey. Physical function was measured by a PROMIS-scaled composite score. Thirty-nine (16.4%) participants reported loneliness. Vulnerability factors for loneliness included age (RR = 1.08, 95% CI 1.02-1.14); impairment with instrumental activities of daily living (RR = 2.08, 95% CI 1.14-3.80); vision impairment (RR = 2.09, 95% CI 1.10-3.97); depression (RR = 1.34, 95% CI 1.25-1.43); and anxiety (RR = 1.92, 95% CI 1.55-2.39). Significant resilience factors included high cognitive functioning (RR = 0.88, 95% CI 0.83-0.94); large social network size (RR = 0.92, 95% CI 0.88-0.96); technology use (RR = 0.81, 95% CI 0.73-0.90); and social and physical activity engagement (RR = 0.91, 95% CI 0.85-0.98). Interaction analyses showed that larger social network size moderated the effect of loneliness on physical function (protective interaction effect, RR = 0.64, 95% CI 0.15-1.13, p <.01), and activity engagement moderated the effect of loneliness on mental health (protective interaction effect, RR = 0.65, 95% CI 0.25-1.05, p <.001). Resilience factors may mitigate the adverse health outcomes associated with loneliness. Interventions to enhance resilience may help to diminish the detrimental effects of loneliness and hold great importance for vulnerable older adults.

Identifiants

pubmed: 37940227
pii: S1064-7481(23)00373-1
doi: 10.1016/j.jagp.2023.07.015
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1102-1113

Subventions

Organisme : NIA NIH HHS
ID : R33 AG071744
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG044518
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Published by Elsevier Inc.

Auteurs

Julianna Liu (J)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA.

Ray Yun Gou (RY)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA.

Richard N Jones (RN)

Department of Psychiatry and Human Behavior (RNJ), Brown University, Providence, RI.

Eva M Schmitt (EM)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA.

Eran Metzger (E)

Department of Psychiatry (EM), Beth Israel Deaconess Medical Center, Boston, MA.

Patricia A Tabloski (PA)

Connell School of Nursing (PAT), Boston College, Chestnut Hill, MA.

Franchesca Arias (F)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA; Harvard Medical School (FA, TTH, TGT, ERM, TF, SKI), Boston, MA; Department of Medicine (FA, TTH), Brigham and Women's Hospital, Boston, MA.

Tammy T Hshieh (TT)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA; Harvard Medical School (FA, TTH, TGT, ERM, TF, SKI), Boston, MA; Department of Medicine (FA, TTH), Brigham and Women's Hospital, Boston, MA.

Thomas G Travison (TG)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA; Harvard Medical School (FA, TTH, TGT, ERM, TF, SKI), Boston, MA.

Edward R Marcantonio (ER)

Harvard Medical School (FA, TTH, TGT, ERM, TF, SKI), Boston, MA; Divisions of General Medicine and Gerontology (ERM), Beth Israel Deaconess Medical Center, Boston, MA.

Tamara Fong (T)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA; Harvard Medical School (FA, TTH, TGT, ERM, TF, SKI), Boston, MA; Department of Neurology (TF), Beth Israel Deaconess Medical Center, Boston, MA. Electronic address: tfong@bidmc.harvard.edu.

Sharon K Inouye (SK)

Aging Brain Center (JL, RYG, EMS, FA, TTH, TGT, TF, SKI), Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA; Harvard Medical School (FA, TTH, TGT, ERM, TF, SKI), Boston, MA; Department of Medicine (SKI), Beth Israel Deaconess Medical Center, Boston, MA.

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Classifications MeSH