Journal article
Age‐Related Changes in the Clinical Picture of Long COVID
Journal of the American Geriatrics Society (JAGS), Vol.73(10), pp.3123-3137
10/2025
DOI: 10.1111/jgs.70043
PMID: 40888500
Abstract
Background This study evaluated the impact of aging on the frequency and prevalent symptoms of Long COVID, also termed post‐acute sequelae of SARS‐CoV‐2, using a previously developed Long COVID research index (LCRI) of 41 self‐reported symptoms in which those with 12 or more points were classified as likely to have Long COVID. Methods We analyzed community‐dwelling participants ≥ 60 years old (2662 with prior infection, 461 controls) compared to participants 18–59 years (7549 infected, 728 controls) in the Researching COVID to Enhance Recovery adult (RECOVER‐Adult) cohort ≥ 135 days post‐onset. Results Compared to the Age 18–39 group, the adjusted odds of LCRI ≥ 12 were higher for the Age 40–49 group (odds ratio [OR] = 1.40, 95% confidence intervals [CI] = 1.21–1.61, p < 0.001) and 50–59 group (OR = 1.31, CI = 1.14–1.51, p < 0.001), similar for the Age 60–69 group (OR = 1.09, CI = 0.93–1.27, p = 0.299), and lower for the ≥ 70 group (OR = 0.68, CI = 0.54–0.85, p < 0.001). Participants ≥ 70 years had smaller adjusted differences between infected and uninfected symptom prevalence rates than those aged 18–39 for the following symptoms: hearing loss, fatigue, pain (including joint, back, chest pain and headache), post‐exertional malaise, sleep disturbance, hair loss, palpitations, and sexual desire/capacity, making these symptoms less discriminating for Long COVID in older adults than in younger. Symptom clustering, as described in Thaweethai et al. (JAMA 2023) also exhibited age‐related shifts: clusters 1 (anosmia and ageusia) and 2 (gastrointestinal, chronic cough and palpitations, without anosmia, ageusia or brain fog) were more likely, and clusters 3 (brain fog, but no loss of smell or taste) and 4 (a mix of symptoms) less likely to be found in older adults (relative risk ratios for clusters 3–4 ranging from 0.10–0.34, p < 0.001 vs. 18–39 year‐olds). Conclusions Within the limits of this observational study, we conclude that in community‐dwelling older adults, aging alters the prevalence and pattern of reported Long COVID. Distribution of Long COVID/PASC symptom clusters by age group, with clusters 1 and 2 denoting milder and 3 and 4 more severe symptom clusters as defined by Thaweethai et al. (JAMA 2023).
Details
- Title: Subtitle
- Age‐Related Changes in the Clinical Picture of Long COVID
- Creators
- Mindy J. Fain - University of ArizonaBenjamin D. Horne - Intermountain HealthcareLeora I. Horwitz - New York UniversityTanayott Thaweethai - Harvard UniversityMeredith Greene - Regenstrief InstituteMady Hornig - Northwell HealthAriela R. Orkaby - Brigham and Women's HospitalClifford Rosen - MaineHealthChristine S. Ritchie - Massachusetts General HospitalHassan Ashktorab - Howard UniversityNina Blachman - New York UniversityHassan Brim - Howard UniversitySarah Emerson - Providence Sacred Heart Medical CenterNathan Erdmann - University of Alabama at BirminghamKristine M. Erlandson - University of Colorado AnschutzGabriel Erausquin - University of Texas Health Sciences CenterTamara Fong - Beth Israel Deaconess Medical CenterLinda N. Geng - Stanford UniversityHoward S. Gordon - Jesse Brown VA Medical CenterJacqueline Rutter Gully - RECOVER Patient Advocate & Caregiver, Dysautonomia InternationalJennifer Hadlock - University of WashingtonJenny Han - Emory UniversityWeixing Huang - Harvard UniversityPrasanna Jagannathan - Stanford UniversityJ. Daniel Kelly - San Francisco VA Medical CenterJonathan D. Klein - University of Illinois ChicagoJerry A. Krishnan - University of Illinois ChicagoEmily B. Levitan - University of Alabama at BirminghamGrace A. McComsey - Case Western Reserve UniversityDylan McDonald - University of WashingtonAoyjai P. Montgomery - University of Alabama at BirminghamLisa O'Brien - RECOVER Patient Representative, Utah Covid‐19 Long HaulersIghovwerha Ofotokun - Emory UniversityThomas F. Patterson - The University of Texas at San Antonio Health Science CenterMichael J. Peluso - University of California, San FranciscoPriscilla Pemu - Morehouse School of MedicineAlice Perlowski - RECOVER Patient Representative, Blooming MagnoliaEric M. Reiman - Banner Alzheimer’s InstituteMartine Sanon - Mount Sinai HospitalSudha Seshadri - The University of Texas at San Antonio Health Science CenterJudd Shellito - Louisiana State University Health Sciences Center New OrleansZaki A. Sherif - Howard UniversityCecilia Shikuma - University of Hawaiʻi at MānoaNora G. Singer - MetroHealthUpinder Singh - Stanford MedicineJoel D. Trinity - University of UtahJuan Wisnivesky - Icahn School of Medicine at Mount SinaiMargot Gage Witvliet - Lamar UniversityAndrea Foulkes - Harvard UniversityJanko Ž. Nikolich - University of Arizonathe RECOVER consortium
- Resource Type
- Journal article
- Publication Details
- Journal of the American Geriatrics Society (JAGS), Vol.73(10), pp.3123-3137
- DOI
- 10.1111/jgs.70043
- PMID
- 40888500
- NLM abbreviation
- J Am Geriatr Soc
- ISSN
- 0002-8614
- eISSN
- 1532-5415
- Publisher
- John Wiley & Sons, Inc
- Number of pages
- 15
- Grant note
- O. Wayne Rollins Foundation National Heart, Lung, and Blood Institute (OT2HL161841; OT2HL161847) National Institute on Aging (P30AG066546; P30AG072980; R56AG074467) William Randolph Hearst Foundations National Center for Advancing Translational Sciences (UM1TR004409; UM1TR004528)
- Language
- English
- Date published
- 10/2025
- Academic Unit
- Internal Medicine
- Record Identifier
- 9985244659302771
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