Circulating Cell-Free Genomic DNA Is Associated with an Increased Risk of Dementia and with Change in Cognitive and Physical Function

Article type: Research Article

Authors: Nidadavolu, Lolita S.^a | Feger, Danielle^b | Wu, Yuqiong^a | Grodstein, Francine^c | Gross, Alden L.^{a; b} | Bennett, David A.^c | Walston, Jeremy D.^a | Oh, Esther S.^{a; *; 1} | Abadir, Peter M.^{a; *; 1}

Affiliations: [a] Johns Hopkins University School of Medicine, Division of Geriatric Medicine and Gerontology, Baltimore, MD, USA | [b] Johns Hopkins University Center on Aging and Health, Baltimore, MD, USA | [c] Rush Alzheimer’s Disease Center, Rush University Medical Center, Chicago, IL, USA

Correspondence: [*] Correspondence to: Esther Oh, MD, PhD, Johns Hopkins University School of Medicine, Division of Geriatric Medicine and Gerontology, Johns Hopkins Asthma and Allergy Center, 5501 Hopkins Bayview Circle, Baltimore, MD 21224, USA. Tel.: +1 410 550 1318; E-mail: [email protected] and Peter M. Abadir, MD, Johns Hopkins University School of Medicine, Division of Geriatric Medicine and Gerontology, Johns Hopkins Asthma and Allergy Center, 5501 Hopkins Bayview Circle, Baltimore, MD 21224, USA. Tel.: +1 410 550 5436; E-mail: [email protected].

Note: [1] These authors contributed equally to this work.

Abstract: Background:Altered cell homeostasis, seen in cognitive decline and frailty, leads to cell death and turnover, releasing circulating cell-free DNA (ccf-DNA). Objective:The goal of this study is to determine if serum genomic cell-free DNA (ccf-gDNA) is associated with physical and cognitive decline in older adults. Methods:We used serum from 631 community-dwelling individuals from the Religious Orders Study or Rush Memory and Aging Project who were without cognitive impairment at baseline. ccf-gDNA fragments in serum were quantified using digital PCR. An array of cognitive and physical traits, risk of dementia, global cognition, and frailty at or nearest the time of blood draw were regressed on ccf-DNA, with adjustment for age, sex, race, and education. Results:Cross-sectionally, higher ccf-gDNA levels were associated with lower global cognition score and slower gait speed at the evaluation nearest to blood draw. Higher ccf-gDNA levels were associated with increased odds of incident dementia (OR 1.27, 95% CI 1.05, 1.54). Longitudinally, higher levels of ccf-gDNA were associated with steeper general cognitive decline and worsening frailty over eight years of follow up. Conclusion:This study demonstrates that ccf-gDNA fragments have utility for identifying persons at higher risk of developing dementia and worsening cognition and frailty.

Keywords: Cell-free DNA, cell death, cognitive dysfunction, dementia, frailty

DOI: 10.3233/JAD-220301

Journal: Journal of Alzheimer's Disease, vol. 89, no. 4, pp. 1233-1240, 2022