Baseline Neurocognitive Impairment (NCI) Is Associated With Incident Frailty but Baseline Frailty Does Not Predict Incident NCI in Older Persons With Human Immunodeficiency Virus (HIV)

Author:

Masters Mary Clare1ORCID,Perez Jeremiah2,Wu Kunling2,Ellis Ronald J3ORCID,Goodkin Karl4,Koletar Susan L5,Andrade Adriana6,Yang Jingyan7,Brown Todd T8,Palella Frank J1,Sacktor Ned8,Tassiopoulos Katherine2,Erlandson Kristine M9

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA

2. Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA

3. University of California, San Diego, San Diego, California, USA

4. University of Nebraska Medical Center, Omaha, Omaha, Nebraska, USA

5. The Ohio State University, Columbus, Ohio, USA

6. DHHS/NIH/NIAID/DAIDS, Rockville, Maryland, USA

7. Columbia University, New York, New York, USA

8. Johns Hopkins University, Baltimore, Maryland, USA

9. University of Colorado- Anschutz Medical Campus, Aurora, Colorado, USA

Abstract

Abstract Background Neurocognitive impairment (NCI) and frailty are more prevalent among persons with human immunodeficiency virus (HIV, PWH) compared to those without HIV. Frailty and NCI often overlap with one another. Whether frailty precedes declines in neurocognitive function among PWH or vice versa has not been well established. Methods AIDS Clinical Trials Group (ACTG) A5322 is an observational cohort study of older PWH. Participants undergo annual assessments for NCI and frailty. ACTG A5322 participants who developed NCI as indexed by tests of impaired executive functioning and processing speed during the first 3 years were compared to persons who maintained normal cognitive function; those who demonstrated resolution of NCI were compared to those who had persistent NCI. Participants were similarly compared by frailty trajectory. We fit multinomial logistic regression models to assess associations between baseline covariates (including NCI) and frailty, and associations between baseline covariates (including frailty) and NCI. Results In total, 929 participants were included with a median age of 51 years (interquartile range [IQR] 46–56). At study entry, 16% had NCI, and 6% were frail. Over 3 years, 6% of participants developed NCI; 5% developed frailty. NCI was associated with development of frailty (odds ratio [OR] = 2.06; 95% confidence interval [CI] = .94, 4.48; P = .07). Further adjustment for confounding strengthened this association (OR = 2.79; 95% CI = 1.21, 6.43; P = .02). Baseline frailty however was not associated with NCI development. Conclusions NCI was associated with increased risk of frailty, but frailty was not associated with development of NCI. These findings suggest that the presence of NCI in PWH should prompt monitoring for the development of frailty and interventions to prevent frailty in this population.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

National Institute on Aging

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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