Plasma Biomarkers of Alzheimer Disease in Women With and Without HIV

Author:

Li Xuantao1,Yucel Recai1,Clervius Helene23,Kamalakar Kundun4,Zetterberg Henrik56789,Blennow Kaj56,Zhang Jinbing10,Adimora Adaora1112,Collins Lauren F.13,Fischl Margaret14,Kassaye Seble15,Maki Pauline161718,Seaberg Eric1910,Sharma Anjali2021,Vance David22,Gustafson Deborah R.25

Affiliation:

1. Department of Epidemiology and Biostatistics, Temple University, Philadelphia, Pennsylvania

2. Department of Neurology, State University of New York Downstate Health Sciences University, Brooklyn

3. Downstate Neurology at One Brooklyn Health, Brookdale Hospital, Brooklyn, New York

4. School of Public Health, State University of New York Downstate Health Sciences University, Brooklyn

5. Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden

6. Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden

7. Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, United Kingdom

8. UK Dementia Research Institute at UCL, London, United Kingdom

9. Hong Kong Center for Neurodegenerative Diseases, Clear Water Bay, Hong Kong, China

10. Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland

11. Department of Medicine, School of MedicineUniversity of North Carolina at Chapel Hill

12. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill

13. Division of Infectious Diseases, Emory University, Atlanta, Georgia

14. Division of Infectious Diseases, Department of Medicine, University of Miami, Miami, Florida

15. Department of Medicine, Division of Infectious Diseases, Georgetown University Medical Center, Washington, DC

16. Department of Psychiatry, University of Illinois College of Medicine, Chicago

17. Department of Psychology, University of Illinois College of Medicine, Chicago

18. Department of Obstetrics and Gynecology, University of Illinois College of Medicine, Chicago

19. Wisconsin Alzheimer’s Disease Research Center, University of Wisconsin School of Medicine and Public Health, University of Wisconsin, Madison

20. Division of General Internal Medicine, Albert Einstein College of Medicine, New York, New York

21. Division of Infectious Diseases, Albert Einstein College of Medicine, New York, New York

22. Department of Acute, Chronic and Continuing Care, University of Alabama at Birmingham

Abstract

ImportanceBlood-based biomarkers associated with increased risk of Alzheimer disease (AD) are understudied in people living with and without HIV, particularly women.ObjectiveTo determine whether baseline or 1-year changes in plasma amyloid-β40 (Aβ40), Aβ42, ratio of Aβ42 to Aβ40, total tau (t-tau), phosphorylated tau 231 (p-tau231), glial fibrillary acidic protein (GFAP), and/or neurofilament light chain (NFL) are associated with neuropsychological performance (NP) among women living with HIV (WLWH) and women living without HIV (WLWOH).Design, Setting, and ParticipantsThis longitudinal, prospective, cohort study with 1-year repeated clinical measures (NP only measured once) and biospecimen collection occurred between 2017 and 2019. Participants were women aged 40 years or older from 10 clinical research sites in cities across the US that were part of the Women’s Interagency HIV Study. Data analysis was conducted from April to December 2022.ExposureLaboratory-confirmed HIV status and AD biomarkers.Main Outcomes and MeasuresSociodemographically adjusted NP T-scores (attention and working memory, executive function, processing speed, memory, learning, verbal fluency, motor function, and global performance) were the primary outcomes. Baseline and 1-year fasting plasma Aβ40, Aβ42, t-tau, p-tau231, GFAP, and NFL levels were measured and analyzed using multivariable linear regression.ResultsThe study consisted of 307 participants (294 aged ≥50 years [96%]; 164 African American or Black women [53%]; 214 women with a high school education or higher [70%]; 238 women who were current or former smokers [78%]; and 236 women [77%] who were overweight or obese [body mass index >25]) including 209 WLWH and 98 WLWOH. Compared with WLWOH at baseline, WLWH performed worse on learning (mean [SD] T-score 47.8 [11.3] vs 51.4 [10.5]), memory (mean [SD] T-score 48.3 [11.6] vs 52.4 [10.2]), verbal fluency (mean [SD] T-score 48.3 [9.8] vs 50.7 [8.5]), and global (mean [SD] T-score 49.2 [6.8] vs 51.1 [5.9]) NP assessments. Baseline median Aβ40, GFAP, and NFL levels were higher among WLWH vs WLWOH. There were no differences in 1-year biomarker change by HIV serostatus. Lower learning, memory, and motor NP were associated with 1-year Aβ40 increase; lower learning and motor with Aβ42 increase; lower motor with p-tau231 increase; and lower processing speed, verbal fluency and motor with NFL increase in the entire sample. Among WLWH, a 1-year increase in Aβ40 from baseline to follow-up was associated with worse learning, memory, and global NP; a 1-year increase in t-tau with worse executive function; and a 1-year increase in NFL with worse processing speed. Among WLWOH, a 1-year increase in Aβ40 and Aβ42 were associated with poorer memory performance and NFL was associated with poorer motor performance.Conclusions and RelevanceThese findings suggest that increases in certain plasma AD biomarkers are associated with NP in WLWH and WLWOH and may be associated with later onset of AD, and measuring these biomarkers could be a pivotal advancement in monitoring aging brain health and development of AD among women with and without HIV.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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1. Error in Byline;JAMA Network Open;2024-01-09

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