# A cross-cohort comparison of the prevalence and clinical significance of Alzheimer’s disease biomarkers in people with versus without HIV

**Authors:** Lillian Ham, Olivia Villers, Judith D. Lobo, Tyler R. Bell, Debralee Cookson, Douglas Galasko, Scott L. Letendre, Mark W. Bondi, David J. Moore, Erin E. Sundermann

PMC · DOI: 10.1007/s13365-026-01309-7 · Journal of Neurovirology · 2026-03-25

## TL;DR

This study compares Alzheimer’s disease biomarkers in people with and without HIV, finding that HIV is linked to higher amyloid levels, but not to other markers like tau.

## Contribution

The study provides new insights into how HIV affects Alzheimer’s biomarkers, independent of cognitive impairment status.

## Key findings

- HIV status was associated with higher odds of Aβ42 and Aβ42/Aβ40 positivity in CSF, regardless of aMCI status.
- aMCI status was linked to higher odds of p-tau181 positivity, regardless of HIV status.
- No HIV-disease characteristics were related to AD biomarker positivity.

## Abstract

With over half of people with HIV (PWH) in the U.S. entering older adulthood, identifying markers to distinguish Alzheimer’s disease (AD) and its precursor, amnestic mild cognitive impairment (aMCI), from other forms of neurocognitive impairment among PWH is urgent. We examined how HIV and aMCI status relate to AD CSF biomarkers in adult PWH and people without HIV (PWoH) characterized for aMCI. We included 80 PWH from the National NeuroHIV Tissue Consortium and 80 PWoH from the Wisconsin Registry for Alzheimer’s Prevention. Binary logistic regressions of AD-related CSF biomarker positivity (Aβ42, Aβ42/Aβ40, t-tau, p-tau181, Aβ42/t-tau) were conducted with HIV serostatus, aMCI status, HIV x aMCI interaction, and demographic covariates. Among PWH, we examined how HIV-disease characteristics relate to AD biomarker positivity. No HIV x aMCI interactions were detected. Regardless of aMCI status, having HIV was associated with higher odds of CSF Aβ42 (OR = 7.97) and Aβ42/Aβ40 (OR = 6.06) positivity, suggesting increased cerebral Aβ plaque burden. Regardless of HIV serostatus, having aMCI was associated with higher odds of CSF p-tau181 positivity (OR = 3.64). Neither HIV nor aMCI status related to Aβ42/t-tau positivity. No HIV-disease characteristics related to AD biomarker positivity. Higher CSF Aβ positivity in PWH versus PWoH, regardless of aMCI status, suggests that HIV disease promotes amyloidosis; however, whether positive CSF biomarkers in PWH raises risk for future cognitive impairment and AD remains to be explored longitudinally. Like PWoH, elevated CSF p-tau181 among PWH may indicate increased risk for AD-related memory impairment.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}
- **Diseases:** cognitive impairment (MESH:D003072), Mental Illnesses (MESH:D001523), plaques (MESH:D003773), neurodegeneration (MESH:D019636), neurocognitive impairment (MESH:D019965), diabetes (MESH:D003920), AIDS (MESH:D000163), HIV (MESH:D015658), infection (MESH:D007239), neurofibrillary tangles (MESH:D055956), aMCI (MESH:D060825), axonal injury (MESH:D001480), amyloidosis (MESH:D000686), death (MESH:D003643), HAND (MESH:D016263), AD (MESH:D000544), amyloid (MESH:C000718787), MSD (MESH:D052517), hypertension (MESH:D006973), MDD (MESH:D003865), DSM-IV (MESH:D006011), inflammation (MESH:D007249), neuronal injury (MESH:D009410), episodic memory impairment (MESH:D008569), Dementia (MESH:D003704), cerebrovascular disease (MESH:D002561), opportunistic infections (MESH:D009894), NNTC (MESH:D017695)
- **Chemicals:** p-tau181 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC13018001