DNA from multiple viral species is associated with Alzheimer's disease risk.

TitleDNA from multiple viral species is associated with Alzheimer's disease risk.
Publication TypeJournal Article
Year of Publication2023
AuthorsTejeda M, Farrell J, Zhu C, Wetzler L, Lunetta KL, Bush WS, Martin ER, San Wang L-, Schellenberg GD, Pericak-Vance MA, Haines JL, Farrer LA, Sherva R
JournalAlzheimers Dement
Date Published08/2023
ISSN1552-5279
Abstract

INTRODUCTION: Multiple infectious agents, including viruses, bacteria, fungi, and protozoa, have been linked to Alzheimer's disease (AD) risk by independent lines of evidence. We explored this association by comparing the frequencies of viral species identified in a large sample of AD cases and controls.

METHODS: DNA sequence reads that did not align to the human genome in sequences were mapped to viral reference sequences, quantified, and then were tested for association with AD in whole exome sequences (WES) and whole genome sequences (WGS) datasets.

RESULTS: Several viruses were significant predictors of AD according to the machine learning classifiers. Subsequent regression analyses showed that herpes simplex type 1 (HSV-1) (odds ratio [OR] = 3.71, p = 8.03 × 10-4) and human papillomavirus 71 (HPV-71; OR = 3.56, p = 0.02), were significantly associated with AD after Bonferroni correction. The phylogenetic-related cluster of Herpesviridae was significantly associated with AD in several strata of the data (p < 0.01).

DISCUSSION: Our results support the hypothesis that viral infection, especially HSV-1, is associated with AD risk.

DOI10.1002/alz.13414
Alternate JournalAlzheimers Dement
PubMed ID37578203
Grant ListU01 AG032984 / AG / NIA NIH HHS / United States
R01 AG033193 / AG / NIA NIH HHS / United States
U01AG049506 / HL / NHLBI NIH HHS / United States
U01AG049507 / HL / NHLBI NIH HHS / United States
/ AG / NIA NIH HHS / United States
RF1 AG057519 / NH / NIH HHS / United States
R01 AG048927 / NH / NIH HHS / United States
U19 AG068753 / NH / NIH HHS / United States
U01 AG062602 / NH / NIH HHS / United States
R01-AG076002 / NH / NIH HHS / United States