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Temporal Cognitive Decline Associated With Exposure to Infectious Agents in a Population-based, Aging Cohort

Nimgaonkar, Vishwajit L. MD, PhD; Yolken, Robert H. MD, PhD; Wang, Tianxiu MS; Chang, Chung-Chou H. PhD; McClain, Lora BS; McDade, Eric DO; Snitz, Beth E. PhD; Ganguli, Mary MD

Alzheimer Disease & Associated Disorders: July–September 2016 - Volume 30 - Issue 3 - p 216–222
doi: 10.1097/WAD.0000000000000133
Original Articles

Background: Numerous cross-sectional studies have related exposure to neurotropic infectious agents with cognitive dysfunction in older adults, however, the temporal sequence is uncertain.

Methods: In a representative, well-characterized, population-based aging cohort, we determined whether the temporal trajectories of multiple cognitive domains are associated with exposure to cytomegalovirus (CMV), Herpes Simplex virus, type 1 (HSV-1), Herpes Simplex virus, type 2 (HSV-2), or Toxoplasma gondii (TOX). Complex attention, executive functions, memory, language, and visuospatial function were assessed annually for 5 years among consenting individuals. Study entry IgG antibody titers indexing exposure to each infectious agent were examined in relation to slopes of subsequent temporal cognitive decline using multiple linear regressions adjusted for potential confounders.

Results: The IgG levels for HSV-2 were significantly associated with baseline cognitive domain scores (N=1022 participants). Further, the IgG levels for HSV-2, TOX, and CMV, but not HSV-1 were significantly associated with greater temporal cognitive decline that varied by type of infection.

Conclusions: Exposure to CMV, HSV-2, or TOX is associated with cognitive deterioration in older individuals, independent of general age–related variables. An increased understanding of the role of infectious agents in cognitive decline may lead to new methods for its prevention and treatment.

Departments of *Psychiatry

Medicine

Neurology, University of Pittsburgh School of Medicine

Departments of Human Genetics

§Biostatistics

#Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA

Department of Pediatrics, Stanley Division of Neurovirology, Johns Hopkins University School of Medicine, Baltimore, MD

Supported in part by Grants # R01 AG02365 and K07 AG044395 and AG020677 from the National Institute on Aging (NIA); MH09375 from NIMH; and 07R-1712 from the Stanley Medical Research Institute.

The authors declare no conflicts of interest.

Reprints: Vishwajit L. Nimgaonkar, MD, PhD, TDH, Room 441, 3811 O’Hara Street, Pittsburgh, PA 15208 (e-mail: nimga@pitt.edu).

Received April 9, 2015

Accepted November 17, 2015

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