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Seropositivity to herpes simplex virus antibodies and risk of Alzheimer's disease: a population-based cohort study.

Abstract : BACKGROUND: Herpes Simplex Virus (HSV) infection has been proposed as a possible risk factor of Alzheimer's Disease (AD) notably because it is neurotropic, ubiquitous in the general population and able to establish lifelong latency in the host. The fact that HSV was present in elderly subjects with AD suggests that the virus could be a co-factor of the disease. We investigated the risk of developing AD in anti-HSV immunoglobulin G (IgG) positive subjects (indicator of a lifelong infection to HSV) and IgM-positive subjects (indicator of primary infection or reactivation of the virus) in a longitudinal population-based cohort of elderly subjects living in the community. METHODS: Cox proportional hazard models were used to study the risk of developing AD according to the presence or not of anti-HSV IgG and IgM antibodies, assessed in the sera of 512 elderly initially free of dementia followed for 14 years. RESULTS: During the follow-up, 77 incident AD cases were diagnosed. Controlled for age, gender, educational level and Apolipoprotein E4 (APOE4) status, IgM-positive subjects showed a significant higher risk of developing AD (HR = 2.55; 95% CI [1.38-4.72]), although no significant increased risk was observed in IgG-positive subjects (HR = 1.67; 95%CI [0.75-3.73]). No modification effect with APOE4 status was found. CONCLUSION: Reactivation of HSV seropositivity is highly correlated with incident AD. HSV chronic infection may therefore be contributive to the progressive brain damage characteristic of AD.
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Contributor : Evelyne Mouillet <>
Submitted on : Tuesday, November 4, 2008 - 12:05:23 PM
Last modification on : Friday, October 23, 2020 - 4:53:52 PM
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Luc Letenneur, Karine Pérès, Hervé Fleury, Isabelle Garrigue, Pascale Barberger-Gateau, et al.. Seropositivity to herpes simplex virus antibodies and risk of Alzheimer's disease: a population-based cohort study.. PLoS ONE, Public Library of Science, 2008, 3 (11), pp.e3637. ⟨10.1371/journal.pone.0003637⟩. ⟨inserm-00336499⟩



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