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2011
- handle: 10670/1.q369im
- inserm-00657059
- doi: 10.1371/journal.pone.0029480
- PUBMED: 22216291
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info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0029480
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info:eu-repo/semantics/altIdentifier/pmid/22216291
info:eu-repo/semantics/OpenAccess
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Catherine Féart et al., « Association between IgM Anti-Herpes Simplex Virus and Plasma Amyloid-Beta Levels. », HAL-SHS : sciences de l'information, de la communication et des bibliothèques, ID : 10.1371/journal.pone.0029480
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OBJECTIVE: Herpes simplex virus (HSV) reactivation has been identified as a possible risk factor for Alzheimer's disease (AD) and plasma amyloid-beta (Aβ) levels might be considered as possible biomarkers of the risk of AD. The aim of our study was to investigate the association between anti-HSV antibodies and plasma Aβ levels. METHODS: The study sample consisted of 1222 subjects (73.9 y in mean) from the Three-City cohort. IgM and IgG anti-HSV antibodies were quantified using an ELISA kit, and plasma levels of Aβ(1-40) and Aβ(1-42) were measured using an xMAP-based assay technology. Cross-sectional analyses of the associations between anti-HSV antibodies and plasma Aβ levels were performed by multi-linear regression. RESULTS: After adjustment for study center, age, sex, education, and apolipoprotein E-e4 polymorphism, plasma Aβ(1-42) and Aβ(1-40) levels were specifically inversely associated with anti-HSV IgM levels (β = -20.7, P = 0.001 and β = -92.4, P = 0.007, respectively). In a sub-sample with information on CLU- and CR1-linked SNPs genotyping (n = 754), additional adjustment for CR1 or CLU markers did not modify these associations (adjustment for CR1 rs6656401, β = -25.6, P = 0.002 for Aβ(1-42) and β = -132.7, P = 0.002 for Aβ(1-40;) adjustment for CLU rs2279590, β = -25.6, P = 0.002 for Aβ(1-42) and β = -134.8, P = 0.002 for Aβ(1-40)). No association between the plasma Aβ(1-42)-to-Aβ(1-40) ratio and anti-HSV IgM or IgG were evidenced. CONCLUSION: High anti-HSV IgM levels, markers of HSV reactivation, are associated with lower plasma Aβ(1-40) and Aβ(1-42) levels, which suggest a possible involvement of the virus in the alterations of the APP processing and potentially in the pathogenesis of AD in human.