Association between IgM anti-herpes simplex virus and plasma amyloid-beta levels |
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Authors: | Féart Catherine Helmer Catherine Fleury Hervé Béjot Yannick Ritchie Karen Amouyel Philippe Schraen-Maschke Susanna Buée Luc Lambert Jean-Charles Letenneur Luc Dartigues Jean-François |
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Institution: | INSERM, U897, Bordeaux, France. catherine.feart@isped.u-bordeaux2.fr |
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Abstract: | ObjectiveHerpes 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.MethodsThe 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 Aβ1–40 and Aβ1–42 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.ResultsAfter adjustment for study center, age, sex, education, and apolipoprotein E-e4 polymorphism, plasma Aβ1–42 and Aβ1–40 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 Aβ1–42 and β?=??132.7, P?=?0.002 for Aβ1–40; adjustment for CLU rs2279590, β?=??25.6, P?=?0.002 for Aβ1–42 and β?=??134.8, P?=?0.002 for Aβ1–40). No association between the plasma Aβ1–42-to-Aβ1–40 ratio and anti-HSV IgM or IgG were evidenced.ConclusionHigh anti-HSV IgM levels, markers of HSV reactivation, are associated with lower plasma Aβ1–40 and Aβ1–42 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. |
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