CRP gene haplotypes, serum CRP, and cerebral small-vessel disease: the Rotterdam Scan Study and the MEMO Study.

نویسندگان

  • Christiane Reitz
  • Klaus Berger
  • Moniek P M de Maat
  • Monika Stoll
  • Frauke Friedrichs
  • Isabella Kardys
  • Jacqueline C M Witteman
  • Monique M B Breteler
چکیده

BACKGROUND AND PURPOSE It remains unclear whether C-reactive protein (CRP) is a serum marker for atherothrombotic disease or a causal factor in the pathogenesis of atherosclerosis. We explored the association between CRP gene variations and cerebral small-vessel disease (SVD) in the Rotterdam Scan Study (N=1035) and the MEMO Study (N=268). METHODS Common haplotypes within the CRP gene were determined by genotype-tagging single-nucleotide polymorphisms. Then their relation with periventricular and subcortical white matter lesions and the prevalence of lacunar brain infarcts was explored by regression analyses. RESULTS There was no association between CRP haplotypes and measures of cerebral SVD in either study. There was no effect modification of the association between serum CRP levels and measures of SVD by CRP haplotypes. CONCLUSIONS Our observations suggest that CRP is not causally involved in the pathogenesis of SVD.

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عنوان ژورنال:
  • Stroke

دوره 38 8  شماره 

صفحات  -

تاریخ انتشار 2007