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Stroke. 2011 Nov;42(11):3297-9. doi: 10.1161/STROKEAHA.111.623090. Epub 2011 Aug 25.

Replication study of chr17q25 with cerebral white matter lesion volume.

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1
Department of Epidemiology, Erasmus MC University Medical Center, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.

Abstract

BACKGROUND AND PURPOSE:

Recently, the first genomewide association study on cerebral white matter lesion burden identified chr17q25 to be significantly associated with white matter lesions. We report on the first independent replication study of this genetic association.

METHODS:

In a population-based cohort study, we investigated the association between the 6 genomewide significant single nucleotide polymorphisms at that locus and cerebral white matter lesion volume on MRI, measured quantitatively, adjusted for age, sex, and intracranial volume. Adjustments for ApoE4 carriership and cardiovascular risk factors were evaluated separately. Finally, we performed a meta-analysis of all published data for the single most significant single nucleotide polymorphism, rs3744028.

RESULTS:

The risk alleles of all the 6 single nucleotide polymorphisms were significantly associated with white matter lesion volume with P=1.1*10(-3) for rs3744028, adjusted for age, sex, and intracranial volume. Additional adjustments only had minor influence on these associations. A meta-analysis with all published data for rs3744028 resulted in a probability value of 5.3*10(-17).

CONCLUSIONS:

This study further establishes chr17q25 as a novel genetic locus for WML volume.

PMID:
21868733
DOI:
10.1161/STROKEAHA.111.623090
[Indexed for MEDLINE]
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