PT  - JOURNAL ARTICLE
AU  - M.H. Sombekke
AU  - M.M. Vellinga
AU  - B.M.J. Uitdehaag
AU  - F. Barkhof
AU  - C.H. Polman
AU  - D. Arteta
AU  - D. Tejedor
AU  - A. Martinez
AU  - J.B.A. Crusius
AU  - A.S. Peña
AU  - J.J.G. Geurts
AU  - H. Vrenken
TI  - Genetic Correlations of Brain Lesion Distribution in Multiple Sclerosis: An Exploratory Study
AID  - 10.3174/ajnr.A2352
DP  - 2011 Mar 23
TA  - American Journal of Neuroradiology
4099  - http://www.ajnr.org/content/early/2011/03/24/ajnr.A2352.short
4100  - http://www.ajnr.org/content/early/2011/03/24/ajnr.A2352.full
AB  - BACKGROUND AND PURPOSE: In MS, the total brain lesion volume and spatial distribution of lesions across the brain vary widely among individual patients. We hypothesized that spatial distribution may be partially driven by genetic predisposition, and we aimed to explore relations among candidate genes and the spatial distribution of white matter brain lesions in MS. MATERIAL AND METHODS: Genotypes of 69 SNPs in 208 patients with MS were related to the spatial distribution of T2 brain lesions. Lesions were manually outlined on MR images, and binary lesion masks were produced and registered to a common space. With Randomise software, the lesion masks were related to genotype by using a voxelwise nonparametric GLM approach, followed by clusterwise analysis. We used a DNA chip with SNPs selected from the literature on MS susceptibility, severity, and phenotypes. RESULTS: For 11 of these SNPs, 1 of the genotypes expressed significant clusters of increased or decreased lesion probability in varying, predominantly periventricular, brain regions. When we statistically controlled the voxelwise analyses for effects of total brain lesion volume, only 1 SNP remained significant: rs2227139, located within the MHC class II region. This SNP retained its periventricular cluster of significantly increased lesion probability for the heterozygote genotype. CONCLUSIONS: Heterozygosity of rs2227139 (MHC class II region) is associated with increased right frontal periventricular lesion probability (P < .01). Ten other SNPs showed associations between genotype and spatial lesion distribution that are partly explained by total lesion volume.