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- W2116731299 abstract "Abstract Introduction We recently showed that tagging single‐nucleotide polymorphisms across the SNCA locus were significantly associated with increased risk for Lewy body (LB) pathology in Alzheimer's disease (AD) cases. However, the actual genetic variant(s) that underlie the observed associations remain elusive. Methods We used a bioinformatics algorithm to catalog structural variants in a region of SNCA intron 4, followed by phased sequencing. We performed a genetic association analysis in autopsy series of LB variant of Alzheimer's disease (LBV/AD) cases compared with AD‐only controls. We investigated the biological functions by expression analysis using temporal‐cortex samples. Results We identified four distinct haplotypes within a highly polymorphic low‐complexity cytosine‐thymine (CT)‐rich region. We showed that a specific haplotype conferred risk to develop LBV/AD. We demonstrated that the CT‐rich site acts as an enhancer element, where the risk haplotype was significantly associated with elevated levels of SNCA messenger RNA. Discussion We have discovered a novel haplotype in a CT‐rich region in SNCA that contributes to LB pathology in AD patients, possibly via cis ‐regulation of the gene expression." @default.
- W2116731299 created "2016-06-24" @default.
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- W2116731299 date "2015-06-13" @default.
- W2116731299 modified "2023-10-16" @default.
- W2116731299 title "A cytosine‐thymine (CT)‐rich haplotype in intron 4 of <i>SNCA</i> confers risk for Lewy body pathology in Alzheimer's disease and affects <i>SNCA</i> expression" @default.
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- W2116731299 doi "https://doi.org/10.1016/j.jalz.2015.05.011" @default.
- W2116731299 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4630109" @default.
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