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• W2963119504 abstract "Abstract Objective We aimed to study the role of coding VPS13C variants in a large cohort of late-onset PD (LOPD) patients. Methods VPS13C and its untranslated regions were sequenced using targeted next-generation sequencing in 1,567 PD patients and 1,667 controls from 3 cohorts. Association tests of rare potential homozygous and compound heterozygous variants and burden tests for rare heterozygous variants were performed. Common variants were analyzed using logistic regression adjusted for age and sex in each of the cohorts, followed by a meta-analysis. Results No bi-allelic carriers of rare VPS13C variants were found among patients and two carriers of compound heterozygous variants were found in two controls. There was no statistically significant burden of rare (MAF<1%) or very rare (MAF<0.1%) coding VPS13C variants in PD. A VPS13C haplotype including the p.R153H-p.I398I-p.I1132V-p.Q2376Q variants was nominally associated with a reduced risk for PD (meta-analysis of the tagging SNP p.I1132V (OR=0.48, 95%CI=0.28-0.82, p =0.0052). This haplotype was not in linkage disequilibrium (LD) with the known genome-wide association study (GWAS) top hit. Conclusions Our results do not support a role for rare heterozygous or bi-allelic VPS13C variants in LOPD. Additional genetic replication and functional studies are needed to examine the role of the haplotype identified here associated with reduced risk for PD." @default.
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• W2963119504 date "2019-07-20" @default.
• W2963119504 modified "2023-10-01" @default.
• W2963119504 title "Analysis of common and rare <i>VPS13C</i> variants in late onset Parkinson disease" @default.
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• W2963119504 doi "https://doi.org/10.1101/705533" @default.
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