Dataset Information

Association of low-frequency and rare coding variants with information processing speed.

ABSTRACT: Measures of information processing speed vary between individuals and decline with age. Studies of aging twins suggest heritability may be as high as 67%. The Illumina HumanExome Bead Chip genotyping array was used to examine the association of rare coding variants with performance on the Digit-Symbol Substitution Test (DSST) in community-dwelling adults participating in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. DSST scores were available for 30,576 individuals of European ancestry from nine cohorts and for 5758 individuals of African ancestry from four cohorts who were older than 45 years and free of dementia and clinical stroke. Linear regression models adjusted for age and gender were used for analysis of single genetic variants, and the T5, T1, and T01 burden tests that aggregate the number of rare alleles by gene were also applied. Secondary analyses included further adjustment for education. Meta-analyses to combine cohort-specific results were carried out separately for each ancestry group. Variants in RNF19A reached the threshold for statistical significance (p = 2.01 × 10^-6) using the T01 test in individuals of European descent. RNF19A belongs to the class of E3 ubiquitin ligases that confer substrate specificity when proteins are ubiquitinated and targeted for degradation through the 26S proteasome. Variants in SLC22A7 and OR51A7 were suggestively associated with DSST scores after adjustment for education for African-American participants and in the European cohorts, respectively. Further functional characterization of its substrates will be required to confirm the role of RNF19A in cognitive function.

SUBMITTER: Bressler J

PROVIDER: S-EPMC8643353 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature

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Association of low-frequency and rare coding variants with information processing speed.

Bressler Jan J Davies Gail G Smith Albert V AV Saba Yasaman Y Bis Joshua C JC Jian Xueqiu X Hayward Caroline C Yanek Lisa L Smith Jennifer A JA Mirza Saira S SS Wang Ruiqi R Adams Hieab H H HHH Becker Diane D Boerwinkle Eric E Campbell Archie A Cox Simon R SR Eiriksdottir Gudny G Fawns-Ritchie Chloe C Gottesman Rebecca F RF Grove Megan L ML Guo Xiuqing X Hofer Edith E Kardia Sharon L R SLR Knol Maria J MJ Koini Marisa M Lopez Oscar L OL Marioni Riccardo E RE Nyquist Paul P Pattie Alison A Polasek Ozren O Porteous David J DJ Rudan Igor I Satizabal Claudia L CL Schmidt Helena H Schmidt Reinhold R Sidney Stephen S Simino Jeannette J Smith Blair H BH Turner Stephen T ST van der Lee Sven J SJ Ware Erin B EB Whitmer Rachel A RA Yaffe Kristine K Yang Qiong Q Zhao Wei W Gudnason Vilmundur V Launer Lenore J LJ Fitzpatrick Annette L AL Psaty Bruce M BM Fornage Myriam M Arfan Ikram M M van Duijn Cornelia M CM Seshadri Sudha S Mosley Thomas H TH Deary Ian J IJ

Translational psychiatry 20211204 1

Measures of information processing speed vary between individuals and decline with age. Studies of aging twins suggest heritability may be as high as 67%. The Illumina HumanExome Bead Chip genotyping array was used to examine the association of rare coding variants with performance on the Digit-Symbol Substitution Test (DSST) in community-dwelling adults participating in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. DSST scores were available for 30,576 in ...[more]

PMID: 34864818

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Project description:Genome-wide association studies (GWASs) have identified loci contributing to total serum bilirubin level. However, no exome-wide approaches have been performed to address this question. Using exome-wide approach, we assessed the influence of protein-coding variants on unconjugated, conjugated, and total serum bilirubin levels in a well-characterized cohort of 773 ambulatory elderly subjects from Italy. Coding variants were replicated in 227 elderly subjects from the same area. We identified 4 missense rare (minor allele frequency, MAF < 0.5%) and low-frequency (MAF, 0.5%-5%) coding variants located in the first exon of the UGT1A1 gene, which encodes for the substrate-binding domain (rs4148323 [MAF = 0.06%; p.Gly71Arg], rs144398951 [MAF = 0.06%; p.Ile215Val], rs35003977 [MAF = 0.78%; p.Val225Gly], and rs57307513 [MAF = 0.06%; p.Ser250Pro]). These variants were in strong linkage disequilibrium with 3 intronic UGT1A1 variants (rs887829, rs4148325, rs6742078), which were significantly associated with total bilirubin level (P = 2.34 × 10(-34), P = 7.02 × 10(-34), and P = 8.27 × 10(-34)), as well as unconjugated, and conjugated bilirubin levels. We also identified UGT1A6 variants in association with total (rs6759892, p.Ser7Ala, P = 1.98 × 10(-26); rs2070959, p.Thr181Ala, P = 2.87 × 10(-27); and rs1105879, p.Arg184Ser, P = 3.27 × 10(-29)), unconjugated, and conjugated bilirubin levels. All UGT1A1 intronic variants (rs887829, rs6742078, and rs4148325) and UGT1A6 coding variants (rs6759892, rs2070959, and rs1105879) were significantly associated with gallstone-related cholecystectomy risk. The UGT1A6 variant rs2070959 (p.Thr181Ala) was associated with the highest risk of gallstone-related cholecystectomy (OR, 4.58; 95% CI, 1.58-13.28; P = 3.21 × 10(-3)). Using an exome-wide approach we identified coding variants on UGT1A1 and UGT1A6 genes in association with serum bilirubin level and hyperbilirubinemia risk in elderly subjects. UGT1A1 intronic single-nucleotide polymorphisms (SNPs) (rs6742078, rs887829, rs4148324) serve as proxy markers for the low-frequency and rare UGT1A1 variants, thereby providing mechanistic explanation to the relationship between UGT1A1 intronic SNPs and the UGT1A1 enzyme activity. UGT1A1 and UGT1A6 variants might be potentially associated with gallstone-related cholecystectomy risk.

Dataset Information

Association of low-frequency and rare coding variants with information processing speed.

Publications

Association of low-frequency and rare coding variants with information processing speed.

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