Literature DB >> 23067351

High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.

Laura J Rasmussen-Torvik1, Jennifer A Pacheco, Russell A Wilke, William K Thompson, Marylyn D Ritchie, Abel N Kho, Arun Muthalagu, M Geoff Hayes, Loren L Armstrong, Douglas A Scheftner, John T Wilkins, Rebecca L Zuvich, David Crosslin, Dan M Roden, Joshua C Denny, Gail P Jarvik, Christopher S Carlson, Iftikhar J Kullo, Suzette J Bielinski, Catherine A McCarty, Rongling Li, Teri A Manolio, Dana C Crawford, Rex L Chisholm.   

Abstract

Only one low-density lipoprotein cholesterol (LDL-C) genome-wide association study (GWAS) has been previously reported in -African Americans. We performed a GWAS of LDL-C in African Americans using data extracted from electronic medical records (EMR) in the eMERGE network. African Americans were genotyped on the Illumina 1M chip. All LDL-C measurements, prescriptions, and diagnoses of concomitant disease were extracted from EMR. We created two analytic datasets; one dataset having median LDL-C calculated after the exclusion of some lab values based on comorbidities and medication (n= 618) and another dataset having median LDL-C calculated without any exclusions (n= 1,249). SNP rs7412 in APOE was strongly associated with LDL-C in both datasets (p < 5 × 10(-8) ). In the dataset with exclusions, a decrease of 20.0 mg/dL per minor allele was observed. The effect size was attenuated (12.3 mg/dL) in the dataset without any lab values excluded. Although other signals in APOE have been detected in previous GWAS, this large and important SNP association has not been well detected in large GWAS because rs7412 was not included on many genotyping arrays. Use of median LDL-C extracted from EMR after exclusions for medications and comorbidities increased the percentage of trait variance explained by genetic variation.
© 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23067351      PMCID: PMC3521536          DOI: 10.1111/j.1752-8062.2012.00446.x

Source DB:  PubMed          Journal:  Clin Transl Sci        ISSN: 1752-8054            Impact factor:   4.689


  31 in total

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3.  Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.

Authors:  Joshua C Denny; Dana C Crawford; Marylyn D Ritchie; Suzette J Bielinski; Melissa A Basford; Yuki Bradford; High Seng Chai; Lisa Bastarache; Rebecca Zuvich; Peggy Peissig; David Carrell; Andrea H Ramirez; Jyotishman Pathak; Russell A Wilke; Luke Rasmussen; Xiaoming Wang; Jennifer A Pacheco; Abel N Kho; M Geoffrey Hayes; Noah Weston; Martha Matsumoto; Peter A Kopp; Katherine M Newton; Gail P Jarvik; Rongling Li; Teri A Manolio; Iftikhar J Kullo; Christopher G Chute; Rex L Chisholm; Eric B Larson; Catherine A McCarty; Daniel R Masys; Dan M Roden; Mariza de Andrade
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Review 4.  Association of apolipoprotein E genotypes with lipid levels and coronary risk.

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6.  Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

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Journal:  Nat Genet       Date:  2008-12-07       Impact factor: 38.330

7.  Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Authors:  Stephen D Turner; Richard L Berg; James G Linneman; Peggy L Peissig; Dana C Crawford; Joshua C Denny; Dan M Roden; Catherine A McCarty; Marylyn D Ritchie; Russell A Wilke
Journal:  PLoS One       Date:  2011-05-11       Impact factor: 3.240

8.  Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability.

Authors:  Serena Sanna; Bingshan Li; Antonella Mulas; Carlo Sidore; Hyun M Kang; Anne U Jackson; Maria Grazia Piras; Gianluca Usala; Giuseppe Maninchedda; Alessandro Sassu; Fabrizio Serra; Maria Antonietta Palmas; William H Wood; Inger Njølstad; Markku Laakso; Kristian Hveem; Jaakko Tuomilehto; Timo A Lakka; Rainer Rauramaa; Michael Boehnke; Francesco Cucca; Manuela Uda; David Schlessinger; Ramaiah Nagaraja; Gonçalo R Abecasis
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9.  Newly identified loci that influence lipid concentrations and risk of coronary artery disease.

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Journal:  Nat Genet       Date:  2008-01-13       Impact factor: 38.330

10.  Common variants at 30 loci contribute to polygenic dyslipidemia.

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Journal:  Nat Genet       Date:  2008-12-07       Impact factor: 38.330

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  33 in total

1.  Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.

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Journal:  Eur J Hum Genet       Date:  2015-07-01       Impact factor: 4.246

2.  Development of reusable logic for determination of statin exposure-time from electronic health records.

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3.  PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.

Authors:  Jacqueline C Kirby; Peter Speltz; Luke V Rasmussen; Melissa Basford; Omri Gottesman; Peggy L Peissig; Jennifer A Pacheco; Gerard Tromp; Jyotishman Pathak; David S Carrell; Stephen B Ellis; Todd Lingren; Will K Thompson; Guergana Savova; Jonathan Haines; Dan M Roden; Paul A Harris; Joshua C Denny
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4.  Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.

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5.  Association of exome sequences with plasma C-reactive protein levels in >9000 participants.

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Review 6.  Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.

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7.  Common Genetic Variants Influence Circulating Vitamin D Levels in Inflammatory Bowel Diseases.

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Review 8.  Pleiotropy in complex traits: challenges and strategies.

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