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GWAS Study

Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.

Teslovich TM, Kim DS, Yin X et al.

29481666 PubMed ID
GWAS Study Type
11136 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TT
Teslovich TM
KD
Kim DS
YX
Yin X
SA
Stancáková A
JA
Jackson AU
WM
Wielscher M
NA
Naj A
PJ
Perry JRB
HJ
Huyghe JR
SH
Stringham HM
DJ
Davis JP
RC
Raulerson CK
WR
Welch RP
FC
Fuchsberger C
LA
Locke AE
SX
Sim X
CP
Chines PS
NN
Narisu N
KA
Kangas AJ
SP
Soininen P
AM
Ala-Korpela M
GV
Gudnason V
MS
Musani SK
JM
Jarvelin MR
SG
Schellenberg GD
SE
Speliotes EK
KJ
Kuusisto J
CF
Collins FS
BM
Boehnke M
LM
Laakso M
MK
Mohlke KL
Chapter II

Abstract

Summary of the research findings

Comprehensive metabolite profiling captures many highly heritable traits, including amino acid levels, which are potentially sensitive biomarkers for disease pathogenesis. To better understand the contribution of genetic variation to amino acid levels, we performed single variant and gene-based tests of association between nine serum amino acids (alanine, glutamine, glycine, histidine, isoleucine, leucine, phenylalanine, tyrosine, and valine) and 16.6 million genotyped and imputed variants in 8545 non-diabetic Finnish men from the METabolic Syndrome In Men (METSIM) study with replication in Northern Finland Birth Cohort (NFBC1966). We identified five novel loci associated with amino acid levels (P = < 5×10-8): LOC157273/PPP1R3B with glycine (rs9987289, P = 2.3×10-26); ZFHX3 (chr16:73326579, minor allele frequency (MAF) = 0.42%, P = 3.6×10-9), LIPC (rs10468017, P = 1.5×10-8), and WWOX (rs9937914, P = 3.8×10-8) with alanine; and TRIB1 with tyrosine (rs28601761, P = 8×10-9). Gene-based tests identified two novel genes harboring missense variants of MAF <1% that show aggregate association with amino acid levels: PYCR1 with glycine (Pgene = 1.5×10-6) and BCAT2 with valine (Pgene = 7.4×10-7); neither gene was implicated by single variant association tests. These findings are among the first applications of gene-based tests to identify new loci for amino acid levels. In addition to the seven novel gene associations, we identified five independent signals at established amino acid loci, including two rare variant signals at GLDC (rs138640017, MAF=0.95%, Pconditional = 5.8×10-40) with glycine levels and HAL (rs141635447, MAF = 0.46%, Pconditional = 9.4×10-11) with histidine levels. Examination of all single variant association results in our data revealed a strong inverse relationship between effect size and MAF (Ptrend<0.001). These novel signals provide further insight into the molecular mechanisms of amino acid metabolism and potentially, their perturbations in disease.

8,545 Finnish ancestry males

Chapter III

Study Statistics

Key metrics and study information

11136
Total Participants
GWAS
Study Type
Yes
Replicated
2,591 Finnish ancestry individuals
Replication Participants
European
Ancestry
Finland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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