Genome-wide analysis study of gestational diabetes mellitus and related pathogenic factors in a Chinese Han population

Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and gluco...

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Published inBMC pregnancy and childbirth Vol. 23; no. 1; pp. 856 - 9
Main Authors Yue, Shufan, Pei, Ling, Lai, Fenghua, Xiao, Huangmeng, Li, Zeting, Zeng, Rui, Chen, Li, Chen, Wenzhan, Liu, Huiling, Li, Yanbing, Xiao, Haipeng, Cao, Xiaopei
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Abstract Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and glucose traits remain limited in China. This study aimed to identify genes associated with GDM susceptibility in Chinese Han women and validate those findings using clinical data during pregnancy and postpartum period. A genome-wide association study (GWAS) of 398 Chinese Han women (199 each with and without GDM) was conducted and associations between single nucleotide polymorphisms (SNPs) and glucose metabolism were identified by searching public databases. Relationships between filtered differential SNPs and glucose metabolism were verified using clinical data during pregnancy. The GDM group were followed up postpartum to evaluate the progression of glucose metabolism. We identified five novel SNPs with genome-wide significant associations with GDM: rs62069863 in TRPV3 gene and rs2232016 in PRMT6 gene were positive correlated with 1 h plasma glucose (1hPG) and 2 h plasma glucose (2hPG), rs1112718 in HHEX/EXOC6 gene and rs10460009 in LPIN2 gene were positive associated with fasting plasma glucose, 1hPG and 2hPG, rs927316 in GLIS3 gene was negative correlated with 2hPG. Of the 166 GDM women followed up postpartum, rs62069863 in TRPV3 gene was positively associated with fasting insulin, homoeostasis model assessment of insulin resistance. The variants of rs62069863 in TRPV3 gene, rs2232016 in PRMT6 gene, rs1112718 in HHEX/EXOC6 gene, rs927316 in GLIS3 gene, and rs10460009 in LPIN2 gene were newly-identified susceptibility loci for GDM in the Chinese Han population. TRPV3 was associated with worse insulin resistance postpartum. This study was registered in the Chinese Clinical Trial Registry. ChiCTR2100043762. Date of first registration: 28/02/2021.
AbstractList BackgroundGestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and glucose traits remain limited in China. This study aimed to identify genes associated with GDM susceptibility in Chinese Han women and validate those findings using clinical data during pregnancy and postpartum period.MethodsA genome-wide association study (GWAS) of 398 Chinese Han women (199 each with and without GDM) was conducted and associations between single nucleotide polymorphisms (SNPs) and glucose metabolism were identified by searching public databases. Relationships between filtered differential SNPs and glucose metabolism were verified using clinical data during pregnancy. The GDM group were followed up postpartum to evaluate the progression of glucose metabolism.ResultsWe identified five novel SNPs with genome-wide significant associations with GDM: rs62069863 in TRPV3 gene and rs2232016 in PRMT6 gene were positive correlated with 1 h plasma glucose (1hPG) and 2 h plasma glucose (2hPG), rs1112718 in HHEX/EXOC6 gene and rs10460009 in LPIN2 gene were positive associated with fasting plasma glucose, 1hPG and 2hPG, rs927316 in GLIS3 gene was negative correlated with 2hPG. Of the 166 GDM women followed up postpartum, rs62069863 in TRPV3 gene was positively associated with fasting insulin, homoeostasis model assessment of insulin resistance.ConclusionsThe variants of rs62069863 in TRPV3 gene, rs2232016 in PRMT6 gene, rs1112718 in HHEX/EXOC6 gene, rs927316 in GLIS3 gene, and rs10460009 in LPIN2 gene were newly-identified susceptibility loci for GDM in the Chinese Han population. TRPV3 was associated with worse insulin resistance postpartum.Trial registrationThis study was registered in the Chinese Clinical Trial Registry. Trial registration number: ChiCTR2100043762. Date of first registration: 28/02/2021.
Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and glucose traits remain limited in China. This study aimed to identify genes associated with GDM susceptibility in Chinese Han women and validate those findings using clinical data during pregnancy and postpartum period. A genome-wide association study (GWAS) of 398 Chinese Han women (199 each with and without GDM) was conducted and associations between single nucleotide polymorphisms (SNPs) and glucose metabolism were identified by searching public databases. Relationships between filtered differential SNPs and glucose metabolism were verified using clinical data during pregnancy. The GDM group were followed up postpartum to evaluate the progression of glucose metabolism. We identified five novel SNPs with genome-wide significant associations with GDM: rs62069863 in TRPV3 gene and rs2232016 in PRMT6 gene were positive correlated with 1 h plasma glucose (1hPG) and 2 h plasma glucose (2hPG), rs1112718 in HHEX/EXOC6 gene and rs10460009 in LPIN2 gene were positive associated with fasting plasma glucose, 1hPG and 2hPG, rs927316 in GLIS3 gene was negative correlated with 2hPG. Of the 166 GDM women followed up postpartum, rs62069863 in TRPV3 gene was positively associated with fasting insulin, homoeostasis model assessment of insulin resistance. The variants of rs62069863 in TRPV3 gene, rs2232016 in PRMT6 gene, rs1112718 in HHEX/EXOC6 gene, rs927316 in GLIS3 gene, and rs10460009 in LPIN2 gene were newly-identified susceptibility loci for GDM in the Chinese Han population. TRPV3 was associated with worse insulin resistance postpartum. This study was registered in the Chinese Clinical Trial Registry. ChiCTR2100043762. Date of first registration: 28/02/2021.
Abstract Background Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and glucose traits remain limited in China. This study aimed to identify genes associated with GDM susceptibility in Chinese Han women and validate those findings using clinical data during pregnancy and postpartum period. Methods A genome-wide association study (GWAS) of 398 Chinese Han women (199 each with and without GDM) was conducted and associations between single nucleotide polymorphisms (SNPs) and glucose metabolism were identified by searching public databases. Relationships between filtered differential SNPs and glucose metabolism were verified using clinical data during pregnancy. The GDM group were followed up postpartum to evaluate the progression of glucose metabolism. Results We identified five novel SNPs with genome-wide significant associations with GDM: rs62069863 in TRPV3 gene and rs2232016 in PRMT6 gene were positive correlated with 1 h plasma glucose (1hPG) and 2 h plasma glucose (2hPG), rs1112718 in HHEX/EXOC6 gene and rs10460009 in LPIN2 gene were positive associated with fasting plasma glucose, 1hPG and 2hPG, rs927316 in GLIS3 gene was negative correlated with 2hPG. Of the 166 GDM women followed up postpartum, rs62069863 in TRPV3 gene was positively associated with fasting insulin, homoeostasis model assessment of insulin resistance. Conclusions The variants of rs62069863 in TRPV3 gene, rs2232016 in PRMT6 gene, rs1112718 in HHEX/EXOC6 gene, rs927316 in GLIS3 gene, and rs10460009 in LPIN2 gene were newly-identified susceptibility loci for GDM in the Chinese Han population. TRPV3 was associated with worse insulin resistance postpartum. Trial registration This study was registered in the Chinese Clinical Trial Registry. Trial registration number: ChiCTR2100043762. Date of first registration: 28/02/2021.
Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and glucose traits remain limited in China. This study aimed to identify genes associated with GDM susceptibility in Chinese Han women and validate those findings using clinical data during pregnancy and postpartum period.BACKGROUNDGestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the pathogenesis of GDM, and associations vary by ethnicity. However, related studies about the relationship between the susceptibility genes and glucose traits remain limited in China. This study aimed to identify genes associated with GDM susceptibility in Chinese Han women and validate those findings using clinical data during pregnancy and postpartum period.A genome-wide association study (GWAS) of 398 Chinese Han women (199 each with and without GDM) was conducted and associations between single nucleotide polymorphisms (SNPs) and glucose metabolism were identified by searching public databases. Relationships between filtered differential SNPs and glucose metabolism were verified using clinical data during pregnancy. The GDM group were followed up postpartum to evaluate the progression of glucose metabolism.METHODSA genome-wide association study (GWAS) of 398 Chinese Han women (199 each with and without GDM) was conducted and associations between single nucleotide polymorphisms (SNPs) and glucose metabolism were identified by searching public databases. Relationships between filtered differential SNPs and glucose metabolism were verified using clinical data during pregnancy. The GDM group were followed up postpartum to evaluate the progression of glucose metabolism.We identified five novel SNPs with genome-wide significant associations with GDM: rs62069863 in TRPV3 gene and rs2232016 in PRMT6 gene were positive correlated with 1 h plasma glucose (1hPG) and 2 h plasma glucose (2hPG), rs1112718 in HHEX/EXOC6 gene and rs10460009 in LPIN2 gene were positive associated with fasting plasma glucose, 1hPG and 2hPG, rs927316 in GLIS3 gene was negative correlated with 2hPG. Of the 166 GDM women followed up postpartum, rs62069863 in TRPV3 gene was positively associated with fasting insulin, homoeostasis model assessment of insulin resistance.RESULTSWe identified five novel SNPs with genome-wide significant associations with GDM: rs62069863 in TRPV3 gene and rs2232016 in PRMT6 gene were positive correlated with 1 h plasma glucose (1hPG) and 2 h plasma glucose (2hPG), rs1112718 in HHEX/EXOC6 gene and rs10460009 in LPIN2 gene were positive associated with fasting plasma glucose, 1hPG and 2hPG, rs927316 in GLIS3 gene was negative correlated with 2hPG. Of the 166 GDM women followed up postpartum, rs62069863 in TRPV3 gene was positively associated with fasting insulin, homoeostasis model assessment of insulin resistance.The variants of rs62069863 in TRPV3 gene, rs2232016 in PRMT6 gene, rs1112718 in HHEX/EXOC6 gene, rs927316 in GLIS3 gene, and rs10460009 in LPIN2 gene were newly-identified susceptibility loci for GDM in the Chinese Han population. TRPV3 was associated with worse insulin resistance postpartum.CONCLUSIONSThe variants of rs62069863 in TRPV3 gene, rs2232016 in PRMT6 gene, rs1112718 in HHEX/EXOC6 gene, rs927316 in GLIS3 gene, and rs10460009 in LPIN2 gene were newly-identified susceptibility loci for GDM in the Chinese Han population. TRPV3 was associated with worse insulin resistance postpartum.This study was registered in the Chinese Clinical Trial Registry.TRIAL REGISTRATIONThis study was registered in the Chinese Clinical Trial Registry.ChiCTR2100043762. Date of first registration: 28/02/2021.TRIAL REGISTRATION NUMBERChiCTR2100043762. Date of first registration: 28/02/2021.
ArticleNumber 856
Author Yue, Shufan
Liu, Huiling
Cao, Xiaopei
Li, Zeting
Xiao, Haipeng
Pei, Ling
Zeng, Rui
Lai, Fenghua
Xiao, Huangmeng
Chen, Li
Chen, Wenzhan
Li, Yanbing
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CitedBy_id crossref_primary_10_1021_acs_est_4c03221
crossref_primary_10_3390_metabo14090508
crossref_primary_10_3390_ani14192874
crossref_primary_10_2174_0118715303288107240227074611
crossref_primary_10_1210_clinem_dgae838
Cites_doi 10.1007/s00439-011-1080-z
10.3390/nu14081543
10.2337/dc09-1848
10.1111/acer.13888
10.1038/nature15394
10.1038/s41598-020-78164-x
10.1016/j.febslet.2009.05.039
10.2337/db12-1692
10.2337/db13-0949
10.1530/JME-16-0232
10.1016/j.stem.2022.12.003
10.1186/s12944-020-01398-1
10.3389/fnut.2022.919357
10.1126/scisignal.2004479
10.1038/s41572-019-0098-8
10.1210/en.2014-1831
10.1186/s12933-016-0338-0
10.1164/rccm.201408-1426OC
10.1038/s41588-018-0241-6
10.1038/nature24277
10.1007/s00125-018-4637-8
10.1371/journal.pgen.1003532
10.1016/j.bbrc.2015.08.069
10.1152/ajpcell.00210.2017
10.1093/database/baaa030
10.2337/db11-1034
10.1093/nar/gkp122
10.5582/bst.2016.01226
10.2337/db07-0338
10.2337/dc18-1646
10.1515/cclm-2021-0643
10.21873/invivo.11621
10.12688/wellcomeopenres.17294.1
10.1016/j.cca.2021.09.004
10.1007/s10815-023-02843-7
10.1080/15548627.2019.1569931
10.1074/jbc.REV119.008351
10.3390/jcm11102737
10.1200/JCO.2008.18.7906
10.3389/fimmu.2023.1197490
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Issue 1
Keywords Gestational Diabetes Mellitus
GWAS
SNP
Susceptibility gene
Language English
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References K Goueslard (6167_CR4) 2016; 15
AS Dimas (6167_CR26) 2014; 63
E Jamaspishvili (6167_CR23) 2019; 66
X Sun (6167_CR10) 2021; 523
GTEx Consortium (6167_CR21) 2017; 550
SY Cheung (6167_CR31) 2015; 156
SH Kwak (6167_CR13) 2012; 61
HD McIntyre (6167_CR3) 2019; 5
XM Zhang (6167_CR9) 2020; 10
Y Cheng (6167_CR37) 2023; 30
M Skrzypski (6167_CR32) 2017; 11
E Vitacolonna (6167_CR11) 2022; 14
S He (6167_CR16) 2023; 40
BE Metzger (6167_CR15) 2010; 33
E Israel (6167_CR20) 2015; 191
YS Aulchenko (6167_CR41) 2007; 56
N Sriboonvorakul (6167_CR8) 2022; 11
HAPO Study Cooperative Research Group (6167_CR1) 2009; 358
Z Li (6167_CR6) 2020; 2020
Y Liu (6167_CR12) 2022; 11
X Wen (6167_CR28) 2017; 58
HS Han (6167_CR35) 2014; 7
MJ Ahn (6167_CR19) 2012; 131
B Matli (6167_CR17) 2021; 59
YS Yang (6167_CR29) 2009; 37
A Klip (6167_CR40) 2019; 294
KS Jung (6167_CR43) 2020; 2020
TC Nogueira (6167_CR30) 2013; 9
B Zhong (6167_CR33) 2019; 33
S Choi (6167_CR36) 2019; 15
M Ding (6167_CR22) 2018; 61
WL Lowe Jr (6167_CR2) 2019; 42
PH Sudmant (6167_CR42) 2015; 526
C Wang (6167_CR7) 2020; 35
D Major-Smith (6167_CR44) 2023; 6
A Mahajan (6167_CR38) 2018; 50
H Sano (6167_CR39) 2015; 465
MG Hayes (6167_CR14) 2013; 62
T Sawatani (6167_CR34) 2019; 316
N Watanabe (6167_CR27) 2009; 583
S Park (6167_CR25) 2018; 42
YT Huang (6167_CR18) 2009; 27
L Pei (6167_CR5) 2020; 19
JT Jackson (6167_CR24) 2023; 14
References_xml – volume: 131
  start-page: 365
  year: 2012
  ident: 6167_CR19
  publication-title: Hum Genet
  doi: 10.1007/s00439-011-1080-z
– volume: 14
  start-page: 1543
  year: 2022
  ident: 6167_CR11
  publication-title: Nutrients
  doi: 10.3390/nu14081543
– volume: 33
  start-page: 676
  year: 2010
  ident: 6167_CR15
  publication-title: Diabetes Care
  doi: 10.2337/dc09-1848
– volume: 42
  start-page: 2326
  year: 2018
  ident: 6167_CR25
  publication-title: Alcohol Clin Exp Res
  doi: 10.1111/acer.13888
– volume: 526
  start-page: 75
  year: 2015
  ident: 6167_CR42
  publication-title: Nature
  doi: 10.1038/nature15394
– volume: 10
  start-page: 21223
  year: 2020
  ident: 6167_CR9
  publication-title: Sci Rep
  doi: 10.1038/s41598-020-78164-x
– volume: 583
  start-page: 2108
  year: 2009
  ident: 6167_CR27
  publication-title: FEBS Lett
  doi: 10.1016/j.febslet.2009.05.039
– volume: 62
  start-page: 3282
  year: 2013
  ident: 6167_CR14
  publication-title: Diabetes
  doi: 10.2337/db12-1692
– volume: 63
  start-page: 2158
  year: 2014
  ident: 6167_CR26
  publication-title: Diabetes
  doi: 10.2337/db13-0949
– volume: 58
  start-page: R73
  year: 2017
  ident: 6167_CR28
  publication-title: J Mol Endocrinol
  doi: 10.1530/JME-16-0232
– volume: 30
  start-page: 69
  year: 2023
  ident: 6167_CR37
  publication-title: Cell Stem Cell
  doi: 10.1016/j.stem.2022.12.003
– volume: 19
  start-page: 220
  year: 2020
  ident: 6167_CR5
  publication-title: Lipids Health Dis
  doi: 10.1186/s12944-020-01398-1
– volume: 11
  start-page: 919357
  year: 2022
  ident: 6167_CR12
  publication-title: Front Nutr
  doi: 10.3389/fnut.2022.919357
– volume: 7
  start-page: ra19
  year: 2014
  ident: 6167_CR35
  publication-title: Sci Signal
  doi: 10.1126/scisignal.2004479
– volume: 5
  start-page: 47
  year: 2019
  ident: 6167_CR3
  publication-title: Nat Rev Dis Prim
  doi: 10.1038/s41572-019-0098-8
– volume: 35
  start-page: 1
  year: 2020
  ident: 6167_CR7
  publication-title: J Matern Fetal Neonatal Med
– volume: 156
  start-page: 2074
  year: 2015
  ident: 6167_CR31
  publication-title: Endocrinology
  doi: 10.1210/en.2014-1831
– volume: 15
  start-page: 15
  year: 2016
  ident: 6167_CR4
  publication-title: Cardiovasc Diabetol
  doi: 10.1186/s12933-016-0338-0
– volume: 191
  start-page: 530
  year: 2015
  ident: 6167_CR20
  publication-title: Am J Respir Crit Care Med
  doi: 10.1164/rccm.201408-1426OC
– volume: 50
  start-page: 1505
  year: 2018
  ident: 6167_CR38
  publication-title: Nat Genet
  doi: 10.1038/s41588-018-0241-6
– volume: 550
  start-page: 204
  year: 2017
  ident: 6167_CR21
  publication-title: Nature
  doi: 10.1038/nature24277
– volume: 61
  start-page: 1758
  year: 2018
  ident: 6167_CR22
  publication-title: Diabetologia
  doi: 10.1007/s00125-018-4637-8
– volume: 9
  start-page: e1003532
  year: 2013
  ident: 6167_CR30
  publication-title: PLoS Genet
  doi: 10.1371/journal.pgen.1003532
– volume: 465
  start-page: 601
  year: 2015
  ident: 6167_CR39
  publication-title: Biochem Biophys Res Commun
  doi: 10.1016/j.bbrc.2015.08.069
– volume: 316
  start-page: C434
  year: 2019
  ident: 6167_CR34
  publication-title: Am J Physiol Cell Physiol
  doi: 10.1152/ajpcell.00210.2017
– volume: 2020
  start-page: baaa030
  year: 2020
  ident: 6167_CR43
  publication-title: Database (Oxford)
  doi: 10.1093/database/baaa030
– volume: 61
  start-page: 531
  year: 2012
  ident: 6167_CR13
  publication-title: Diabetes
  doi: 10.2337/db11-1034
– volume: 37
  start-page: 2529
  year: 2009
  ident: 6167_CR29
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gkp122
– volume: 11
  start-page: 9
  year: 2017
  ident: 6167_CR32
  publication-title: Biosci Trends
  doi: 10.5582/bst.2016.01226
– volume: 56
  start-page: 3020
  year: 2007
  ident: 6167_CR41
  publication-title: Diabetes
  doi: 10.2337/db07-0338
– volume: 42
  start-page: 372
  year: 2019
  ident: 6167_CR2
  publication-title: Diabetes Care
  doi: 10.2337/dc18-1646
– volume: 59
  start-page: 1844
  year: 2021
  ident: 6167_CR17
  publication-title: Clin Chem Lab Med
  doi: 10.1515/cclm-2021-0643
– volume: 33
  start-page: 1431
  year: 2019
  ident: 6167_CR33
  publication-title: In Vivo
  doi: 10.21873/invivo.11621
– volume: 6
  start-page: 283
  year: 2023
  ident: 6167_CR44
  publication-title: Wellcome Open Res
  doi: 10.12688/wellcomeopenres.17294.1
– volume: 523
  start-page: 87
  year: 2021
  ident: 6167_CR10
  publication-title: Clin Chim Acta
  doi: 10.1016/j.cca.2021.09.004
– volume: 40
  start-page: 1983
  year: 2023
  ident: 6167_CR16
  publication-title: J Assist Reprod Genet
  doi: 10.1007/s10815-023-02843-7
– volume: 15
  start-page: 1069
  year: 2019
  ident: 6167_CR36
  publication-title: Autophagy
  doi: 10.1080/15548627.2019.1569931
– volume: 294
  start-page: 11369
  year: 2019
  ident: 6167_CR40
  publication-title: J Biol Chem
  doi: 10.1074/jbc.REV119.008351
– volume: 11
  start-page: 2737
  issue: 10
  year: 2022
  ident: 6167_CR8
  publication-title: J Clin Med
  doi: 10.3390/jcm11102737
– volume: 27
  start-page: 2660
  year: 2009
  ident: 6167_CR18
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2008.18.7906
– volume: 358
  start-page: 1991
  year: 2009
  ident: 6167_CR1
  publication-title: N Engl J Med
– volume: 2020
  start-page: 3076463
  year: 2020
  ident: 6167_CR6
  publication-title: J Diab Res
– volume: 66
  start-page: 679
  year: 2019
  ident: 6167_CR23
  publication-title: Acta Biochim Pol
– volume: 14
  start-page: 1197490
  year: 2023
  ident: 6167_CR24
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2023.1197490
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Snippet Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in the...
BackgroundGestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are important in...
Abstract Background Gestational diabetes mellitus (GDM) affects the metabolism of both the mother and fetus during and after pregnancy. Genetic factors are...
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SubjectTerms Blood Glucose - metabolism
Body mass index
Deoxyribonucleic acid
Diabetes, Gestational - epidemiology
DNA
Ethnicity
Female
Genes
Genome-Wide Association Study
Genomes
Gestational diabetes
Gestational Diabetes Mellitus
Glucose
Glucose - metabolism
GWAS
Humans
Insulin resistance
Insulin Resistance - genetics
Metabolism
Nuclear Proteins - genetics
Obesity
Plasma
Polymorphism, Single Nucleotide
Pregnancy
Protein-Arginine N-Methyltransferases - genetics
Quality control
Regression analysis
SNP
Susceptibility gene
Womens health
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Title Genome-wide analysis study of gestational diabetes mellitus and related pathogenic factors in a Chinese Han population
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