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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 in: | BMC pregnancy and childbirth 2023-12, Vol.23 (1), p.856-856, Article 856 |
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description | 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. |
doi_str_mv | 10.1186/s12884-023-06167-3 |
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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.</description><identifier>ISSN: 1471-2393</identifier><identifier>EISSN: 1471-2393</identifier><identifier>DOI: 10.1186/s12884-023-06167-3</identifier><identifier>PMID: 38087213</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>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</subject><ispartof>BMC pregnancy and childbirth, 2023-12, Vol.23 (1), p.856-856, Article 856</ispartof><rights>2023. The Author(s).</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-f87b1a1b4b1ccf9870957d98979060df8f3c4f8b742b3c4dc59ef653eb2a5db03</citedby><cites>FETCH-LOGICAL-c564t-f87b1a1b4b1ccf9870957d98979060df8f3c4f8b742b3c4dc59ef653eb2a5db03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10714520/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2902116642?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38087213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yue, Shufan</creatorcontrib><creatorcontrib>Pei, Ling</creatorcontrib><creatorcontrib>Lai, Fenghua</creatorcontrib><creatorcontrib>Xiao, Huangmeng</creatorcontrib><creatorcontrib>Li, Zeting</creatorcontrib><creatorcontrib>Zeng, Rui</creatorcontrib><creatorcontrib>Chen, Li</creatorcontrib><creatorcontrib>Chen, Wenzhan</creatorcontrib><creatorcontrib>Liu, Huiling</creatorcontrib><creatorcontrib>Li, Yanbing</creatorcontrib><creatorcontrib>Xiao, Haipeng</creatorcontrib><creatorcontrib>Cao, Xiaopei</creatorcontrib><title>Genome-wide analysis study of gestational diabetes mellitus and related pathogenic factors in a Chinese Han population</title><title>BMC pregnancy and childbirth</title><addtitle>BMC Pregnancy Childbirth</addtitle><description>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.</description><subject>Blood Glucose - metabolism</subject><subject>Body mass index</subject><subject>Deoxyribonucleic acid</subject><subject>Diabetes, Gestational - epidemiology</subject><subject>DNA</subject><subject>Ethnicity</subject><subject>Female</subject><subject>Genes</subject><subject>Genome-Wide Association Study</subject><subject>Genomes</subject><subject>Gestational diabetes</subject><subject>Gestational Diabetes Mellitus</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>GWAS</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - genetics</subject><subject>Metabolism</subject><subject>Nuclear Proteins - genetics</subject><subject>Obesity</subject><subject>Plasma</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Pregnancy</subject><subject>Protein-Arginine N-Methyltransferases - genetics</subject><subject>Quality control</subject><subject>Regression analysis</subject><subject>SNP</subject><subject>Susceptibility gene</subject><subject>Womens health</subject><issn>1471-2393</issn><issn>1471-2393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1vEzEQhlcIREvhD3BAlrhwWfDX-uOEUARtpUpc4Gx57XHiaLMOtrdV_j1uUqqW04xm3nk0Hr9d957gz4Qo8aUQqhTvMWU9FkTInr3ozgmXpKdMs5dP8rPuTSlbjIlUA37dnTGFlaSEnXe3lzCnHfR30QOys50OJRZU6uIPKAW0hlJtjak1kI92hAoF7WCaYl1K03uUYbIVPNrbuklrmKNDwbqackFxRhatNnGGAujKzmif9st0xL3tXgU7FXj3EC-63z--_1pd9Tc_L69X3256Nwhe-6DkSCwZ-UicC1pJrAfptdJSY4F9UIE5HtQoOR1b5t2gIYiBwUjt4EfMLrrrE9cnuzX7HHc2H0yy0RwLKa-NzTW6CYwOTjnQFJijnHKrBPGayhD4QKwgpLG-nlj7ZdyBdzDXbKdn0OedOW7MOt0agiXhA73f5tMDIac_Szut2cXi2jXtDGkphmpMNdcDFk368T_pNi25fcNJRYgQnDYVPalcTqVkCI_bEGzuPWJOHjHNI-boEcPa0Ien73gc-WcK9heeBLlc</recordid><startdate>20231212</startdate><enddate>20231212</enddate><creator>Yue, Shufan</creator><creator>Pei, Ling</creator><creator>Lai, Fenghua</creator><creator>Xiao, Huangmeng</creator><creator>Li, Zeting</creator><creator>Zeng, Rui</creator><creator>Chen, Li</creator><creator>Chen, Wenzhan</creator><creator>Liu, Huiling</creator><creator>Li, Yanbing</creator><creator>Xiao, Haipeng</creator><creator>Cao, Xiaopei</creator><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20231212</creationdate><title>Genome-wide analysis study of gestational diabetes mellitus and related pathogenic factors in a Chinese Han population</title><author>Yue, Shufan ; Pei, Ling ; Lai, Fenghua ; Xiao, Huangmeng ; Li, Zeting ; Zeng, Rui ; Chen, Li ; Chen, Wenzhan ; Liu, Huiling ; Li, Yanbing ; Xiao, Haipeng ; Cao, Xiaopei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-f87b1a1b4b1ccf9870957d98979060df8f3c4f8b742b3c4dc59ef653eb2a5db03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Blood Glucose - metabolism</topic><topic>Body mass index</topic><topic>Deoxyribonucleic acid</topic><topic>Diabetes, Gestational - epidemiology</topic><topic>DNA</topic><topic>Ethnicity</topic><topic>Female</topic><topic>Genes</topic><topic>Genome-Wide Association Study</topic><topic>Genomes</topic><topic>Gestational diabetes</topic><topic>Gestational Diabetes Mellitus</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>GWAS</topic><topic>Humans</topic><topic>Insulin resistance</topic><topic>Insulin Resistance - genetics</topic><topic>Metabolism</topic><topic>Nuclear Proteins - genetics</topic><topic>Obesity</topic><topic>Plasma</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Pregnancy</topic><topic>Protein-Arginine N-Methyltransferases - genetics</topic><topic>Quality control</topic><topic>Regression analysis</topic><topic>SNP</topic><topic>Susceptibility gene</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yue, Shufan</creatorcontrib><creatorcontrib>Pei, Ling</creatorcontrib><creatorcontrib>Lai, Fenghua</creatorcontrib><creatorcontrib>Xiao, Huangmeng</creatorcontrib><creatorcontrib>Li, Zeting</creatorcontrib><creatorcontrib>Zeng, Rui</creatorcontrib><creatorcontrib>Chen, Li</creatorcontrib><creatorcontrib>Chen, Wenzhan</creatorcontrib><creatorcontrib>Liu, Huiling</creatorcontrib><creatorcontrib>Li, Yanbing</creatorcontrib><creatorcontrib>Xiao, Haipeng</creatorcontrib><creatorcontrib>Cao, Xiaopei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC pregnancy and childbirth</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yue, Shufan</au><au>Pei, Ling</au><au>Lai, Fenghua</au><au>Xiao, Huangmeng</au><au>Li, Zeting</au><au>Zeng, Rui</au><au>Chen, Li</au><au>Chen, Wenzhan</au><au>Liu, Huiling</au><au>Li, Yanbing</au><au>Xiao, Haipeng</au><au>Cao, Xiaopei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-wide analysis study of gestational diabetes mellitus and related pathogenic factors in a Chinese Han population</atitle><jtitle>BMC pregnancy and childbirth</jtitle><addtitle>BMC Pregnancy Childbirth</addtitle><date>2023-12-12</date><risdate>2023</risdate><volume>23</volume><issue>1</issue><spage>856</spage><epage>856</epage><pages>856-856</pages><artnum>856</artnum><issn>1471-2393</issn><eissn>1471-2393</eissn><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.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>38087213</pmid><doi>10.1186/s12884-023-06167-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 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 |
title | Genome-wide analysis study of gestational diabetes mellitus and related pathogenic factors in a Chinese Han population |
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