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The visfatin gene is associated with glucose and lipid metabolism in a Chinese population
Aims Visfatin is a newly discovered adipokine found in abundance in visceral fat. It lowers plasma glucose in humans and mice. In this study, we explored the relationships between the plasma level of visfatin and genetic single nucleotide polymorphisms (SNPs) and Type 2 diabetes mellitus (T2DM) and...
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Published in: | Diabetic medicine 2006-09, Vol.23 (9), p.967-973 |
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container_title | Diabetic medicine |
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creator | Jian, W.-X. Luo, T.-H. Gu, Y.-Y. Zhang, H.-L. Zheng, S. Dai, M. Han, J.-F. Zhao, Y. Li, G. Luo, M. |
description | Aims Visfatin is a newly discovered adipokine found in abundance in visceral fat. It lowers plasma glucose in humans and mice. In this study, we explored the relationships between the plasma level of visfatin and genetic single nucleotide polymorphisms (SNPs) and Type 2 diabetes mellitus (T2DM) and anthropometric and metabolic parameters in Chinese subjects.
Methods Oral glucose tolerance tests (OGTT) and biochemical assays for plasma insulin, lipid profiles and serum visfatin were performed in 241 newly diagnosed T2DM patients, subjects with impaired glucose regulation (IGR), and normal glucose tolerant subjects more than 40 years of age. Genotyping for three SNP loci: −1535C/T, rs2058539 and rs10953502 were performed using the allele‐specific real‐time PCR method.
Results Visfatin levels were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, visfatin levels were significantly lower in obese than normal‐weight subjects (13.66 ± 0.87 vs. 15.46 ± 0.47 ng/ml, P = 0.03). There was suggestively significant correlation between visfatin level and body mass index (r = –0.17 P = 0.07) and waist–hip ratio (r = 0.16 P = 0.08) in male subjects, but not in female subjects. Allele and common haplotype frequencies of the three SNP loci were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, significant associations were found between these three SNP loci and plasma glucose concentration at 0 and 120 min during OGTT, the area under the response curve for plasma glucose, and triglyceride and total cholesterol levels.
Conclusions Serum visfatin levels may be related to visceral obesity in men, and the visfatin gene may account for variation of glucose and lipid parameters in Chinese subjects. |
doi_str_mv | 10.1111/j.1464-5491.2006.01909.x |
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Methods Oral glucose tolerance tests (OGTT) and biochemical assays for plasma insulin, lipid profiles and serum visfatin were performed in 241 newly diagnosed T2DM patients, subjects with impaired glucose regulation (IGR), and normal glucose tolerant subjects more than 40 years of age. Genotyping for three SNP loci: −1535C/T, rs2058539 and rs10953502 were performed using the allele‐specific real‐time PCR method.
Results Visfatin levels were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, visfatin levels were significantly lower in obese than normal‐weight subjects (13.66 ± 0.87 vs. 15.46 ± 0.47 ng/ml, P = 0.03). There was suggestively significant correlation between visfatin level and body mass index (r = –0.17 P = 0.07) and waist–hip ratio (r = 0.16 P = 0.08) in male subjects, but not in female subjects. Allele and common haplotype frequencies of the three SNP loci were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, significant associations were found between these three SNP loci and plasma glucose concentration at 0 and 120 min during OGTT, the area under the response curve for plasma glucose, and triglyceride and total cholesterol levels.
Conclusions Serum visfatin levels may be related to visceral obesity in men, and the visfatin gene may account for variation of glucose and lipid parameters in Chinese subjects.</description><identifier>ISSN: 0742-3071</identifier><identifier>EISSN: 1464-5491</identifier><identifier>DOI: 10.1111/j.1464-5491.2006.01909.x</identifier><identifier>PMID: 16922702</identifier><identifier>CODEN: DIMEEV</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Anthropometry ; Asian Continental Ancestry Group - genetics ; association ; Biological and medical sciences ; Blood Glucose - metabolism ; China ; Cytokines - blood ; Cytokines - genetics ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - ethnology ; Diabetes Mellitus, Type 2 - etiology ; Diabetes Mellitus, Type 2 - genetics ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Genotype ; Glucose Tolerance Test - methods ; Humans ; Insulin - blood ; Lipid Metabolism - genetics ; Male ; Medical sciences ; Middle Aged ; Nicotinamide Phosphoribosyltransferase ; Obesity - blood ; Obesity - complications ; Obesity - ethnology ; oral glucose tolerance test ; Polymorphism, Single Nucleotide ; Sex Factors ; single nucleotide polymorphism ; Type 2 diabetes mellitus ; visfatin</subject><ispartof>Diabetic medicine, 2006-09, Vol.23 (9), p.967-973</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4669-75bd54bc723e759e87bd379851b4bf3e63ed1f293ee3d0df00054dd14bf179503</citedby><cites>FETCH-LOGICAL-c4669-75bd54bc723e759e87bd379851b4bf3e63ed1f293ee3d0df00054dd14bf179503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18035915$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16922702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jian, W.-X.</creatorcontrib><creatorcontrib>Luo, T.-H.</creatorcontrib><creatorcontrib>Gu, Y.-Y.</creatorcontrib><creatorcontrib>Zhang, H.-L.</creatorcontrib><creatorcontrib>Zheng, S.</creatorcontrib><creatorcontrib>Dai, M.</creatorcontrib><creatorcontrib>Han, J.-F.</creatorcontrib><creatorcontrib>Zhao, Y.</creatorcontrib><creatorcontrib>Li, G.</creatorcontrib><creatorcontrib>Luo, M.</creatorcontrib><title>The visfatin gene is associated with glucose and lipid metabolism in a Chinese population</title><title>Diabetic medicine</title><addtitle>Diabet Med</addtitle><description>Aims Visfatin is a newly discovered adipokine found in abundance in visceral fat. It lowers plasma glucose in humans and mice. In this study, we explored the relationships between the plasma level of visfatin and genetic single nucleotide polymorphisms (SNPs) and Type 2 diabetes mellitus (T2DM) and anthropometric and metabolic parameters in Chinese subjects.
Methods Oral glucose tolerance tests (OGTT) and biochemical assays for plasma insulin, lipid profiles and serum visfatin were performed in 241 newly diagnosed T2DM patients, subjects with impaired glucose regulation (IGR), and normal glucose tolerant subjects more than 40 years of age. Genotyping for three SNP loci: −1535C/T, rs2058539 and rs10953502 were performed using the allele‐specific real‐time PCR method.
Results Visfatin levels were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, visfatin levels were significantly lower in obese than normal‐weight subjects (13.66 ± 0.87 vs. 15.46 ± 0.47 ng/ml, P = 0.03). There was suggestively significant correlation between visfatin level and body mass index (r = –0.17 P = 0.07) and waist–hip ratio (r = 0.16 P = 0.08) in male subjects, but not in female subjects. Allele and common haplotype frequencies of the three SNP loci were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, significant associations were found between these three SNP loci and plasma glucose concentration at 0 and 120 min during OGTT, the area under the response curve for plasma glucose, and triglyceride and total cholesterol levels.
Conclusions Serum visfatin levels may be related to visceral obesity in men, and the visfatin gene may account for variation of glucose and lipid parameters in Chinese subjects.</description><subject>Adult</subject><subject>Aged</subject><subject>Anthropometry</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>association</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>China</subject><subject>Cytokines - blood</subject><subject>Cytokines - genetics</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - ethnology</subject><subject>Diabetes Mellitus, Type 2 - etiology</subject><subject>Diabetes Mellitus, Type 2 - genetics</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Genotype</subject><subject>Glucose Tolerance Test - methods</subject><subject>Humans</subject><subject>Insulin - blood</subject><subject>Lipid Metabolism - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nicotinamide Phosphoribosyltransferase</subject><subject>Obesity - blood</subject><subject>Obesity - complications</subject><subject>Obesity - ethnology</subject><subject>oral glucose tolerance test</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Sex Factors</subject><subject>single nucleotide polymorphism</subject><subject>Type 2 diabetes mellitus</subject><subject>visfatin</subject><issn>0742-3071</issn><issn>1464-5491</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkM1u1DAUhS0EokPhFZA3sEvwbxwvWKChtJWmZVOEWFlOfNPx4PwQJ3T69nU6o3YJ3tjS_b7jq4MQpiSn6Xza5VQUIpNC05wRUuSEaqLz_Qu0ehq8RCuiBMs4UfQEvYlxRwhlmuvX6IQWmjFF2Ar9utkC_utjYyff4VvoAPuIbYx97e0EDt_5aYtvw1z3EbDtHA5-8A63MNmqDz62OHkWr7e-g0QM_TCHlNV3b9GrxoYI7473Kfrx7exmfZFtvp9frr9ssloUhc6UrJwUVa0YByU1lKpyXOlS0kpUDYeCg6NN2huAO-IaQogUztE0pEpLwk_Rx0PuMPZ_ZoiTaX2sIQTbQT9HU5RKMcb_DVItCiYeE8sDWI99jCM0Zhh9a8d7Q4lZ-jc7s9RslprN0r957N_sk_r--MdcteCexWPhCfhwBGysbWhG29U-PnMl4VJTmbjPB-7OB7j_7wXM16uz5ZX87OD7OMH-ybfjb1MorqT5eX1u-JW-vuBSmA1_AFWnr1U</recordid><startdate>200609</startdate><enddate>200609</enddate><creator>Jian, W.-X.</creator><creator>Luo, T.-H.</creator><creator>Gu, Y.-Y.</creator><creator>Zhang, H.-L.</creator><creator>Zheng, S.</creator><creator>Dai, M.</creator><creator>Han, J.-F.</creator><creator>Zhao, Y.</creator><creator>Li, G.</creator><creator>Luo, M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200609</creationdate><title>The visfatin gene is associated with glucose and lipid metabolism in a Chinese population</title><author>Jian, W.-X. ; Luo, T.-H. ; Gu, Y.-Y. ; Zhang, H.-L. ; Zheng, S. ; Dai, M. ; Han, J.-F. ; Zhao, Y. ; Li, G. ; Luo, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4669-75bd54bc723e759e87bd379851b4bf3e63ed1f293ee3d0df00054dd14bf179503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anthropometry</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>association</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - metabolism</topic><topic>China</topic><topic>Cytokines - blood</topic><topic>Cytokines - genetics</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - ethnology</topic><topic>Diabetes Mellitus, Type 2 - etiology</topic><topic>Diabetes Mellitus, Type 2 - genetics</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Genotype</topic><topic>Glucose Tolerance Test - methods</topic><topic>Humans</topic><topic>Insulin - blood</topic><topic>Lipid Metabolism - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nicotinamide Phosphoribosyltransferase</topic><topic>Obesity - blood</topic><topic>Obesity - complications</topic><topic>Obesity - ethnology</topic><topic>oral glucose tolerance test</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Sex Factors</topic><topic>single nucleotide polymorphism</topic><topic>Type 2 diabetes mellitus</topic><topic>visfatin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jian, W.-X.</creatorcontrib><creatorcontrib>Luo, T.-H.</creatorcontrib><creatorcontrib>Gu, Y.-Y.</creatorcontrib><creatorcontrib>Zhang, H.-L.</creatorcontrib><creatorcontrib>Zheng, S.</creatorcontrib><creatorcontrib>Dai, M.</creatorcontrib><creatorcontrib>Han, J.-F.</creatorcontrib><creatorcontrib>Zhao, Y.</creatorcontrib><creatorcontrib>Li, G.</creatorcontrib><creatorcontrib>Luo, M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetic medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jian, W.-X.</au><au>Luo, T.-H.</au><au>Gu, Y.-Y.</au><au>Zhang, H.-L.</au><au>Zheng, S.</au><au>Dai, M.</au><au>Han, J.-F.</au><au>Zhao, Y.</au><au>Li, G.</au><au>Luo, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The visfatin gene is associated with glucose and lipid metabolism in a Chinese population</atitle><jtitle>Diabetic medicine</jtitle><addtitle>Diabet Med</addtitle><date>2006-09</date><risdate>2006</risdate><volume>23</volume><issue>9</issue><spage>967</spage><epage>973</epage><pages>967-973</pages><issn>0742-3071</issn><eissn>1464-5491</eissn><coden>DIMEEV</coden><abstract>Aims Visfatin is a newly discovered adipokine found in abundance in visceral fat. It lowers plasma glucose in humans and mice. In this study, we explored the relationships between the plasma level of visfatin and genetic single nucleotide polymorphisms (SNPs) and Type 2 diabetes mellitus (T2DM) and anthropometric and metabolic parameters in Chinese subjects.
Methods Oral glucose tolerance tests (OGTT) and biochemical assays for plasma insulin, lipid profiles and serum visfatin were performed in 241 newly diagnosed T2DM patients, subjects with impaired glucose regulation (IGR), and normal glucose tolerant subjects more than 40 years of age. Genotyping for three SNP loci: −1535C/T, rs2058539 and rs10953502 were performed using the allele‐specific real‐time PCR method.
Results Visfatin levels were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, visfatin levels were significantly lower in obese than normal‐weight subjects (13.66 ± 0.87 vs. 15.46 ± 0.47 ng/ml, P = 0.03). There was suggestively significant correlation between visfatin level and body mass index (r = –0.17 P = 0.07) and waist–hip ratio (r = 0.16 P = 0.08) in male subjects, but not in female subjects. Allele and common haplotype frequencies of the three SNP loci were similar in T2DM patients, IGR and normal glucose tolerant subjects. However, significant associations were found between these three SNP loci and plasma glucose concentration at 0 and 120 min during OGTT, the area under the response curve for plasma glucose, and triglyceride and total cholesterol levels.
Conclusions Serum visfatin levels may be related to visceral obesity in men, and the visfatin gene may account for variation of glucose and lipid parameters in Chinese subjects.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16922702</pmid><doi>10.1111/j.1464-5491.2006.01909.x</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Anthropometry Asian Continental Ancestry Group - genetics association Biological and medical sciences Blood Glucose - metabolism China Cytokines - blood Cytokines - genetics Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - ethnology Diabetes Mellitus, Type 2 - etiology Diabetes Mellitus, Type 2 - genetics Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Female Genotype Glucose Tolerance Test - methods Humans Insulin - blood Lipid Metabolism - genetics Male Medical sciences Middle Aged Nicotinamide Phosphoribosyltransferase Obesity - blood Obesity - complications Obesity - ethnology oral glucose tolerance test Polymorphism, Single Nucleotide Sex Factors single nucleotide polymorphism Type 2 diabetes mellitus visfatin |
title | The visfatin gene is associated with glucose and lipid metabolism in a Chinese population |
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