Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes
Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes Signe S. Torekov 1 2 , Lesli H. Larsen 1 3 , Charlotte Glümer 1 4 , Knut Borch-Johnsen 1 4 5 , Torben Jørgensen 4 , Jens J. Holst 6 , Ole D. Madsen 1 2 , Torben Hansen 1 and Oluf Pedersen 1 5...
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creator | TOREKOV, Signe S LARSEN, Lesli H GLÜMER, Charlotte BORCH-JOHNSEN, Knut JØRGENSEN, Torben HOLST, Jens J MADSEN, Ole D HANSEN, Torben PEDERSEN, Oluf |
description | Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes
Signe S. Torekov 1 2 ,
Lesli H. Larsen 1 3 ,
Charlotte Glümer 1 4 ,
Knut Borch-Johnsen 1 4 5 ,
Torben Jørgensen 4 ,
Jens J. Holst 6 ,
Ole D. Madsen 1 2 ,
Torben Hansen 1 and
Oluf Pedersen 1 5
1 Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
2 Faculty of Health Science, University of Copenhagen, Copenhagen, Denmark
3 Danish Epidemiology Science Centre and Research Unit for Dietary Studies at the Institute of Preventive Medicine, Copenhagen
University Hospital, Copenhagen, Denmark
4 Research Centre for Prevention and Health, Glostrup University Hospital, Glostrup, Denmark
5 Faculty of Health Science, University of Aarhus, Aarhus, Denmark
6 Department of Medical Physiology, University of Copenhagen, Denmark
Address correspondence and reprint requests to Signe S. Torekov, MSc, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820,
Gentofte, Denmark. E-mail: skto{at}steno.dk
Abstract
We tested the hypothesis that variants in the gene encoding the prepropeptide YY ( PYY ) associate with type 2 diabetes and/or obesity. Mutation analyses of DNA from 84 patients with obesity and familial type
2 diabetes identified two polymorphisms, IVS3 + 68C>T and Arg72Thr, and one rare variant, +151C>A of PYY . The common allele of the Arg72Thr variant associated with type 2 diabetes with an allele frequency of the Arg allele of
0.667 (95% CI 0.658–0.677) among 4,639 glucose-tolerant subjects and 0.692 (0.674–0.710) among 1,326 patients with type 2
diabetes ( P = 0.005, odds ratio 1.19 [95% CI 1.05–1.35]). The same polymorphism associated with overweight (25 ≤ BMI < 30 kg/m 2 ) ( P = 0.018, 1.15 [1.02–1.28]). In quantitative trait analyses of a population-based sample of 6,022 subjects, the Arg allele
was associated with an increased plasma glucose level 2 h after an oral glucose tolerance test (OGTT) ( P = 0.03), an increased area under the curve for the post-OGTT plasma glucose level ( P = 0.03), and a lower insulinogenic index ( P = 0.01). In conclusion, the common Arg allele of the PYY Arg72Thr variant modestly associates with type 2 diabetes and with type 2 diabetes–related quantitative traits.
HPLC, high-performance liquid chromatography
OGTT, oral glucose tolerance test
NPY, neuropeptide Y
PYY, peptide YY
UTR, untranslated region
Footnotes
O.D.M. is employed by, holds stock in, and has received grant support from Novo Nordisk.
Accepted Apri |
doi_str_mv | 10.2337/diabetes.54.7.2261 |
format | Article |
fullrecord | <record><control><sourceid>gale_highw</sourceid><recordid>TN_cdi_gale_incontextgauss_8GL_A134380199</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A134380199</galeid><sourcerecordid>A134380199</sourcerecordid><originalsourceid>FETCH-LOGICAL-c646t-46bccbcbb94ee679227cd33bb7baa6295c7b38839b89fb3ba74f14a71d58a753</originalsourceid><addsrcrecordid>eNqF0u-L0zAYB_Aiijen_4AvJCgKIp350TbNyznP82BwInvhvQpJ-rTLXZfOpPO8_97UVcZkKHlRCJ_vk6TPkyTPCZ5Rxvj7yioNPYRZns34jNKCPEgmRDCRMsq_PUwmGBOaEi74WfIkhBuMcRHX4-SM5KJklJFJcnv-w1bgDKCuRsqheQidsaq3nUMfoL8DcKhfA5r7hlM0b1tof9Nh7wts-xhG19cxWaFLZzyoABX6asPtgFb3W0AUfRzv-TR5VKs2wLPxO01Wn85Xi8_p8uricjFfpqbIij7NCm2MNlqLDKDgglJuKsa05lqpgorccM3KkgldilozrXhWk0xxUuWl4jmbJm_2Zbe--76D0MuNDQbaVjnodkHGkiXDZfZfSDjjWLCh4su_4E238y6-QVJSZGVOI5smr_aoUS1I6-qu98oMFeWcsIyVmIhBpSdUAw68ajsHtY3bR352wsdVwcaak4G3R4FoevjZN2oXgiwvlv-6zGhNF9vcgIxNWVwde7r3xncheKjl1tuN8veSYDmMpPwzkjLPJJfDSMbQi_Hn7fQGqkNknMEIXo9ABaPa2itnbDi4QjDMiqFd7_ZubZv1nfVwOO3Esb8A0JX0wQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>216485209</pqid></control><display><type>article</type><title>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>TOREKOV, Signe S ; LARSEN, Lesli H ; GLÜMER, Charlotte ; BORCH-JOHNSEN, Knut ; JØRGENSEN, Torben ; HOLST, Jens J ; MADSEN, Ole D ; HANSEN, Torben ; PEDERSEN, Oluf</creator><creatorcontrib>TOREKOV, Signe S ; LARSEN, Lesli H ; GLÜMER, Charlotte ; BORCH-JOHNSEN, Knut ; JØRGENSEN, Torben ; HOLST, Jens J ; MADSEN, Ole D ; HANSEN, Torben ; PEDERSEN, Oluf</creatorcontrib><description>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes
Signe S. Torekov 1 2 ,
Lesli H. Larsen 1 3 ,
Charlotte Glümer 1 4 ,
Knut Borch-Johnsen 1 4 5 ,
Torben Jørgensen 4 ,
Jens J. Holst 6 ,
Ole D. Madsen 1 2 ,
Torben Hansen 1 and
Oluf Pedersen 1 5
1 Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
2 Faculty of Health Science, University of Copenhagen, Copenhagen, Denmark
3 Danish Epidemiology Science Centre and Research Unit for Dietary Studies at the Institute of Preventive Medicine, Copenhagen
University Hospital, Copenhagen, Denmark
4 Research Centre for Prevention and Health, Glostrup University Hospital, Glostrup, Denmark
5 Faculty of Health Science, University of Aarhus, Aarhus, Denmark
6 Department of Medical Physiology, University of Copenhagen, Denmark
Address correspondence and reprint requests to Signe S. Torekov, MSc, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820,
Gentofte, Denmark. E-mail: skto{at}steno.dk
Abstract
We tested the hypothesis that variants in the gene encoding the prepropeptide YY ( PYY ) associate with type 2 diabetes and/or obesity. Mutation analyses of DNA from 84 patients with obesity and familial type
2 diabetes identified two polymorphisms, IVS3 + 68C>T and Arg72Thr, and one rare variant, +151C>A of PYY . The common allele of the Arg72Thr variant associated with type 2 diabetes with an allele frequency of the Arg allele of
0.667 (95% CI 0.658–0.677) among 4,639 glucose-tolerant subjects and 0.692 (0.674–0.710) among 1,326 patients with type 2
diabetes ( P = 0.005, odds ratio 1.19 [95% CI 1.05–1.35]). The same polymorphism associated with overweight (25 ≤ BMI < 30 kg/m 2 ) ( P = 0.018, 1.15 [1.02–1.28]). In quantitative trait analyses of a population-based sample of 6,022 subjects, the Arg allele
was associated with an increased plasma glucose level 2 h after an oral glucose tolerance test (OGTT) ( P = 0.03), an increased area under the curve for the post-OGTT plasma glucose level ( P = 0.03), and a lower insulinogenic index ( P = 0.01). In conclusion, the common Arg allele of the PYY Arg72Thr variant modestly associates with type 2 diabetes and with type 2 diabetes–related quantitative traits.
HPLC, high-performance liquid chromatography
OGTT, oral glucose tolerance test
NPY, neuropeptide Y
PYY, peptide YY
UTR, untranslated region
Footnotes
O.D.M. is employed by, holds stock in, and has received grant support from Novo Nordisk.
Accepted April 21, 2005.
Received December 22, 2004.
DIABETES</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/diabetes.54.7.2261</identifier><identifier>PMID: 15983231</identifier><identifier>CODEN: DIAEAZ</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Arginine - genetics ; Biological and medical sciences ; Body Mass Index ; Diabetes Mellitus, Type 2 - epidemiology ; Diabetes Mellitus, Type 2 - genetics ; Diabetes. Impaired glucose tolerance ; DNA - genetics ; DNA Mutational Analysis ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Female ; Genetic aspects ; Genetic code ; Humans ; Male ; Medical sciences ; Obesity - genetics ; Observations ; Odds Ratio ; Pedigree ; Peptide YY - genetics ; Polymorphism, Genetic ; Risk Factors ; Sequence Deletion ; Type 2 diabetes</subject><ispartof>Diabetes (New York, N.Y.), 2005-07, Vol.54 (7), p.2261-2265</ispartof><rights>2005 INIST-CNRS</rights><rights>COPYRIGHT 2005 American Diabetes Association</rights><rights>Copyright American Diabetes Association Jul 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c646t-46bccbcbb94ee679227cd33bb7baa6295c7b38839b89fb3ba74f14a71d58a753</citedby><cites>FETCH-LOGICAL-c646t-46bccbcbb94ee679227cd33bb7baa6295c7b38839b89fb3ba74f14a71d58a753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16930364$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15983231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TOREKOV, Signe S</creatorcontrib><creatorcontrib>LARSEN, Lesli H</creatorcontrib><creatorcontrib>GLÜMER, Charlotte</creatorcontrib><creatorcontrib>BORCH-JOHNSEN, Knut</creatorcontrib><creatorcontrib>JØRGENSEN, Torben</creatorcontrib><creatorcontrib>HOLST, Jens J</creatorcontrib><creatorcontrib>MADSEN, Ole D</creatorcontrib><creatorcontrib>HANSEN, Torben</creatorcontrib><creatorcontrib>PEDERSEN, Oluf</creatorcontrib><title>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes</title><title>Diabetes (New York, N.Y.)</title><addtitle>Diabetes</addtitle><description>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes
Signe S. Torekov 1 2 ,
Lesli H. Larsen 1 3 ,
Charlotte Glümer 1 4 ,
Knut Borch-Johnsen 1 4 5 ,
Torben Jørgensen 4 ,
Jens J. Holst 6 ,
Ole D. Madsen 1 2 ,
Torben Hansen 1 and
Oluf Pedersen 1 5
1 Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
2 Faculty of Health Science, University of Copenhagen, Copenhagen, Denmark
3 Danish Epidemiology Science Centre and Research Unit for Dietary Studies at the Institute of Preventive Medicine, Copenhagen
University Hospital, Copenhagen, Denmark
4 Research Centre for Prevention and Health, Glostrup University Hospital, Glostrup, Denmark
5 Faculty of Health Science, University of Aarhus, Aarhus, Denmark
6 Department of Medical Physiology, University of Copenhagen, Denmark
Address correspondence and reprint requests to Signe S. Torekov, MSc, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820,
Gentofte, Denmark. E-mail: skto{at}steno.dk
Abstract
We tested the hypothesis that variants in the gene encoding the prepropeptide YY ( PYY ) associate with type 2 diabetes and/or obesity. Mutation analyses of DNA from 84 patients with obesity and familial type
2 diabetes identified two polymorphisms, IVS3 + 68C>T and Arg72Thr, and one rare variant, +151C>A of PYY . The common allele of the Arg72Thr variant associated with type 2 diabetes with an allele frequency of the Arg allele of
0.667 (95% CI 0.658–0.677) among 4,639 glucose-tolerant subjects and 0.692 (0.674–0.710) among 1,326 patients with type 2
diabetes ( P = 0.005, odds ratio 1.19 [95% CI 1.05–1.35]). The same polymorphism associated with overweight (25 ≤ BMI < 30 kg/m 2 ) ( P = 0.018, 1.15 [1.02–1.28]). In quantitative trait analyses of a population-based sample of 6,022 subjects, the Arg allele
was associated with an increased plasma glucose level 2 h after an oral glucose tolerance test (OGTT) ( P = 0.03), an increased area under the curve for the post-OGTT plasma glucose level ( P = 0.03), and a lower insulinogenic index ( P = 0.01). In conclusion, the common Arg allele of the PYY Arg72Thr variant modestly associates with type 2 diabetes and with type 2 diabetes–related quantitative traits.
HPLC, high-performance liquid chromatography
OGTT, oral glucose tolerance test
NPY, neuropeptide Y
PYY, peptide YY
UTR, untranslated region
Footnotes
O.D.M. is employed by, holds stock in, and has received grant support from Novo Nordisk.
Accepted April 21, 2005.
Received December 22, 2004.
DIABETES</description><subject>Arginine - genetics</subject><subject>Biological and medical sciences</subject><subject>Body Mass Index</subject><subject>Diabetes Mellitus, Type 2 - epidemiology</subject><subject>Diabetes Mellitus, Type 2 - genetics</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>DNA - genetics</subject><subject>DNA Mutational Analysis</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Genetic code</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Obesity - genetics</subject><subject>Observations</subject><subject>Odds Ratio</subject><subject>Pedigree</subject><subject>Peptide YY - genetics</subject><subject>Polymorphism, Genetic</subject><subject>Risk Factors</subject><subject>Sequence Deletion</subject><subject>Type 2 diabetes</subject><issn>0012-1797</issn><issn>1939-327X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0u-L0zAYB_Aiijen_4AvJCgKIp350TbNyznP82BwInvhvQpJ-rTLXZfOpPO8_97UVcZkKHlRCJ_vk6TPkyTPCZ5Rxvj7yioNPYRZns34jNKCPEgmRDCRMsq_PUwmGBOaEi74WfIkhBuMcRHX4-SM5KJklJFJcnv-w1bgDKCuRsqheQidsaq3nUMfoL8DcKhfA5r7hlM0b1tof9Nh7wts-xhG19cxWaFLZzyoABX6asPtgFb3W0AUfRzv-TR5VKs2wLPxO01Wn85Xi8_p8uricjFfpqbIij7NCm2MNlqLDKDgglJuKsa05lqpgorccM3KkgldilozrXhWk0xxUuWl4jmbJm_2Zbe--76D0MuNDQbaVjnodkHGkiXDZfZfSDjjWLCh4su_4E238y6-QVJSZGVOI5smr_aoUS1I6-qu98oMFeWcsIyVmIhBpSdUAw68ajsHtY3bR352wsdVwcaak4G3R4FoevjZN2oXgiwvlv-6zGhNF9vcgIxNWVwde7r3xncheKjl1tuN8veSYDmMpPwzkjLPJJfDSMbQi_Hn7fQGqkNknMEIXo9ABaPa2itnbDi4QjDMiqFd7_ZubZv1nfVwOO3Esb8A0JX0wQ</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>TOREKOV, Signe S</creator><creator>LARSEN, Lesli H</creator><creator>GLÜMER, Charlotte</creator><creator>BORCH-JOHNSEN, Knut</creator><creator>JØRGENSEN, Torben</creator><creator>HOLST, Jens J</creator><creator>MADSEN, Ole D</creator><creator>HANSEN, Torben</creator><creator>PEDERSEN, Oluf</creator><general>American Diabetes Association</general><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>8GL</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes</title><author>TOREKOV, Signe S ; LARSEN, Lesli H ; GLÜMER, Charlotte ; BORCH-JOHNSEN, Knut ; JØRGENSEN, Torben ; HOLST, Jens J ; MADSEN, Ole D ; HANSEN, Torben ; PEDERSEN, Oluf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c646t-46bccbcbb94ee679227cd33bb7baa6295c7b38839b89fb3ba74f14a71d58a753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Arginine - genetics</topic><topic>Biological and medical sciences</topic><topic>Body Mass Index</topic><topic>Diabetes Mellitus, Type 2 - epidemiology</topic><topic>Diabetes Mellitus, Type 2 - genetics</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>DNA - genetics</topic><topic>DNA Mutational Analysis</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Genetic code</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Obesity - genetics</topic><topic>Observations</topic><topic>Odds Ratio</topic><topic>Pedigree</topic><topic>Peptide YY - genetics</topic><topic>Polymorphism, Genetic</topic><topic>Risk Factors</topic><topic>Sequence Deletion</topic><topic>Type 2 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TOREKOV, Signe S</creatorcontrib><creatorcontrib>LARSEN, Lesli H</creatorcontrib><creatorcontrib>GLÜMER, Charlotte</creatorcontrib><creatorcontrib>BORCH-JOHNSEN, Knut</creatorcontrib><creatorcontrib>JØRGENSEN, Torben</creatorcontrib><creatorcontrib>HOLST, Jens J</creatorcontrib><creatorcontrib>MADSEN, Ole D</creatorcontrib><creatorcontrib>HANSEN, Torben</creatorcontrib><creatorcontrib>PEDERSEN, Oluf</creatorcontrib><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>Gale In Context: High School</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>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</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>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TOREKOV, Signe S</au><au>LARSEN, Lesli H</au><au>GLÜMER, Charlotte</au><au>BORCH-JOHNSEN, Knut</au><au>JØRGENSEN, Torben</au><au>HOLST, Jens J</au><au>MADSEN, Ole D</au><au>HANSEN, Torben</au><au>PEDERSEN, Oluf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><addtitle>Diabetes</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>54</volume><issue>7</issue><spage>2261</spage><epage>2265</epage><pages>2261-2265</pages><issn>0012-1797</issn><eissn>1939-327X</eissn><coden>DIAEAZ</coden><abstract>Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes
Signe S. Torekov 1 2 ,
Lesli H. Larsen 1 3 ,
Charlotte Glümer 1 4 ,
Knut Borch-Johnsen 1 4 5 ,
Torben Jørgensen 4 ,
Jens J. Holst 6 ,
Ole D. Madsen 1 2 ,
Torben Hansen 1 and
Oluf Pedersen 1 5
1 Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
2 Faculty of Health Science, University of Copenhagen, Copenhagen, Denmark
3 Danish Epidemiology Science Centre and Research Unit for Dietary Studies at the Institute of Preventive Medicine, Copenhagen
University Hospital, Copenhagen, Denmark
4 Research Centre for Prevention and Health, Glostrup University Hospital, Glostrup, Denmark
5 Faculty of Health Science, University of Aarhus, Aarhus, Denmark
6 Department of Medical Physiology, University of Copenhagen, Denmark
Address correspondence and reprint requests to Signe S. Torekov, MSc, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820,
Gentofte, Denmark. E-mail: skto{at}steno.dk
Abstract
We tested the hypothesis that variants in the gene encoding the prepropeptide YY ( PYY ) associate with type 2 diabetes and/or obesity. Mutation analyses of DNA from 84 patients with obesity and familial type
2 diabetes identified two polymorphisms, IVS3 + 68C>T and Arg72Thr, and one rare variant, +151C>A of PYY . The common allele of the Arg72Thr variant associated with type 2 diabetes with an allele frequency of the Arg allele of
0.667 (95% CI 0.658–0.677) among 4,639 glucose-tolerant subjects and 0.692 (0.674–0.710) among 1,326 patients with type 2
diabetes ( P = 0.005, odds ratio 1.19 [95% CI 1.05–1.35]). The same polymorphism associated with overweight (25 ≤ BMI < 30 kg/m 2 ) ( P = 0.018, 1.15 [1.02–1.28]). In quantitative trait analyses of a population-based sample of 6,022 subjects, the Arg allele
was associated with an increased plasma glucose level 2 h after an oral glucose tolerance test (OGTT) ( P = 0.03), an increased area under the curve for the post-OGTT plasma glucose level ( P = 0.03), and a lower insulinogenic index ( P = 0.01). In conclusion, the common Arg allele of the PYY Arg72Thr variant modestly associates with type 2 diabetes and with type 2 diabetes–related quantitative traits.
HPLC, high-performance liquid chromatography
OGTT, oral glucose tolerance test
NPY, neuropeptide Y
PYY, peptide YY
UTR, untranslated region
Footnotes
O.D.M. is employed by, holds stock in, and has received grant support from Novo Nordisk.
Accepted April 21, 2005.
Received December 22, 2004.
DIABETES</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>15983231</pmid><doi>10.2337/diabetes.54.7.2261</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0012-1797 |
ispartof | Diabetes (New York, N.Y.), 2005-07, Vol.54 (7), p.2261-2265 |
issn | 0012-1797 1939-327X |
language | eng |
recordid | cdi_gale_incontextgauss_8GL_A134380199 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Arginine - genetics Biological and medical sciences Body Mass Index Diabetes Mellitus, Type 2 - epidemiology Diabetes Mellitus, Type 2 - genetics Diabetes. Impaired glucose tolerance DNA - genetics DNA Mutational Analysis Endocrine pancreas. Apud cells (diseases) Endocrinopathies Female Genetic aspects Genetic code Humans Male Medical sciences Obesity - genetics Observations Odds Ratio Pedigree Peptide YY - genetics Polymorphism, Genetic Risk Factors Sequence Deletion Type 2 diabetes |
title | Evidence of an Association Between the Arg72 Allele of the Peptide YY and Increased Risk of Type 2 Diabetes |
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