The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine

The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine Susanne R. de Rooij , MSC 1 , Rebecca C. Painter , MD, MSC 1 , David I.W. Phillips , PHD, FRCP 2 , Clive Osmond , PHD 2 , Michael...

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Veröffentlicht in:Diabetes care 2006-05, Vol.29 (5), p.1052-1057
Hauptverfasser: de Rooij, Susanne R., Painter, Rebecca C., Phillips, David I.W., Osmond, Clive, Tanck, Michael W.T., Defesche, Joep C., Bossuyt, Patrick M.M., Michels, Robert P.J., Bleker, Otto P., Roseboom, Tessa J.
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container_end_page 1057
container_issue 5
container_start_page 1052
container_title Diabetes care
container_volume 29
creator de Rooij, Susanne R.
Painter, Rebecca C.
Phillips, David I.W.
Osmond, Clive
Tanck, Michael W.T.
Defesche, Joep C.
Bossuyt, Patrick M.M.
Michels, Robert P.J.
Bleker, Otto P.
Roseboom, Tessa J.
description The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine Susanne R. de Rooij , MSC 1 , Rebecca C. Painter , MD, MSC 1 , David I.W. Phillips , PHD, FRCP 2 , Clive Osmond , PHD 2 , Michael W.T. Tanck , PHD 1 , Joep C. Defesche , PHD 3 , Patrick M.M. Bossuyt , PHD 1 , Robert P.J. Michels , MD, PHD 4 , Otto P. Bleker , MD, PHD, FRCOG 5 and Tessa J. Roseboom , PHD 1 1 Department of Clinical Epidemiology and Biostatistics, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 2 Medical Research Council Epidemiology Resource Centre at the University of Southampton, Southampton, U.K 3 Department of Vascular Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 4 Department of Internal Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 5 Department of Obstetrics and Gynaecology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands Address correspondence and reprint requests to Susanne de Rooij, MSc, Academic Medical Centre, Department of Clinical Epidemiology and Biostatistics, Room nr J1B-210-1, Meibergdreef 9, P.O. Box 22660, 1100 DD, Amsterdam, Netherlands. E-mail: s.r.derooij{at}amc.uva.nl Abstract OBJECTIVE —An adverse fetal environment may permanently modify the effects of specific genes on glucose tolerance, insulin secretion, and insulin sensitivity. In the present study, we assessed a possible interaction of the peroxisome proliferator–activated receptor (PPAR)-γ2 Pro12Ala polymorphism with prenatal exposure to famine on glucose and insulin metabolism. RESEARCH DESIGN AND METHODS —We measured plasma glucose and insulin concentrations after an oral glucose tolerance test and determined the PPAR-γ2 genotype among 675 term singletons born around the time of the 1944–1945 Dutch famine. RESULTS —A significant interaction effect between exposure to famine during midgestation and the PPAR-γ2 Pro12Ala polymorphism was found on the prevalence of impaired glucose tolerance and type 2 diabetes. The Ala allele of the PPAR-γ2 gene was associated with a higher prevalence of impaired glucose tolerance and type 2 diabetes but only in participants who had been prenatally exposed to famine during midgestation. Similar interactions were found for area under the curve for insulin and insulin increment ratio, which were lower for Ala carriers exposed
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Painter , MD, MSC 1 , David I.W. Phillips , PHD, FRCP 2 , Clive Osmond , PHD 2 , Michael W.T. Tanck , PHD 1 , Joep C. Defesche , PHD 3 , Patrick M.M. Bossuyt , PHD 1 , Robert P.J. Michels , MD, PHD 4 , Otto P. Bleker , MD, PHD, FRCOG 5 and Tessa J. Roseboom , PHD 1 1 Department of Clinical Epidemiology and Biostatistics, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 2 Medical Research Council Epidemiology Resource Centre at the University of Southampton, Southampton, U.K 3 Department of Vascular Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 4 Department of Internal Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 5 Department of Obstetrics and Gynaecology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands Address correspondence and reprint requests to Susanne de Rooij, MSc, Academic Medical Centre, Department of Clinical Epidemiology and Biostatistics, Room nr J1B-210-1, Meibergdreef 9, P.O. Box 22660, 1100 DD, Amsterdam, Netherlands. E-mail: s.r.derooij{at}amc.uva.nl Abstract OBJECTIVE —An adverse fetal environment may permanently modify the effects of specific genes on glucose tolerance, insulin secretion, and insulin sensitivity. In the present study, we assessed a possible interaction of the peroxisome proliferator–activated receptor (PPAR)-γ2 Pro12Ala polymorphism with prenatal exposure to famine on glucose and insulin metabolism. RESEARCH DESIGN AND METHODS —We measured plasma glucose and insulin concentrations after an oral glucose tolerance test and determined the PPAR-γ2 genotype among 675 term singletons born around the time of the 1944–1945 Dutch famine. RESULTS —A significant interaction effect between exposure to famine during midgestation and the PPAR-γ2 Pro12Ala polymorphism was found on the prevalence of impaired glucose tolerance and type 2 diabetes. The Ala allele of the PPAR-γ2 gene was associated with a higher prevalence of impaired glucose tolerance and type 2 diabetes but only in participants who had been prenatally exposed to famine during midgestation. Similar interactions were found for area under the curve for insulin and insulin increment ratio, which were lower for Ala carriers exposed to famine during midgestation. CONCLUSIONS —The effects of the PPAR-γ2 Pro12Ala polymorphism on glucose and insulin metabolism may be modified by prenatal exposure to famine during midgestation. This is possibly due to a combined deficit in insulin secretion, as conferred by pancreatic β-cell maldevelopment and carrier type of the Ala allele in the PPAR-γ2 gene. AUC, area under the curve HOMA-IR, homeostasis model assessment of insulin resistance OGTT, oral glucose tolerance test PPAR, peroxisome proliferator–activated receptor Footnotes A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted February 8, 2006. Received October 18, 2005. DIABETES CARE</description><identifier>ISSN: 0149-5992</identifier><identifier>EISSN: 1935-5548</identifier><identifier>DOI: 10.2337/dc05-1993</identifier><identifier>PMID: 16644636</identifier><language>eng</language><publisher>American Diabetes Association</publisher><subject>Diabetes ; Genetic aspects ; Genetic polymorphisms</subject><ispartof>Diabetes care, 2006-05, Vol.29 (5), p.1052-1057</ispartof><rights>COPYRIGHT 2006 American Diabetes Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2913-c166cf527d1efdb66ceda3e662608997c41eea119c2b91548a193a97cd820fe23</citedby><cites>FETCH-LOGICAL-c2913-c166cf527d1efdb66ceda3e662608997c41eea119c2b91548a193a97cd820fe23</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></links><search><creatorcontrib>de Rooij, Susanne R.</creatorcontrib><creatorcontrib>Painter, Rebecca C.</creatorcontrib><creatorcontrib>Phillips, David I.W.</creatorcontrib><creatorcontrib>Osmond, Clive</creatorcontrib><creatorcontrib>Tanck, Michael W.T.</creatorcontrib><creatorcontrib>Defesche, Joep C.</creatorcontrib><creatorcontrib>Bossuyt, Patrick M.M.</creatorcontrib><creatorcontrib>Michels, Robert P.J.</creatorcontrib><creatorcontrib>Bleker, Otto P.</creatorcontrib><creatorcontrib>Roseboom, Tessa J.</creatorcontrib><title>The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine</title><title>Diabetes care</title><description>The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine Susanne R. de Rooij , MSC 1 , Rebecca C. Painter , MD, MSC 1 , David I.W. Phillips , PHD, FRCP 2 , Clive Osmond , PHD 2 , Michael W.T. Tanck , PHD 1 , Joep C. Defesche , PHD 3 , Patrick M.M. Bossuyt , PHD 1 , Robert P.J. Michels , MD, PHD 4 , Otto P. Bleker , MD, PHD, FRCOG 5 and Tessa J. Roseboom , PHD 1 1 Department of Clinical Epidemiology and Biostatistics, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 2 Medical Research Council Epidemiology Resource Centre at the University of Southampton, Southampton, U.K 3 Department of Vascular Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 4 Department of Internal Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 5 Department of Obstetrics and Gynaecology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands Address correspondence and reprint requests to Susanne de Rooij, MSc, Academic Medical Centre, Department of Clinical Epidemiology and Biostatistics, Room nr J1B-210-1, Meibergdreef 9, P.O. Box 22660, 1100 DD, Amsterdam, Netherlands. E-mail: s.r.derooij{at}amc.uva.nl Abstract OBJECTIVE —An adverse fetal environment may permanently modify the effects of specific genes on glucose tolerance, insulin secretion, and insulin sensitivity. In the present study, we assessed a possible interaction of the peroxisome proliferator–activated receptor (PPAR)-γ2 Pro12Ala polymorphism with prenatal exposure to famine on glucose and insulin metabolism. RESEARCH DESIGN AND METHODS —We measured plasma glucose and insulin concentrations after an oral glucose tolerance test and determined the PPAR-γ2 genotype among 675 term singletons born around the time of the 1944–1945 Dutch famine. RESULTS —A significant interaction effect between exposure to famine during midgestation and the PPAR-γ2 Pro12Ala polymorphism was found on the prevalence of impaired glucose tolerance and type 2 diabetes. The Ala allele of the PPAR-γ2 gene was associated with a higher prevalence of impaired glucose tolerance and type 2 diabetes but only in participants who had been prenatally exposed to famine during midgestation. Similar interactions were found for area under the curve for insulin and insulin increment ratio, which were lower for Ala carriers exposed to famine during midgestation. CONCLUSIONS —The effects of the PPAR-γ2 Pro12Ala polymorphism on glucose and insulin metabolism may be modified by prenatal exposure to famine during midgestation. This is possibly due to a combined deficit in insulin secretion, as conferred by pancreatic β-cell maldevelopment and carrier type of the Ala allele in the PPAR-γ2 gene. AUC, area under the curve HOMA-IR, homeostasis model assessment of insulin resistance OGTT, oral glucose tolerance test PPAR, peroxisome proliferator–activated receptor Footnotes A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted February 8, 2006. Received October 18, 2005. DIABETES CARE</description><subject>Diabetes</subject><subject>Genetic aspects</subject><subject>Genetic polymorphisms</subject><issn>0149-5992</issn><issn>1935-5548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNptkU1uEzEUxy0EomlhwQ28BWlaf8xMxsuoSkOkIipUxHLkeJ4zRh47sp3S7rgD52DFPXoITsILQawqL-z39-_99T4IecPZuZByfjEY1lRcKfmMzLiSTdU0dfeczBivVdUoJU7Iac5fGWN13XUvyQlv27puZTsjP29HoEtrwZRMo6UFw5sUuVh4TW-if5hi2o0uT_8_IcV7l-P0l_POQtIlpt_ffyxMcXe6wEA_gYEditXjL0FXEIDGQFd-b2KGi3XIe-8C_QBFb9AArdehoIsp9IsrI9pC0EV7urzfxbxPQEukV3pyAV6RF1b7DK__3Wfk89Xy9vJ9df1xtb5cXFdGKC4rg_0Z24j5wMEOGwxg0BLaVrSsU2puag6gOVdGbBTHWWmcmkZ96ASzIOQZqY6-W-2hd8HGgvVtsZOkfQxgHcoLXrdszhsukT9_gsczwOTMkwlvjwkmxZwT2H6X3KTTQ89Zf9hpf9hpf9gpsu-O7Oi24zeXoB-c3kCBfHgYjYJQPcKsEfIP0YWkwg</recordid><startdate>20060501</startdate><enddate>20060501</enddate><creator>de Rooij, Susanne R.</creator><creator>Painter, Rebecca C.</creator><creator>Phillips, David I.W.</creator><creator>Osmond, Clive</creator><creator>Tanck, Michael W.T.</creator><creator>Defesche, Joep C.</creator><creator>Bossuyt, Patrick M.M.</creator><creator>Michels, Robert P.J.</creator><creator>Bleker, Otto P.</creator><creator>Roseboom, Tessa J.</creator><general>American Diabetes Association</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20060501</creationdate><title>The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine</title><author>de Rooij, Susanne R. ; Painter, Rebecca C. ; Phillips, David I.W. ; Osmond, Clive ; Tanck, Michael W.T. ; Defesche, Joep C. ; Bossuyt, Patrick M.M. ; Michels, Robert P.J. ; Bleker, Otto P. ; Roseboom, Tessa J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2913-c166cf527d1efdb66ceda3e662608997c41eea119c2b91548a193a97cd820fe23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Diabetes</topic><topic>Genetic aspects</topic><topic>Genetic polymorphisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Rooij, Susanne R.</creatorcontrib><creatorcontrib>Painter, Rebecca C.</creatorcontrib><creatorcontrib>Phillips, David I.W.</creatorcontrib><creatorcontrib>Osmond, Clive</creatorcontrib><creatorcontrib>Tanck, Michael W.T.</creatorcontrib><creatorcontrib>Defesche, Joep C.</creatorcontrib><creatorcontrib>Bossuyt, Patrick M.M.</creatorcontrib><creatorcontrib>Michels, Robert P.J.</creatorcontrib><creatorcontrib>Bleker, Otto P.</creatorcontrib><creatorcontrib>Roseboom, Tessa J.</creatorcontrib><collection>CrossRef</collection><jtitle>Diabetes care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Rooij, Susanne R.</au><au>Painter, Rebecca C.</au><au>Phillips, David I.W.</au><au>Osmond, Clive</au><au>Tanck, Michael W.T.</au><au>Defesche, Joep C.</au><au>Bossuyt, Patrick M.M.</au><au>Michels, Robert P.J.</au><au>Bleker, Otto P.</au><au>Roseboom, Tessa J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine</atitle><jtitle>Diabetes care</jtitle><date>2006-05-01</date><risdate>2006</risdate><volume>29</volume><issue>5</issue><spage>1052</spage><epage>1057</epage><pages>1052-1057</pages><issn>0149-5992</issn><eissn>1935-5548</eissn><abstract>The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine Susanne R. de Rooij , MSC 1 , Rebecca C. Painter , MD, MSC 1 , David I.W. Phillips , PHD, FRCP 2 , Clive Osmond , PHD 2 , Michael W.T. Tanck , PHD 1 , Joep C. Defesche , PHD 3 , Patrick M.M. Bossuyt , PHD 1 , Robert P.J. Michels , MD, PHD 4 , Otto P. Bleker , MD, PHD, FRCOG 5 and Tessa J. Roseboom , PHD 1 1 Department of Clinical Epidemiology and Biostatistics, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 2 Medical Research Council Epidemiology Resource Centre at the University of Southampton, Southampton, U.K 3 Department of Vascular Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 4 Department of Internal Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands 5 Department of Obstetrics and Gynaecology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands Address correspondence and reprint requests to Susanne de Rooij, MSc, Academic Medical Centre, Department of Clinical Epidemiology and Biostatistics, Room nr J1B-210-1, Meibergdreef 9, P.O. Box 22660, 1100 DD, Amsterdam, Netherlands. E-mail: s.r.derooij{at}amc.uva.nl Abstract OBJECTIVE —An adverse fetal environment may permanently modify the effects of specific genes on glucose tolerance, insulin secretion, and insulin sensitivity. In the present study, we assessed a possible interaction of the peroxisome proliferator–activated receptor (PPAR)-γ2 Pro12Ala polymorphism with prenatal exposure to famine on glucose and insulin metabolism. RESEARCH DESIGN AND METHODS —We measured plasma glucose and insulin concentrations after an oral glucose tolerance test and determined the PPAR-γ2 genotype among 675 term singletons born around the time of the 1944–1945 Dutch famine. RESULTS —A significant interaction effect between exposure to famine during midgestation and the PPAR-γ2 Pro12Ala polymorphism was found on the prevalence of impaired glucose tolerance and type 2 diabetes. The Ala allele of the PPAR-γ2 gene was associated with a higher prevalence of impaired glucose tolerance and type 2 diabetes but only in participants who had been prenatally exposed to famine during midgestation. Similar interactions were found for area under the curve for insulin and insulin increment ratio, which were lower for Ala carriers exposed to famine during midgestation. CONCLUSIONS —The effects of the PPAR-γ2 Pro12Ala polymorphism on glucose and insulin metabolism may be modified by prenatal exposure to famine during midgestation. This is possibly due to a combined deficit in insulin secretion, as conferred by pancreatic β-cell maldevelopment and carrier type of the Ala allele in the PPAR-γ2 gene. AUC, area under the curve HOMA-IR, homeostasis model assessment of insulin resistance OGTT, oral glucose tolerance test PPAR, peroxisome proliferator–activated receptor Footnotes A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted February 8, 2006. Received October 18, 2005. DIABETES CARE</abstract><pub>American Diabetes Association</pub><pmid>16644636</pmid><doi>10.2337/dc05-1993</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Diabetes
Genetic aspects
Genetic polymorphisms
title The Effects of the Pro12Ala Polymorphism of the Peroxisome Proliferator–Activated Receptor-γ2 Gene on Glucose/Insulin Metabolism Interact With Prenatal Exposure to Famine
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