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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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 |
doi_str_mv | 10.2337/dc05-1993 |
format | Article |
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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><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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language | eng |
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source | EZB-FREE-00999 freely available EZB journals |
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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