Effect of ENPP1/PC-1-K121Q and PPARγ-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population

被引:32
作者
Bouhaha, R. [1 ]
Meyre, D. [3 ,4 ]
Kamoun, H. Abid [2 ]
Ennafaa, H. [1 ]
Vaillant, E. [3 ,4 ]
Sassi, R. [1 ]
Baroudi, T. [1 ]
Vatin, V. [3 ,4 ]
Froguel, P. [3 ,4 ,5 ]
Elgaaied, A. [1 ]
Vaxillaire, M. [3 ,4 ]
机构
[1] Fac Sci Tunis, Lab Genet Immunol & Human Pathol, Tunis 2092, Tunisia
[2] Hop Charles Nicolle, Tunis, Tunisia
[3] Univ Lille 2, Inst Pasteur, CNRS 8090, Lille, France
[4] Univ Lille 2, Inst Pasteur, Inst Biol, Lille, France
[5] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Genom Med, London SW7 2AZ, England
基金
英国医学研究理事会;
关键词
ENPP1; PPAR gamma; diabetes; overweight; Tunisians;
D O I
10.1016/j.diabres.2008.06.004
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Diabetes mellitus is the most common chronic metabolic disease. The raising diabetes epidemic is unfolding as an interaction between several environmental factors and a genetic predisposition. The aim of the current study was to evaluate the role of the PPAR gamma-Pro12Ala and ENPP1-K121Q polymorphisms on type 2 diabetes (T2D) risk in a case-control study in the Tunisian population. To assess for any association of ENPP1-K121Q and PPAR gamma-Pro12Ala polymorphisms with T2D risk, we analysed the genotypic and allelic distributions of each variant in the studied cohort. Our results support that the genetic variation at ENPP1-K121Q predisposes to T2D in the Tunisian population after adjustment on gender, age and BMI status (OR = 1.55, 95%CI [1.11-2.16], p = 0.007). Conversely, the PPAR-y-Pro12Ala variant seems not to have a significant effect on T2D risk in our Tunisian cohort. However, the minor A-allele would convey protection against overweight in the Tunisian population. In fact, the over weighted subjects showed a significantly lower frequency of A-allele than lean controls (OR = 0.49, 95%CI [0.25-0.97], p = 0.02). in conclusion, our findings support the hypothesis that ENPP1-121Q is involved in the genetic susceptibility of T2D in the Tunisian population, while the PPAR gamma-12Ala allele may confer protection against overweight. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:278 / 283
页数:6
相关论文
共 51 条
[1]
ENPP1/PC-1 K121Q polymorphism and genetic susceptibility to type 2 diabetes [J].
Abate, N ;
Chandalia, M ;
Satija, P ;
Adams-Huet, B ;
Grundy, SM ;
Sandeep, S ;
Radha, V ;
Deepa, R ;
Mohan, V .
DIABETES, 2005, 54 (04) :1207-1213
[2]
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes [J].
Altshuler, D ;
Hirschhorn, JN ;
Klannemark, M ;
Lindgren, CM ;
Vohl, MC ;
Nemesh, J ;
Lane, CR ;
Schaffner, SF ;
Bolk, S ;
Brewer, C ;
Tuomi, T ;
Gaudet, D ;
Hudson, TJ ;
Daly, M ;
Groop, L ;
Lander, ES .
NATURE GENETICS, 2000, 26 (01) :76-80
[3]
Testing for population subdivision and association in four case-control studies [J].
Ardlie, KG ;
Lunetta, KL ;
Seielstad, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (02) :304-311
[4]
New polymorphism of ENPP1 (PC-1) is associated with increased risk of type 2 diabetes among obese individuals [J].
Bochenski, Jacek ;
Placha, Grzegorz ;
Wanic, Krzysztof ;
Malecki, Maciej ;
Sieradzki, Jacek ;
Warram, James H. ;
Krolewski, Andrzej S. .
DIABETES, 2006, 55 (09) :2626-2630
[5]
Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns [J].
Bonnycastle, Lori L. ;
Willer, Cristen J. ;
Conneely, Karen N. ;
Jackson, Anne U. ;
Burrill, Cecily P. ;
Watanabe, Richard M. ;
Chines, Peter S. ;
Narisu, Narisu ;
Scott, Laura J. ;
Enloe, Sareena T. ;
Swift, Amy J. ;
Duren, William L. ;
Stringham, Heather M. ;
Erdos, Michael R. ;
Riebow, Nancy L. ;
Buchanan, Thomas A. ;
Valle, Timo T. ;
Tuomilehto, Jaakko ;
Bergman, Richard N. ;
Mohlke, Karen L. ;
Boehnke, Michael ;
Collins, Francis S. .
DIABETES, 2006, 55 (09) :2534-2540
[6]
The peroxisome proliferator activated receptorγ2 (PPARγ2) Pro12Ala variant:: lack of association with type 2 diabetes in obese and non obese Tunisian patients [J].
Bouassida, KZ ;
Chouchane, L ;
Jellouli, K ;
Chérif, S ;
Haddad, S ;
Gabbouj, S ;
Danguir, J .
DIABETES & METABOLISM, 2005, 31 (02) :119-123
[7]
The global diabetes pandemic: the Tunisian experience [J].
Bouguerra, R. ;
Alberti, H. ;
Salem, L. B. ;
Rayana, C. B. ;
Atti, J. E. ;
Gaigi, S. ;
Slama, C. B. ;
Zouari, B. ;
Alberti, K. .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2007, 61 (02) :160-165
[8]
Cauchi S, 2006, DIABETES, V55, P3635
[9]
TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis [J].
Cauchi, Stephane ;
El Achhab, Younes ;
Choquet, Helene ;
Dina, Christian ;
Krempler, Franz ;
Weitgasser, Raimund ;
Nejjari, Chakib ;
Patsch, Wolfgang ;
Chikri, Mohamed ;
Meyre, David ;
Froguel, Philippe .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2007, 85 (07) :777-782
[10]
TCF7L2 variation predicts hyperglycentia incidence in a French general population -: The Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study [J].
Cauchi, Stephane ;
Meyre, David ;
Choquet, Helene ;
Dina, Christian ;
Born, Catherine ;
Marre, Michel ;
Balkau, Beverley ;
Froguel, Philippe .
DIABETES, 2006, 55 (11) :3189-3192