2009, Number 2
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Rev Esp Med Quir 2009; 14 (2)
Proposal for identifying genomic disorders to gestational diabetes in Mexican population
Silva XCA, Escobedo AF, Tusie LMT
Language: Spanish
References: 34
Page: 83-87
PDF size: 234.25 Kb.
ABSTRACT
Diabetes mellitus is among the primary mortality and morbidity causes in Mexico. Genetic factors play a fundamental role in the development of this entity. In the past few years due to the recognition and study of families with monogenic forms of diabetes and dyslipidemias associated with development of atherosclerosis, several genes and loci have been associated with this condition through genetic linkage studies. These studies have provided evidence of the genetic heterogeneity that exists and the type of genes involved in different ethnic groups. The study of Mexican families with early-onset diabetes gestational showed the participation of different genetic loci associated with these conditions in the Mexican population. These findings show the value of gene mapping strategies in the identification of the genetic component in these entities in our population.
REFERENCES
Secretaria de Salud, Dirección General de Epidemiología. México, 1999.
Gleicher Norbert. Medicina clínica en obstetricia. Diabetes y Embarazo. Panamericana, 1989.
Arias F. Guía práctica para el embarazo y el parto de alto riesgo. Diabetes y embarazo. 2ª ed. Madrid: Mosby/Doyma.
Cabero RL. Tratado de ginecología, obstetricia y medicina de la reproducción. Diabetes y embarazo. Sociedad Española de Ginecología y Obstetricia. Tomo 1. 1ª ed. Panamericana, 2003.
Cabero RL. Riesgo obstétrico elevado. Diabetes y gestación. 1ª ed. Masson, 1996.
American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care 2004;27(Suppl. 1):S5-S10.
Grupo de Estudio sobre Diabetes Mellitus. Diabetes y embarazo. Importancia diagnóstica. Rev Med IMSS 1992;30:35-39.
Forsbach G, Contreras-Soto JJ, Fong G, Flores G, Moreno O. Prevalence of gestational diabetes and macrosomic newborns in a Mexican population. Diabetes Care 1988;11(3):235-8.
McLellan JA, Barrow BA, Levy JC, Hammersley MS, et al. Prevalence of diabetes mellitus and impaired glucose tolerance in parents of women with gestational diabetes. Diabetologia 1995;38(6):693-8.
Rodrigues S, Robinson EJ, Ghezzo H, Gray-Donald K. Interaction of body weight and ethnicity on risk of gestational diabetes mellitus. Am J Clin Nutr 1999;70(6):1083-9.
Savona-Ventura C, Azzopardi J, Sant R. Risk factors for gestational diabetes mellitus in the Maltese population: a population based study. Int J Risk Safety Med 2000;13:1-7.
Gloyn AL, Weedon MN, Owen KR, Turner MJ, et al. Large scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCJNJ11 E23K variant is associated with type 2 diabetes. Diabetes 2003;52(2):568-72.
Leipold H, Knöfler M, Gruber C, Haslinger P, et al. Calpain-10 haplotype combination and association with gestational diabetes mellitus. Obstet Gynecol 2004;103(6):1235-40.
Ellard S, Beards F, Allen LIS, Shepherd M, et al. A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria. Diabetologia 2000;43:250-3.
Hitman GA, Sudagani J. Searching for genes in diabetes and the metabolic syndrome. Int J Clin Pract Suppl 2004;143:3-8.
Frayling TM. Genome-wide association studies provide new insights into type 2 diabetes aetiology. Nat Rev Genet 2007;8(9):657-62.
Grant SF, Thorleifsson G, Reynisdottir I, Beneditsson R, et al. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat Genet 2006;38(3):320-3.
Yamagata K, Furuta H, Oda N, Kaisaki PJ, et al. Mutations in the hepatocyte nuclear factor-4 alpha gene in maturity-onset diabetes on the young (MODY1). Nature 1996;384(6608):458-60.
Hani EH, Stoffers DA, Chevre JC, Durand E, Froguel P. Defective mutations in the insulin promoter factor (IPF-1) gene in late-onset type 2 diabetes mellitus. J Clin Invest 1999;104:R41-R48.
Shaat N, Karlsson E, Lernmark A, Ivarsson S, et al. Common variants in MODY genes increase the risk of gestational diabetes mellitus. Diabetologia 2006;49:1545-51.
Muller YL, Infante AM, Hanson RL, Love-Gregory L, et al. Variants in hepatocyte nuclear factor 4alpha are modestly associated with type 2 diabetes in Pima indians. Diabetes 2005;54:3035-9.
Weedon MN, Owen KR, Shields B, Hitman G, et al. Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population. Diabetes 2004;53:3002-6.
Vaxillaire M, Dina C, Lobbens S, Dechaume A, et al. Effect of common polymorphisms in the HNF4alpha promoter on susceptibility to type 2 diabetes in the French Caucasian population. Diabetologia 2005;48:440-4.
Winckler W, Graham RR, De Bakker PI, Sun M, et al. Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people. Diabetes 2005;54:886-92.
Weissglas-Volkov D, Huertas-Vazquez A, Suviolahti E, Lee J, et al. Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome. Diabetes 2006,55(7):1970-7.
Salonen JT, Uimari P, Aalto JM, Pirskanen M, et al. Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. Am J Hum Genet 2007;81(2):338-45.
Groves CJ, Zeggini E, Minton J, Frayling TM, et al. Association analysis of 6736 U.K. subjects provides replication and confirms TCFT7L2 as a type 2 diabetes susceptibility gene with substantial effect on individual risk. Diabetes 2006;55:2640-4.
Damcott CM, Pollin TI, Reinhart LJ, Ott SH, et al. Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance. Diabetes 2006;55:2654-9.
Scott LJ, Bonnycastle C, Willer CJ, Sprau AG, et al Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. Diabetes 2006;55:2649-53.
Van Vliet-Ostaptchouk JV, Shiri-Sversdlov R, Zhernakova A, Strengman E, et al. Association of variants of transcription factor 7-like 2 (TCF7L2) with susceptibility to type 2 diabetes in the Dutch Breda cohort. Diabetologia 2007;50(1):59-62.
Villarreal-Molina MT, Aguilar-Salinas CA, Rodríguez-Cruz M, Riaño D, et al, The ABCA1 R230 variant affects HDLcholesterol levels and body mass index in the Mexican population: association with obesity and obesity-related comorbidities. Diabetes 2007;56:1881-7.
Villarreal-Molina MT, Arellano-Campos O, Dorantes-Flores MT, Villalobos-Comparan M, et al. The Metabolic Study Group Association of the ABCA1 R230C variant with earlyonset type 2 diabetes and its interaction with obesity in the Mexican population. Diabetes 2008;57:509-13.
Attie AD, Kastelein JP, Hayden MR. Pivotal role of ABCA1 in reverse cholesterol transport influencing HDL levels and susceptibility to atherosclerosis. J Lipid Res 2001;42:1717-26.
Brunham LR, Kruit JK, Pape TD, Parks JS, et al. Tissuespecific induction of intestinal ABCA1 expression with a liver X receptor agonist raises plasma HDL cholesterol levels. Cir Res 2006;99(7):672-4.