BIENERTOVÁ VAŠKŮ, Julie, Anna VAŠKŮ, Zuzana DOSTÁLOVÁ and Petr BIENERT. ASSOCIATION OF LEPTIN GENETIC POLYMORPHISM -2548 G/A WITH GESTATIONAL DIABETES. Genes and Nutrition. New Century Health Publishers, 2006, 2/2006, No 2, p. 117-124, 5 pp. ISSN 1555-8932.
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Basic information
Original name ASSOCIATION OF LEPTIN GENETIC POLYMORPHISM -2548 G/A WITH GESTATIONAL DIABETES
Name in Czech Asociace genetického polymorfismu -2548 G/A v genu pro leptin s gestačním diabetem
Authors BIENERTOVÁ VAŠKŮ, Julie (203 Czech Republic, guarantor), Anna VAŠKŮ (203 Czech Republic), Zuzana DOSTÁLOVÁ (203 Czech Republic) and Petr BIENERT (203 Czech Republic).
Edition Genes and Nutrition, New Century Health Publishers, 2006, 1555-8932.
Other information
Original language English
Type of outcome Article in a journal
Field of Study Genetics and molecular biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
WWW URL
RIV identification code RIV/00216224:14110/06:00017421
Organization unit Faculty of Medicine
UT WoS 000258559500006
Keywords in English Gestational Diabetes Mellitus; Leptin; Polymorphism; Preeclampsia
Tags gestational diabetes mellitus, leptin, polymorphism, preeclampsia
Tags International impact, Reviewed
Changed by Changed by: prof. MUDr. Anna Vašků, CSc., učo 122. Changed: 18/6/2009 08:15.
Abstract
The aim of this study was to investigate possible associations of -2548 G/A polymorphism in leptin gene promoter and pregnancy-associated diseases with abnormal fetal growth such as preeclampsia and gestational diabetes. The study was also focused on whether it is rather maternal or fetal variants that determines the pathological growth status. Peripheral or cord blood samples obtained from 49 preeclamptic women and their 39 newborns, 53 healthy controls and their 53 healthy newborns and 48 patients with gestational diabetes mellitus were evaluated for leptin gene (LEP) locus -2548 genotypes. The significantly higher risk for gestational diabetes mellitus was observed in the presence of an allele (AA and AG genotypes) against carriers of GG genotype (OR=2.84, 95%CI 1.14-7.07, p=0.02). There is a significant risk of diabetes mellitus associated to A allele (OR=1.79, 95%CI 1.02-3.14, p=0.03). Furthermore, evaluations of preeclamptic patients data revealed a significant association of genotype distribution and delivery and spontaneous abortion rate, where the GG carriers performed the highest pregnancy rate while the AG carriers performed the lowest spontaneous abortion rate. Our results support the hypothesis for -2548 G/A leptin gene polymorphism involvement in ethiopathogenesis of pregnancy-associated diseases with abnormal fetal growth, especially gestational diabetes mellitus.
Abstract (in Czech)
Získaná data naznačují, ze variabilita v genu pro leptin, konkrétně definovaný polymorfismus -2548 G/A se může uplatnit jako etiopatogenetický faktor při vzniku gestačního diabetu nebo obecně při poruchách fetálního růstu.
Links
MSM 141100002, plan (intention)Name: Molekulární patofyziologie multigenních chorob
Investor: Ministry of Education, Youth and Sports of the CR, Molecular pathophysiology of multigene diseases
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