The Common C49620T Polymorphism in the Sulfonylurea Receptor Gene SUR1 (ABCC8) in Patients with Gestational Diabetes and Subsequent GlucoseMetabolism Abnormalities

被引:4
作者
Moleda, Piotr [1 ]
Binczak-Kuleta, Agnieszka [2 ]
Homa, Katarzyna [1 ]
Safranow, Krzysztof [3 ]
Celewicz, Zbigniew [4 ]
Syrenicz, Anhelli [5 ]
Stefanski, Adam [1 ]
Fronczyk, Aneta [1 ]
Majkowska, Lilianna [1 ]
机构
[1] Pomeranian Med Univ, Dept Diabetol & Internal Dis, Szczecin, Poland
[2] Pomeranian Med Univ, Chair Clin Biochem & Lab Diagnost, Szczecin, Poland
[3] Pomeranian Med Univ, Chair Biochem & Med Chem, Szczecin, Poland
[4] Pomeranian Med Univ, Dept Maternal Fetal Med & Gynecol, Szczecin, Poland
[5] Pomeranian Med Univ, Dept Endocrinol Metab & Internal Dis, Szczecin, Poland
关键词
IMPAIRED GLUCOSE-TOLERANCE; HIGH PREVALENCE; MELLITUS; WOMEN; VARIANTS; RISK; MUTATIONS; NIDDM;
D O I
10.1155/2012/712617
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim. The aim of this study is to investigate the relationship between the common C49620T polymorphism in the sulfonylurea receptor (SUR1) gene and glucose metabolism, beta-cell secretory function and insulin resistance in women with a history of gestational diabetes (GDM). Material and Methods. Study group included 199 women, diagnosed GDM within the last 5-12 years and control group of comparable 50 women in whom GDM was excluded during pregnancy. Blood glucose and insulin levels were measured during oral glucose tolerance test. Indices of insulin resistance (HOMA-IR) and beta-cell function (HOMA %B) were calculated. In all patients, the C49620T polymorphism in intron 15 of the SUR1 gene was determined. Results. The distribution of the studied polymorphism in the two groups did not differ from each other (chi(2) = 0.34, P = 0.8425). No association between the distribution of polymorphisms and coexisting glucose metabolism disorders (chi(2) = 7,13, P = 0, 3043) was found. No association was also observed between the polymorphism and HOMA %B or HOMA-IR. Conclusions. The polymorphism C49620T in the SUR1 gene is not associated with insulin resistance and/or insulin secretion in women with a history of GDM and does not affect the development of GDM, or the development of glucose intolerance in the studied population.
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页数:7
相关论文
共 31 条
  • [1] 17β-Estradiol Modulates Apoptosis in Pancreatic β-Cells by Specific Involvement of the Sulfonylurea Receptor (SUR) Isoform SUR1
    Ackermann, Stefanie
    Hiller, Sabrina
    Osswald, Hartmut
    Loesle, Martina
    Grenz, Almut
    Hambrock, Annette
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (08) : 4905 - 4913
  • [2] [Anonymous], DIABETOL DOSW KLIN
  • [3] Risk Factors for Type 2 Diabetes Among Women with Gestational Diabetes: A Systematic Review
    Baptiste-Roberts, Kesha
    Barone, Bethany B.
    Gary, Tiffany L.
    Golden, Sherita H.
    Wilson, Lisa M.
    Bass, Eric B.
    Nicholson, Wanda K.
    [J]. AMERICAN JOURNAL OF MEDICINE, 2009, 122 (03) : 207 - U34
  • [4] Type 2 diabetes mellitus after gestational diabetes: a systematic review and meta-analysis
    Bellamy, Leanne
    Casas, Juan-Pablo
    Hingorani, Aroon D.
    Williams, David
    [J]. LANCET, 2009, 373 (9677) : 1773 - 1779
  • [5] Pancreatic B-cell defects in gestational diabetes: Implications for the pathogenesis and prevention of type 2 diabetes
    Buchanan, TA
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (03) : 989 - 993
  • [6] Gestational diabetes mellitus
    Buchanan, TA
    Xiang, AH
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (03) : 485 - 491
  • [7] INSULIN SENSITIVITY AND B-CELL RESPONSIVENESS TO GLUCOSE DURING LATE PREGNANCY IN LEAN AND MODERATELY OBESE WOMEN WITH NORMAL GLUCOSE-TOLERANCE OR MILD GESTATIONAL DIABETES
    BUCHANAN, TA
    METZGER, BE
    FREINKEL, N
    BERGMAN, RN
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1990, 162 (04) : 1008 - 1014
  • [8] Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population
    Cho, Y. M.
    Kim, T. H.
    Lim, S.
    Choi, S. H.
    Shin, H. D.
    Lee, H. K.
    Park, K. S.
    Jang, H. C.
    [J]. DIABETOLOGIA, 2009, 52 (02) : 253 - 261
  • [9] DORNER G, 1987, EXP CLIN ENDOCRINOL, V89, P84
  • [10] A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria
    Ellard, S
    Beards, F
    Allen, LIS
    Shepherd, M
    Ballantyne, E
    Harvey, R
    Hattersley, AT
    [J]. DIABETOLOGIA, 2000, 43 (02) : 250 - 253