Khan Imran Ali, Movva Sireesha, Shaik Noor Ahmad, Chava Srinivas, Jahan Parveen, Mukkavali Kamal Kiran, Kamineni Vasundhara, Hasan Qurratulain, Rao Pragna
Department of Genetics and Molecular Medicine, Kamineni Hospitals, LB Nagar, Hyderabad 500068, India ; Department of Genetics, Vasavi Medical and Research Centre, Lakdikapool, Hyderabad 500004, India ; Department of Genetics and Biotechnology, Osmania University, Tarnaka, Hyderabad 500007, India.
Department of Genetics, Vasavi Medical and Research Centre, Lakdikapool, Hyderabad 500004, India.
Meta Gene. 2014 Apr 17;2:299-306. doi: 10.1016/j.mgene.2014.03.001. eCollection 2014 Dec.
Type 2 Diabetes Mellitus (T2DM) and Gestational Diabetes Mellitus (GDM) are part of a heterogeneous and complex metabolic group of disorders that share common pathophysiological circumstances, including β-cell dysfunction and insulin resistance. The protein Calpain 10 (CAPN10) plays a role in glucose metabolism, pancreatic β-cell insulin secretion, and thermogenesis.
Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) based genotyping of CAPN10 (rs2975760) polymorphism was carried out in T2DM and GDM with suitable controls for each of the pathologies from the same population. Genomic DNA was isolated from 787 participants, including 250 cases of T2DM, 287 pregnant women, of which 137 were identified as having GDM and the remaining 150 were confirmed as non-GDM, and 250 healthy control volunteers, and association analysis was carried out for genotypes and alleles.
In the present study, T2DM was compared with healthy controls and was not found to be associated with the CAPN10 C allele (odds ratio, OR: 1.09; 95% CI = 0.8011-1.484; p = 0.5821). GDM also did not show any association when compared with non-GDM (OR: 1.124; 95% CI = 0.7585-1.667; p = 0.5606) respectively.
Our study suggests that the CAPN10 (rs2975760) polymorphism scrutinized in this study is not associated with T2DM and GDM.
2型糖尿病(T2DM)和妊娠期糖尿病(GDM)是一组异质性且复杂的代谢紊乱疾病,它们具有共同的病理生理情况,包括β细胞功能障碍和胰岛素抵抗。钙蛋白酶10(CAPN10)蛋白在葡萄糖代谢、胰腺β细胞胰岛素分泌及产热过程中发挥作用。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对来自同一人群的T2DM和GDM患者以及每种疾病相应的合适对照进行CAPN10(rs2975760)多态性基因分型。从787名参与者中分离出基因组DNA,其中包括250例T2DM患者、287名孕妇(其中137例被诊断为GDM,其余150例被确认为非GDM)以及250名健康对照志愿者,并对基因型和等位基因进行关联分析。
在本研究中,将T2DM患者与健康对照进行比较,未发现其与CAPN10 C等位基因相关(优势比,OR:1.09;95%置信区间=0.8011 - 1.484;p = 0.5821)。将GDM患者与非GDM患者进行比较时,也未显示出任何相关性(OR:1.124;95%置信区间=0.7585 - 1.667;p = 0.5606)。
我们的研究表明,本研究中所检测的CAPN10(rs2975760)多态性与T2DM和GDM无关。