Radha Venkatesan, Kanthimathi Sekar, Anjana Ranjit Mohan, Mohan Viswanathan
Madras Diabetes Research Foundation, WHO Collaborating Centre for Noncommunicable Diseases Prevention and Control, Chennai, India.
Madras Diabetes Research Foundation, WHO Collaborating Centre for Noncommunicable Diseases Prevention and Control, Chennai, India and Dr. Mohan's Diabetes Specialities Centre, WHO Collaborating Centre for Noncommunicable Diseases Prevention and Control, Chennai, India.
J Pak Med Assoc. 2016 Sep;66(9 Suppl 1):S11-4.
Gestational diabetes mellitus (GDM) has now become a major public health problem because of its prevalence and its associated complications during pregnancy. Earlier studies have suggested that type 2 diabetes mellitus (T2DM) and GDM might have similar pathophysiology, such as increased insulin resistance, decreased insulin secretion resulting in hyperglycaemia. Evidence for a genetic basis of GDM has been poorly understood. To some extent, the current advancement in genomic techniques has thrown better light on the genetics of GDM. Based on the candidate gene approach and genome wide association studies, genetic loci in several genes that are responsible for insulin secretion, insulin resistance, lipid and glucose metabolism and other pathways have shown association with the GDM susceptibility. Understanding the possible underlying genetic factors of GDM would help us in gaining knowledge on the pathophysiologic mechanism of the disease.
妊娠糖尿病(GDM)因其在孕期的患病率及其相关并发症,现已成为一个主要的公共卫生问题。早期研究表明,2型糖尿病(T2DM)和GDM可能具有相似的病理生理学,如胰岛素抵抗增加、胰岛素分泌减少导致高血糖。GDM的遗传基础证据一直未得到充分理解。在某种程度上,基因组技术的当前进展使人们对GDM的遗传学有了更好的了解。基于候选基因方法和全基因组关联研究,几个负责胰岛素分泌、胰岛素抵抗、脂质和葡萄糖代谢以及其他途径的基因中的遗传位点已显示与GDM易感性相关。了解GDM可能的潜在遗传因素将有助于我们了解该疾病的病理生理机制。