Bahíllo Curieses P, Hermoso López F, Garrote Molpeceres R, Zurita Muñoz O, Campos Barros A
Departamento de Endocrinología Pediátrica, Hospital Clínico Universitario, Valladolid, España.
An Pediatr (Barc). 2011 Oct;75(4):273-6. doi: 10.1016/j.anpedi.2011.05.009. Epub 2011 Jun 22.
Glucokinase is one of the most important regulators of fasting glucose levels. There are several mutations in the glucokinase gene (GCK) which are linked with monogenic diabetes. Recently, a polymorphism in its promoter has been described, which is associated with impaired fasting glucose levels. We present a 7 years and 7 months old boy with overweight and a familial background of diabetes in two previous generations. In the oral glucose tolerance test, he had impaired fasting glucose levels and after two hours, with a high insulin response. Laboratory abnormalities improved after weight loss, but he maintains a slight fasting hyperglycaemia. The molecular study of the most common monogenic diabetes forms, MODY subtypes 1, 2, and 3, was negative. The allelic variant G/A was however detected at the GCK promoter polymorphism rs1799884.
葡萄糖激酶是空腹血糖水平最重要的调节因子之一。葡萄糖激酶基因(GCK)存在多种突变,这些突变与单基因糖尿病有关。最近,有人描述了其启动子中的一种多态性,它与空腹血糖水平受损有关。我们报告一名7岁7个月大的超重男孩,其家族有两代糖尿病病史。在口服葡萄糖耐量试验中,他空腹血糖水平受损,两小时后胰岛素反应较高。体重减轻后实验室异常情况有所改善,但他仍维持轻微的空腹高血糖。对最常见的单基因糖尿病类型,即青少年发病的成年型糖尿病(MODY)1、2和3型的分子研究结果为阴性。然而,在GCK启动子多态性rs1799884处检测到等位基因变体G/A。