Froguel P, Velho G
Inserm U358, Paris, France.
Curr Opin Pediatr. 1994 Aug;6(4):482-5. doi: 10.1097/00008480-199408000-00022.
Maturity-onset diabetes of the young (MODY) is an autosomal dominant-subtype of noninsulin-dependent diabetes mellitus, characterized by an early age of onset. MODY is considered a model for genetic studies of noninsulin-dependent diabetes mellitus because of the availability of large multigenerational families, which make linkage analyses possible. So far, two MODY susceptibility loci have been reported, one unknown gene on chromosome 20q, and glucokinase on chromosome 7q. Glucokinase mutations appear to be the most common cause of MODY in the European population, being found in 60% of the families investigated. This form of diabetes results from a primary defect in insulin secretion due to the reduced enzymatic activity of the mutant glucokinase. The search for a third MODY gene will provide a better understanding of diabetes in childhood.
青少年发病的成年型糖尿病(MODY)是常染色体显性遗传的非胰岛素依赖型糖尿病的一个亚型,其特征为发病年龄较早。由于存在大型多代家族,使得连锁分析成为可能,因此MODY被视为非胰岛素依赖型糖尿病基因研究的一个模型。到目前为止,已报道了两个MODY易感基因座,一个位于20号染色体上的未知基因,另一个是位于7号染色体上的葡萄糖激酶。在欧洲人群中,葡萄糖激酶突变似乎是MODY最常见的病因,在所研究的家族中有60%发现了这种突变。这种糖尿病是由于突变的葡萄糖激酶酶活性降低导致胰岛素分泌的原发性缺陷所致。寻找第三个MODY基因将有助于更好地理解儿童糖尿病。