Chen Miao-Pei, Chung Fu-Mei, Chang Dao-Ming, Tsai Jack C-R, Huang Han-Fen, Shin Shyi-Jang, Lee Yau-Jiunn
Department of Clinical Research, Pingtung Christian Hospital, Pingtung, 90000 Taiwan.
Rev Diabet Stud. 2006 Spring;3(1):21-30. doi: 10.1900/RDS.2006.3.21. Epub 2006 May 10.
Ectoenzyme nucleotide pyrophosphate phosphodiesterase 1 (ENPP1) is known to influence insulin sensitivity by inhibiting insulin receptor signaling. A DNA polymorphism in the ENPP1 gene at exon 4 (K121Q) was demonstrated to be associated with insulin resistance, type 2 diabetes mellitus (T2DM), and a risk of early myocardial infarction, albeit with controversy. Our aim was to investigate any association of ENPP1 K121Q alleles with T2DM, features of the metabolic syndrome, and diabetic cardiovascular complications in a Chinese population of Han origin.
The ENPP1 K121Q polymorphism was determined by a restriction fragment-length polymorphism-polymerase chain reaction in 1,862 patients with T2DM and 844 non-diabetic subjects.
The genotype distributions or Q-allele frequency were not statistically different between the diabetic and non-diabetic groups. The anthropometric parameters, systolic and diastolic blood pressures, lipid profiles, and serum creatinine levels of subjects with different ENPP1 K121Q polymorphisms were not statistically different in the two groups or even in the pooled data. When sub-group analyses of diabetic subjects were stratified according to BMI levels (greater or less than 27), gender, age of diabetes onset (older or younger than 60 years), and the presence or absence of a diabetic family history; this polymorphism was still not associated with T2DM. Nor was the ENPP1 K121Q polymorphism associated with the prevalence of coronary artery disease and ischemic cerebrovascular disease in patients with T2DM.
The ENPP1 K121Q polymorphism is not related to T2DM, features of the metabolic syndrome, or diabetic macrovascular complications in a Chinese population.
已知胞外核苷酸焦磷酸磷酸二酯酶1(ENPP1)通过抑制胰岛素受体信号传导来影响胰岛素敏感性。尽管存在争议,但已证明ENPP1基因第4外显子的一个DNA多态性(K121Q)与胰岛素抵抗、2型糖尿病(T2DM)以及早期心肌梗死风险相关。我们的目的是研究ENPP1 K121Q等位基因与中国汉族人群的T2DM、代谢综合征特征以及糖尿病心血管并发症之间的任何关联。
采用限制性片段长度多态性-聚合酶链反应法对1862例T2DM患者和844例非糖尿病受试者进行ENPP1 K121Q多态性检测。
糖尿病组和非糖尿病组之间的基因型分布或Q等位基因频率无统计学差异。在两组甚至合并数据中,具有不同ENPP1 K121Q多态性的受试者的人体测量参数、收缩压和舒张压、血脂谱以及血清肌酐水平均无统计学差异。当根据BMI水平(大于或小于27)、性别、糖尿病发病年龄(大于或小于60岁)以及是否有糖尿病家族史对糖尿病受试者进行亚组分析时;这种多态性仍与T2DM无关。ENPP1 K121Q多态性也与T2DM患者的冠状动脉疾病和缺血性脑血管疾病患病率无关。
在中国人群中,ENPP1 K121Q多态性与T2DM、代谢综合征特征或糖尿病大血管并发症无关。