首页 | 本学科首页   官方微博 | 高级检索  
     

中国妊娠期血糖异常人群葡萄糖激酶基因突变初步筛查
引用本文:王志新,平凡,张茜,郑佳,李明敏,刘一静,张化冰,于淼,李文慧,肖新华. 中国妊娠期血糖异常人群葡萄糖激酶基因突变初步筛查[J]. 中华糖尿病杂志, 2014, 0(6): 397-401
作者姓名:王志新  平凡  张茜  郑佳  李明敏  刘一静  张化冰  于淼  李文慧  肖新华
作者单位:中国医学科学院北京协和医学院北京协和医院内分泌科卫生部内分泌重点实验室,100730
基金项目:国家自然科学基金项目(81170736);卫生部内分泌重点实验室面上项目;“国家临床重点专科”资助课题;卫生部·诺和诺德糖尿病研究英才基金
摘    要:目的 初步明确中国妊娠期血糖异常人群中葡萄糖激酶(GCK)基因突变情况.方法 回顾性选择2005年7月至2008年5月在北京协和医院进行妊娠期血糖筛查并进行了口服葡萄糖耐量试验(OGTT)和糖化血红蛋白(HbA1c)检测的妊娠妇女.以空腹血糖在5.5~ 10.0 mmol/L、OGTT试验2h与0h血糖差值小于4.6 mmol/L且HbA1c值小于8.0%作为筛选条件,对满足所有条件者进行GCK基因外显子区和启动子区-71G>C的突变筛查.结果 共纳入577例受试者,符合GCK基因检测条件者30例,可获得标本数17例,发现1例GCK基因突变致青少年的成人起病型糖尿病2型(MODY2)患者和1处非编码区新变异.该MODY2患者6号外显子区c.626 C>T(NM_000162.3)突变导致第209位编码氨基酸从苏氨酸变为甲硫氨酸(p.T209M,NP_000153.1).推测中国妊娠期血糖异常人群GCK最小突变率为0.27%,估测中国总人群中MODY2的最小患病率为21/10万.结论 中国妊娠期血糖异常的人群中GCK基因突变并不常见.

关 键 词:糖尿病,妊娠  妊娠期糖代谢异常  青少年的成人起病型糖尿病2型  葡萄糖激酶基因突变  Maturity-onset  diabetes  of  the  young  type  2

Preliminary screening of mutations in the glucokinase gene in Chinese gestational subjects with abnormal glucose metabolism
Wang Zhixin,Ping Fan,Zhang Qian,Zheng Jia,Li Mingmin,Liu Yijing,Zhang Huabing,Yu Miao,Li Wenhui,Xiao Xinhua. Preliminary screening of mutations in the glucokinase gene in Chinese gestational subjects with abnormal glucose metabolism[J]. CHINESE JOURNAL OF DIABETES MELLITUS, 2014, 0(6): 397-401
Authors:Wang Zhixin  Ping Fan  Zhang Qian  Zheng Jia  Li Mingmin  Liu Yijing  Zhang Huabing  Yu Miao  Li Wenhui  Xiao Xinhua
Affiliation:. (Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Key Laboratory of Ministry of Health, Beijing 100730, China)
Abstract:Objective To preliminarily assess the rate of glucokinase (GCK) gene mutation in Chinese gestational subjects with abnormal glucose metabolism.Methods We retrospectively analyzed Chinese gestational subjects who received oral glucose tolerance test and glycosylated hemoglobin A1c (HbA1c) detection in Peking Union Medical College Hospital (PUMCH) from July 2005 to May 2008.Subjects were selected for direct sequencing of GCK gene if they met the following three criteria:(1) fasting plasma glucose was between 5.5 and 10.0 mmol/L; (2) a small increase (〈 4.6 mmol/L) in plasma glucose 2 hours after an oral glucose load ; (3) HbA1 c was below 8.0%.Results A total of 577 subjects were collected in this study,in which 30 subjects met the criteria for GCK gene mutation testing.Of the 17 subjects whose DNA samples were obtainable,one case of maturity-onset diabetes of the young type 2 (MODY2) with GCK gene mutation c.626 C 〉 T(NM_000162.3) in exon6 and one case with previously unreported variation in noncoding region had been found.The mutation c.626C 〉 T(NM_000162.3) resulted in the substitution of methionine for threonine in amino acid 209 (p.T209M,NP_000153.1).It was estimated the minimum GCK gene mutation rate was 0.27% in Chinese gestational subjects with abnormal glucose metabolism,and the minimum prevalence of MODY2 was 21/100 000 in Chinese population.Conclusion The GCK gene mutations are not common in Chinese gestational subjects with abnormal glucose metabolism.
Keywords:Diabetes,gestational  Abnormal glucose metabolism in pregnancy  Glucokinase gene mutation
本文献已被 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号