国际眼科纵览 ›› 2014, Vol. 38 ›› Issue (4): 236-241.doi: 103706/ cma.j.issn.16735803201404005

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我国TGFBI基因相关性角膜营养不良的研究现状

梁庆丰 潘志强   

  1. 100730 首都医科大学附属北京同仁医院 北京同仁眼科中心 北京市眼科研究所 眼科学与视觉科学北京市重点实验室
  • 收稿日期:2014-04-18 出版日期:2014-08-22 发布日期:2014-09-02
  • 通讯作者: 潘志强,Email:panyj0526@sina.com E-mail:panyj0526@sina.com

Current study situation of TGFBI Gene related corneal dystrophy in China

LIANG Qing-feng, PAN Zhi-qiang   

  1. eijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Key laboratory of Ophthalmology and Visual Science, Beijing Tongren Hospital, Capital Medical University, 100730 Beijing, China
  • Received:2014-04-18 Online:2014-08-22 Published:2014-09-02
  • Contact: PAN Zhiqiang, Email: panyj0526@sina.com E-mail:panyj0526@sina.com

摘要: TGFBI是最常见的角膜营养不良致病基因,角膜营养不良家系在TGFBI基因上的突变已发现33种,TGFBI基因表达的产物角膜上皮蛋白(keratoepithelin, KE蛋白)沉积于患者角膜中。1998-2014年中国人角膜营养不良TGFBI基因突变类型已报告17种,约71个家系445例患者,其中由R555W突变导致的Ⅰ型颗粒状角膜营养不良占28.2%,由R124H突变导致的Ⅱ型颗粒状角膜营养不良占239%,而Thiel\|Behnke角膜营养不良家系在中国人较少见(5%)。

Abstract: Genotypic analysis has revealed that TGFBI gene is the most important and common pathogenic gene to corneal dystrophy. Tirty\|three mutations of TGFBI gene had been reported in corneal dystrophy families. Keratoepithelin protein (KE protein) expressed by TGFBI gene was always deposited in the different layer of the cornea. In Chinese corneal dystrophy families, 17 TGFBI gene mutations (445 cases, 71 families) were detected from 1998 to 2014. Among them, 28.2% mutations were R555W which induced granular corneal dystrophy type Ⅰ(GCDⅠ), 23.9% mutations were R124H related to granular corneal dystrophy type Ⅱ (GCDⅡ), and 5% mutations were reltaed to Thiel\|Behnke corneal dystrophy.