Percy Alan K, Lane Jane B, Childers Jerry, Skinner Steve, Annese Fran, Barrish Judy, Caeg Erwin, Glaze Daniel G, MacLeod Patrick
Civitan International Research Center, University of Alabama at Birmingham, 35294-0021, USA.
J Child Neurol. 2007 Dec;22(12):1338-41. doi: 10.1177/0883073807308715.
The International Rett Syndrome Association (IRSA) North American database is the first comprehensive compilation of information in the United States and Canada on individuals with Rett syndrome or with another diagnosis in association with MECP2 mutations. The database contains specific information by diagnosis, mutation status, and mutation type and frequency on 1928 participants. Among the 1928 participants, 85.5% were typical, 13.4% were atypical, and 1.1% had MECP2 mutations but did not have Rett syndrome. MECP2 mutations were identified in 914 of 1059 participants (86%): 799 of 870 (92%) participants with typical Rett syndrome had an MECP2 mutation, 94 of 162 (58%) with atypical Rett syndrome had a mutation, and all 21 individuals diagnosed as Not Rett syndrome had a mutation. Missense-type mutations (39.0%) were slightly more common than nonsense type (35.1%). Individual mutation frequency for the 8 common mutations varied from 11.9% for T158M to 4.4% for R106W; large deletions accounted for 6.4% and C-terminal truncations occurred in 8.8%. The remaining mutations (14.3%) occurred singly or in small numbers. This database provides a unique resource for expanding our understanding of Rett syndrome, for comparison with other national databases, and for future study including organization of clinical trials based on the expected emergence of fundamental therapies.
国际瑞特综合征协会(IRSA)北美数据库是美国和加拿大首个关于患有瑞特综合征或伴有与MECP2突变相关的其他诊断的个体信息的综合汇编。该数据库包含了1928名参与者按诊断、突变状态、突变类型和频率分类的具体信息。在这1928名参与者中,85.5%为典型病例,13.4%为非典型病例,1.1%有MECP2突变但不患有瑞特综合征。在1059名参与者中有914名(86%)检测到MECP2突变:870名典型瑞特综合征参与者中有799名(92%)有MECP2突变,162名非典型瑞特综合征参与者中有94名(58%)有突变,所有21名被诊断为非瑞特综合征的个体均有突变。错义型突变(39.0%)比无义型突变(35.1%)略为常见。8种常见突变的个体突变频率从T158M的11.9%到R106W的4.4%不等;大片段缺失占6.4%,C末端截短占8.8%。其余突变(14.3%)为单个或少量出现。该数据库为扩展我们对瑞特综合征的理解、与其他国家数据库进行比较以及未来研究(包括基于预期出现的基础疗法组织临床试验)提供了独特的资源。