法布里病
医学
疾病
内科学
表征(材料科学)
多中心研究
法布里病
物理
光学
随机对照试验
作者
Maarten Arends,Christoph Wanner,Derralynn Hughes,Atul Mehta,Daniel Oder,Oliver Watkinson,Perry Elliott,Gabor E. Linthorst,Frits A. Wijburg,Marieke Biegstraaten,Carla E. M. Hollak
出处
期刊:Journal of The American Society of Nephrology
日期:2016-12-15
卷期号:28 (5): 1631-1641
被引量:318
标识
DOI:10.1681/asn.2016090964
摘要
Fabry disease leads to renal, cardiac, and cerebrovascular manifestations. Phenotypic differences between classically and nonclassically affected patients are evident, but there are few data on the natural course of classical and nonclassical disease in men and women. To describe the natural course of Fabry disease stratified by sex and phenotype, we retrospectively assessed event-free survival from birth to the first clinical visit (before enzyme replacement therapy) in 499 adult patients (mean age 43 years old; 41% men; 57% with the classical phenotype) from three international centers of excellence. We classified patients by phenotype on the basis of characteristic symptoms and enzyme activity. Men and women with classical Fabry disease had higher event rate than did those with nonclassical disease (hazard ratio for men, 5.63, 95% confidence interval, 3.17 to 10.00;
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