The risk of cardiomyopathy in inherited epidermolysis bullosa

被引:41
作者
Fine, J. -D. [1 ,2 ,3 ]
Hall, M. [1 ,2 ]
Weiner, M. [1 ,4 ]
Li, K. -P. [5 ]
Suchindran, C. [5 ]
机构
[1] Natl Epidermolysis Bullosa Registry, Nashville, TN USA
[2] Vanderbilt Univ, Sch Med, Dept Med Dermatol, Nashville, TN 37203 USA
[3] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37203 USA
[4] Univ N Carolina, Dept Dermatol, Chapel Hill, NC 27514 USA
[5] Univ N Carolina, Dept Biostat, Chapel Hill, NC 27514 USA
关键词
cardiomyopathy; congestive heart failure; epidermolysis bullosa;
D O I
10.1111/j.1365-2133.2008.08697.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Case reports have suggested that cardiomyopathy may be a complication of recessive dystrophic epidermolysis bullosa (RDEB). Objective To determine the risk of congestive heart failure (CHF) or cardiomyopathy in each major EB subtype. Methods These data represent systematic case findings and data collection performed throughout the continental United States from 1986 through 2002, by the National Epidermolysis Bullosa Registry. Study design is cross-sectional (n = 3280) with a nested randomly sampled longitudinal subcohort (n = 450). Frequencies of CHF and cardiomyopathy were determined by patient self-reporting, medical histories and review of medical records. In those who died, death certificates were reviewed and histories obtained from surviving family. Cumulative risks were stratified by cause and EB subtype. Results Cardiomyopathy was reported as early as within the first year of life. In patients having no other known risk factors for CHF or cardiomyopathy, the highest risk of cardiomyopathy was seen among patients with Hallopeau-Siemens RDEB (RDEB-HS), with a cumulative risk of 4.51% on or after age 20 years. The cumulative risk of cardiomyopathy was only 1.14% and 0.40% in non-Herlitz junctional EB (JEB) and non-Hallopeau-Siemens RDEB, respectively, and was not observed in any other EB subtype. When patients with coexistent chronic renal failure were included, the cumulative risk for RDEB-HS rose to 18.86% by age 35 years. About 30% of our patients affected with RDEB-HS died of CHF or cardiomyopathy, even those with no other known risk factors. Conclusions CHF and cardiomyopathy are uncommon complications in both major RDEB subtypes and non-Herlitz JEB, and may be fatal.
引用
收藏
页码:677 / 682
页数:6
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