Functional MASP2 gene polymorphism in patients with history of rheumatic fever

被引:15
|
作者
Schafranski, Marcelo Derbli [1 ]
Ferraria, Lilian Pereira [1 ]
Scherner, Daniela [1 ]
Torres, Renato [2 ]
de Messias-Reason, Iara Jose [1 ]
机构
[1] Univ Fed Parana, Hosp Clin, Dept Anat Med, BR-80060000 Curitiba, Parana, Brazil
[2] Hosp Pequeno Principe, Dept Pediat Cardiol, Curitiba, Parana, Brazil
关键词
complement; rheumatic fever; rheumatic heart disease; MASP2; gene;
D O I
10.1016/j.humimm.2007.11.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study we investigated whether partial or total MASP-2 deficiencies resulting from Asp105Gly mutation are associated with rheumatic fever (RF) and chronic rheumatic heart disease (RHD). The Asp105Gly MASP2 mutation (D105G) was detected by polymerase chain reaction-restriction fragment length polymorphism in 148 patients (43 men and 105 women; mean age 39.1 +/- 14.4 years) with a history of RF, including 106 (73%) with RHD and 42 (27%) without cardiac sequelae, and 129 control subjects (52 men and 77 women, mean age 38.4 +/- 12.2 years). The D105G mutation was detected in four patients with RHD (3.77%) and in five control subjects (3.88%), all in the heterozygous state. None of the patients without cardiac sequelae had the mutation. No significant difference was found in the frequency of the mutant allele between the groups (p < 0.6). These results suggest that the D105G mutation in the MASP2 gene does not play a major role in the pathogenesis of RF. Whether D105G plays a rote in the development of RHD should be ascertained in future studies. (c) 2008 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 44
页数:4
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