| Literature DB >> 25318078 |
Sandra Jeremias dos Santos Catarino1, Angelica Beate Winter Boldt2, Marcia Holsbach Beltrame1, Renato Mitsunori Nisihara1, Marcelo Derbli Schafranski3, Iara Jose de Messias-Reason4.
Abstract
MASP-2 is a key protein of the lectin pathway of complement system. Several MASP2 polymorphisms were associated with MASP-2 serum levels or functional activity. Here we investigated a possible association between MASP2 polymorphisms and MASP-2 serum levels with the susceptibility to rheumatic fever (RF) and rheumatic heart disease (RHD). We haplotyped 11 MASP2 polymorphisms with multiplex sequence-specific PCR in 145 patients with history of RF from south Brazil (103 with RHD and 42 without cardiac lesion [RFo]) and 342 healthy controls. MASP-2 levels were determined by ELISA. The low MASP-2 producing p.377A and p.439H variants were negatively associated with RF (P=0.02, OR=0.36) and RHD (P=0.01, OR=0.25). In contrast, haplotypes that share the intron 9 - exon 12 g.1961795C, p.371D, p.377V and p.439R polymorphisms increased the susceptibility to RHD (P=0.02, OR=4.9). MASP-2 levels were associated with MASP2 haplotypes and were lower in patients (P<0.0001), which may reflect protein consumption due to complement activation. MASP2 gene polymorphisms and protein levels seem to play an important role in the development of RF and establishment of RHD.Entities:
Keywords: Haplotype-specific genotyping; MASP2; Polymorphism; Rheumatic fever; Rheumatic heart disease
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Year: 2014 PMID: 25318078 DOI: 10.1016/j.humimm.2014.10.003
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850