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
相关论文
共 16 条
  • [1] Complement activation after oxidative stress -: Role of the lectin complement pathway
    Collard, CD
    Väkevä, A
    Morrissey, MA
    Agah, A
    Rollins, SA
    Reenstra, WR
    Buras, JA
    Meri, S
    Stahl, GL
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (05) : 1549 - 1556
  • [2] The association between mannan-binding lectin gene polymorphism and clinical leprosy: New insight into an old paradigm
    de Messias-Reason, Iara J.
    Boldt, Angelica B. W.
    Moraes Braga, Anna Carolina
    Seeling Stahlke, Ewalda Von Rosen
    Dornelles, Luciana
    Pereira-Ferrari, Lilian
    Kremsner, Peter G.
    Kun, Juergen F. J.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2007, 196 (09) : 1379 - 1385
  • [3] Mannan-binding lectin plasma levels in leprosy: deficiency confers protection against the lepromatous but not the tuberculoid forms
    Dornelles, L. N.
    Pereira-Ferrari, L.
    Messias-Reason, I.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2006, 145 (03) : 463 - 468
  • [4] Garred P, 2000, J RHEUMATOL, V27, P26
  • [5] Why inorganic salts decrease the TiO2 photocatalytic efficiency
    Guillard, C
    Puzenat, E
    Lachheb, H
    Houas, A
    Herrmann, JM
    [J]. INTERNATIONAL JOURNAL OF PHOTOENERGY, 2005, 7 (01) : 1 - 9
  • [6] Mannose-binding lectin (MBL) and vascular complications in diabetes
    Hansen, TK
    [J]. HORMONE AND METABOLIC RESEARCH, 2005, 37 : S95 - S98
  • [7] Inhibition of mannose-binding lectin reduces postischemic myocardial reperfusion injury
    Jordan, JE
    Montalto, MC
    Stahl, GL
    [J]. CIRCULATION, 2001, 104 (12) : 1413 - 1418
  • [8] MCKAY I, 2001, NEW ENGL J MED, V344, P1058
  • [9] A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS
    MILLER, SA
    DYKES, DD
    POLESKY, HF
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (03) : 1215 - 1215
  • [10] Heart valve structure: a predisposing factor for rheumatic heart disease
    Nayar, S.
    Nayar, P. G.
    Cherian, K. M.
    [J]. HEART, 2006, 92 (08) : 1151 - 1152