Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema

被引:50
作者
Duan, Qing Ling [1 ,2 ,3 ,4 ]
Binkley, Karen [5 ]
Rouleau, Guy A. [1 ,2 ,3 ]
机构
[1] Univ Montreal, Ctr Excellence Neurom, Montreal, PQ, Canada
[2] CHU Montreal, Montreal, PQ, Canada
[3] Hop St Justine, Montreal, PQ H3T 1C5, Canada
[4] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[5] Univ Toronto, Dept Med, Div Clin Immunol & Allergy, Toronto, ON, Canada
关键词
Estrogen-dependent inherited angioedema; bradykinin; coagulation Factor XII; angiotensin I-converting enzyme; aminopeptidase P; HORMONE REPLACEMENT THERAPY; HEREDITARY ANGIOEDEMA; POSTMENOPAUSAL WOMEN; HYPERSENSITIVITY REACTIONS; ESSENTIAL-HYPERTENSION; NORMAL C1-INHIBITOR; AMINOPEPTIDASE-P; ACE; METABOLISM; INHIBITOR;
D O I
10.1016/j.jaci.2008.12.010
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Recent studies reported a gain-of-function mutation in the gene encoding coagulation Factor XII (F12) among 5 German and French families with estrogen-associated angioedema who share a common ancestor. The role of this factor, additional pathways that might contribute to increased bradykinin levels, or both remain to be determined in other families with estrogen-dependent or estrogen-associated inherited angioedema. Objective: The purpose of this study was to determine whether mutations in F12 and polymorphisms in the genes encoding aminopeptidase P (APP) and angiotensin I-converting enzyme (ACE), which have been associated with increased bradykinin levels, contribute to estrogen-dependent inherited angioedema in a large family of Italian origin. Methods: We screened the coding regions of F12 and the gene encoding membrane-bound APP (XPNPEP2), for genetic variants in the 3 affected female subjects. In addition, we genotyped this family for the insertion/deletion polymorphism in the ACE gene, which accounts for variable ACE levels. Results: The 3 affected female subjects all have the threonine-to-lysine (Thre328Lys) mutation, which is associated with higher Factor XII activity. In addition, they have at least one A allele of rs3788853 at the XPNPEP2 locus, which is associated with lower APP activity, and at least one I allele in ACE, which is associated with reduced ACE activity. Conclusion: A missense mutation in F12 is present in the 3 affected female subjects of this family with estrogen-dependent inherited angioedema. In addition, these affected females have polymorphisms associated with lower levels of both APP and ACE, the major enzymes responsible for bradykinin degradation. Thus, our study suggests that multiple genes might contribute to estrogen-dependent or estrogen-associated inherited angioedema and explain some of the observed heterogeneity. (J Allergy Clin Immunol 2009;123:906-10.)
引用
收藏
页码:906 / 910
页数:5
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