Classification and biological diagnostic of angioedema diseases

被引:4
作者
Drouet, C. [1 ]
Ponard, D. [2 ]
Monnier, N. [3 ]
Lunardi, J. [3 ]
Bosson, J. -L. [4 ]
机构
[1] Univ Grenoble 1, CHU Grenoble, Ctr Reference Angioedeme, GREPI TIMC IMAG CNRS 5525, F-38043 Grenoble, France
[2] CHU Grenoble, Ctr Reference Angioedeme, Immunol Lab, F-38043 Grenoble, France
[3] CHU Grenoble, Ctr Reference Angioedeme, Lab Biochim & Genet Mol, F-38043 Grenoble, France
[4] Univ Grenoble 1, CHU Grenoble, CIC Inserm, TIMC IMAG CNRS 5525, F-38043 Grenoble, France
来源
REVUE FRANCAISE D ALLERGOLOGIE ET D IMMUNOLOGIE CLINIQUE | 2008年 / 48卷 / 06期
关键词
Angioedema; Kinins; Kininogenase; Kininase; C1; Inhibitor; Complement;
D O I
10.1016/j.allerg.2008.02.004
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The angioedema disease represents a situation associated with production or accumulation of kinins at the endothelial cell surface. A classification of the different forms of the disease can be proposed upon the bases of the metabolic failure, either from the increased proteolytic activities towards kininogens (decreased control by C1 Inhibitor, escape to this control) or from the kinin accumulation associated with the decreased catabolism. The diagnostic Must describe the failure of the C1 Inhibitor control, the gain of function of the kinin-producing kininogenases or the decreased activities of the proteases needed for kinin catabolism (kininases). (c) 2008 Elsevier Masson SAS.
引用
收藏
页码:441 / 446
页数:6
相关论文
共 31 条
[1]   ANGIOEDEMA INDUCED BY THE ANGIOTENSIN-II BLOCKER LOSARTAN [J].
ACKER, CG ;
GREENBERG, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (23) :1572-1572
[2]   ACQUIRED C1 INHIBITOR (C1-INH) DEFICIENCY TYPE-II - REPLACEMENT THERAPY WITH C1-INH AND ANALYSIS OF PATIENTS C1-INH AND ANTI-C1-INH AUTOANTIBODIES [J].
ALSENZ, J ;
LAMBRIS, JD ;
BORK, K ;
LOOS, M .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (06) :1794-1799
[3]   Angiotensin-converting enzyme inhibitor-related angioedema: how to deal with it [J].
Beltrami, Laura ;
Zingale, Lorenza. C. ;
Carugo, Stefano ;
Cicardi, Marco .
EXPERT OPINION ON DRUG SAFETY, 2006, 5 (05) :643-649
[4]  
Binkley KE, 2000, J ALLERGY CLIN IMMUN, V106, P546
[5]   Estrogen-dependent inherited angioedema [J].
Binkley, KE ;
Davis, AE .
TRANSFUSION AND APHERESIS SCIENCE, 2003, 29 (03) :215-219
[6]   Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men [J].
Bork, K ;
Gül, D ;
Dewald, G .
BRITISH JOURNAL OF DERMATOLOGY, 2006, 154 (03) :542-545
[7]   Hereditary angioedema with normal C1-inhibitor activity in women [J].
Bork, K ;
Barnstedt, SE ;
Koch, P ;
Traupe, H .
LANCET, 2000, 356 (9225) :213-217
[8]   A case of hereditary angio-oedema type III presenting with C1-inhibitor cleavage and a missense mutation in the F12 gene [J].
Bouillet, L. ;
Ponard, D. ;
Rousset, H. ;
Cichon, S. ;
Drouet, C. .
BRITISH JOURNAL OF DERMATOLOGY, 2007, 156 (05) :1063-1065
[9]   Non-histaminic angioedema management: diagnostic and therapeutic interest of tranexamic acid [J].
Bouillet, L ;
Ponard, D ;
Douet, C ;
Massot, C .
REVUE DE MEDECINE INTERNE, 2004, 25 (12) :924-926
[10]   Dipeptidyl peptidase IV in angiotensin-converting enzyme inhibitor-associated angioedema [J].
Byrd, James Brian ;
Touzin, Karine ;
Sile, Saba ;
Gainer, James V. ;
Yu, Chang ;
Nadeau, John ;
Adam, Albert ;
Brown, Nancy J. .
HYPERTENSION, 2008, 51 (01) :141-147