HLA-A*31:01 and different types of carbamazepine-induced severe cutaneous adverse reactions: an international study and meta-analysis

被引:181
作者
Genin, E. [1 ]
Chen, D-P [2 ,3 ]
Hung, S-I [4 ]
Sekula, P. [5 ]
Schumacher, M. [5 ]
Chang, P-Y [2 ,3 ]
Tsai, S-H [2 ,3 ]
Wu, T-L [2 ,3 ]
Bellon, T. [6 ]
Tamouza, R. [7 ,8 ]
Fortier, C. [7 ,8 ]
Toubert, A. [7 ,8 ]
Charron, D. [7 ,8 ]
Hovnanian, A. [8 ]
Wolkenstein, P.
Chung, W-H [9 ]
Mockenhaupt, M. [10 ]
Roujeau, J-C [11 ]
机构
[1] Univ Paris Diderot, Inst Univ Hematol, St Louis Hosp, Inserm U946, Paris, France
[2] Chang Gung Mem Hosp, Dept Lab Med, Taoyuan, Taiwan
[3] Chang Gung Univ, Coll Med, Dept Med Biotechnol & Lab Sci, Taipei 105, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Infect & Immun Res Ctr, Inst Pharmacol, Taipei 112, Taiwan
[5] Univ Freiburg, Med Ctr, Inst Med Biometry & Med Informat, D-79106 Freiburg, Germany
[6] Hosp Univ La Paz IdiPAZ, Res Unit, Madrid, Spain
[7] St Louis Hosp, Jean Dausset Lab, Paris, France
[8] Univ Paris Diderot, St Louis Hosp, Inst Univ Hematol, Inserm UMRS 940, Paris, France
[9] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp, Dept Dermatol,Drug Hypersensit Clin & Res Ctr, Taipei 105, Taiwan
[10] Univ Freiburg, Med Ctr, Dept Dermatol, Dokumentat Zentrum Schwerer Hautreaktionen dZH, D-79104 Freiburg, Germany
[11] Univ Paris Est, Hop Henri Mondor, Serv Dermatol, Creteil, France
关键词
carbamazepine; drug reaction with eosinophilia and systemic symptoms; human leukocyte antigen; severe cutaneous adverse reactions; Stevens-Johnson syndrome; toxic epidermal necrolysis; STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; GENOME-WIDE ASSOCIATION; HLA-B-ASTERISK-1502; ALLELE; DRUG-REACTIONS; HYPERSENSITIVITY SYNDROME; SYSTEMIC SYMPTOMS; DRESS SYNDROME; T-CELLS; HLA-B;
D O I
10.1038/tpj.2013.40
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
HLA-A*31:01 was reported to be associated with carbamazepine (CBZ)-induced severe cutaneous adverse reactions (SCAR), including drug reaction with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). We conducted an international study using consensus diagnosis criteria to enroll a total of 93 patients with CBZ-SCAR from Europe or Asia. We found that HLA-A*31:01 showed a significant association with CBZ-DRESS in Europeans (P< 0.001; odds ratio (OR) (95% confidence interval (CI) = 57.6 (11.0-340)), and the strong association was also found in Chinese (P<0.001; OR (95% Cl) = 23.0 (4.2-125)). However, HLA-A*31:01 had no association with CBZ-SJS/TEN in neither Chinese nor Europeans. By comparison, HLA-B*15:02 showed a strong association with CBZ-SJS/TEN in Chinese (P<0.001, OR (95% CI = 58.1 (17.6-192)). A meta-analysis of this and other published studies confirmed that in all populations, HLA-A*31:01 had an extremely strong association with CBZ-DRESS (P<0.001, a pooled OR (95% Cl) = 13.2 (8.4-20.8)), but a much weaker association with CBZ-SJS/TEN (P=0.01, OR (95% CI) = 3.94 (1.4-11.5)). Our data revealed that HLA-A*31:01 is a specific predictor for CBZ-DRESS but not for CBZ-SJS/TEN. More studies are needed to investigate the genetic determinant of CBZ-SJS/TEN in Europeans. Considering the potential clinical utility, the cost-effectiveness of the combined HLA-A*31:01 and HLA-B*15:02 genetic test to prevent CBZ-SCAR in Chinese needs further investigation.
引用
收藏
页码:281 / 288
页数:8
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