Association of HLA-B*5801 allele and allopurinol-induced stevens johnson syndrome and toxic epidermal necrolysis: a systematic review and meta-analysis

被引:153
|
作者
Somkrua, Ratchadaporn [1 ]
Eickman, Elizabeth E. [2 ]
Saokaew, Surasak [3 ]
Lohitnavy, Manupat [4 ]
Chaiyakunapruk, Nathorn [1 ,4 ,5 ,6 ]
机构
[1] Naresuan Univ, CPOR, Phitsanulok, Thailand
[2] Univ Nebraska, Med Ctr, Dept Pharm Practice, Omaha, NE USA
[3] Univ Phayao, Sch Pharm, Phayao, Thailand
[4] Naresuan Univ, Fac Pharmaceut Sci, Dept Pharm Practice, Phitsanulok, Thailand
[5] Univ Queensland, Sch Populat Hlth, Brisbane, Qld, Australia
[6] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
来源
BMC MEDICAL GENETICS | 2011年 / 12卷
关键词
Human leukocyte antigen; severe cutaneous reaction; Stevens-Johnson syndrome; toxic epidermal necrolysis; allopurinol; meta-analysis; CUTANEOUS ADVERSE-REACTIONS; MEDIUM-TERM BIOASSAY; HLA-B LOCUS; DRUG HYPERSENSITIVITY; JAPANESE PATIENTS; ERYTHEMA MULTIFORME; FOCI; POPULATION; HEXACHLOROBENZENE; HETEROGENEITY;
D O I
10.1186/1471-2350-12-118
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Despite some studies suggesting a possible association between human leukocyte antigen, HLA-B*5801 and allopurinol induced Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN), the evidence of association and its magnitude remain inconclusive. This study aims to systematically review and meta-analyze the association between HLA-B*5801 allele and allopurinol-induced SJS/TEN. Methods: A comprehensive search was performed in databases including MEDLINE, Pre-MEDLINE, Cochrane Library, EMBASE, International Pharmaceutical Abstracts (IPA), CINAHL, PsychInfo, the WHO International, Clinical Trial Registry, and ClinicalTrial.gov from their inceptions to June 2011. Only studies investigating association between HLA-B*5801 with allopurinol-induced SJS/TEN were included. All studies were extracted by two independent authors. The primary analysis was the carrier frequency of HLA-B*5801 comparison between allopurinol-induced SJS/TEN cases and each comparative group. The pooled odds ratios were calculated using a random effect model. Results: A total of 4 studies with 55 SJS/TEN cases and 678 matched-controls (allopurinol-tolerant control) was identified, while 5 studies with 69 SJS/TEN cases and 3378 population-controls (general population) were found. SJS/TEN cases were found to be significantly associated with HLA-B*5801 allele in both groups of studies with matched-control (OR 96.60, 95%CI 24.49-381.00, p < 0.001) and population-control (OR 79.28, 95%CI 41.51-151.35, p < 0.001). Subgroup analysis for Asian and Non-Asian population yielded similar findings. Conclusion: We found a strong and significant association between HLA-B*5801 and allopurinol-induced SJS/TEN. Therefore, HLA-B*5801 allele screening may be considered in patients who will be treated with allopurinol.
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页数:10
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