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DOI 10.2217/pgs-2021-0156

Медицинская библиотека · Pharmacogenomics · 2022

Allopurinol-induced severe cutaneous adverse reactions in Vietnamese: the role of HLA alleles and other risk factors.

Ha Pham Tran Thu, Tran Quang Binh, Chu Chi Hieu, Nga Do Thi Quynh, Nguyen Hoang Anh, Nguyen Dinh Van, Phung Thanh Huong

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Aim: To reveal the association of three class I HLA alleles, including HLA-A*33:03, HLA-B*58:01 and HLA-C*03:02, and allopurinol-induced severe cutaneous adverse reactions (SCARs) in Vietnamese patients.

Methods

A case-control study on 100 allopurinol-induced SCARs patients, 183 tolerant controls and 810 population controls was performed. The HLA-A*33:03 and HLA-C*03:02 alleles were detected with the nested allele-specific PCR method; the HLA-B*58:01 allele was detected with the sequence-specific primer PCR method.

Results

There were strong associations between HLA-B*58:01 and HLA-C*03:02 and allopurinol-induced SCARs. Specific associations were found between HLA-B*58:01 and Stevens-Johnson syndrome/toxic epidermal necrolysis and between HLA-C*03:02 and drug reaction with eosinophilia and systemic symptoms, with a gene dosage effect. The multivariate regression analysis indicated two significant independent risk factors: HLA-B*58:01/HLA-C*03:02 and estimated glomerular filtration rate <60 ml/min/1.73 m2. The specificity, positive predictive value and negative predictive value of HLA-B*58:01 testing were higher than the HLA-C*03:02 or the multiplex testing, especially in patients with impaired renal function.

Conclusion

The results supported pre-treatment HLA-B*58:01 testing in Vietnamese patients with declined renal function to prevent SCARs.

Для цитирования: Ha Pham Tran Thu, Tran Quang Binh, Chu Chi Hieu, Nga Do Thi Quynh, Nguyen Hoang Anh, Nguyen Dinh Van, Phung Thanh Huong. Allopurinol-induced severe cutaneous adverse reactions in Vietnamese: the role of HLA alleles and other risk factors.. Pharmacogenomics. 2022. DOI: 10.2217/pgs-2021-0156.

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