Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study

Abstract Objective The aim of this study was to investigate risk factors for cutaneous adverse reactions (CARs) in Kinh Vietnamese. Methods All patients were prospectively recruited in Ho Chi Minh City. Presence of the HLA-B*58:01 allele was determined by real-time PCR-sequence-specific amplificatio...

Full description

Bibliographic Details
Main Authors: Minh Duc Do, Thao Phuong Mai, Anh Duy Do, Quang Dinh Nguyen, Nghia Hieu Le, Linh Gia Hoang Le, Vu Anh Hoang, Anh Ngoc Le, Hung Quoc Le, Pascal Richette, Matthieu Resche-Rigon, Thomas Bardin
Format: Article
Language:English
Published: BMC 2020-08-01
Series:Arthritis Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13075-020-02273-1
_version_ 1818415118901313536
author Minh Duc Do
Thao Phuong Mai
Anh Duy Do
Quang Dinh Nguyen
Nghia Hieu Le
Linh Gia Hoang Le
Vu Anh Hoang
Anh Ngoc Le
Hung Quoc Le
Pascal Richette
Matthieu Resche-Rigon
Thomas Bardin
author_facet Minh Duc Do
Thao Phuong Mai
Anh Duy Do
Quang Dinh Nguyen
Nghia Hieu Le
Linh Gia Hoang Le
Vu Anh Hoang
Anh Ngoc Le
Hung Quoc Le
Pascal Richette
Matthieu Resche-Rigon
Thomas Bardin
author_sort Minh Duc Do
collection DOAJ
description Abstract Objective The aim of this study was to investigate risk factors for cutaneous adverse reactions (CARs) in Kinh Vietnamese. Methods All patients were prospectively recruited in Ho Chi Minh City. Presence of the HLA-B*58:01 allele was determined by real-time PCR-sequence-specific amplification by using the PG5801 Detection Kit (Pharmigene, Taipei). Patients with severe (SCARs) and mild (MCARs) CARs and controls were compared for differences in features prospectively collected, and odds ratios (ORs) with 95% confidence intervals (CIs) were estimated. Results On comparing 32 patients with SCARs and 395 tolerant controls, we identified eight strong risk factors: increased age (OR 15.1 [95% CI 5.8–40.1], P < 0.0001), female sex (OR 333 [40–43,453], P < 0.0001), allopurinol for asymptomatic hyperuricemia (OR 955 [120–125,847], P < 0.0001), allopurinol starting dose > 150 mg (OR 316 [101–122], P < 0.0001), diuretics intake (OR 304 [35–40,018], P < 0.0001), eGFR < 60 ml/min/1.73 m2 (OR 100 [32–353], P < 0.0001), history of allopurinol-induced skin reaction (OR 78 [6–10,808], P = 0.004), and HLA-B*58:01 carriage (OR 147 [45–746], P < 0.0001). HLA-B*58:01 allele frequency in controls was 7.3%. For MCARs (n = 74), risk factors were eGFR < 60 ml/min/1.73 m2 (OR 4.9 [1.61–14.6], P = 0.006), history of allopurinol-induced skin reaction (OR 27 [2–3777], P = 0.01), and asymptomatic hyperuricemia (OR 27 [2–3777], P = 0.01). Conclusion This study confirmed 8 risk factors, including HLA-B*58:01, for SCARs and identified 3 risk factors for MCARs in Kinh Vietnamese. HLA-B*58:01 genotyping could guide the indication for allopurinol in Kinh Vietnamese patients with gout.
first_indexed 2024-12-14T11:29:55Z
format Article
id doaj.art-0b2a8f26f4b6475dbd2572047530e7a2
institution Directory Open Access Journal
issn 1478-6362
language English
last_indexed 2024-12-14T11:29:55Z
publishDate 2020-08-01
publisher BMC
record_format Article
series Arthritis Research & Therapy
spelling doaj.art-0b2a8f26f4b6475dbd2572047530e7a22022-12-21T23:03:20ZengBMCArthritis Research & Therapy1478-63622020-08-0122111010.1186/s13075-020-02273-1Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control studyMinh Duc Do0Thao Phuong Mai1Anh Duy Do2Quang Dinh Nguyen3Nghia Hieu Le4Linh Gia Hoang Le5Vu Anh Hoang6Anh Ngoc Le7Hung Quoc Le8Pascal Richette9Matthieu Resche-Rigon10Thomas Bardin11Center for Molecular Biomedicine, University of Medicine and PharmacyDepartment of Physiology, Pathophysiology and Immunology, Faculty of Medicine, University of Medicine and PharmacyDepartment of Physiology, Pathophysiology and Immunology, Pham Ngoc Thach University of MedicineFrench Vietnamese Research Center on Gout and Chronic Diseases, Vien Gut Medical CentreFrench Vietnamese Research Center on Gout and Chronic Diseases, Vien Gut Medical CentreCenter for Molecular Biomedicine, University of Medicine and PharmacyCenter for Molecular Biomedicine, University of Medicine and PharmacyDepartment of Scientific Research, Cho Ray HospitalDepartment of Tropical Disease, Cho Ray HospitalUniversité de Paris, U1132, INSERMUniversité de Paris, ECSTRRA Team U1153, INSERMFrench Vietnamese Research Center on Gout and Chronic Diseases, Vien Gut Medical CentreAbstract Objective The aim of this study was to investigate risk factors for cutaneous adverse reactions (CARs) in Kinh Vietnamese. Methods All patients were prospectively recruited in Ho Chi Minh City. Presence of the HLA-B*58:01 allele was determined by real-time PCR-sequence-specific amplification by using the PG5801 Detection Kit (Pharmigene, Taipei). Patients with severe (SCARs) and mild (MCARs) CARs and controls were compared for differences in features prospectively collected, and odds ratios (ORs) with 95% confidence intervals (CIs) were estimated. Results On comparing 32 patients with SCARs and 395 tolerant controls, we identified eight strong risk factors: increased age (OR 15.1 [95% CI 5.8–40.1], P < 0.0001), female sex (OR 333 [40–43,453], P < 0.0001), allopurinol for asymptomatic hyperuricemia (OR 955 [120–125,847], P < 0.0001), allopurinol starting dose > 150 mg (OR 316 [101–122], P < 0.0001), diuretics intake (OR 304 [35–40,018], P < 0.0001), eGFR < 60 ml/min/1.73 m2 (OR 100 [32–353], P < 0.0001), history of allopurinol-induced skin reaction (OR 78 [6–10,808], P = 0.004), and HLA-B*58:01 carriage (OR 147 [45–746], P < 0.0001). HLA-B*58:01 allele frequency in controls was 7.3%. For MCARs (n = 74), risk factors were eGFR < 60 ml/min/1.73 m2 (OR 4.9 [1.61–14.6], P = 0.006), history of allopurinol-induced skin reaction (OR 27 [2–3777], P = 0.01), and asymptomatic hyperuricemia (OR 27 [2–3777], P = 0.01). Conclusion This study confirmed 8 risk factors, including HLA-B*58:01, for SCARs and identified 3 risk factors for MCARs in Kinh Vietnamese. HLA-B*58:01 genotyping could guide the indication for allopurinol in Kinh Vietnamese patients with gout.http://link.springer.com/article/10.1186/s13075-020-02273-1GoutAllopurinolSkin reactionsKinh VietnameseRisk factorsHLA-B*58:01
spellingShingle Minh Duc Do
Thao Phuong Mai
Anh Duy Do
Quang Dinh Nguyen
Nghia Hieu Le
Linh Gia Hoang Le
Vu Anh Hoang
Anh Ngoc Le
Hung Quoc Le
Pascal Richette
Matthieu Resche-Rigon
Thomas Bardin
Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study
Arthritis Research & Therapy
Gout
Allopurinol
Skin reactions
Kinh Vietnamese
Risk factors
HLA-B*58:01
title Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study
title_full Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study
title_fullStr Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study
title_full_unstemmed Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study
title_short Risk factors for cutaneous reactions to allopurinol in Kinh Vietnamese: results from a case-control study
title_sort risk factors for cutaneous reactions to allopurinol in kinh vietnamese results from a case control study
topic Gout
Allopurinol
Skin reactions
Kinh Vietnamese
Risk factors
HLA-B*58:01
url http://link.springer.com/article/10.1186/s13075-020-02273-1
work_keys_str_mv AT minhducdo riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT thaophuongmai riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT anhduydo riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT quangdinhnguyen riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT nghiahieule riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT linhgiahoangle riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT vuanhhoang riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT anhngocle riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT hungquocle riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT pascalrichette riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT matthieurescherigon riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy
AT thomasbardin riskfactorsforcutaneousreactionstoallopurinolinkinhvietnameseresultsfromacasecontrolstudy