Prevalence of Human Leukocyte Antigen (HLA)-B*58:01 and Allopurinol-Induced Adverse Reactions in Filipino Patients in Hawai'i: Implications for Genotyping

被引:0
|
作者
Terashima, Rika [1 ,2 ]
Medina, Alejandro Jude P. [1 ]
Del Mundo, Hans Jesper F. [1 ]
Briones, Ryan Sean S. [1 ]
Aquino, Joseph Arman B. [1 ]
Quiminiano, Ellaine M. [1 ]
Sin, Yuh Miin [1 ]
Bautista, Rhea A. [1 ]
Sonido, Charlie Y. [1 ,3 ]
Yamada, Seiji [1 ,4 ]
机构
[1] Primary Care Clin Hawaii, Waipahu, HI 96797 USA
[2] Stanford Univ, Dept Epidemiol & Populat Hlth, Sch Med, Stanford, CA 94305 USA
[3] AT Still Univ, Sch Osteopath Med Arizona, Mesa, AZ USA
[4] Univ Hawaii, John A Burns Sch Med, Dept Family Med & Community Hlth, Honolulu, HI USA
关键词
adverse drug reactions; allopurinol; Filipino; genotyping; gout; Hawaii; HLA-B*58:01; STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; COST-EFFECTIVENESS; HLA-B-ASTERISK-5801;
D O I
10.1111/1756-185X.70127
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Allopurinol, a first-line treatment for gout and hyperuricemia, is associated with severe cutaneous adverse reactions (SCAR) in individuals carrying the HLA-B*58:01 allele. Genotyping is conditionally recommended in Han Chinese, Korean, and Thai populations with an allele prevalence of 7.4%, and in African Americans at 3.8%. The prevalence in Filipino patients has not been studied. We investigate the prevalence of HLA-B*58:01 among Filipino patients in Hawai'i and evaluate the incidence of allopurinol-induced adverse reactions following genotyping. Methods: We conducted a retrospective chart review of 312 patients who underwent HLA-B*58:01 genotyping at a primary care clinic in Hawai'i between November 2021 and July 2024. After excluding patients with missing ethnicity data, non-Filipino ethnicity, or prior allopurinol use, 237 Filipino patients were included in the analysis. The prevalence of the HLA-B*58:01 allele and the incidence of allopurinol-induced adverse reactions were calculated. Results: Among the 237 Filipino patients, 17 (7.2%) were HLA-B*58:01 positive. A total of 97 patients were started on allopurinol after genotyping and 1 (1.0%) developed mild cutaneous reactions, 0 (0%) developed SCAR, and 2 (2.1%) experienced gastrointestinal symptoms (nausea and diarrhea). Conclusion: The high prevalence of HLA-B*58:01 allele among Filipino patients in Hawai'i suggests that genotyping may be considered before initiating allopurinol treatment. Given no instances of SCAR were observed in patients who were administered allopurinol after undergoing HLA-B*58:01 genotyping, genotyping may play a crucial role in reducing the risk of allopurinol-induced SCAR in this population. Further studies with larger cohorts are suggested to confirm our findings and assess broader clinical utility of genotyping.
引用
收藏
页数:5
相关论文
共 50 条
  • [21] HLA-B*58:01 carrier status of Hmong in Minnesota: first in Hmong genotyping for prevalence of this biomarker of risk for severe cutaneous adverse reactions caused by allopurinol
    Peng Kerui
    Bjork, Jonathan
    Wen Ya-Feng
    Roman, Youssef M.
    Culhane-Pera, Kathleen
    Lo, May Xia
    Gertner, Elie
    Straka, Robert J.
    PHARMACOGENETICS AND GENOMICS, 2020, 30 (02): : 21 - 25
  • [22] Clinical Utility ofHLA-B*58:01Genotyping to Prevent Allopurinol-Induced SJS']JS/TEN
    Lavu, Alekhya
    Thiriveedi, Sneha
    Thomas, Levin
    Khera, Kanav
    Saravu, Kavitha
    Rao, Mahadev
    HOSPITAL PHARMACY, 2021, 56 (06) : 660 - 663
  • [23] Allopurinol induced DRESS in Han Chinese - is routine HLA-B*58:01 genotyping warranted?
    Sheriff, T.
    Daniel, B.
    Murrell, D. F.
    AUSTRALASIAN JOURNAL OF DERMATOLOGY, 2021, 62 : 115 - 115
  • [24] HLA-B*58:01 and allopurinol high dose were associated with allopurinol induced cutaneous adverse drug reactions in Thai population
    Sukasem, C.
    Jantararoungtong, T.
    Kuntawong, P.
    Puangpetch, A.
    Koomdee, N.
    Klaewsongkram, J.
    Rerkpattanapipat, T.
    ALLERGY, 2016, 71 : 205 - 206
  • [25] Prevalence of Human Leukocyte Antigen (HLA)-B*57:01 in HIV-Infected Patients
    Deveci, Aydin
    Coban, Ahmet Yilmaz
    Durupinar, Belma
    MIKROBIYOLOJI BULTENI, 2016, 50 (04): : 544 - 551
  • [26] Allopurinol-Induced Stevens-Johnson Syndrome in Java']Javanese Men With Positive HLA-B*58:01
    Ferdiana, Astri
    Fachiroh, Jajah
    Oktarina, Dyah Ayu Mira
    Irwanto, Astrid
    Mahendra, Caroline
    Febriana, Sri Awalia
    Soebono, Hardyanto
    FRONTIERS IN GENETICS, 2022, 13
  • [27] Validation of a genotyping technique for a surrogate marker of HLA B*58:01 for allopurinol-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in the Japanese population
    Tsukagoshi, Eri
    Nakamura, Ryosuke
    Tanaka, Yoichi
    Maekawa, Keiko
    Hiratsuka, Masahiro
    Asada, Hideo
    Saito, Yoshiro
    DRUG METABOLISM AND PHARMACOKINETICS, 2023, 49
  • [28] Necessity of a human leukocyte antigen-B*58:01 screening test for preventing severe cutaneous adverse reactions
    Sanchez-Garcia, Alberto
    Poma-Saavedra, Fabrizzio
    Garcia-Vilarino, Elena
    Vicente-Pardo, Andrea
    Perez-del-Caz, Maria D.
    PHARMACOGENETICS AND GENOMICS, 2019, 29 (05): : 121 - 121
  • [29] Immunologic basis for allopurinol-induced severe cutaneous adverse reactions: HLA-B*58:01-restricted activation of drug-specific T cells and molecular interaction
    Lin, Chia-Hsien
    Chen, Jung-Kuei
    Ko, Tai-Ming
    Wei, Chun-Yu
    Wu, Jer-Yuarn
    Chung, Wen-Hung
    Chen, Shih-Yang
    Liao, You-Di
    Hung, Shuen-Iu
    Chen, Yuan-Tsong
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (04) : 1063 - +
  • [30] Detection of HLA-B☆58:01, the susceptible allele for allopurinol-induced hypersensitivity, by loop-mediated isothermal amplification
    Kwok, J.
    Kwong, K. M.
    BRITISH JOURNAL OF DERMATOLOGY, 2013, 168 (03) : 526 - 532