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
  • [41] PREVALENCE OF HUMAN LEUKOCYTE ANTIGEN HLA-B☆57:01 IN HIV-INFECTED SUBJECTS IN THE CZECH REPUBLIC
    Jilich, David
    Vrana, Milena
    Snopkova, Svatava
    Sedlacek, Dalibor
    Kapla, Jaroslav
    Rozsypal, Hanus
    Kolcakova, Jitka
    Olbrechtova, Lenka
    Zjevikova, Alena
    Jerhotova, Zdenka
    Maly, Marek
    Stankova, Marie
    Machala, Ladislav
    CENTRAL EUROPEAN JOURNAL OF PUBLIC HEALTH, 2011, 19 (03) : 128 - 130
  • [42] Cost-effectiveness analysis of HLA-B*58:01 genetic testing before initiation of allopurinol therapy to prevent allopurinol-induced Stevens-Johnson syndrome/toxic epidermal necrolysis in a Malaysian population
    Chong, Huey Yi
    Lim, Yi Heng
    Prawjaeng, Juthamas
    Tassaneeyakul, Wichittra
    Mohamed, Zahurin
    Chaiyakunapruk, Nathorn
    PHARMACOGENETICS AND GENOMICS, 2018, 28 (02): : 56 - 67
  • [43] Human leukocyte antigen HLA-B*57:01 status in HIV-1 patients developing hypersensitivity reactions in Benin: a pilot study
    Adechina, Adefounke Prudencia
    Assogba, Yaou Pierrot
    Tchiakpe, Edmond
    Yessoufou, Akadiri
    BMC RESEARCH NOTES, 2024, 17 (01)
  • [44] Rapid and Reliable HLA-B*59:01 Genotyping to Prevent Carbonic Anhydrase Inhibitor-Induced Severe Cutaneous Adverse Reactions
    Huh, Ji Young
    Song, Yong Ju
    Park, Geon
    ANNALS OF CLINICAL AND LABORATORY SCIENCE, 2024, 54 (01): : 101 - 105
  • [45] Human leukocyte antigen (HLA) and pharmacogenetics: screening for HLA-B*57:01 among human immunodeficiency virus-positive patients from southern Alberta
    Berka, Noureddine
    Gill, John M.
    Liacini, Abdelhamid
    O'Bryan, Tyler
    Khan, Faisal M.
    HUMAN IMMUNOLOGY, 2012, 73 (02) : 164 - 167
  • [46] HLA-B☆58:01 Genotype and the Risk of Allopurinol-Associated Severe Cutaneous Adverse Reactions in a Predominately Black or African American Population with Advanced Chronic Kidney Disease
    Ford, Sarah
    Kimball, Pamela
    Gupta, Gaurav
    Shah, Nehal
    ARTHRITIS & RHEUMATOLOGY, 2018, 70
  • [47] HLA-A24:02 increase the risk of allopurinol-induced drug reaction with eosinophilia and systemic symptoms in HLA-B58:01 carriers in a Korean population; a multicenter cross-sectional case-control study
    Kim, Mi-Yeong
    Yun, James
    Kang, Dong-Yoon
    Kim, Tae Hee
    Oh, Min-Kyung
    Lee, Sunggun
    Kang, Min-Gyu
    Nam, Young-Hee
    Choi, Jeong-Hee
    Yang, Min-Suk
    Han, Seung Seok
    Lee, Hajeong
    Cho, Hyun-Jai
    Yang, Jaeseok
    Oh, Kook-Hwan
    Kim, Yon Su
    Jung, Jae Woo
    Lee, Kye Hwa
    Kang, Hye-Ryun
    CLINICAL AND TRANSLATIONAL ALLERGY, 2022, 12 (09)
  • [48] Absence of human leukocyte antigen-B*57:01 amongst patients on antiretroviral therapy in Nigeria: Implications for use of abacavir
    Agbaji, Oche O.
    Akanbi, Maxwell O.
    Otoh, Ihedinachi
    Agaba, Patricia E.
    Akinsola, Rolake
    Okolie, Victoria
    Ugoagwu, Placid O.
    Babadoko, Aliyu A.
    Adediran, Adewumi
    Finomo, Finomo O.
    Abah, Jonah O.
    Muktar, Haruna M.
    Akanmu, Alani S.
    NIGERIAN POSTGRADUATE MEDICAL JOURNAL, 2019, 26 (04) : 195 - 198
  • [49] HLA-B*13:01 Is a Predictive Marker of Dapsone-Induced Severe Cutaneous Adverse Reactions in Thai Patients
    Satapornpong, Patompong
    Pratoomwun, Jirawat
    Rerknimitr, Pawinee
    Klaewsongkram, Jettanong
    Nakkam, Nontaya
    Rungrotmongkol, Thanyada
    Konyoung, Parinya
    Saksit, Niwat
    Mahakkanukrauh, Ajanee
    Amornpinyo, Warayuwadee
    Khunarkornsiri, Usanee
    Tempark, Therdpong
    Wantavornprasert, Kittipong
    Jinda, Pimonpan
    Koomdee, Napatrupron
    Jantararoungtong, Thawinee
    Rerkpattanapipat, Ticha
    Wang, Chuang-Wei
    Naisbitt, Dean
    Tassaneeyakul, Wichittra
    Ariyachaipanich, Manasalak
    Roonghiranwat, Thapana
    Pirmohamed, Munir
    Chung, Wen-Hung
    Sukasem, Chonlaphat
    FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [50] Identification of six novel human leukocyte antigen alleles, HLA-A*24:248, B*46:01:17, B*46:58, C*01:02:22, C*01:02:25 and C*01:91, in Chinese individuals
    Pan, J.
    Chen, L. N.
    Zhuo, X. F.
    Huang, L. P.
    Zheng, Z. Z.
    TISSUE ANTIGENS, 2015, 85 (02): : 132 - U94