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在亚太地区进行HLA - B*58:01筛查是一项道德要求——而不仅仅是成本问题。

HLA-B*58:01 screening in Asia-Pacific is an ethical imperative - not just a cost question.

作者信息

Ng Wei Leik, Tse Emily Tsui Yee, Oka Prawira, Lim Hooi Min, Koh Sky Wei Chee, Ramli Rizawati, Lau Hung Chiun, Lam Benjamin Chih Chiang, Goldsmith Laurie J, Abdullah Adina, Goh Lay Hoon

机构信息

Department of Primary Care Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.

Department of Family Medicine and Primary Care, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

出版信息

J Glob Health. 2025 Aug 22;15:03037. doi: 10.7189/jogh.15.03037.

Abstract

Allopurinol remains the first-line treatment for gout; however, it carries a risk of severe cutaneous adverse reactions (SCARs), particularly among carriers of the HLA-B*58:01 allele. In the Asia-Pacific region, screening practices vary widely due to infrastructure gaps, cost concerns, and differing health policies. For example, while cost-effectiveness analyses have influenced screening decisions in some countries, they often overlook long-term health system burdens and ethical imperatives. Therefore, screenings should not be withheld solely on economic grounds, especially when they can prevent life-threatening outcomes. For that reason, a targeted, risk-based approach that integrates genetic and clinical factors could offer a practical and equitable path forward, improving pharmacogenomic literacy, expanding access to testing, developing regional data-sharing platforms, and involving patients in co-designing screening strategies. Rapid point-of-care testing and integration of screening process with existing care pathway may further support this implementation. However, a coordinated regional effort is needed to ensure safer prescribing and equitable access to pharmacogenomic screening across diverse healthcare settings.

摘要

别嘌醇仍然是痛风的一线治疗药物;然而,它存在严重皮肤不良反应(SCARs)的风险,尤其是在携带HLA - B*58:01等位基因的人群中。在亚太地区,由于基础设施差距、成本担忧以及不同的卫生政策,筛查做法差异很大。例如,虽然成本效益分析在一些国家影响了筛查决策,但它们往往忽视了长期的卫生系统负担和伦理要求。因此,不应仅基于经济原因而不进行筛查,特别是当筛查可以预防危及生命的后果时。出于这个原因,一种整合遗传和临床因素的有针对性的、基于风险的方法可以提供一条切实可行且公平的前进道路,提高药物基因组学素养,扩大检测可及性,开发区域数据共享平台,并让患者参与共同设计筛查策略。即时快速检测以及将筛查过程与现有护理路径相结合可能会进一步支持这一实施。然而,需要区域协调努力,以确保在不同的医疗环境中更安全地开药并公平获得药物基因组学筛查。

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