Thiopurine S-methyltransferase (TPMT) activity cutoffs in the Thai population.

IF 1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY
Pimonpan Jinda, Pimpun Kitpoka, Wimol Thienphopirak, Suwat Chiawchan, Santirhat Prommas, Rattanaporn Sukprasong, Jiratha Rachanakul, Supaporn Wiwattanakul, Orapa Suteerojntrakool, Chansuda Bongsebandhu-Phubhakdi, Therdpong Tempark, Sittiphong Hunthai, Apichaya Puangpetch
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引用次数: 0

Abstract

BackgroundThiopurine S-methyltransferase (TPMT) is crucial for metabolizing thiopurine drugs. This study aimed to establish the cutoff values for TPMT activity in a cohort of healthy individuals. We defined normal TPMT activity ranges and identified clinically applicable thresholds to distinguish individuals with normal TPMT function from those with reduced or deficient activity.MethodsA total of 457 participants, including 207 children and 250 healthy adults without prior thiopurine drug exposure, were enrolled. TPMT activity was measured and common defective genetic variants (TPMT*3A, TPMT*3B, and TPMT*3C) were detected. To determine TPMT activity cutoff values and maximize sensitivity and specificity, receiver operating characteristic curve analysis was employed.ResultsThe cutoff values for TPMT activity in children were ≥52.9 nmol 6-MMP/g Hb/h for persons of the wild type and <52.9 nmol 6-MMP/g Hb/h for individuals who were heterozygous. In adults, the cutoff values were ≥44.6, 31.58-44.5, and <31.58 nmol 6-MMP/g Hb/h for wild-type, heterozygous, and compound heterozygous individuals, respectively. The sensitivity and specificity were 79.29% and 100% in children, whereas, in adults, they were 61.86% and 78.57%, 38.46% and 64.73%, and 100% and 95.98% in the wild-type, heterozygous, and compound heterozygous, respectively.ConclusionsIdentifying TPMT activity cutoff values is crucial for managing patients receiving thiopurine therapy, especially in Thailand. This approach allows for personalized treatment plans and minimizes the risk of adverse drug reactions. Since TPMT activity cutoff values can differ by population and testing methods, it is important to establish specific cutoff values locally.

泰国人群中硫嘌呤s -甲基转移酶(TPMT)活性中断。
背景:硫嘌呤s -甲基转移酶(TPMT)对硫嘌呤类药物的代谢至关重要。本研究旨在建立一个健康个体队列中TPMT活性的临界值。我们定义了正常的TPMT活性范围,并确定了临床适用的阈值,以区分TPMT功能正常的个体与活性降低或缺乏的个体。方法:共纳入457名参与者,包括207名儿童和250名健康成人,之前没有硫嘌呤药物暴露。检测TPMT活性,检测常见缺陷遗传变异(TPMT*3A、TPMT*3B、TPMT*3C)。为了确定TPMT活性临界值并最大限度地提高灵敏度和特异性,采用了受试者工作特征曲线分析。结果:野生型儿童TPMT活性临界值≥52.9 nmol 6-MMP/g Hb/h。结论:确定TPMT活性临界值对于管理接受硫嘌呤治疗的患者至关重要,特别是在泰国。这种方法允许个性化的治疗计划,并最大限度地减少药物不良反应的风险。由于TPMT活性临界值可能因种群和测试方法而异,因此在当地建立特定的临界值非常重要。
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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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