Bushel P R, Fannin R D, Gerrish K, Watkins P B, Paules R S
Microarray and Genome Informatics Group, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Pharmacogenomics J. 2017 Jun;17(3):230-236. doi: 10.1038/tpj.2016.8. Epub 2016 Mar 1.
Acetaminophen can adversely affect the liver especially when overdosed. We used whole blood as a surrogate to identify genes as potential early indicators of an acetaminophen-induced response. In a clinical study, healthy human subjects were dosed daily with 4 g of either acetaminophen or placebo pills for 7 days and evaluated over the course of 14 days. Alanine aminotransferase (ALT) levels for responders to acetaminophen increased between days 4 and 9 after dosing, and 12 genes were detected with expression profiles significantly altered within 24 h. The early responsive genes separated the subjects by class and dose period. In addition, the genes clustered patients who overdosed on acetaminophen apart from controls and also predicted the exposure classifications with 100% accuracy. The responsive genes serve as early indicators of an acetaminophen exposure, and their gene expression profiles can potentially be evaluated as molecular indicators for further consideration.
对乙酰氨基酚可能会对肝脏产生不利影响,尤其是过量服用时。我们使用全血作为替代物来鉴定基因,将其作为对乙酰氨基酚诱导反应的潜在早期指标。在一项临床研究中,健康的人类受试者连续7天每天服用4克对乙酰氨基酚或安慰剂药丸,并在14天的过程中进行评估。对乙酰氨基酚反应者的丙氨酸转氨酶(ALT)水平在给药后第4天至第9天之间升高,并且检测到12个基因的表达谱在24小时内发生了显著变化。早期反应基因按类别和剂量期将受试者区分开来。此外,这些基因将过量服用对乙酰氨基酚的患者与对照组区分开来,并且还以100%的准确率预测了暴露分类。这些反应基因可作为对乙酰氨基酚暴露的早期指标,其基因表达谱有可能作为分子指标进行进一步评估。