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关于哌甲酯潜在诱导基因组损伤的现有证据简要综述。

Brief review of available evidence concerning the potential induction of genomic damage by methylphenidate.

作者信息

Stopper H, Walitza S, Warnke A, Gerlach M

机构信息

Department of Toxicology, University of Wuerzburg, Wuerzburg, Germany.

出版信息

J Neural Transm (Vienna). 2008;115(2):331-4. doi: 10.1007/s00702-007-0829-y. Epub 2007 Nov 12.

Abstract

Children affected by attention deficit/hyperactivity disorder are often treated with methylphenidate (MPH). Two years ago, an increase in genomic damage after 3 months of MPH treatment was reported by researchers from Texas, U.S.A., raising concern about potential carcinogenic effects. In a similar investigation conducted in Wuerzburg, Germany, we did not find a comparable elevation of genomic damage. MPH is not genotoxic in standard test systems, but yielded one positive result in a rodent carcinogenicity study at the highest test dose only (60-fold above therapeutic doses). In conclusion, changes in treatment strategies do not seem justified currently. Larger studies are under way and will hopefully eliminate any remaining doubt about potential genotoxic or carcinogenic consequences of MPH treatment.

摘要

患有注意力缺陷多动障碍的儿童常使用哌甲酯(MPH)进行治疗。两年前,美国得克萨斯州的研究人员报告称,MPH治疗3个月后基因组损伤增加,这引发了人们对潜在致癌作用的担忧。在德国维尔茨堡进行的一项类似调查中,我们并未发现基因组损伤有类似程度的升高。MPH在标准测试系统中没有基因毒性,但仅在啮齿动物致癌性研究的最高测试剂量(高于治疗剂量60倍)下产生了一个阳性结果。总之,目前看来改变治疗策略似乎没有道理。规模更大的研究正在进行,有望消除对MPH治疗潜在基因毒性或致癌后果的任何疑虑。

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