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苯妥英治疗的癫痫患者中姐妹染色单体交换诱导缺乏。

Lack of sister chromatid exchange induction in phenytoin-treated patients with epilepsy.

作者信息

Schaumann B A, Winge V B, Garry V F

机构信息

Research Service, VA Medical Center, Minneapolis, MN 55147.

出版信息

Epilepsia. 1989 Mar-Apr;30(2):240-5. doi: 10.1111/j.1528-1157.1989.tb05461.x.

Abstract

Phenytoin (PHT) has been suspected of having a mutagenic effect with chronic administration, but the existing evidence is equivocal. Contradictory results have been obtained using different testing systems. Sister chromatid exchange (SCE), a sensitive indicator of genotoxic environmental influences, has been used in only a few limited studies of PHT users, with varying results. The present study was designed to evaluate the potential mutagenicity of PHT in a more objective and reliable way than has been done previously. Following careful screening procedures, 16 adult male patients with epilepsy receiving long-term PHT monotherapy and 16 healthy controls were selected for a study of SCE frequencies in peripheral lymphocytes. The patients and controls were matched for sex, age, and smoking habits. Strict exclusionary criteria were observed, including all factors known to affect or suspected of affecting the SCE frequencies. Statistical analyses did not reveal any significant differences between the SCE rates of PHT-treated patients and controls, indicating a lack of PHT mutagenicity as expressed by induction of SCE in adults.

摘要

长期服用苯妥英(PHT)一直被怀疑具有致突变作用,但现有证据并不明确。使用不同的测试系统得到了相互矛盾的结果。姐妹染色单体交换(SCE)是遗传毒性环境影响的一个敏感指标,仅在少数针对服用PHT患者的有限研究中使用过,结果各不相同。本研究旨在以比以往更客观、更可靠的方式评估PHT的潜在致突变性。经过仔细的筛选程序,选择了16名接受长期PHT单一疗法的成年男性癫痫患者和16名健康对照,以研究外周淋巴细胞中的SCE频率。患者和对照在性别、年龄和吸烟习惯方面进行了匹配。严格遵守了排除标准,包括所有已知会影响或怀疑会影响SCE频率的因素。统计分析未显示PHT治疗患者和对照的SCE率之间有任何显著差异,表明在成年人中PHT不会通过诱导SCE表现出致突变性。

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