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他克林给药对阿尔茨海默病患者的肝毒性作用。

Hepatotoxic effects of tacrine administration in patients with Alzheimer's disease.

作者信息

Watkins P B, Zimmerman H J, Knapp M J, Gracon S I, Lewis K W

机构信息

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor.

出版信息

JAMA. 1994 Apr 6;271(13):992-8.

PMID:8139084
Abstract

OBJECTIVE

To characterize the hepatic effects of tacrine treatment in patients with Alzheimer's disease.

DESIGN

Controlled trials of tacrine therapy consisting of two blinded, parallel-group trials; three blinded, enrichment-design trials; and their respective open-label extensions.

SETTING

Multicenter clinical trials in the United States, France, and Canada.

PATIENTS

A total of 2446 men and women at least 50 years of age with a diagnosis of probable Alzheimer's disease of mild to moderate severity and in good health without significant hepatic, cardiovascular, or renal disease.

INTERVENTION

Administration of tacrine vs placebo, with weekly measurement of serum hepatic enzymes.

MAIN OUTCOME MEASURES

Incidence, maximum severity, and timing of event for serum alanine aminotransferase (ALT) elevation.

RESULTS

Among the 2446 patients who received tacrine in clinical trials, ALT levels greater than the upper limit of normal (ULN) occurred on at least one occasion in 1203 patients (49%), ALT levels greater than three times the ULN occurred in 621 patients (25%), and ALT levels greater than 20 times the ULN occurred in 40 patients (2%). The elevated ALT levels were generally asymptomatic and occurred more frequently in women than men. The mean time from initiation of tacrine treatment to first ALT level greater than three times the ULN was 50 days, and 90% of all initial ALT levels greater than three times the ULN occurred during the first 12 weeks of treatment. Of 145 patients who discontinued tacrine treatment because of an ALT level greater than three times the ULN and were rechallenged, 127 (88%) were able to resume long-term therapy with the drug. In all instances, discontinuing tacrine completely reversed elevations in ALT levels, and no deaths related to hepatotoxicity occurred.

CONCLUSIONS

These data suggest that the potential for serious hepatic toxicity can be reduced through careful monitoring of ALT levels in patients who may benefit from tacrine therapy.

摘要

目的

明确他克林治疗阿尔茨海默病患者时对肝脏的影响。

设计

他克林治疗的对照试验,包括两项双盲、平行组试验;三项双盲、富集设计试验;以及各自的开放标签扩展试验。

地点

美国、法国和加拿大的多中心临床试验。

患者

总共2446名年龄至少50岁、被诊断为轻度至中度可能的阿尔茨海默病且身体健康、无明显肝脏、心血管或肾脏疾病的男性和女性。

干预

给予他克林与安慰剂,每周测量血清肝酶。

主要观察指标

血清丙氨酸氨基转移酶(ALT)升高的发生率、最大严重程度及发生时间。

结果

在临床试验中接受他克林治疗的2446名患者中,1203名患者(49%)至少有一次ALT水平高于正常上限(ULN),621名患者(25%)的ALT水平高于ULN的三倍,40名患者(2%)的ALT水平高于ULN的20倍。ALT水平升高通常无症状,且在女性中比男性更常见。从开始他克林治疗到首次ALT水平高于ULN三倍的平均时间为50天,所有初始ALT水平高于ULN三倍的患者中有90%发生在治疗的前12周内。在145名因ALT水平高于ULN三倍而停用他克林治疗并再次接受挑战的患者中,127名(88%)能够恢复使用该药物的长期治疗。在所有情况下,停用他克林可使ALT水平升高完全逆转,且未发生与肝毒性相关的死亡。

结论

这些数据表明,通过仔细监测可能从他克林治疗中获益的患者的ALT水平,可降低严重肝毒性的可能性。

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