Tacrine - A cause of fatal hepatotoxicity?

被引:50
作者
Blackard, WG
Sood, GK
Crowe, DR
Fallon, MB
机构
[1] Univ Alabama, Ctr Liver, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Pathol, Birmingham, AL 35294 USA
关键词
tacrine; hepatotoxicity;
D O I
10.1097/00004836-199801000-00015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Tacrine, an acetyl cholinesterase inhibitor used in the treatment of Alzheimer's disease, often causes reversible abnormalities in liver enzymes, but significant hepatotoxicity is uncommon. We describe fatal hepatic failure associated with tacrine administration. A 75-year-old woman with Alzheimer's disease, taking tacrine for 14 months, developed progressive jaundice. Liver function abnormalities developed during tacrine treatment and led to hepatic failure and death. An extensive evaluation for other etiologies of liver disease was negative. Other potentially hepatotoxic medicines had been administered for at least 2 years before beginning tacrine, and postmortem examination of the liver was consistent with drug-induced hepatotoxicity. Approximately half the patients treated with tacrine have liver enzyme abnormalities develop, primarily in the first 12 weeks of therapy, that resolve with discontinuation of drug or dosage adjustment. Our case of tacrine-associated hepatotoxicity 14 months after the initiation of treatment despite regular biochemical evaluation suggests the potential for delayed and fatal hepatotoxicity with tacrine.
引用
收藏
页码:57 / 59
页数:3
相关论文
共 12 条
[1]  
AMES DJ, 1988, LANCET, V1, P887
[2]   TACRINE (TETRAHYDROAMINOACRIDINE - THA) AND LECITHIN IN SENILE DEMENTIA OF THE ALZHEIMER TYPE - A MULTICENTER TRIAL [J].
CHATELLIER, G ;
LACOMBLEZ, L .
BRITISH MEDICAL JOURNAL, 1990, 300 (6723) :495-499
[3]   A DOUBLE-BLIND, PLACEBO-CONTROLLED MULTICENTER STUDY OF TACRINE FOR ALZHEIMERS-DISEASE [J].
DAVIS, KL ;
THAL, LJ ;
GAMZU, ER ;
DAVIS, CS ;
WOOLSON, RF ;
GRACON, SI ;
DRACHMAN, DA ;
SCHNEIDER, LS ;
WHITEHOUSE, PJ ;
HOOVER, TM ;
MORRIS, JC ;
KAWAS, CH ;
KNOPMAN, DS ;
EARL, NL ;
KUMAR, V ;
DOODY, RS .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (18) :1253-1259
[4]   TACRINE IN ALZHEIMERS-DISEASE [J].
EAGGER, SA ;
LEVY, R ;
SAHAKIAN, BJ .
LANCET, 1991, 337 (8748) :989-992
[5]   A CONTROLLED TRIAL OF TACRINE IN ALZHEIMERS-DISEASE [J].
FARLOW, M ;
GRACON, SI ;
HERSHEY, LA ;
LEWIS, KW ;
SADOWSKY, CH ;
DOLANURENO, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (18) :2523-2529
[6]   The caffeine breath test does not identify patients susceptible to tacrine hepatotoxicity [J].
Fontana, RJ ;
Turgeon, DK ;
Woolf, TF ;
Knapp, MJ ;
Foster, NL ;
Watkins, PB .
HEPATOLOGY, 1996, 23 (06) :1429-1435
[7]   ACUTE HEPATITIS AFTER TETRAHYDROAMINOACRIDINE ADMINISTRATION FOR ALZHEIMERS-DISEASE [J].
HAMMEL, P ;
LARREY, D ;
BERNUAU, J ;
KALAFAT, M ;
FRENEAUX, E ;
BABANY, G ;
DEGOTT, C ;
FELDMANN, G ;
PESSAYRE, D ;
BENHAMOU, JP .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1990, 12 (03) :329-331
[8]   AN INVESTIGATION INTO THE FORMATION OF STABLE, PROTEIN-REACTIVE AND CYTOTOXIC METABOLITES FROM TACRINE IN-VITRO - STUDIES WITH HUMAN AND RAT-LIVER MICROSOMES [J].
MADDEN, S ;
WOOLF, TF ;
POOL, WF ;
PARK, BK .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (01) :13-20
[9]  
PARK BK, 1994, ALZ DIS ASSOC DIS, V8, pS39
[10]   ORAL TETRAHYDROAMINOACRIDINE IN LONG-TERM TREATMENT OF SENILE DEMENTIA, ALZHEIMER TYPE [J].
SUMMERS, WK ;
MAJOVSKI, LV ;
MARSH, GM ;
TACHIKI, K ;
KLING, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (20) :1241-1245