Sheikh N M, Philen R M, Love L A
Center for Food Safety and Applied Nutrition, Food and Drug Administration, Washington, DC, USA.
Arch Intern Med. 1997 Apr 28;157(8):913-9.
Personal health care practices that may include the use of dietary supplements are common in the United States. Products marketed as dietary supplements are diverse and may include botanicals, vitamins, and/or minerals. Chaparral (Larrea tridentata) is a botanical dietary supplement made from a desert shrub and used for its antioxidant properties. Several reports of chaparral-associated hepatitis have been published since 1990, but a complete picture of the clinical presentation is still unclear.
We reviewed the 18 case reports of adverse events associated with the ingestion of chaparral reported to the Food and Drug Administration between 1992 and 1994. These reports were from health care professionals, state health departments, and individual consumers.
Of 18 reports of illnesses associated with the ingestion of chaparral, there was evidence of hepatotoxicity in 13 cases. Clinical presentation, characterized as jaundice with a marked increase in serum liver chemistry values, occurred 3 to 52 weeks after the ingestion of chaparral, and it resolved 1 to 17 weeks after most individuals stopped their intake of chaparral. The predominant pattern of liver injury was characterized as toxic or drug-induced cholestatic hepatitis; in 4 individuals, there was progression to cirrhosis; and in 2 individuals, there was acute fulminant liver failure that required liver transplants.
These data indicate that the use of chaparral may be associated with acute to chronic irreversible liver damage with fulminant hepatic failure, and they underscore the potential for certain dietary supplement ingredients to cause toxic effects on the liver. Health professionals should be encouraged to inquire routinely about the use of dietary supplements and other products, to be alert to potential adverse effects that may be associated with these products, and, finally, to report any serious adverse events associated with these products through the MEDWatch Program of the Food and Drug Administration.
在美国,个人保健行为(可能包括使用膳食补充剂)很常见。作为膳食补充剂销售的产品种类繁多,可能包括植物药、维生素和/或矿物质。拉瑞阿三齿叶(Larrea tridentata)是一种由沙漠灌木制成的植物性膳食补充剂,因其抗氧化特性而被使用。自1990年以来,已经发表了几篇关于拉瑞阿三齿叶相关肝炎的报告,但临床表现的全貌仍不清楚。
我们回顾了1992年至1994年期间向美国食品药品监督管理局报告的18例与摄入拉瑞阿三齿叶相关的不良事件病例报告。这些报告来自医疗保健专业人员、州卫生部门和个人消费者。
在18例与摄入拉瑞阿三齿叶相关的疾病报告中,有13例存在肝毒性证据。临床表现为黄疸伴血清肝酶值显著升高,在摄入拉瑞阿三齿叶后3至52周出现,大多数人停止摄入拉瑞阿三齿叶后1至17周症状缓解。肝损伤的主要模式为中毒性或药物性胆汁淤积性肝炎;4人发展为肝硬化;2人出现急性暴发性肝衰竭,需要进行肝移植。
这些数据表明,使用拉瑞阿三齿叶可能与急性至慢性不可逆肝损伤及暴发性肝衰竭有关,强调了某些膳食补充剂成分对肝脏产生毒性作用的可能性。应鼓励卫生专业人员常规询问患者膳食补充剂及其他产品的使用情况,警惕这些产品可能带来的潜在不良反应,并通过美国食品药品监督管理局的MEDWatch计划报告与这些产品相关的任何严重不良事件。