Björnsson Helgi K, Björnsson Einar S, Avula Bharathi, Khan Ikhlas A, Jonasson Jon G, Ghabril Marwan, Hayashi Paul H, Navarro Victor
Landspitali University Hospital, Reykjavik, Iceland.
National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS, USA.
Liver Int. 2020 Apr;40(4):825-829. doi: 10.1111/liv.14393. Epub 2020 Feb 11.
BACKGROUND & AIMS: Ashwagandha (Withania somnifera) is widely used in Indian Ayurvedic medicine. Several dietary supplements containing ashwagandha are marketed in the US and Europe, but only one case of drug-induced liver injury (DILI) due to ashwagandha has been published. The aim of this case series was to describe the clinical phenotype of suspected ashwagandha-induced liver injury.
Five cases of liver injury attributed to ashwagandha-containing supplements were identified; three were collected in Iceland during 2017-2018 and two from the Drug-Induced Liver Injury Network (DILIN) in 2016. Other causes for liver injury were excluded. Causality was assessed using the DILIN structured expert opinion causality approach.
Among the five patients, three were males; mean age was 43 years (range 21-62). All patients developed jaundice and symptoms such as nausea, lethargy, pruritus and abdominal discomfort after a latency of 2-12 weeks. Liver injury was cholestatic or mixed (R ratios 1.4-3.3). Pruritus and hyperbilirubinaemia were prolonged (5-20 weeks). No patient developed hepatic failure. Liver tests normalized within 1-5 months in four patients. One patient was lost to follow-up. One biopsy was performed, showing acute cholestatic hepatitis. Chemical analysis confirmed ashwagandha in available supplements; no other toxic compounds were identified. No patient was taking potentially hepatotoxic prescription medications, although four were consuming additional supplements, and in one case, rhodiola was a possible causative agent along with ashwagandha.
These cases illustrate the hepatotoxic potential of ashwagandha. Liver injury is typically cholestatic or mixed with severe jaundice and pruritus, but self-limited with liver tests normalizing in 1-5 months.
南非醉茄(Withania somnifera)在印度阿育吠陀医学中被广泛使用。在美国和欧洲,有几种含有南非醉茄的膳食补充剂在市场上销售,但仅有一例因南非醉茄导致的药物性肝损伤(DILI)的病例被报道。本病例系列的目的是描述疑似南非醉茄所致肝损伤的临床表型。
确定了5例因含南非醉茄的补充剂导致肝损伤的病例;其中3例于2017 - 2018年在冰岛收集,2例于2016年来自药物性肝损伤网络(DILIN)。排除了其他肝损伤原因。使用DILIN结构化专家意见因果关系评估方法评估因果关系。
5例患者中,3例为男性;平均年龄43岁(范围21 - 62岁)。所有患者在2 - 12周的潜伏期后出现黄疸以及恶心、乏力、瘙痒和腹部不适等症状。肝损伤为胆汁淤积性或混合型(R值为1.4 - 3.3)。瘙痒和高胆红素血症持续时间较长(5 - 20周)。无患者发生肝衰竭。4例患者的肝功能检查在1 - 5个月内恢复正常。1例患者失访。进行了1例肝活检,显示为急性胆汁淤积性肝炎。化学分析在可用补充剂中确认了南非醉茄成分;未鉴定出其他有毒化合物。尽管4例患者还服用了其他补充剂,但无患者正在服用可能具有肝毒性的处方药,且在1例病例中,红景天与南非醉茄可能是共同致病因素。
这些病例说明了南非醉茄的肝毒性潜力。肝损伤通常为胆汁淤积性或混合型,伴有严重黄疸和瘙痒,但具有自限性,肝功能检查在1 - 5个月内恢复正常。