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Chaparral-associated hepatotoxicity

N M Sheikh1, R M Philen, L A Love

  • 1Center for Food Safety and Applied Nutrition, Food and Drug Administration, Washington, DC, USA.

Archives of Internal Medicine
|April 28, 1997
PubMed
Summary
This summary is machine-generated.

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Chaparral, a botanical dietary supplement, may cause severe liver damage, including irreversible injury and liver failure. Healthcare providers should monitor for adverse effects and report them.

Area of Science:

  • Hepatology
  • Toxicology
  • Integrative Medicine

Background:

  • Dietary supplements, including botanicals like chaparral (Larrea tridentata), are widely used for health purposes.
  • Chaparral is recognized for its antioxidant properties but has been linked to liver injury since 1990.
  • The full clinical spectrum of chaparral-associated hepatitis remains incompletely understood.

Purpose of the Study:

  • To investigate the clinical presentation and outcomes of adverse events linked to chaparral ingestion.
  • To assess the potential for chaparral to cause significant liver damage.

Main Methods:

  • A review of 18 case reports submitted to the Food and Drug Administration (FDA) between 1992 and 1994.
  • Data sources included reports from healthcare professionals, state health departments, and consumers.

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Main Results:

  • Hepatotoxicity was evident in 13 of the 18 reported cases.
  • Liver injury manifested as jaundice and elevated liver enzymes 3–52 weeks post-ingestion, resolving after cessation.
  • The pattern was predominantly toxic or drug-induced cholestatic hepatitis, with 4 cases progressing to cirrhosis and 2 to acute liver failure requiring transplantation.

Conclusions:

  • Chaparral use is associated with potential for acute to chronic, irreversible liver damage, including fulminant hepatic failure.
  • This highlights the risk of toxic effects from certain dietary supplement ingredients.
  • Healthcare professionals should routinely inquire about supplement use, monitor for adverse effects, and report serious events via FDA's MEDWatch Program.