Fanconi syndrome caused by low-dose adefovir dipivoxil

Li-Na Zhu1, Li-Jun Mou2, Ying Hu3

  • 1Department of Nephrology, The Second Affiliated Hospital Binjiang Branch, Zhejiang, China.

Saudi Medical Journal
|March 14, 2014
PubMed

Insights

Low-dose Adefovir dipivoxil (ADV) can cause acquired Fanconi syndrome (FS), even at doses previously thought safe. Monitoring phosphate levels is crucial, as entecavir may be a better alternative than tenofovir for patients experiencing FS.

Area of Science:

  • Nephrology
  • Hepatology
  • Pharmacology

Background:

  • Adefovir dipivoxil (ADV) is an antiviral medication used for chronic hepatitis B.
  • Low-dose ADV (10 mg daily) was previously considered to have a low risk of nephrotoxicity.
  • Acquired Fanconi syndrome (FS) is a generalized proximal tubule dysfunction.

Observation:

  • Three patients (one woman, two men) of Asian ethnicity developed acquired Fanconi syndrome (FS) while on low-dose ADV therapy.
  • Symptoms included bone pain and muscle weakness.
  • Diagnosis was confirmed by electrolyte and phosphate imbalances.

Findings:

  • Patients experienced normalization of serum phosphate after switching from ADV to entecavir, with or without phosphate supplementation.
  • One patient did not show significant improvement after switching to tenofovir, despite phosphate supplementation.
  • Low-dose ADV-induced FS appears to be more prevalent in the Asian population.

Implications:

  • Regular monitoring of urine and serum phosphate is essential for patients on ADV therapy.
  • Entecavir may be a more suitable alternative to ADV than tenofovir for patients developing FS.
  • This study highlights a previously underestimated risk associated with low-dose ADV, necessitating vigilant patient management.

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