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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.
Abstract:
Adefovir dipivoxil (ADV) at a low-dose (10 mg daily), which was previously considered not nephrotoxic, was reported to have induced acquired Fanconi syndrome (FS). We report one 64-year-old Chinese woman and 2 Chinese men (ages 45 and 63 years) with bone pain, and/or muscle weakness on ADV therapy were diagnosed with low-dose ADV-induced FS. The serum phosphate normalized, or nearly normalized in the first and second patients after changing ADV to entecavir with, or without phosphate supplement, but did not improve significantly in the third patient after changing ADV to tenofovir, even though he was supplied with a higher dose of phosphate. Low-dose ADV-related FS is not rare in the Asian population. Regular monitoring of urine and serum phosphate is necessary during therapy with ADV. Prognosis was favorable, however, tenofovir is not a suitable replacement for ADV.
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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