4.2 Article

Adefovir dipivoxil induced hypophosphatemic osteomalacia in chronic hepatitis B: a comparative study of Chinese and foreign case series

期刊

BMC PHARMACOLOGY & TOXICOLOGY
卷 19, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s40360-018-0212-7

关键词

Adefovir dipivoxil; Hypophosphatemia; Osteomalacia; Renal insufficiency; Fanconi syndrome

资金

  1. Special Research Fund of Clinical Medicine of the Chinese Medical Association [13060990484]
  2. Natural Science Foundation of Shandong Province [ZR2015HM074]
  3. Key Research and Development Plan of Shandong Province [2016GSF201014]
  4. Joint Scientific Research Fund of Shandong University [11671315]

向作者/读者索取更多资源

Background: Adefovir dipivoxil (ADV)-induced renal tubular dysfunction and hypophosphatemic osteomalacia (HO) have been given great consideration in the past few years. However, no standard guidance is available due to a lack of powerful evidence from appropriate long-term prospective case-control studies and variations in the definition of renal adverse events. The aim of this study is to clarify clinical features of ADV-related HO in Chinese chronic hepatitis B patients with long-term ADV treatment in Chinese and non-Chinese comparative case series. Methods: Retrieval of case reports was based on Pubmed, CNKI, Wan Fang and VIP databases using the key words adefovir dipivoxil, hypophosphatemia, osteomalacia and Fanconi syndrome. We divided patients into Chinese (C group) and Foreign (F group) groups according to their nationality. Comparisons involving demographics, clinical manifestations, tests, treatment and prognosis were conducted between the two groups. Results: Of the patients screened, 120 Chinese patients were identified in the C group, and 32 non-Chinese patients were identified in the F group. The average age of the C group was younger than that of the F group (51.89 years +/- 10.96 years versus 56.47 years +/- 11.36 years, t =- 2.084, P = 0.039). No significant difference was found in gender (male to female, 3.29:1 versus 3:1, chi(2 )= 0.039, P = 0.844). Although there was no significant difference in the duration of ADV therapy before ostalgia onset, the C group tended to develop adverse events earlier, by 2-3 years, while the F group developed adverse events at 4-5 years (Z =- 1.517, P = 0.129). Prognosis was good after adjustment of the ADV dose and supplemental administration of phosphate and calcitriol. Time to resolution of tubular dysfunction was commenced at the first month, and Chinese patients were more prone to recover in the first 3 months than non-Chinese patients (91.3% of patients in the C group versus 563% in the F group, Z = - 3.013, P = 0.003). Conclusions: Sufficient attention is required for middle-aged males before and during exposure to long-term ADV therapy, regardless of nationality. The clinical picture, laboratory and radiograph alterations are important clues for those patients and are usually characterized by polyarthralgia, renal tubular dysfunction and mineralization defects. Implementation of an early renal tubular injury index is recommended for patients with higher risk, which would prevent further renal injury.

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