Elevation in Serum Concentration of Bone-Specific Alkaline Phosphatase without Elevation in Serum Creatinine Concentration Secondary to Adefovir Dipivoxil Therapy in Chronic Hepatitis B Virus Infection.

Hepatitis research and treatment Pub Date : 2013-01-01 Epub Date: 2013-09-09 DOI:10.1155/2013/739247
Hiroshi Abe, Nobuyoshi Seki, Tomonori Sugita, Yuta Aida, Haruya Ishiguro, Tamihiro Miyazaki, Munenori Itagaki, Satoshi Sutoh, Yoshio Aizawa
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Abstract

Of 168 patients with chronic hepatitis B virus (HBV) infection-related liver disease, 20 patients who had received 100 mg of lamivudine plus 10 mg/day of adefovir dipivoxil (ADV) (ADV group) and 124 patients who had received 0.5 mg/day of entecavir or 100 mg/day of lamivudine (non-ADV group) for >1 year were enrolled. For comparative analyses, 19 well-matched pairs were obtained from the groups by propensity scores. At the time of enrollment, serum creatinine and phosphate concentrations were similar between the ADV and non-ADV groups; however, urinary phosphate (P = 0.0424) and serum bone-specific alkaline phosphatase (BAP) (P = 0.0228) concentrations were significantly higher in the ADV group than in the non-ADV group. Serum BAP was significantly higher at the time of enrollment than before ADV administration in the ADV group (P = 0.0001), although there was no significant change in serum BAP concentration in the non-ADV group. There was a significant positive correlation between the period of ADV therapy and ΔBAP (R (2) = 0.2959, P = 0.0160). Serum BAP concentration increased before increase in serum creatinine concentration and was useful for early detection of adverse events and for developing adequate measures for continuing ADV for chronic HBV infection-related liver disease.

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慢性乙型肝炎病毒感染阿德福韦酯治疗后骨特异性碱性磷酸酶血清浓度升高而血清肌酐浓度未升高
在168例慢性乙型肝炎病毒(HBV)感染相关肝病患者中,20例接受100 mg拉米夫定加10 mg/天阿德福韦酯(ADV)治疗的患者(ADV组)和124例接受0.5 mg/天恩替卡韦或100 mg/天拉米夫定治疗(非ADV组)>1年的患者被纳入研究。为了进行比较分析,根据倾向得分从各组中获得了19对匹配良好的配对。在入组时,ADV组和非ADV组的血清肌酐和磷酸盐浓度相似;然而,ADV组尿磷酸盐(P = 0.0424)和血清骨特异性碱性磷酸酶(BAP) (P = 0.0228)浓度显著高于非ADV组。ADV组患者入组时血清BAP显著高于ADV给药前(P = 0.0001),而非ADV组患者血清BAP浓度无显著变化。ADV治疗时间与ΔBAP呈显著正相关(R (2) = 0.2959, P = 0.0160)。血清BAP浓度在血清肌酐浓度升高之前升高,这有助于早期发现不良事件,并为慢性HBV感染相关肝病的持续ADV制定适当的措施。
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