恩替卡韦和替诺福韦二氧吡酯对慢性乙型肝炎患者骨密度的影响

Yasemin EMÜR GÜNAY, Arif Mansur COŞAR
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摘要

背景/目的:评价慢性乙型肝炎感染(CHB)患者接受恩替卡韦(ETV)或富马酸替诺福韦二氧吡酯(TDF)治疗时药物与骨质疏松的关系。材料和方法:该研究纳入了在2016年至2021年期间接受ETV或TDF治疗至少12个月并在治疗后12个月内接受骨矿物质密度测量(BMD)测量的患者。回顾性分析患者的人口学特征及抗病毒药物使用与骨质减少/骨质疏松的关系。 结果:共纳入170例患者,其中男性92例(54.1%),平均诊断年龄36.57±14.88岁。其中24例(14.1%)接受ETV治疗,146例(85.9%)接受TDF治疗。测量骨密度时的平均年龄为48.62±13.4岁。从诊断到BMD的中位时间为138.5(15-373)个月。男性14例(15.2%)、女性25例(32.1%)出现骨质减少/骨质疏松。骨量减少/骨质疏松症的发生率在女性中显著高于男性(p=0.011)。ETV组与TDF组在骨质减少/骨质疏松发生率上无显著差异(p=0.112)。TDF服用者腰椎骨密度显著增高(p=0.043)。虽然没有患者在治疗开始的12个月内出现BMD,但6例(3.5%)患者在治疗开始后的24个月内出现BMD, 8例(4.7%)患者在治疗开始后的36个月内出现BMD, 25例(14.7%)患者在治疗开始后的60个月内出现BMD。结论:TDF组与ETV组在骨质减少/骨质疏松发生方面无显著差异。发现慢性乙型肝炎患者的骨矿物质测量没有定期和适当地进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Entecavir and Tenofovir Disoproxil on Bone Mineral Density in Chronic Hepatitis B Treatment
Background/Aim:Evaluation of the relationship between drugs and osteoporosis in patients receiving entecavir (ETV) or tenofovir disoproxil fumarate (TDF) treatment for chronic hepatitis B infection (CHB). Material and Method: The study included patients who received ETV or TDF treatment for at least 12 months between 2016 and 2021 and underwent bone mineral densitometry (BMD) measurement within 12 months after treatment. Demographic characteristics of the patients and the association of antiviral drug use with osteopenia/osteoporosis were retrospectively. Results: The study included 170 patients, 92 (54.1%) of whom were male, with a mean age at diagnosis of 36.57 ± 14.88 years. Of the patients, 24 (14.1%) were on ETV and 146 (85.9%) were on TDF. The mean age at BMD measurement was 48.62 ± 13.4 years. The median time from diagnosis to BMD was 138.5 (15-373) months. Osteopenia/osteoporosis was found in 14 (15.2%) of male patients and 25 (32.1%) of female patients. The frequency of osteopenia/osteoporosis was significantly higher in women (p=0.011). There was no significant difference in the frequency of osteopenia/osteoporosis between ETV and TDF (p=0.112). Lumbar spine (LS) BMD was significantly higher in TDF users (p=0.043). While no patient had a BMD within 12 months of treatment initiation, 6 (3.5%) of the patients had a BMD within 24 months, 8 (4.7%) within 36 months and 25 (14.7%) within 60 months of treatment initiation. Conclusion: There was no significant difference in the development of osteopenia/osteoporosis in patients using TDF and ETV. It was found that bone mineral measurements of patients with CHB were not performed regularly and appropriately.
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