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Received:July 02, 2020 Published Online:November 20, 2020
Received:July 02, 2020 Published Online:November 20, 2020
中文摘要: 目的 探讨补肾活血方治疗糖尿病性骨质疏松(DOP)的临床效果。方法 选取2017年1月至2020年 1月在中医科、内分泌科门诊及住院的DOP患者55例,随机分为对照组(n=27)及治疗组(n=28)。对照组在控制其他原发病基础上加用碳酸钙D3 600 mg+骨化三醇胶丸0.5 μg,治疗组在对照组基础上加用补肾活血方,治疗周期为6个月。观察并比较两组治疗前后VAS评分、肝功能[丙氨酸氨基转移酶(ALT)、谷氨酸氨基转移酶(AST)]、骨代谢指标[I型胶原氨基端延长肽(P1NP)、β-I型胶原羧基端肽(β-CTX)]、骨密度(腰椎L1~4及左侧股骨)。结果 与对照组相比,治疗后治疗组VAS评分、β-CTX水平降低,P1NP水平升高,腰椎(L1~4)及左侧股骨骨密度增加,差异有统计学意义(P<0.05,P<0.01)。两组治疗前后肝功能指标比较差异无统计学意义(P>0.05)。结论 补肾活血方可有效缓解DOP患者疼痛,改善骨代谢,增加骨密度,且无明显肝损作用。
Abstract:Objective To investigate the clinical effect of Bushen Huoxue decoction on diabetic osteoporosis (DOP).Methods A total of 55 outpatients or inpatients with DOP who received treatment in the Department of TCM or Endocrinology from January 2017 to January 2020 were randomly divided into control group ( n=27) and treatment group ( n=28).The control group was treated with calcium carbonate and vitamin D3 tablets 600 mg+calcitriol capsules 0.5 μg on the basis of controlling other primary diseases,and the treatment group was added with Bushen Huoxue decoction on the basis of control group.The treatment period was 6 months.The VAS score,liver function [alanine aminotransferase (ALT),glutamate aminotransferase (AST)],bone metabolism index [type I collagen N-terminal lengthening peptide (P1NP),β-I collagen carboxyl terminal peptide (β-CTX)],bone mineral density (BMD) were observed and compared between the two groups before and after treatment.Results Compared with the control group,the VAS score and β-CTX level in the treatment group were decreased,the P1NP level,BMD of lumbar spine (L1-4) and left femur was increased ( P<0.05).There was no significant difference in liver function between the two groups before and after treatment ( P>0.05).Conclusion Bushen Huoxue decoction could relieve pain,improve bone metabolism and increase bone mineral density in patients with DOP without obvious liver damage,which can be used in clinical treatment of DOP.
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基金项目:南京大学医院管理研究所课题研究项目(NDYG2019026)
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