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骨质疏松症患者 denosumab 和 romosozumab 对骨密度和骨转换标志物影响的荟萃分析。

Meta-analysis of the effects of denosumab and romosozumab on bone mineral density and turnover markers in patients with osteoporosis.

机构信息

Department of Joint Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

Front Endocrinol (Lausanne). 2023 Jul 12;14:1188969. doi: 10.3389/fendo.2023.1188969. eCollection 2023.

Abstract

PURPOSE

To assess the alterations in bone mineral density and bone turnover marker concentrations following the administration of denosumab and romosozumab therapies in patients with osteoporosis.

METHODS

PubMed was searched for studies published until January 28, 2023, that investigated the clinical efficacy and bone turnover marker changes of denosumab and romosozumab in the treatment of osteoporosis, with a minimum follow-up of 3 months in each study. Studies were screened, and data on changes in bone mineral density (BMD), P1NP, and TRACP-5b levels after treatment were extracted and included in the analysis.

RESULTS

Six studies were analyzed. At 3 months after treatment, the romosozumab group showed greater changes in lumbar BMD and bone turnover markers. BMD of total hip and femoral neck was relatively delayed. Beginning at 6 to 12 months, romosozumab showed greater changes in bone mineral density and markers of bone turnover.

CONCLUSION

Both romosozumab and denosumab have antiosteoporotic effects, with greater effects on BMD and bone turnover markers observed within 12 months of romosozumab treatment.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/prospero, identifier CRD42023395034.

摘要

目的

评估地舒单抗和罗莫佐单抗治疗骨质疏松症患者后骨密度和骨转换标志物浓度的变化。

方法

检索 PubMed 数据库,截至 2023 年 1 月 28 日,纳入研究地舒单抗和罗莫佐单抗治疗骨质疏松症的临床疗效和骨转换标志物变化的相关研究,每个研究的随访时间至少为 3 个月。筛选研究,并提取治疗后骨密度(BMD)、P1NP 和 TRACP-5b 水平变化的数据进行分析。

结果

共分析了 6 项研究。治疗 3 个月后,罗莫佐单抗组腰椎 BMD 和骨转换标志物的变化更大。全髋和股骨颈的 BMD 相对延迟。从 6 至 12 个月开始,罗莫佐单抗组在骨密度和骨转换标志物方面的变化更大。

结论

地舒单抗和罗莫佐单抗均具有抗骨质疏松作用,罗莫佐单抗治疗 12 个月内对 BMD 和骨转换标志物的作用更大。

系统评价注册

https://www.crd.york.ac.uk/prospero,标识符 CRD42023395034。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/10390296/97a944649012/fendo-14-1188969-g001.jpg

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