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Efficacy of anti-osteoporosis treatment for men with osteoporosis: a meta-analysis

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Journal of Bone and Mineral Metabolism Aims and scope Submit manuscript

Abstract

Introduction

Osteoporosis and fracture are important healthcare problems for men worldwide, which are relevant to severe disability and mortality. This meta-analysis aimed to assess the effectiveness of pharmacological therapy in men with osteoporosis, and to provide evidence-based hints for clinical practice.

Materials and Methods

PubMed, Embase, Web of Science were searched from inception to July 31, 2022. Pooled standardized mean difference (SMD) and relative risk (RR) were calculated. Heterogeneity between included studies and publication bias were detected.

Results

Twenty clinical studies were enrolled in this meta-analysis. The pooled SMD for mean percentage differences of change from baseline in lumbar spine BMD between the treatment group and the control group was 4.95 (95% CI 2.48, 7.42, I2 = 99%, p < 0.0001). For mean percentage differences of change in femoral neck BMD, the overall SMD was 3.08 (95% CI 0.95, 5.20, I2 = 99%, p = 0.0045). For a change in total hip BMD, the overall SMD was 1.06 (95% CI 0.50, 1.63, I2 = 82%, p = 0.0002). The overall RR for incident vertebral fractures was 0.50 (95% CI 0.37, 0.68, I2 = 5%, p = 0.3971). The pooled RR for nonvertebral fractures and clinical fracture were 0.74 (95% CI 0.41, 1.33, I2 = 28%, p = 0.3139) and 0.81 (95% CI 0.54, 1.21, I2 = 0%, p = 0.2992).

Conclusion

Findings in this meta-analysis indicate that pharmacological treatment increases lumbar spine, femoral neck, total hip BMD, and decreases incident vertebral fractures in men with osteoporosis.

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Data avalibality

All data generated or analysed during this study are included in this published article [and its supplementary information files].

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Authors and Affiliations

Authors

Contributions

AD and XF carried out the studies, participated in collecting data, and drafted the manuscript. AD and YH performed the statistical analysis and participated in its design. YH and YH participated in the acquisition, analysis, or interpretation of data. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Aimei Dong.

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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 19 KB)

774_2023_1407_MOESM2_ESM.tiff

Supplementary file2 Figure S1. Forest plots of percentage change in lumbar spine BMD for bisphosphonates and non-bisphosphonates groups. (TIFF 85 KB)

774_2023_1407_MOESM3_ESM.tiff

Supplementary file3 Figure S2. Forest plots of percentage change in femoral neck BMD for bisphosphonates and non-bisphosphonates groups. (TIFF 85 KB)

Supplementary file4 Figure S3. Forest plots of percentage change in total hip BMD. (TIF 130 KB)

774_2023_1407_MOESM5_ESM.tif

Supplementary file5 Figure S4. Forest plots of percentage change in total hip BMD for bisphosphonates and non-bisphosphonates groups. (TIF 132 KB)

774_2023_1407_MOESM6_ESM.tiff

Supplementary file6 Figure S5. Forest plots of RR for incident vertebral fractures for bisphosphonates and non-bisphosphonates groups. (TIFF 141 KB)

Supplementary file7 Figure S6. Forest plots of RR for incident nonvertebral fractures. (TIF 139 KB)

774_2023_1407_MOESM8_ESM.tif

Supplementary file8 Figure S7. Forest plots of RR for incident nonvertebral fractures for bisphosphonates and non-bisphosphonates groups. (TIF 155 KB)

Supplementary file9 Figure S8. Forest plots of RR for incident clinical fractures. (TIF 143 KB)

774_2023_1407_MOESM10_ESM.tif

Supplementary file10 Figure S9. Forest plots of RR for incident clinical fractures for bisphosphonates and non-bisphosphonates groups. (TIF 159 KB)

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Dong, A., Fei, X., Huang, Y. et al. Efficacy of anti-osteoporosis treatment for men with osteoporosis: a meta-analysis. J Bone Miner Metab 41, 258–267 (2023). https://doi.org/10.1007/s00774-023-01407-0

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  • DOI: https://doi.org/10.1007/s00774-023-01407-0

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