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In male osteoporosis, anabolic therapies improved lumbar spine and hip BMD more than antiresorptives at 12 months.

In male osteoporosis, anabolic therapies improved lumbar spine and hip BMD more than antiresorptives…
Photo by Nathan Rimoux / Unsplash
Key Takeaway
Consider anabolic agents for male osteoporosis to maximize lumbar spine and hip BMD gains at 12 months.

This Bayesian network meta-analysis synthesized data from 18 randomized controlled trials involving 19 to 1199 participants each. The study assessed the efficacy and safety of antiresorptive and anabolic therapies for male osteoporosis, focusing on percent changes in lumbar spine, femoral neck, and total hip bone mineral density (BMD) at 12 months. No specific comparator was reported for the primary analysis, and the setting was not detailed.

Regarding primary outcomes, anabolic therapies outperformed antiresorptives for lumbar spine BMD, with a mean difference of 6.62 versus 3.58 (95% CI 5.01–8.23 vs. 2.52–4.64). For total hip BMD, anabolic agents also showed greater efficacy, with a mean difference of 3.53 versus 1.98 (95% CI 2.18–4.89 vs. –1.10–5.06). Conversely, antiresorptives demonstrated modest advantages at the femoral neck, with a mean difference of 1.66 versus 1.43 (95% CI 0.57–2.75 vs. –0.03–2.86).

Safety analysis indicated no significant differences between drug classes for all adverse events or serious adverse events. Discontinuations and tolerability data were not reported. The study represents the first comprehensive drug- and class-level synthesis for male osteoporosis. However, direct comparisons between drug classes are limited, and evidence directly comparing these therapies in male populations remains constrained. Funding sources and conflicts of interest were not reported. Consequently, treatment choices should primarily be guided by efficacy considerations while acknowledging these limitations.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
BackgroundOsteoporosis in men is an increasingly recognized health issue associated with reduced bone mineral density (BMD) and elevated fracture risk. While both antiresorptive and anabolic therapies are recommended in clinical practice, evidence directly comparing these drug classes in male populations remains limited.MethodsWe performed a systematic review and Bayesian network meta-analysis (NMA), registered on PROSPERO (CRD420251151177), to assess the efficacy and safety of pharmacological interventions for male osteoporosis. Randomized controlled trials (RCTs) evaluating alendronate, risedronate, zoledronic acid, denosumab, teriparatide, or abaloparatide were identified from PubMed, Web of Science, and the Cochrane Library through 2025. Primary outcomes included percent change in lumbar spine, femoral neck, and total hip BMD at 12 months. Safety outcomes were all adverse events (AEs) and serious adverse events (SAEs). Category-level meta-analyses were further conducted to compare pooled effects of antiresorptive versus anabolic agents.ResultsEighteen RCTs comprising 19–1199 participants each were included. At the drug level, abaloparatide and teriparatide ranked highest for lumbar spine BMD, while alendronate and abaloparatide demonstrated the most favorable effects for femoral neck and total hip BMD, respectively. Safety profiles were broadly similar, with teriparatide and alendronate showing relatively lower risks of AEs and SAEs. At the class level, anabolic therapies significantly outperformed antiresorptives in improving lumbar spine (MD 6.62, 95% CI 5.01–8.23 vs. 3.58, 95% CI 2.52–4.64) and total hip BMD (3.53, 95% CI 2.18–4.89 vs. 1.98, 95% CI –1.10–5.06), whereas antiresorptives showed modest advantages at the femoral neck (1.66, 95% CI 0.57–2.75 vs. 1.43, 95% CI –0.03–2.86). No significant differences were observed between classes in AEs or SAEs.ConclusionsThis study provides the first comprehensive drug- and class-level synthesis of treatments for male osteoporosis. Anabolic agents confer greater efficacy at the lumbar spine and total hip, while antiresorptives may offer modest benefits at the femoral neck. Safety outcomes were comparable across drug classes, suggesting that treatment choice should primarily be guided by efficacy considerations.Systematic Review Registrationhttps://www.crd.york.ac.uk/prospero/, identifier CRD420251151177.
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