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