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<i>Summary</i> <p>Metformin is widely used for diabetes, but its effects on bone health are uncertain. This meta-analysis study found that it reduces markers of both bone loss and bone formation. It is still unclear whether this benefits or harms bones long term, highlighting the need for larger, longer clinical studies.</p> Purpose <p>Metformin is a widely used antidiabetic drug that has shown potential effects on bone metabolism. However, its impact on bone turnover markers remains unclear. This systematic review and meta-analysis aimed to assess this effect.</p> Methods <p>A comprehensive search was conducted across PubMed, Scopus, Embase, Web of Science, and Cochrane Library databases, identifying clinical trials published up to February 04, 2026, that evaluated the effects of metformin on validated bone turnover markers. The quality and risk of bias were assessed using the Modified Jadad Scale, and Cochrane Collaboration’s risk of bias tool, respectively. A random-effects meta-analysis was performed to estimate the standardized mean difference (SMD) with a 95% confidence interval.</p> Results <p>Fourteen studies met the inclusion criteria, involving diabetic and non-diabetic populations. Metformin significantly reduced both bone resorption, bone formation markers (SMD: −1.28 [95% CI: −2.03, −0.52], <i>I</i><sup>2</sup> = 99.33%), and (−0.18 [−0.28, −0.08], <i>I</i><sup>2</sup> = 67.78%), respectively. These findings suggest a pattern consistent with reduced bone turnover rather than selective modulation of either bone resorption or bone formation. However, substantial statistical heterogeneity was observed across studies, especially for bone resorption markers, limiting the precision and generalizability of pooled estimates.</p> Conclusion <p>Metformin appears to lower overall bone turnover, reducing both bone resorption and bone formation markers. However, given the high heterogeneity across studies and the reliance on surrogate biochemical endpoints rather than fracture or bone mineral density outcomes, the clinical significance of these findings remains uncertain. Larger, long-term trials are needed to determine whether metformin provides real benefits or risks for osteoporosis.</p>

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Impact of metformin on bone turnover markers: a systematic review and meta-analysis of clinical trials

  • 期刊论文

  • 发表日期：

    2026年5月7日

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  • Mohammadreza Heidari,
  • Niloofar Mirdamadi,
  • Pouria Khashayar,
  • Ozra Tabatabaei-Malazy,
  • Marzieh Golabchi,
  • Patricia khashayar

摘要

Summary

Metformin is widely used for diabetes, but its effects on bone health are uncertain. This meta-analysis study found that it reduces markers of both bone loss and bone formation. It is still unclear whether this benefits or harms bones long term, highlighting the need for larger, longer clinical studies.

Purpose

Metformin is a widely used antidiabetic drug that has shown potential effects on bone metabolism. However, its impact on bone turnover markers remains unclear. This systematic review and meta-analysis aimed to assess this effect.

Methods

A comprehensive search was conducted across PubMed, Scopus, Embase, Web of Science, and Cochrane Library databases, identifying clinical trials published up to February 04, 2026, that evaluated the effects of metformin on validated bone turnover markers. The quality and risk of bias were assessed using the Modified Jadad Scale, and Cochrane Collaboration’s risk of bias tool, respectively. A random-effects meta-analysis was performed to estimate the standardized mean difference (SMD) with a 95% confidence interval.

Results

Fourteen studies met the inclusion criteria, involving diabetic and non-diabetic populations. Metformin significantly reduced both bone resorption, bone formation markers (SMD: −1.28 [95% CI: −2.03, −0.52], I2 = 99.33%), and (−0.18 [−0.28, −0.08], I2 = 67.78%), respectively. These findings suggest a pattern consistent with reduced bone turnover rather than selective modulation of either bone resorption or bone formation. However, substantial statistical heterogeneity was observed across studies, especially for bone resorption markers, limiting the precision and generalizability of pooled estimates.

Conclusion

Metformin appears to lower overall bone turnover, reducing both bone resorption and bone formation markers. However, given the high heterogeneity across studies and the reliance on surrogate biochemical endpoints rather than fracture or bone mineral density outcomes, the clinical significance of these findings remains uncertain. Larger, long-term trials are needed to determine whether metformin provides real benefits or risks for osteoporosis.