# Association of metabolic dysfunction-associated steatotic liver disease with bone health in adults: a systematic review and meta-analysis of observational studies

## TL;DR

This study finds that metabolic dysfunction-associated steatotic liver disease is linked to higher femur bone density but also increased fracture risk and lower bone turnover markers in adults.

## Contribution

The study provides a meta-analysis showing a complex relationship between MASLD and bone health, highlighting potential underestimation of fracture risk.

## Key findings

- MASLD is associated with increased femur BMD, especially in women and overweight individuals.
- MASLD significantly increases the risk of osteoporosis and osteoporotic fractures.
- MASLD is linked to decreased bone turnover markers like CTX, OC, and P1NP.

## Abstract

Several studies have explored the effects of metabolic dysfunction-associated steatotic liver disease (MASLD) on bone mineral density (BMD) and bone turnover markers (BTMs) in adults and the risk of osteoporotic fractures. However, the extent of adverse effects of MASLD on bone health remains uncertain. This systematic review and meta-analysis aimed to investigate the effects of MASLD on bone health in adults.

We searched PubMed, Medline, EMBASE, Cochrane Library, and Scopus for observational studies published from inception to June 2025 that reported MASLD effects on bone health.

This meta-analysis indicated that MASLD was associated with increased femur BMD (WMD: 0.03 g/cm2, 95% CI: 0.02 to 0.03, P<0.001), especially in women (WMD: 0.02 g/cm2, 95% CI: 0.01 to 0.04, P = 0.002) and overweight people (WMD: 0.04 g/cm2, 95% CI: 0.01 to 0.06, P = 0.002). MASLD was also significantly associated with increased osteoporosis/osteoporotic fractures (OR: 1.23, 95% CI: 1.13-1.34; P<0.001) and decreased BTMs (CTX: WMD: -0.03 ng/mL, 95% CI: -0.05 to -0.02, P<0.001; OC: WMD: -1.86 ng/mL, 95% CI: -2.69 to -1.03, P<0.001; P1NP: WMD: -4.59 ng/mL, 95% CI: -5.64 to -3.54, P<0.001).

MASLD was significantly associated with increased femur BMD compared to non-MASLD patients, especially in women and overweight individuals. Interestingly, increased risk of OP/osteoporotic fractures and decreased BTMs were significantly associated with MASLD. This may suggest that BMD underestimates the risk of OP/osteoporotic fractures in MASLD patients.