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Prevalence of Osteoporosis in Cirrhosis: A Systematic Review and Meta-Analysis
Open accessAbstract
The prevalence of osteoporosis in individuals with cirrhosis varies based on the diagnostic approach and etiology of the underlying liver disease. This systematic review aims to evaluate the prevalence of osteoporosis in individuals with cirrhosis. Electronic databases were searched for studies reporting the prevalence of osteoporosis among patients with cirrhosis. The primary outcome was the presence of osteoporosis, as determined by a dual-energy x-ray absorptiometry (DEXA) scan. Secondary outcomes were levels of biochemical markers of bone metabolism, including calcium, vitamin D, phosphorus, and parathormone (PTH) levels. A cohort of 836 patients from 10 studies was included in the final analysis. The pooled rate of osteoporosis was 14.80% (95% CI: 14.19-15.49). Pooled levels of biochemical markers of bone metabolism were as follows: calcium 9.09 mg/dL (95% CI: 8.73-9.45), 25-hydroxyvitamin D (25-OH vitamin D) 15.41 ng/mL (95% CI: 14.79-16.03), phosphorus 15.41 mg/dL (95% CI: 2.99-3.51), and PTH 26.58 pg/mL (95% CI: 25.45-27.71). Pooled levels of liver biochemistries were: bilirubin 3.04 mg/dL (95% CI: 2.84-3.25), aspartate aminotransferase (AST) 65.35 U/L (95% CI: 61.39-69.31), alanine aminotransferase (ALT) 50.17 U/L (95% CI: 46.18-54.10), alkaline phosphatase 133.31 U/L (95% CI: 124.89-141.73), and albumin 3.25 g/dL (95% CI: 3.05-3.45). Cirrhosis appears to be associated with an increased risk for osteoporosis, with a pooled prevalence of 15%. This can include men and individuals younger than 50 years of age, a cohort not typically considered to be at an increased risk of osteoporosis. Levels of 25-hydroxyvitamin D and insulin-like growth factor-1 (IGF-1) were also significantly low. Further studies are required to evaluate the risk of osteoporosis based on the etiology and stage of cirrhosis, especially in younger males, to incorporate this into future prediction models for fragility fractures.
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![Figure 2 Forest plot showing the individual study rates of osteoporosis in relation to the pooled rate. Source: [15-22]. Note: This image is the author's own creation.](/paper-figures/f716b453832b433ca0f2fe33e542675c/prevalence-of-osteoporosis-in-cirrhosis-a-systematic-review-and-meta-analysis-figure-2.jpg)
![Figure 3 Forest plot showing the individual study proportions of calcium (mg/dL) in relation to the pooled level. Source: [15,17,18,20,22-24]. Note: This image is the author's own creation.](/paper-figures/17e6ed0198c141c9bda75a5c889e1156/prevalence-of-osteoporosis-in-cirrhosis-a-systematic-review-and-meta-analysis-figure-3.jpg)

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“hepatocyte-derived RANKL, up-regulated under inflammatory conditions, represents a direct liver-to-bone endocrine signal that promotes osteoclast-mediated resorption [93,94]”
From Interorgan Communications in Skeletal Pathophysiology: From Molecular Pathways to Multidisciplinary Therapies (2026) · cites this paper as [93]
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Guidelines on the management of osteoporosis associated with chronic liver disease
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Cited by
Gan, D., Qin, L., & Xiao, G. (2026) · Research · doi:10.34133/research.1319 · Cited by 1
Metadata
- Authors
- Kang, J., Gopakumar, H., & Puli, S. R.
- Affiliations
- Peoria campus of the University of Illinois System (US)
- Corresponding author
- Gopakumar, Harishankar
- Venue
- Cureus
- Published
- 2023-01-12
- Volume
- 15
- Issue
- 1
- Pages
- e33721-e33721
- ISSN
- 2168-8184 (ISSN-L)
- PMC
- PMC9922208
- OpenAlex
- W4315767602
- Cited by
- 12
- References
- 4
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 1 · 2023: 5
- FWCI
- 0.52
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by
- Locations
- Cureus (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Keywords
- osteoporosis, liver cirrhosis, prevalence, bone metabolism, vitamin D, parathyroid hormone, calcium, phosphorus, liver function tests, alkaline phosphatase, aspartate aminotransferase, albumin, bone mineral density, dual-energy X-ray absorptiometry, liver disease etiology, sex differences, age differences, comorbidities
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