Association Between Nonalcoholic Fatty Liver Disease and Reduced Bone Mineral Density in Children: A Meta-Analysis
- PMID: 30706504
- DOI: 10.1002/hep.30538
Association Between Nonalcoholic Fatty Liver Disease and Reduced Bone Mineral Density in Children: A Meta-Analysis
Abstract
Recent cross-sectional studies have examined the association between nonalcoholic fatty liver disease (NAFLD) and bone mineral density (BMD) in children or adolescents, but these have produced conflicting results. We performed a systematic review and meta-analysis of these published studies to quantify the magnitude of the association, if any, between NAFLD and BMD. We searched publication databases from January 2000 to September 2018, using predefined keywords to identify relevant observational studies conducted in children or adolescents in whom NAFLD was diagnosed either by imaging or by histology and BMD Z score was measured by dual-energy X-ray absorptiometry. Data from selected studies were extracted, and a meta-analysis was performed using random-effects modeling. A total of eight observational cross-sectional or case-control studies enrolling 632 children and adolescents (mean age 12.8 years), 357 of whom had NAFLD, were included in the final analysis. Meta-analysis showed significant differences in whole-body or lumbar BMD Z scores between children/adolescents with and without NAFLD (n = 6 studies; pooled weighted mean difference [WMD], -0.48; 95% confidence interval [CI], -0.74 to -0.21; I2 = 55.5%), as well as between those with biopsy-confirmed nonalcoholic steatohepatitis (NASH) and those with no-NASH (n = 4 studies; pooled WMD, -0.27; 95% CI, -0.40 to -0.13; I2 = 0%). The aforementioned WMDs in BMD Z scores were independent of common clinical risk factors, such as age, sex, race/ethnicity, and body mass index. Sensitivity analyses did not modify these findings. Funnel plot and Egger test did not reveal significant publication bias. Conclusion: This meta-analysis shows that the presence and severity of NAFLD are significantly associated with reduced whole-body BMD Z scores in children and adolescents; however, the observational design of the studies included does not allow for proving causality.
© 2019 by the American Association for the Study of Liver Diseases.
Comment in
-
Letter to the Editor: Bone Health in Nonalcoholic Fatty Liver Disease: A Mechanistic Insight.Hepatology. 2019 Nov;70(5):1872. doi: 10.1002/hep.30776. Hepatology. 2019. PMID: 31099070 No abstract available.
Similar articles
-
Systematic review with meta-analysis: non-alcoholic fatty liver disease is associated with a history of osteoporotic fractures but not with low bone mineral density.Aliment Pharmacol Ther. 2019 Feb;49(4):375-388. doi: 10.1111/apt.15087. Epub 2019 Jan 1. Aliment Pharmacol Ther. 2019. PMID: 30600540
-
Adipokines and C-reactive protein in relation to bone mineralization in pediatric nonalcoholic fatty liver disease.World J Gastroenterol. 2013 Jul 7;19(25):4007-14. doi: 10.3748/wjg.v19.i25.4007. World J Gastroenterol. 2013. PMID: 23840146 Free PMC article.
-
Association Between Primary Hypothyroidism and Nonalcoholic Fatty Liver Disease: A Systematic Review and Meta-Analysis.Thyroid. 2018 Oct;28(10):1270-1284. doi: 10.1089/thy.2018.0257. Epub 2018 Aug 30. Thyroid. 2018. PMID: 30084737
-
Association between nonalcoholic fatty liver disease and colorectal tumours in asymptomatic adults undergoing screening colonoscopy: a systematic review and meta-analysis.Metabolism. 2018 Oct;87:1-12. doi: 10.1016/j.metabol.2018.06.004. Epub 2018 Jun 20. Metabolism. 2018. PMID: 29935236
-
Histologic Severity of Nonalcoholic Fatty Liver Disease Associates with Reduced Bone Mineral Density in Children.Dig Dis Sci. 2023 Feb;68(2):644-655. doi: 10.1007/s10620-022-07563-z. Epub 2022 Jun 7. Dig Dis Sci. 2023. PMID: 35672623 Free PMC article.
Cited by
-
Low bone mineral density is associated with fatty liver disease and respiratory illness in a pediatric mortality sample.Osteoporos Int. 2023 Jul;34(7):1231-1239. doi: 10.1007/s00198-023-06760-4. Epub 2023 Apr 21. Osteoporos Int. 2023. PMID: 37083968
-
Association between fatty liver index and controlled attenuation parameters as markers of metabolic dysfunction-associated fatty liver disease and bone mineral density: observational and two-sample Mendelian randomization studies.Osteoporos Int. 2024 Apr;35(4):679-689. doi: 10.1007/s00198-023-06996-0. Epub 2024 Jan 15. Osteoporos Int. 2024. PMID: 38221591
-
Non-alcoholic fatty liver disease is associated with decreased bone mineral density in upper Egyptian patients.Sci Rep. 2023 Mar 16;13(1):4353. doi: 10.1038/s41598-023-31256-w. Sci Rep. 2023. PMID: 36928441 Free PMC article.
-
Increased risk of non-alcoholic fatty liver disease fibrosis is closely associated with osteoporosis in women but not in men with type 2 diabetes.Endocr Connect. 2022 Oct 12;11(11):e220174. doi: 10.1530/EC-22-0174. Print 2022 Nov 1. Endocr Connect. 2022. PMID: 36129166 Free PMC article.
-
A Review of the Increasing Prevalence of Metabolic-Associated Fatty Liver Disease (MAFLD) in Children and Adolescents Worldwide and in Mexico and the Implications for Public Health.Med Sci Monit. 2021 Aug 30;27:e934134. doi: 10.12659/MSM.934134. Med Sci Monit. 2021. PMID: 34456329 Free PMC article. Review.
References
-
- Fleet SE, Lefkowitch JH, Lavine JE. Current concepts in pediatric nonalcoholic fatty liver disease. Gastroenterol Clin North Am 2017;46:217-231.
-
- Mann JP, Valenti L, Scorletti E, Byrne CD, Nobili V. Nonalcoholic fatty liver disease in children. Semin Liver Dis 2018;38:1-13.
-
- Selvakumar PKC, Kabbany MN, Nobili V, Alkhouri N. Nonalcoholic fatty liver disease in children: hepatic and extrahepatic complications. Pediatr Clin North Am 2017;64:659-675.
-
- Byrne CD, Targher G. NAFLD: a multisystem disease. J Hepatol 2015;62(Suppl. 1):S47-S64.
-
- Younossi Z, Anstee QM, Marietti M, Hardy T, Henry L, Eslam M, et al. Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention. Nat Rev Gastroenterol Hepatol 2018;15:11-20.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical