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The Association of Nonalcoholic Fatty Liver Disease with Bone Mineral Density in Type 2 Diabetes

Overview
Journal Eur J Med Res
Publisher Biomed Central
Specialty General Medicine
Date 2022 Aug 7
PMID 35934712
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Abstract

Objective: We examined the association between nonalcoholic fatty liver disease and lumbar spine bone mineral density in individuals with and without type 2 diabetes.

Methods: The lumbar BMD of 1088 subjects was measured using dual-energy X-ray absorptiometry (DXA). Liver fat content was quantified via B-mode ultrasound. Multivariable linear regression was used to study the association between NAFLD and lumbar BMD in participants with and without T2DM.

Results: The lumbar BMD in the T2DM group and the non-diabetes group was higher in the NAFLD group than in the non-NAFLD group (P < 0.001). Multivariate regression analysis in the T2DM group showed that after adjusting for confounders, the positive association between lumbar spine BMD and NAFLD remained (P = 0.027). In the non-diabetes group, after adjusting for confounders, the association between NAFLD and lumbar spine BMD disappeared.

Conclusions: The relationship between nonalcoholic fatty liver disease and lumbar bone mineral density may differ in individuals with and without diabetes. The effect of nonalcoholic fatty liver disease on bone mineral density needs to be evaluated in different clinical contexts.

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References
1.
Campos R, de Piano A, da Silva P, Carnier J, Sanches P, Corgosinho F . The role of pro/anti-inflammatory adipokines on bone metabolism in NAFLD obese adolescents: effects of long-term interdisciplinary therapy. Endocrine. 2012; 42(1):146-56. DOI: 10.1007/s12020-012-9613-3. View

2.
Haukeland J, Dahl T, Yndestad A, Gladhaug I, Loberg E, Haaland T . Fetuin A in nonalcoholic fatty liver disease: in vivo and in vitro studies. Eur J Endocrinol. 2011; 166(3):503-10. DOI: 10.1530/EJE-11-0864. View

3.
Lebeaupin C, Vallee D, Hazari Y, Hetz C, Chevet E, Bailly-Maitre B . Endoplasmic reticulum stress signalling and the pathogenesis of non-alcoholic fatty liver disease. J Hepatol. 2018; 69(4):927-947. DOI: 10.1016/j.jhep.2018.06.008. View

4.
Cui Z, Xuan R, Yang Y . Serum fetuin A level is associated with nonalcoholic fatty liver disease in Chinese population. Oncotarget. 2018; 8(63):107149-107156. PMC: 5739803. DOI: 10.18632/oncotarget.22361. View

5.
Sato M, Kamada Y, Takeda Y, Kida S, Ohara Y, Fujii H . Fetuin-A negatively correlates with liver and vascular fibrosis in nonalcoholic fatty liver disease subjects. Liver Int. 2015; 35(3):925-35. DOI: 10.1111/liv.12478. View