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Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea

OBJECTIVES: The aim of this retrospective cohort study was to investigate whether non-alcoholic fatty liver disease (NAFLD) was associated with incident bone mineral density (BMD) decrease. METHODS: This study included 4536 subjects with normal BMD at baseline. NAFLD was defined as the presence of f...

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Autores principales: Sung, Jisun, Ryu, Seungho, Song, Yun-Mi, Cheong, Hae-Kwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Preventive Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569013/
https://www.ncbi.nlm.nih.gov/pubmed/33070506
http://dx.doi.org/10.3961/jpmph.20.089
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author Sung, Jisun
Ryu, Seungho
Song, Yun-Mi
Cheong, Hae-Kwan
author_facet Sung, Jisun
Ryu, Seungho
Song, Yun-Mi
Cheong, Hae-Kwan
author_sort Sung, Jisun
collection PubMed
description OBJECTIVES: The aim of this retrospective cohort study was to investigate whether non-alcoholic fatty liver disease (NAFLD) was associated with incident bone mineral density (BMD) decrease. METHODS: This study included 4536 subjects with normal BMD at baseline. NAFLD was defined as the presence of fatty liver on abdominal ultrasonography without significant alcohol consumption or other causes. Decreased BMD was defined as a diagnosis of osteopenia, osteoporosis, or BMD below the expected range for the patient’s age based on dual-energy X-ray absorptiometry. Cox proportional hazards models were used to estimate the hazard ratio of incident BMD decrease in subjects with or without NAFLD. Subgroup analyses were conducted according to the relevant factors. RESULTS: Across 13 354 person-years of total follow-up, decreased BMD was observed in 606 subjects, corresponding to an incidence of 45.4 cases per 1000 person-years (median follow-up duration, 2.1 years). In the model adjusted for age and sex, the hazard ratio was 0.65 (95% confidence interval, 0.51 to 0.82), and statistical significance disappeared after adjustment for body mass index (BMI) and cardiometabolic factors. In the subgroup analyses, NAFLD was associated with a lower risk of incident BMD decrease in females even after adjustment for confounders. The direction of the effect of NAFLD on the risk of BMD decrease changed depending on BMI category and body fat percentage, although the impact was statistically insignificant. CONCLUSIONS: NAFLD had a significant protective effect on BMD in females. However, the effects may vary depending on BMI category or body fat percentage.
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spelling pubmed-75690132020-10-23 Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea Sung, Jisun Ryu, Seungho Song, Yun-Mi Cheong, Hae-Kwan J Prev Med Public Health Original Article OBJECTIVES: The aim of this retrospective cohort study was to investigate whether non-alcoholic fatty liver disease (NAFLD) was associated with incident bone mineral density (BMD) decrease. METHODS: This study included 4536 subjects with normal BMD at baseline. NAFLD was defined as the presence of fatty liver on abdominal ultrasonography without significant alcohol consumption or other causes. Decreased BMD was defined as a diagnosis of osteopenia, osteoporosis, or BMD below the expected range for the patient’s age based on dual-energy X-ray absorptiometry. Cox proportional hazards models were used to estimate the hazard ratio of incident BMD decrease in subjects with or without NAFLD. Subgroup analyses were conducted according to the relevant factors. RESULTS: Across 13 354 person-years of total follow-up, decreased BMD was observed in 606 subjects, corresponding to an incidence of 45.4 cases per 1000 person-years (median follow-up duration, 2.1 years). In the model adjusted for age and sex, the hazard ratio was 0.65 (95% confidence interval, 0.51 to 0.82), and statistical significance disappeared after adjustment for body mass index (BMI) and cardiometabolic factors. In the subgroup analyses, NAFLD was associated with a lower risk of incident BMD decrease in females even after adjustment for confounders. The direction of the effect of NAFLD on the risk of BMD decrease changed depending on BMI category and body fat percentage, although the impact was statistically insignificant. CONCLUSIONS: NAFLD had a significant protective effect on BMD in females. However, the effects may vary depending on BMI category or body fat percentage. Korean Society for Preventive Medicine 2020-09 2020-07-17 /pmc/articles/PMC7569013/ /pubmed/33070506 http://dx.doi.org/10.3961/jpmph.20.089 Text en Copyright © 2020 The Korean Society for Preventive Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sung, Jisun
Ryu, Seungho
Song, Yun-Mi
Cheong, Hae-Kwan
Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea
title Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea
title_full Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea
title_fullStr Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea
title_full_unstemmed Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea
title_short Relationship Between Non-alcoholic Fatty Liver Disease and Decreased Bone Mineral Density: A Retrospective Cohort Study in Korea
title_sort relationship between non-alcoholic fatty liver disease and decreased bone mineral density: a retrospective cohort study in korea
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569013/
https://www.ncbi.nlm.nih.gov/pubmed/33070506
http://dx.doi.org/10.3961/jpmph.20.089
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