Cargando…

The Factors Affecting Bone Density in Cirrhosis

BACKGROUND: Bone loss is common in cirrhosis. However, the prevalence of osteopenia and osteoporosis has been heterogeneous in different reports. Reduction in bone formation with or without increase in bone resorption appears to be responsible for bone loss in these patients. OBJECTIVES: We aimed to...

Descripción completa

Detalles Bibliográficos
Autores principales: Hajiabbasi, Asghar, Shafaghi, Afshin, Fayazi, Haniyeh Sadat, Shenavar Masooleh, Irandokht, Hedayati Emami, Mohammad Hassan, Ghavidel Parsa, Pooneh, Amir Maafi, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428083/
https://www.ncbi.nlm.nih.gov/pubmed/25977695
http://dx.doi.org/10.5812/hepatmon.15(4)2015.26871
_version_ 1782370834823774208
author Hajiabbasi, Asghar
Shafaghi, Afshin
Fayazi, Haniyeh Sadat
Shenavar Masooleh, Irandokht
Hedayati Emami, Mohammad Hassan
Ghavidel Parsa, Pooneh
Amir Maafi, Alireza
author_facet Hajiabbasi, Asghar
Shafaghi, Afshin
Fayazi, Haniyeh Sadat
Shenavar Masooleh, Irandokht
Hedayati Emami, Mohammad Hassan
Ghavidel Parsa, Pooneh
Amir Maafi, Alireza
author_sort Hajiabbasi, Asghar
collection PubMed
description BACKGROUND: Bone loss is common in cirrhosis. However, the prevalence of osteopenia and osteoporosis has been heterogeneous in different reports. Reduction in bone formation with or without increase in bone resorption appears to be responsible for bone loss in these patients. OBJECTIVES: We aimed to investigate bone loss in patients with cirrhosis at different anatomical sites and key factors that might affect it. PATIENTS AND METHODS: In this cross-sectional study, 97 patients with cirrhosis who were referred to Razi Hospital, Rasht, Iran, from 2008 to 2010, were studied. Cirrhosis was diagnosed using biopsy and/or clinical and paraclinical findings. Bone mineral densitometry was done in L2 through L4 lumbar spine (LS) and femoral neck (FN), using dual-energy X-ray absorptiometry (DEXA) (QDR 1000, Hologic DEXA Inc, Waltham, Massachusetts, the United States). Statistical analysis was performed using SPSS 18. A P value < 0.05 was considered statistically significant. RESULTS: A total of 97 patients with cirrhosis (55.7% male) and the mean age of 51 ± 13 years and median body mass index (BMI) of 22.7 kg/m(2) were recruited over a two-year period. Etiologies of cirrhosis were hepatitis C (40.2%), hepatitis B (26.8%), cryptogenic (21.6%), and other causes (11.4%). Child A, B, and C, were seen in 16.5%, 47.4%, and 36.1% of patients, respectively. The DEXA results were abnormal in 78.4% of our participants (osteopenia, 45.4%; osteoporosis, 33%). BMI and calculated glomerular filtration rate (GFRc) had moderate positive and Child score had moderate negative significant correlation with T score in both anatomical sites. There was no significant association between abnormal DEXA and the causes of cirrhosis. The univariate analysis showed that the risk of abnormal results in DEXA was significantly higher in those with low BMI, current smoking, higher Child score, and low GFRc; however, in multivariate analysis, the abnormal results were more frequent in those with lower vitamin D, higher Child score, and less GFRc. CONCLUSIONS: Abnormal DEXA was highly prevalent among patients with cirrhosis. The risk of this finding was increased by lower vitamin D levels, advanced disease, and impaired renal function.
format Online
Article
Text
id pubmed-4428083
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Kowsar
record_format MEDLINE/PubMed
spelling pubmed-44280832015-05-14 The Factors Affecting Bone Density in Cirrhosis Hajiabbasi, Asghar Shafaghi, Afshin Fayazi, Haniyeh Sadat Shenavar Masooleh, Irandokht Hedayati Emami, Mohammad Hassan Ghavidel Parsa, Pooneh Amir Maafi, Alireza Hepat Mon Research Article BACKGROUND: Bone loss is common in cirrhosis. However, the prevalence of osteopenia and osteoporosis has been heterogeneous in different reports. Reduction in bone formation with or without increase in bone resorption appears to be responsible for bone loss in these patients. OBJECTIVES: We aimed to investigate bone loss in patients with cirrhosis at different anatomical sites and key factors that might affect it. PATIENTS AND METHODS: In this cross-sectional study, 97 patients with cirrhosis who were referred to Razi Hospital, Rasht, Iran, from 2008 to 2010, were studied. Cirrhosis was diagnosed using biopsy and/or clinical and paraclinical findings. Bone mineral densitometry was done in L2 through L4 lumbar spine (LS) and femoral neck (FN), using dual-energy X-ray absorptiometry (DEXA) (QDR 1000, Hologic DEXA Inc, Waltham, Massachusetts, the United States). Statistical analysis was performed using SPSS 18. A P value < 0.05 was considered statistically significant. RESULTS: A total of 97 patients with cirrhosis (55.7% male) and the mean age of 51 ± 13 years and median body mass index (BMI) of 22.7 kg/m(2) were recruited over a two-year period. Etiologies of cirrhosis were hepatitis C (40.2%), hepatitis B (26.8%), cryptogenic (21.6%), and other causes (11.4%). Child A, B, and C, were seen in 16.5%, 47.4%, and 36.1% of patients, respectively. The DEXA results were abnormal in 78.4% of our participants (osteopenia, 45.4%; osteoporosis, 33%). BMI and calculated glomerular filtration rate (GFRc) had moderate positive and Child score had moderate negative significant correlation with T score in both anatomical sites. There was no significant association between abnormal DEXA and the causes of cirrhosis. The univariate analysis showed that the risk of abnormal results in DEXA was significantly higher in those with low BMI, current smoking, higher Child score, and low GFRc; however, in multivariate analysis, the abnormal results were more frequent in those with lower vitamin D, higher Child score, and less GFRc. CONCLUSIONS: Abnormal DEXA was highly prevalent among patients with cirrhosis. The risk of this finding was increased by lower vitamin D levels, advanced disease, and impaired renal function. Kowsar 2015-04-25 /pmc/articles/PMC4428083/ /pubmed/25977695 http://dx.doi.org/10.5812/hepatmon.15(4)2015.26871 Text en Copyright © 2015, Kowsar Corp. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Research Article
Hajiabbasi, Asghar
Shafaghi, Afshin
Fayazi, Haniyeh Sadat
Shenavar Masooleh, Irandokht
Hedayati Emami, Mohammad Hassan
Ghavidel Parsa, Pooneh
Amir Maafi, Alireza
The Factors Affecting Bone Density in Cirrhosis
title The Factors Affecting Bone Density in Cirrhosis
title_full The Factors Affecting Bone Density in Cirrhosis
title_fullStr The Factors Affecting Bone Density in Cirrhosis
title_full_unstemmed The Factors Affecting Bone Density in Cirrhosis
title_short The Factors Affecting Bone Density in Cirrhosis
title_sort factors affecting bone density in cirrhosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428083/
https://www.ncbi.nlm.nih.gov/pubmed/25977695
http://dx.doi.org/10.5812/hepatmon.15(4)2015.26871
work_keys_str_mv AT hajiabbasiasghar thefactorsaffectingbonedensityincirrhosis
AT shafaghiafshin thefactorsaffectingbonedensityincirrhosis
AT fayazihaniyehsadat thefactorsaffectingbonedensityincirrhosis
AT shenavarmasoolehirandokht thefactorsaffectingbonedensityincirrhosis
AT hedayatiemamimohammadhassan thefactorsaffectingbonedensityincirrhosis
AT ghavidelparsapooneh thefactorsaffectingbonedensityincirrhosis
AT amirmaafialireza thefactorsaffectingbonedensityincirrhosis
AT hajiabbasiasghar factorsaffectingbonedensityincirrhosis
AT shafaghiafshin factorsaffectingbonedensityincirrhosis
AT fayazihaniyehsadat factorsaffectingbonedensityincirrhosis
AT shenavarmasoolehirandokht factorsaffectingbonedensityincirrhosis
AT hedayatiemamimohammadhassan factorsaffectingbonedensityincirrhosis
AT ghavidelparsapooneh factorsaffectingbonedensityincirrhosis
AT amirmaafialireza factorsaffectingbonedensityincirrhosis