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Osteoporos Int ; 30(6): 1195-1204, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30788527

ABSTRACT

Liver cirrhosis leads to bone loss. To date, information on bone quality (three-dimensional microarchitecture) and, thus, bone strength is scarce. We observed decreased bone quality at both assessed sites, independent of disease severity. Therefore, all patients should undergo early-stage screening for osteoporosis. INTRODUCTION: Recent studies found low bone mineral density in cirrhosis, but data on bone microstructure are scarce. This study assessed weight-bearing and non-weight-bearing bones in patients with cirrhosis and healthy controls. The primary objective was to evaluate trabecular and cortical microarchitecture. METHODS: This was a single-center study in patients with recently diagnosed hepatic cirrhosis. Thirty-two patients and 32 controls participated in this study. After determining the type of cirrhosis, the parameters of bone microarchitecture were assessed by high-resolution peripheral quantitative computed tomography. RESULTS: Both cortical and trabecular microarchitectures showed significant alterations. At the radius, trabecular bone volume fraction was 17% lower (corrected p = 0.028), and, at the tibia, differences were slightly more pronounced. Trabecular bone volume fraction was 19% lower (p = 0.024), cortical bone mineral density 7% (p = 0.007), and cortical thickness 28% (p = 0.001), while cortical porosity was 32% higher (p = 0.023), compared to controls. Areal bone mineral density was lower (lumbar spine - 13%, total hip - 11%, total body - 9%, radius - 17%, and calcaneus - 26%). There was no correlation between disease severity and microarchitecture. Areal bone mineral density (aBMD) measured by dual-energy X-ray absorptiometry (DXA) correlated well with parameters of cortical and trabecular microarchitecture. CONCLUSIONS: Hepatic cirrhosis deteriorates both trabecular and cortical microarchitecture, regardless of disease severity. Areal bone mineral density is diminished at all sites as a sign of generalized affection. In patients with hepatic cirrhosis, regardless of its origin or disease severity, aBMD measurements are an appropriate tool for osteologic screening.


Subject(s)
Bone Remodeling/physiology , Liver Cirrhosis/pathology , Liver Cirrhosis/physiopathology , Radius/pathology , Tibia/pathology , Aged , Biomarkers/blood , Bone Density , Cancellous Bone/diagnostic imaging , Cancellous Bone/pathology , Case-Control Studies , Cortical Bone/diagnostic imaging , Cortical Bone/pathology , Female , Humans , Liver Cirrhosis/diagnostic imaging , Liver Cirrhosis, Alcoholic/diagnostic imaging , Liver Cirrhosis, Alcoholic/pathology , Liver Cirrhosis, Alcoholic/physiopathology , Male , Middle Aged , Porosity , Radius/diagnostic imaging , Tibia/diagnostic imaging , Tomography, X-Ray Computed/methods , Weight-Bearing/physiology
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