Disease duration and stage influence bone microstructure in patients with primary biliary cholangitis

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Disease duration and stage influence bone microstructure in patients with primary biliary cholangitis. / Schmidt, Tobias; Schmidt, Constantin; Schmidt, Felix N; Butscheidt, Sebastian; Mussawy, Haider; Hubert, Jan; Hawellek, Thelonius; Oehler, Nicola; Barvencik, Florian; Lohse, Ansgar W; Schinke, Thorsten; Schramm, Christoph; Amling, Michael; Rolvien, Tim.

in: J BONE MINER RES, Jahrgang 33, Nr. 6, 06.2018, S. 1011-1019.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{1a99e3f02ea445cfae746ff804436485,
title = "Disease duration and stage influence bone microstructure in patients with primary biliary cholangitis",
abstract = "Primary biliary cholangitis (PBC) is known to be a major risk factor for osteoporosis reflected by a reduction of bone mineral density (BMD). However, both the extent of the macro- and microstructural alterations of bone as well as the causative factors are unknown. We have retrospectively analyzed a total of 96 patients with PBC and 53 healthy controls matched for age, sex and body mass index. In addition to dual-energy X-ray absorptiometry (DXA) measurements at the lumbar spine and hip, high-resolution peripheral quantitative computed tomography (HR-pQCT) was used to assess the geometric, volumetric and microstructural changes of bone at the distal radius and tibia. Furthermore, serum analyses and measures of disease duration and stage including transient elastography were performed. Total, cortical and trabecular volumetric BMD as well as geometric parameters were significantly reduced in PBC patients. Microstructural analysis revealed a significantly lower cortical thickness (p < 0.001) and bone volume per tissue volume (p < 0.001) in the radius and tibia but unchanged trabecular number in patients with PBC (radius: p = 0.42; tibia: p = 0.12). Multivariate regression models pointed out that disease duration and stage are the primary factors that are independently associated with bone loss in PBC. A subgroup analysis of patients with additional autoimmune hepatitis (AIH) revealed no significant changes in bone structure compared to PBC only. Taken together, PBC patients demonstrate severe alterations in bone microstructure that are positively associated with disease duration and stage. By applying high-resolution peripheral quantitative computed tomography in the distal radius and tibia, a combined bone loss syndrome expressed by a predominant decrease in BMD and cortical thickness could be detected. This article is protected by copyright. All rights reserved.",
keywords = "Journal Article",
author = "Tobias Schmidt and Constantin Schmidt and Schmidt, {Felix N} and Sebastian Butscheidt and Haider Mussawy and Jan Hubert and Thelonius Hawellek and Nicola Oehler and Florian Barvencik and Lohse, {Ansgar W} and Thorsten Schinke and Christoph Schramm and Michael Amling and Tim Rolvien",
note = "This article is protected by copyright. All rights reserved.",
year = "2018",
month = jun,
doi = "10.1002/jbmr.3410",
language = "English",
volume = "33",
pages = "1011--1019",
journal = "J BONE MINER RES",
issn = "0884-0431",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Disease duration and stage influence bone microstructure in patients with primary biliary cholangitis

AU - Schmidt, Tobias

AU - Schmidt, Constantin

AU - Schmidt, Felix N

AU - Butscheidt, Sebastian

AU - Mussawy, Haider

AU - Hubert, Jan

AU - Hawellek, Thelonius

AU - Oehler, Nicola

AU - Barvencik, Florian

AU - Lohse, Ansgar W

AU - Schinke, Thorsten

AU - Schramm, Christoph

AU - Amling, Michael

AU - Rolvien, Tim

N1 - This article is protected by copyright. All rights reserved.

PY - 2018/6

Y1 - 2018/6

N2 - Primary biliary cholangitis (PBC) is known to be a major risk factor for osteoporosis reflected by a reduction of bone mineral density (BMD). However, both the extent of the macro- and microstructural alterations of bone as well as the causative factors are unknown. We have retrospectively analyzed a total of 96 patients with PBC and 53 healthy controls matched for age, sex and body mass index. In addition to dual-energy X-ray absorptiometry (DXA) measurements at the lumbar spine and hip, high-resolution peripheral quantitative computed tomography (HR-pQCT) was used to assess the geometric, volumetric and microstructural changes of bone at the distal radius and tibia. Furthermore, serum analyses and measures of disease duration and stage including transient elastography were performed. Total, cortical and trabecular volumetric BMD as well as geometric parameters were significantly reduced in PBC patients. Microstructural analysis revealed a significantly lower cortical thickness (p < 0.001) and bone volume per tissue volume (p < 0.001) in the radius and tibia but unchanged trabecular number in patients with PBC (radius: p = 0.42; tibia: p = 0.12). Multivariate regression models pointed out that disease duration and stage are the primary factors that are independently associated with bone loss in PBC. A subgroup analysis of patients with additional autoimmune hepatitis (AIH) revealed no significant changes in bone structure compared to PBC only. Taken together, PBC patients demonstrate severe alterations in bone microstructure that are positively associated with disease duration and stage. By applying high-resolution peripheral quantitative computed tomography in the distal radius and tibia, a combined bone loss syndrome expressed by a predominant decrease in BMD and cortical thickness could be detected. This article is protected by copyright. All rights reserved.

AB - Primary biliary cholangitis (PBC) is known to be a major risk factor for osteoporosis reflected by a reduction of bone mineral density (BMD). However, both the extent of the macro- and microstructural alterations of bone as well as the causative factors are unknown. We have retrospectively analyzed a total of 96 patients with PBC and 53 healthy controls matched for age, sex and body mass index. In addition to dual-energy X-ray absorptiometry (DXA) measurements at the lumbar spine and hip, high-resolution peripheral quantitative computed tomography (HR-pQCT) was used to assess the geometric, volumetric and microstructural changes of bone at the distal radius and tibia. Furthermore, serum analyses and measures of disease duration and stage including transient elastography were performed. Total, cortical and trabecular volumetric BMD as well as geometric parameters were significantly reduced in PBC patients. Microstructural analysis revealed a significantly lower cortical thickness (p < 0.001) and bone volume per tissue volume (p < 0.001) in the radius and tibia but unchanged trabecular number in patients with PBC (radius: p = 0.42; tibia: p = 0.12). Multivariate regression models pointed out that disease duration and stage are the primary factors that are independently associated with bone loss in PBC. A subgroup analysis of patients with additional autoimmune hepatitis (AIH) revealed no significant changes in bone structure compared to PBC only. Taken together, PBC patients demonstrate severe alterations in bone microstructure that are positively associated with disease duration and stage. By applying high-resolution peripheral quantitative computed tomography in the distal radius and tibia, a combined bone loss syndrome expressed by a predominant decrease in BMD and cortical thickness could be detected. This article is protected by copyright. All rights reserved.

KW - Journal Article

U2 - 10.1002/jbmr.3410

DO - 10.1002/jbmr.3410

M3 - SCORING: Journal article

C2 - 29470841

VL - 33

SP - 1011

EP - 1019

JO - J BONE MINER RES

JF - J BONE MINER RES

SN - 0884-0431

IS - 6

ER -