Micro-scale assessment of bone quality changes in adult cadaveric men with congestive hepatopathy.


Journal

Histochemistry and cell biology
ISSN: 1432-119X
Titre abrégé: Histochem Cell Biol
Pays: Germany
ID NLM: 9506663

Informations de publication

Date de publication:
Dec 2022
Historique:
accepted: 13 06 2022
pubmed: 19 7 2022
medline: 15 12 2022
entrez: 18 7 2022
Statut: ppublish

Résumé

Congestive hepatopathy (CH) is a chronic liver disease (CLD) caused by impaired hepatic venous blood outflow, most frequently resulting from congestive heart failure. Although it is known that heart failure and CLDs contribute to increased risk for age-related fractures, an assessment of CH-induced skeletal alterations has not been made to date. The aim of our study was to characterize changes in bone quality in adult male cadavers with pathohistologically confirmed CH compared with controls without liver disease. The anterior mid-transverse part of the fifth lumbar vertebral body was collected from 33 adult male cadavers (age range 43-89 years), divided into the CH group (n = 15) and the control group (n = 18). We evaluated trabecular and cortical micro-architecture and bone mineral content (using micro-computed tomography), bone mechanical competence (using Vickers micro-hardness tester), vertebral cellular indices (osteocyte lacunar network and bone marrow adiposity), and osteocytic sclerostin and connexin 43 expression levels (using immunohistochemistry staining and analysis). Deterioration in trabecular micro-architecture, reduced trabecular and cortical mineral content, and decreased Vickers microhardness were noted in the CH group (p < 0.05). Reduced total number of osteocytes and declined connexin 43 expression levels (p < 0.05) implied that harmed mechanotransduction throughout the osteocyte network might be present in CH. Moreover, elevated expression levels of sclerostin by osteocytes could indicate the role of sclerostin in mediating low bone formation in individuals with CH. Taken together, these micro-scale bone alterations suggest that vertebral strength could be compromised in men with CH, implying that vertebral fracture risk assessment and subsequent therapy may need to be considered in these patients. However, further research is required to confirm the clinical relevance of our findings.

Identifiants

pubmed: 35849203
doi: 10.1007/s00418-022-02128-7
pii: 10.1007/s00418-022-02128-7
doi:

Substances chimiques

Connexin 43 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

583-593

Subventions

Organisme : Science Fund of the Republic of Serbia
ID : 7749444
Organisme : Alexander von Humboldt-Stiftung
ID : 3.4-1162414-SRB-IP

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Jelena Jadzic (J)

Center of Bone Biology, Institute of Anatomy, Faculty of Medicine, University of Belgrade, Dr. Subotica no. 4/II, 11000, Belgrade, Serbia.

Nada Tomanovic (N)

Institute of Pathology, Faculty of Medicine, University of Belgrade, Dr. Subotica no. 1, Belgrade, Serbia.

Danica Djukic (D)

Institute of Forensic Medicine, Faculty of Medicine , University of Belgrade, Deligradska no. 31a, Belgrade, Serbia.

Vladimir Zivkovic (V)

Institute of Forensic Medicine, Faculty of Medicine , University of Belgrade, Deligradska no. 31a, Belgrade, Serbia.

Slobodan Nikolic (S)

Institute of Forensic Medicine, Faculty of Medicine , University of Belgrade, Deligradska no. 31a, Belgrade, Serbia.

Marija Djuric (M)

Center of Bone Biology, Institute of Anatomy, Faculty of Medicine, University of Belgrade, Dr. Subotica no. 4/II, 11000, Belgrade, Serbia.

Petar Milovanovic (P)

Center of Bone Biology, Institute of Anatomy, Faculty of Medicine, University of Belgrade, Dr. Subotica no. 4/II, 11000, Belgrade, Serbia.

Danijela Djonic (D)

Center of Bone Biology, Institute of Anatomy, Faculty of Medicine, University of Belgrade, Dr. Subotica no. 4/II, 11000, Belgrade, Serbia. danijela.djonic@med.bg.ac.rs.

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