Micro-scale vertebral features in postmenopausal women with alcohol-associated and metabolic-associated fatty liver disease: ex vivo bone quality analyses

• Published in: Journal of endocrinological investigation 2024-01, Vol.47 (1), p.131-140
• Main Authors: Jadzic, J., Milovanovic, P., Tomanovic, N., Zivkovic, V., Djukic, D., Nikolic, S., Djuric, M., Djonic, D.
• Format: Article
• Language: English
• Subjects: Adipose tissue; Body mass index; Bone marrow; Computed tomography; Endocrinology; Epidemiology; Fatty liver; Internal Medicine; Liver diseases; Mechanical properties; Medicine; Medicine & Public Health; Metabolic Diseases; Metabolism; Original Article; Post-menopause; Vertebrae
• ISSN: 1720-8386; 0391-4097; 1720-8386
• DOI: 10.1007/s40618-023-02130-3

Purpose Although epidemiological studies indicate increased fracture risk in women with alcohol-associated liver disease (AALD) and metabolic-associated fatty liver disease (MAFLD), data about their micro-scale bone features are still limited. We aimed to characterize bone quality changes in the anterior mid-transverse part of the first lumbar vertebral body collected from 32 adult postmenopausal females. Based on pathohistological assessment of the liver tissue, individuals were divided into AALD ( n  = 13), MAFLD ( n  = 9), and control group ( n  = 10). Methods We analyzed trabecular and cortical micro-architecture (using micro-computed tomography), bone mechanical properties (using Vickers microhardness tester), osteocyte lacunar network and bone marrow adiposity morphology (using optic microscopy). Data were adjusted to elude the covariant effects of advanced age and body mass index on our results. Results Our data indicated a minor trend toward deteriorated bone quality in MAFLD women, presented in impaired trabecular and cortical micro-architectural integrity, which could be associated with bone marrow adiposity alterations noted in these women. Additionally, we observed a significant decline in micro-architectural, mechanical, and osteocyte lacunar features in lumbar vertebrae collected from the AALD group. Lastly, our data indicated that vertebral bone deterioration was more prominent in the AALD group than in the MAFLD group. Conclusion Our data suggested that MAFLD and AALD are factors that could play a part in compromised vertebral strength of postmenopausal women. Also, our data contribute to understanding the multifactorial nature of bone fragility in these patients and highlight the necessity for developing more effective patient-specific diagnostic, preventive, and therapeutic strategies. Graphical abstract