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DOI 10.1002/ajhb.24130

Медицинская библиотека · American journal of human biology : the official journal of the Human Biology Council · 2024

Bone density in postmenopausal women with scoliosis is associated with markers of degenerative joint disease.

Ganji Elahe, Burshell Alan, Khicha Amisha, Lee Katharine M N

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Аннотация

PURPOSE: Bone mineral density (BMD) measured with dual x-ray absorptiometry (DXA) is the clinical standard for the diagnosis of osteoporosis and prediction of bone fracture risk. In the aging skeleton, osteoporosis is often concomitantly present with degenerative joint disease (DJD).

METHODS

In this study, we evaluated tissue-level changes in the differentially loaded concave (CC) and convex (CV) sides of the lumbar spine in a sample of postmenopausal women with scoliosis. We used a cumulative degeneration score to assess osteophyte formation, the severity of sclerotic morphology, and marrow changes as markers of DJD in the lumbar spine and examined the correlation between markers of DJD and BMD.

RESULTS

More severe osteophyte growth and sclerosis were present on the CC side of the spine. The degenerative score (DS) was higher on the CC side of the lumbar spine compared with the CV side. While CC BMD was positively correlated with CC DS and marrow, CV DS was not correlated with CV BMD. Marrow changes were correlated with DS on the CC lumbar spine.

CONCLUSION

These results highlight the importance of mechanoadaptive as well as broader inflammatory processes in the manifestation of degenerative changes and local mineral deposition at the lumbar spine. DXA-based BMD measurement of osteoporosis need to be contextualized within the biomechanical and degenerative conditions of a joint rather than using a strict threshold cutoff.

Для цитирования: Ganji Elahe, Burshell Alan, Khicha Amisha, Lee Katharine M N. Bone density in postmenopausal women with scoliosis is associated with markers of degenerative joint disease.. American journal of human biology : the official journal of the Human Biology Council. 2024. DOI: 10.1002/ajhb.24130.

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