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Expression of Estrogen Receptor Alpha and Evaluation of Histological Degeneration Scores in Fibroblasts of Hypertrophied Ligamentum Flavum: A Qualitative Study.

Authors :
Westhoff CC
Peterlein CD
Daniel H
Paletta JR
Moll R
Ramaswamy A
Lakemeier S
Source :
Biomolecules [Biomolecules] 2021 Nov 24; Vol. 11 (12). Date of Electronic Publication: 2021 Nov 24.
Publication Year :
2021

Abstract

The most common spinal disorder in elderly is lumbar spinal stenosis (LSS), resulting partly from ligamentum flavum (LF) hypertrophy. Its pathophysiology is not completely understood. The present study wants to elucidate the role of estrogen receptor α (ER α) in fibroblasts of hypertrophied LF. LF samples of 38 patients with LSS were obtained during spinal decompression. Twelve LF samples from patients with disk herniation served as controls. Hematoxylin & Eosin (H&E) and Elastica stains and immunohistochemistry for ER α were performed. The proportions of fibrosis, loss and/or degeneration of elastic fibers and proliferation of collagen fibers were assessed according to the scores of Sairyo and Okuda. Group differences in the ER α and Sairyo and Okuda scores between patients and controls, male and female sex and absence and presence of additional orthopedic diagnoses were assessed with the Mann-Whitney U test. There was a tendency towards higher expression of ER α in LF fibroblasts in the hypertrophy group ( p = 0.065). The Sairyo and Okuda scores were more severe for the hypertrophy group but, in general, not statistically relevant. There was no statistically relevant correlation between the expression of ER α and sex ( p = 0.326). ER α expression was higher in patients with osteochondrosis but not statistically significant ( p = 0.113). In patients with scoliosis, ER α expression was significantly lower ( p = 0.044). LF hypertrophy may be accompanied by a higher expression of ER α in fibroblasts. No difference in ER α expression was observed regarding sex. Further studies are needed to clarify the biological and clinical significance of these findings.

Details

Language :
English
ISSN :
2218-273X
Volume :
11
Issue :
12
Database :
MEDLINE
Journal :
Biomolecules
Publication Type :
Academic Journal
Accession number :
34944396
Full Text :
https://doi.org/10.3390/biom11121752