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Multifocal Glucocorticoid-Associated Osteonecrosis: Clinical Characteristics and Systemic Molecular Features
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Background: Multifocal osteonecrosis involving three or more anatomical sites is an uncommon but severe manifestation of glucocorticoid-associated osteonecrosis and may be associated with systemic clinical backgrounds. This study investigated the clinical characteristics and exploratory serum proteomic profiles of multifocal osteonecrosis using clinical and proteomic analyses. Methods: We analyzed 107 patients who underwent surgery for osteonecrosis of the femoral head between 2019 and 2024. Whole-body MRI was used to detect multifocal lesions. Patients were classified into glucocorticoid-related osteonecrosis of the femoral head (GO) and multifocal glucocorticoid-related osteonecrosis (MGO). Clinical variables were compared, and multivariate logistic regression identified clinical factors associated with multifocal osteonecrosis. Serum proteomic profiling using nanoLC–MS/MS was performed as an exploratory analysis to compare protein expression among GO, MGO, and osteoarthritis controls. Results: Multifocal osteonecrosis was identified in 31 patients (29.0%). Patients with MGO were younger (42.6 vs. 50.9 years, p = 0.021) and had higher glucocorticoid doses (59.5 vs. 48.5 mg, p = 0.005). Hematologic diseases (OR 14.51, 95% CI 3.42–86.69, p < 0.001) and skin manifestations (OR 3.17, 95% CI 1.05–10.44, p = 0.046) were independently associated with multifocal osteonecrosis. Exploratory proteomic analysis showed protein expression patterns related to fibrinolysis, coagulation, inflammation, and vascular homeostasis in MGO. Conclusions: Multifocal osteonecrosis was associated with systemic clinical backgrounds and showed exploratory vascular- or coagulation-related proteomic patterns within glucocorticoid-associated osteonecrosis.
Title: Multifocal Glucocorticoid-Associated Osteonecrosis: Clinical Characteristics and Systemic Molecular Features
Description:
Background: Multifocal osteonecrosis involving three or more anatomical sites is an uncommon but severe manifestation of glucocorticoid-associated osteonecrosis and may be associated with systemic clinical backgrounds.
This study investigated the clinical characteristics and exploratory serum proteomic profiles of multifocal osteonecrosis using clinical and proteomic analyses.
Methods: We analyzed 107 patients who underwent surgery for osteonecrosis of the femoral head between 2019 and 2024.
Whole-body MRI was used to detect multifocal lesions.
Patients were classified into glucocorticoid-related osteonecrosis of the femoral head (GO) and multifocal glucocorticoid-related osteonecrosis (MGO).
Clinical variables were compared, and multivariate logistic regression identified clinical factors associated with multifocal osteonecrosis.
Serum proteomic profiling using nanoLC–MS/MS was performed as an exploratory analysis to compare protein expression among GO, MGO, and osteoarthritis controls.
Results: Multifocal osteonecrosis was identified in 31 patients (29.
0%).
Patients with MGO were younger (42.
6 vs.
50.
9 years, p = 0.
021) and had higher glucocorticoid doses (59.
5 vs.
48.
5 mg, p = 0.
005).
Hematologic diseases (OR 14.
51, 95% CI 3.
42–86.
69, p < 0.
001) and skin manifestations (OR 3.
17, 95% CI 1.
05–10.
44, p = 0.
046) were independently associated with multifocal osteonecrosis.
Exploratory proteomic analysis showed protein expression patterns related to fibrinolysis, coagulation, inflammation, and vascular homeostasis in MGO.
Conclusions: Multifocal osteonecrosis was associated with systemic clinical backgrounds and showed exploratory vascular- or coagulation-related proteomic patterns within glucocorticoid-associated osteonecrosis.
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