Systemic Inflammation in Hip Fracture and Osteoarthritis: Insights into Pathways of Immunoporosis

Inflammaging has been implicated in age-related bone loss and fragility fractures through immune-mediated effects on bone turnover. We aimed to explore the relationship between systemic inflammatory markers and bone health in older adults, focusing on the differences between patients with osteoporotic fractures and non-fractured controls. We retrospectively analyzed 40 older patients (20 with hip fractures and 20 with osteoarthritis without prior fragility fractures). We compared routine inflammatory markers, including red cell distribution width (RDW), C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR), systemic immune-inflammation index (SII), and the composite CRP-albumin-lymphocyte index (CALLY), between groups. Bone mineral density (BMD) at the hip, lumbar spine, and wrist, as well as the FRAX score, were assessed. Correlations between inflammatory markers, BMD, and FRAX scores were evaluated using Spearman's coefficient. Patients with fractures exhibited significantly elevated CRP (66.2 ± 70.3 vs. 3.8 ± 4.0 mg/L, <i>p</i> = 0.0008) and SII (1399.7 ± 1143.4 vs. 751.4 ± 400.8, <i>p</i> = 0.025) compared to controls. RDW, NLR, and CALLY scores did not differ significantly between the groups. Higher CRP levels were associated with lower BMD at all sites (hip: r ≈ -0.63, <i>p</i> = 0.002; spine: r ≈ -0.60, <i>p</i> = 0.005; wrist: r ≈ -0.60, <i>p</i> = 0.005). No significant correlations were observed between the SII and BMD or FRAX values. Elevated systemic inflammation, particularly indicated by CRP and SII, was associated with osteoporotic fracture status and low bone density in our cohort. These findings support the concept that inflammatory pathways may contribute to osteoporosis and fracture risk and suggest that inflammatory markers could serve as adjunctive tools in fracture risk assessment. Further studies are required to clarify the causality and evaluate whether targeting chronic inflammation can improve bone health in older adults.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-09-19
DOI
https://doi.org/10.3390/ijms26189138
Citations
4
Primary Topic
Bone and Joint Diseases
Type
article
Field-Weighted Citation Impact
6.89
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article

Systemic Inflammation in Hip Fracture and Osteoarthritis: Insights into Pathways of Immunoporosis

Bernardo Abel Cedeño‐Veloz, Fabrício Zambom-Ferraresi, Alejandro Rodríguez-García, Nicolás Martínez‐Velilla et al.
4 citations
International Journal of Molecular Sciences
Bone and Joint Diseases
6.89
article

Systemic Inflammation in Hip Fracture and Osteoarthritis: Insights into Pathways of Immunoporosis

Bernardo Abel Cedeño‐Veloz, Fabrício Zambom-Ferraresi, Alejandro Rodríguez-García, Nicolás Martínez‐Velilla, Juan José Lasarte, Soledad Domínguez-Mendoza, Irene Guruceaga-Eguillor, Virginia Ruiz-Izquieta
article en
4 citations

Abstract

Inflammaging has been implicated in age-related bone loss and fragility fractures through immune-mediated effects on bone turnover. We aimed to explore the relationship between systemic inflammatory markers and bone health in older adults, focusing on the differences between patients with osteoporotic fractures and non-fractured controls. We retrospectively analyzed 40 older patients (20 with hip fractures and 20 with osteoarthritis without prior fragility fractures). We compared routine inflammatory markers, including red cell distribution width (RDW), C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR), systemic immune-inflammation index (SII), and the composite CRP-albumin-lymphocyte index (CALLY), between groups. Bone mineral density (BMD) at the hip, lumbar spine, and wrist, as well as the FRAX score, were assessed. Correlations between inflammatory markers, BMD, and FRAX scores were evaluated using Spearman's coefficient. Patients with fractures exhibited significantly elevated CRP (66.2 ± 70.3 vs. 3.8 ± 4.0 mg/L, <i>p</i> = 0.0008) and SII (1399.7 ± 1143.4 vs. 751.4 ± 400.8, <i>p</i> = 0.025) compared to controls. RDW, NLR, and CALLY scores did not differ significantly between the groups. Higher CRP levels were associated with lower BMD at all sites (hip: r ≈ -0.63, <i>p</i> = 0.002; spine: r ≈ -0.60, <i>p</i> = 0.005; wrist: r ≈ -0.60, <i>p</i> = 0.005). No significant correlations were observed between the SII and BMD or FRAX values. Elevated systemic inflammation, particularly indicated by CRP and SII, was associated with osteoporotic fracture status and low bone density in our cohort. These findings support the concept that inflammatory pathways may contribute to osteoporosis and fracture risk and suggest that inflammatory markers could serve as adjunctive tools in fracture risk assessment. Further studies are required to clarify the causality and evaluate whether targeting chronic inflammation can improve bone health in older adults.

International Journal of Molecular SciencesVol. 26(18)
Universidad Pública de Navarra (UPNA) (ES), Instituto de Salud Carlos III (ES), Navarrabiomed (ES), Universidad de Navarra (ES)
Openalex Percentile: Top 3%
Bone and Joint Diseases
6.89
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