ReviewCell biochemistry and biophysics2025
Bone and Cardiometabolic Connection: Crosstalk between Osteoporosis and Atherosclerosis.
Review in Cell biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Sex-specific associations between carotid plaque and bone mineral density in patients with type 2 diabetes: a retrospective cross-sectional study.Biology of sex differences · 2026Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The crosstalk between osteoporosis and atherosclerosis has gained substantial attention due to the shared risk factors and pathophysiological mechanisms underlying both conditions. Osteoporosis, marked by the diminished bone mineral density (BMD), augmented risk for fractures and atherosclerosis, and accumulation of plaques within the arterial walls, are together prevalent in the aging populations. This review highlights the intricate crosstalk between these two conditions, focusing on the role of inflammatory biomarkers, genetic predispositions, and metabolic alterations. We have analyzed reported studies on common pathways such as the osteoprotegerin (OPG)/receptor activator of nuclear factor-κB (NF-κB) (RANK)/receptor activator of NF-κB ligand (RANKL) (OPG/RANK/RANKL) signaling pathway and systemic inflammation in the human subjects and animal and cell culture models, which contribute to both bone resorption and vascular calcification. Additionally, we have explored impact of chronic diseases such as the chronic kidney disease (CKD) on exacerbation of both osteoporosis and atherosclerosis through changes in mineral metabolism. Therapeutic interventions targeting these shared mechanisms including the actions of bisphosphonates, romosozumab, denosumab, and anti-inflammatory agents are discussed for their efficacies to mitigate simultaneously the bone loss and vascular calcification. This comprehensive overview on current understanding of the relationship between osteoporosis and atherosclerosis discloses the unmet need for a targeted research approach that precisely addresses the interdependent nature of these conditions towards improving the outcomes in patients encountering both diseases.
Indexed as
Identifiers
40801976What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.