ReviewFrontiers in immunology2026
The role of the neuro-immune-bone axis in osteoporosis: from bone remodeling imbalance to multi-system interactions.
Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Osteoporosis is a systemic metabolic bone disease characterized by decreased bone mass, destruction of bone microstructure, and increased risk of fractures. Traditional views mainly attribute it to an imbalance between osteoblast-mediated bone formation and osteoclast-mediated bone resorption, but increasing evidence suggests that the pathogenesis and progression of osteoporosis are also regulated by complex interactions among the nervous system, immune system, and skeletal system. The neuro-immune-bone axis provides an important framework for integrating the bidirectional regulation between innervation, immune microenvironment, and bone remodeling process. This article systematically reviews the basis of interactions among sensory nerves, sympathetic nerves, immune cells, and bone cells in bone homeostasis, with a focus on the roles of sympathetic nerve activation, sensory neuropeptide imbalance, and immune inflammatory remodeling in the progression of osteoporosis. Furthermore, this article compares the differential imbalance patterns of this axis in postmenopausal osteoporosis, age-related osteoporosis, and secondary osteoporosis, and accordingly discusses its potential significance for disease classification and risk identification. At the therapeutic level, this article further distinguishes between clinically well-established management strategies and mechanistic interventions still in the exploratory stage. The former includes guideline-recommended anti-osteoporosis drugs, exercise, nutritional support, fall prevention, and control of primary diseases; the latter includes strategies such as sympathetic nerve regulation, CGRP-related interventions, Treg/Th17 balance regulation, and macrophage polarization, which are currently mainly based on animal experiments, mechanistic studies, observational evidence, or early translational research and cannot yet be considered routine clinical treatment. Therefore, the neuro-immune-bone axis is currently more suitable as a theoretical framework to explain the heterogeneity of osteoporosis and guide mechanistic research, and its practical value in precise classification, treatment selection, and clinical decision-making still requires further validation through prospective cohort and intervention trials. By integrating existing evidence, this article aims to offer a theoretical foundation for understanding the multi-system interaction mechanisms of osteoporosis, establishing an evidence stratification framework, and exploring future individualized interventions.
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.