New evidence on the controversy over the correlation between vertebral osteoporosis and intervertebral disc degeneration: a systematic review of relevant animal studies.

Abstract

OBJECTIVE: The effect of vertebral osteoporosis on disc degeneration remains controversial. The aim of this study was to conduct a systematic review and meta-analysis of relevant animal studies to shed more light on the effects and mechanisms of vertebral osteoporosis on disc degeneration and to promote the resolution of the controversy. METHODS: The PubMed, Cochrane Library, and Embase databases were searched for studies that met the inclusion criteria. Basic information and data were extracted from the included studies and data were analyzed using STATA 15.1 software. This study was registered on INPLASY with the registration number INPLASY202370099 and https://doi.org/10.37766/inplasy2023.7.0099 . RESULTS: A total of 13 studies were included in our study. Both animals, rats and mice, were covered. Meta-analysis results showed in disc height index (DHI) (P&#x2009;<&#x2009;0.001), histological score (P&#x2009;<&#x2009;0.001), number of osteoblasts in the endplate (P&#x2009;=&#x2009;0.043), number of osteoclasts in the endplate (P&#x2009;<&#x2009;0.001), type I collagen (P&#x2009;<&#x2009;0.001), type II collagen (P&#x2009;<&#x2009;0.001), aggrecan (P&#x2009;<&#x2009;0.001), recombinant a disintegrin and metalloproteinase with thrombospondin-4 (ADAMTS-4) (P&#x2009;<&#x2009;0.001), matrix metalloproteinase-1 (MMP-1) (P&#x2009;<&#x2009;0.001), MMP-3 (P&#x2009;<&#x2009;0.001), MMP-13 (P&#x2009;<&#x2009;0.001), the difference between the osteoporosis group and the control group was statistically significant. In terms of disc volume, the difference between the osteoporosis group and the control group was not statistically significant (P&#x2009;=&#x2009;0.459). CONCLUSION: Our study shows that vertebral osteoporosis may exacerbate disc degeneration. Abnormal bone remodeling caused by vertebral osteoporosis disrupts the structural integrity of the endplate, leading to impaired nutrient supply to the disc, increased expression of catabolic factors, and decreased levels of type II collagen and aggrecan may be one of the potential mechanisms.