Objective: This study investigates the correlation between magnetic resonance diffusion tensor imaging (DTI) parameters and biochemical composition in degenerative intervertebral disc nucleus pulposus tissue, offering a potential reference for the clinical diagnosis and efficacy evaluation of intervertebral disc degeneration.
Methods: Human lumbar intervertebral disc nucleus pulposus tissue samples were collected via full endoscopic minimally invasive surgery. DTI was employed to quantitatively measure fractional anisotropy (FA) and apparent diffusion coefficient (ADC) values in the degenerative nucleus pulposus, examining the relationship between Pfirrmann grading and these DTI parameters. Western blotting was used to detect the expression levels of aquaporin 1 (AQP1) and aquaporin 3 (AQP3) in the degenerative tissue. The glycosaminoglycan (GAG) content was quantified using the dimethylmethylene blue (DMMB) colorimetric assay, and collagen content was assessed with the Sircol soluble collagen assay kit. The relationship between Pfirrmann grading and biochemical composition was also analyzed. Finally, correlation analysis was performed between the FA and ADC values from the human nucleus pulposus tissue and their GAG and collagen contents.
Results: A total of 39 patients (19 males, 20 females) with lumbar disc herniation (LDH), averaging 54.41 years of age, were included. As the degree of Pfirrmann degeneration increased, FA values rose, while ADC values continuously declined. Concurrently, as degeneration progressed, expression of AQP1 and AQP3 proteins decreased, GAG content significantly diminished, and collagen content increased. FA values exhibited a moderate negative correlation with GAG content (r = -0.5974, P < 0.0001) and a strong positive correlation with collagen content (r = 0.8694, P < 0.0001). ADC values showed a moderate positive correlation with GAG content (r = 0.6873, P < 0.0001) and a strong negative correlation with collagen content (r = -0.8502, P < 0.0001).
Conclusion: The FA and ADC values derived from magnetic resonance DTI, along with the protein expression levels of AQPs, can reflect the severity of intervertebral disc degeneration to a certain extent. Additionally, the content of glycosaminoglycans and collagen in the nucleus pulposus of the intervertebral disc correlates with the FA and ADC values of the DTI parameters. Therefore, magnetic resonance DTI quantitative imaging provides a means to assess the biochemical composition changes within the intervertebral discs, offering valuable insights for the clinical diagnosis and evaluation of therapeutic efficacy in intervertebral disc degenerative diseases.
Trial Registration: Chinese Clinical Trial Registry, ChiCTR2000041151, Registered on 19 December, 2020, https://www.chictr.org.cn/showproj.html?proj=206119 .
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http://dx.doi.org/10.1186/s12891-025-08382-9 | DOI Listing |
Zhong Nan Da Xue Xue Bao Yi Xue Ban
October 2024
Department of Spine Surgery, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Objectives: With the aging population, the incidence of intervertebral disc degeneration (IDD) is increasing every year. The pathogenesis of IDD is complex, and there are currently no effective treatment options. This study aims to investigate the specific function and underlying mechanism of zinc finger protein 667 (ZNF667) in the inflammatory damage of nucleus pulposus cells in IDD.
View Article and Find Full Text PDFBMC Musculoskelet Disord
March 2025
Department of Radiology, Zigong Fourth People's Hospital, Zigong, 643000, Sichuan Province, China.
Background: Low back pain(LBP) is very common among the population, and intervertebral disc(IVD) degeneration is considered to be the most common cause of LBP, but the pathophysiological process between IVD degeneration and LBP is not very clear. We conducted this study to clarify the interplay between quantitative magnetic resonance imaging (MRI) parameters, including q-Dixon and T2 mapping, and clinical symptomatology in patients with LBP.
Methods: All LBP patients underwent lumbar spine MRI, encompassing q-Dixon and T2 mapping.
Spine (Phila Pa 1976)
March 2025
Chicago Anesthesia Pain Specialists, Chicago, IL, USA.
Study Design: An exploratory analysis of a randomized, double-blind, sham-controlled, phase 3 study.
Objective: To evaluate the impact of SI-6603 (condoliase) on health-related quality of life (HRQoL)-related outcomes in patients with lumbar disc herniation (LDH)-associated radicular leg pain from the Discovery 6603 study (NCT03607838).
Summary Of Background Data: Condoliase is a novel chemonucleolytic agent that selectively degrades chondroitin sulfate in the nucleus pulposus.
Cell Signal
March 2025
Department of Orthopedics, Second Hospital of Shanxi Medical University, Taiyuan 030001, China. Electronic address:
Background: Intervertebral disc degeneration (IVDD) is a significant contributor to lower back pain (LBP), affecting approximately 80 % of the global population. The RalA inhibitor BQU57 plays a role in various cellular functions; however, its impact on nucleus pulposus cell (NPC) degeneration remains unclear.
Methods: This study employed a combination of bioinformatics analysis and experimental validation to investigate the role of RALA in IVDD and its inhibitor BQU57 in its therapeutic potential.
During skeletal growth, there is an increased secretion of lactate by glycolytic nucleus pulposus (NP) cells of the intervertebral disc. To investigate the role of this anion, we generated annulus fibrosus (AF) and endplate (EP) specific ( ) mice. Histological and spatial transcriptomic studies indicated significant disc degeneration in , characterized by NP cell loss and delayed EP maturation.
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