Related Experiment Video
Updated: Jan 7, 2026

11:22
Microbiota Analysis Using Two-step PCR and Next-generation 16S rRNA Gene Sequencing
Published on: October 15, 2019
31.0K
Gut microbiome dysbiosis implicates the gut-bone axis in Modic changes: a metagenomic case-control study
Binbin Lan1, Yu Liang1, Zhongxian Zhou1
1Department of Spine and Osteopathy Ward, The Second People's Hospital of Nanning, The Third Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Frontiers in Microbiology
|December 31, 2025
Summary
Gut microbial dysbiosis is linked to Modic changes (MCs), a cause of low back pain (LBP). Reduced gut bacteria diversity and altered pathways suggest a gut-bone axis role in MCs.
Area of Science:
- Microbiology
- Gastroenterology
- Orthopedics
Background:
- Modic changes (MCs) are vertebral lesions associated with discogenic low back pain (LBP).
- The pathogenesis of MCs is poorly understood, with emerging links between gut dysbiosis and systemic inflammation.
- The role of gut microbiome in MC development has not been previously investigated.
Purpose of the Study:
- To characterize the gut microbiome composition in patients with MCs.
- To identify specific microbial and metabolic features associated with MCs.
- To explore the relationship between gut microbiome alterations and MC severity.
Main Methods:
- A case-control study utilizing shotgun metagenomic sequencing on fecal samples from 31 MC patients and 25 healthy controls.
- Analysis of microbial alpha and beta diversity, differential taxa abundance, and functional pathways (KEGG).
- Correlation analysis between microbial features and clinical markers like C-reactive protein (CRP) and Pfirrmann grade.
Main Results:
- Patients with MCs exhibited significantly reduced gut microbial alpha diversity compared to controls.
- Distinct microbial communities were observed between MC patients and controls, with specific taxa like *unclassified_Parabacteroides* and *Bacteroides uniformis* identified as discriminative.
- Enrichment of quorum sensing and glycerolipid metabolism pathways was found in MC patients, correlating with elevated CRP and higher Pfirrmann grade.
Conclusions:
- Gut microbial dysbiosis is associated with MCs, characterized by decreased diversity and altered metabolic pathways.
- These findings suggest a potential role for the gut-bone axis in the pathogenesis of MCs.
- The study highlights potential novel microbial and metabolic targets for diagnosing and treating LBP associated with MCs.
Related Concept Videos
Bone Disorders
5.0K
Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
5.0K
Osteoclasts in Bone Remodeling
3.8K
Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during...
3.8K
Bone Remodeling
40.2K
Bone remodeling is a continuous and balanced process of bone resorption by osteoclasts and bone formation by osteoblasts. In adults, it helps maintain bone mass and calcium homeostasis. While mechanical stress can stimulate turnover as part of the normal maintenance and reparative process, several hormones also regulate bone remodeling.
40.2K
