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Updated: Oct 30, 2025

Evaluation of Blood-Brain Barrier Breakdown in a Mouse Model of Mild Traumatic Brain Injury
Published on: October 18, 2024
Blood-brain barrier dysfunction significantly correlates with serum matrix metalloproteinase-7 (MMP-7) following
Paul Nichols1, Javier Urriola2, Stephanie Miller3
1Department of Neurosurgery, Royal Brisbane and Women's Hospital, Australia.
Objectives:
To determine if radiological evidence of blood brain barrier (BBB) dysfunction, measured using Dynamic Contrast Enhanced MRI (DCE-MRI), correlates with serum matrix metalloproteinase (MMP) levels in traumatic brain injury (TBI) patients, and thereby, identify a potential biomarker for BBB dysfunction.
Patients And Methods:
20 patients with a mild, moderate, or severe TBI underwent a DCE-MRI scan and BBB dysfunction was interpreted from KTrans. KTrans is a measure of capillary permeability that reflects the efflux of gadolinium contrast into the extra-cellar space. The serum samples were concurrently collected and later analysed for MMP-1, -2, -7, -9, and -10 levels using an ELISA assay. Statistical correlations between MMP levels and the KTrans value were calculated. Multiple testing was corrected using the Benjamin-Hochberg method to control the false-discovery rate (FDR).
Results:
Serum MMP-1 values ranged from 1.5 to 49.6 ng/ml (12 ± 12.7), MMP-2 values from 58.3 to 174.1 ng/ml (109.5 ± 26.7), MMP-7 from 1.5 to 31.5 ng/mL (10 ± 7.4), MMP-9 from 128.6 to 1917.5 ng/ml (647.7 ± 749.6) and MMP-10 from 0.1 to 0.6 ng/mL (0.3 ± 0.2). Non-parametric Spearman correlation analysis on the data showed significant positive relationship between KTrans and MMP-7 (r = 0.55, p < 0.01). Correlations were also found between KTrans and MMP-1 (r = 0.74, p < 0.0002) and MMP-2 (r = 0.5, p < 0.025) but the actual MMP values were not above reference ranges, limiting the interpretation of results. Statistically significant correlations between KTrans and either MMP-9 or -10 were not found.
Conclusion:
This is the first study to show a correlation between DCE measures and MMP values in patients with a TBI. Our results support the suggestion that serum MMP-7 may be considered as a peripheral biomarker quantifying BBB dysfunction in TBI patients.
Insights
Matrix metalloproteinase-7 (MMP-7) levels in traumatic brain injury (TBI) patients correlate with blood brain barrier (BBB) dysfunction detected by Dynamic Contrast Enhanced MRI. MMP-7 shows potential as a peripheral biomarker for BBB changes after TBI.
Area of Science:
- Neuroimaging
- Biomarker Discovery
- Traumatic Brain Injury Research
Background:
- Traumatic brain injury (TBI) can cause blood brain barrier (BBB) dysfunction.
- Assessing BBB integrity is crucial for TBI patient management.
- Current methods for evaluating BBB dysfunction in TBI may require novel biomarkers.
Purpose of the Study:
- To investigate the correlation between radiological evidence of BBB dysfunction using Dynamic Contrast Enhanced MRI (DCE-MRI) and serum matrix metalloproteinase (MMP) levels in TBI patients.
- To identify a potential peripheral biomarker for quantifying BBB dysfunction in TBI.
Main Methods:
- 20 TBI patients underwent DCE-MRI to assess BBB dysfunction via KTrans measurements.
- Serum samples were analyzed for MMP-1, -2, -7, -9, and -10 levels using ELISA.
- Statistical correlation analyses (Spearman) were performed between KTrans values and MMP levels, with FDR correction.
Main Results:
- A significant positive correlation was observed between KTrans and serum MMP-7 levels (r=0.55, p<0.01).
- Correlations were also found between KTrans and MMP-1 (r=0.74, p<0.0002) and MMP-2 (r=0.5, p<0.025), though MMP values were within reference ranges.
- No statistically significant correlations were found between KTrans and MMP-9 or MMP-10.
Conclusions:
- This study demonstrates a correlation between DCE-MRI measures of BBB dysfunction and serum MMP levels in TBI patients.
- Serum MMP-7 is proposed as a potential peripheral biomarker for quantifying BBB dysfunction in TBI.
- Further research may validate MMP-7's utility in clinical TBI management.

