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Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
Cumulative Risk of Metabolic Syndrome Correlated with the Coexistence of (-1306C/T) and Altered Circulating MMP2
S S Yadav1, R K Mandal2, M K Singh3
1Department of Pharmacology and Therapeutics, King George's Medical University, Lucknow.
Background:
Interindividual genetic variations and environmental factors both play pivotal roles in the pathogenesis of metabolic syndrome (MetS). The rationale of this study conducted was to analyze the association of Matrix Metalloproteinase (MMP) gene variants, MMP-1 (-1607 1G/2G) and MMP-2 (-1306 C/T) with susceptibility to MetS and its effect on serum MMP level.
Methods:
Study involved 370 subjects with 1:1 distribution of cases and controls. Patients were recruited according to modified NCEP-ATP III criteria for MetS. Clinical, biochemical analysis, PCR-RFLP and ELISA methods were employed for genotyping and estimation of serum MMP level.
Results:
Significantly (p<0.001) higher Serum MMP-2 (39.13±19.96 ng/ml) was detected in cases as compared to controls. The MMP-2 (-1306 C/T) was significantly associated with the risk of MetS. The variant genotype TT was significantly associated with increased risk of MetS. (p=0.032; OR=2.31; 95%CI=1.07-4.97). No significant association of MMP-1(-1607 1G/2G) was found with risk of MetS.
Conclusion:
Our study concluded that presence of MMP-2 (-1306 C/T) might be associated the risk of MetS. Serum MMP2 level was significantly higher in patients and correlated with clinical parameters of MetS. Clinical implication of the work may help to identify the individuals with high risk of MetS and further complications.
Insights
Genetic variations in Matrix Metalloproteinase-2 (MMP-2) are linked to metabolic syndrome (MetS) risk. Elevated serum MMP-2 levels were observed in MetS patients, suggesting a potential biomarker for disease susceptibility.
Area of Science:
- Genetics
- Biochemistry
- Metabolic Diseases
Background:
- Metabolic syndrome (MetS) pathogenesis involves genetic and environmental factors.
- Matrix Metalloproteinases (MMPs) are implicated in various physiological processes.
- Investigating MMP gene variants' role in MetS susceptibility is crucial.
Purpose of the Study:
- To analyze the association of Matrix Metalloproteinase (MMP) gene variants, specifically MMP-1 (-1607 1G/2G) and MMP-2 (-1306 C/T), with MetS susceptibility.
- To evaluate the effect of these gene variants on serum MMP levels.
- To determine potential clinical implications for MetS risk identification.
Main Methods:
- Study included 370 subjects with a 1:1 case-control distribution.
- MetS diagnosis based on modified NCEP-ATP III criteria.
- Genotyping performed using PCR-RFLP; serum MMP levels measured by ELISA.
Main Results:
- Serum MMP-2 levels were significantly higher in MetS cases (p<0.001).
- The MMP-2 (-1306 C/T) variant, particularly the TT genotype, was significantly associated with increased MetS risk (p=0.032; OR=2.31).
- No significant association was found between MMP-1 (-1607 1G/2G) and MetS risk.
Conclusions:
- The MMP-2 (-1306 C/T) gene variant may be associated with an increased risk of developing MetS.
- Elevated serum MMP-2 levels in MetS patients correlate with clinical parameters.
- This research may aid in identifying individuals at high risk for MetS and its complications.
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