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Functional polymorphism of matrix metalloproteinase-9 (MMP9) gene is not associated with schizophrenia and with its
Przemyslaw Bienkowski1, Jerzy Samochowiec2, Justyna Pelka-Wysiecka2
1Department of Pharmacology, Institute of Psychiatry and Neurology, Warszawa, Poland.
Background:
The deficit subtype of schizophrenia is hypothesized to constitute a pathophysiologically distinct subgroup of schizophrenia patients suffering from enduring, idiopathic negative symptoms and various neuropsychological deficits. Matrix metalloproteinases (MMPs) are extracellularly acting endopeptidases the substrates of which are matrix and adhesion molecules. Recently, MMP9 has been shown to be involved in various forms of synaptic plasticity, learning and memory consolidation. The primary aim of the present study was to evaluate associations between the functional MMP-9 -1562C/T gene polymorphism and the deficit and non-deficit subtypes of schizophrenia.
Methods:
The study was conducted between 2009 and 2012. Deficit schizophrenia was diagnosed using the SDS. The sample consisted of 468 patients, Caucasians, of Polish descent with ICD 10 diagnosis of schizophrenia: 189 [51% males] were included in a non-deficit subgroup, 279 patients [53% males] were included in a deficit subgroup. The control group consisted of 532 subjects, Caucasians, of Polish descent [51% males]. MMP-9 -1562C/T gene polymorphism was genotyped using the fluorescence resonance energy transfer (FRET) method and the Light Cycler System 2.0.
Results:
The frequencies of genotypes and alleles did not differ between the schizophrenia patients and control group. The deficit and non-deficit patients did not differ in terms of the genotype and allele frequencies. No differences were found in genotype and allele frequencies between the deficit patients and the controls and between the non-deficit patients and the controls.
Conclusion:
We found no evidence for the association between the functional MMP-9 -1562C/T gene polymorphism and deficit/non-deficit subtypes of schizophrenia.
Insights
This study found no association between the MMP-9 -1562C/T gene polymorphism and schizophrenia subtypes. The genetic variations did not differ between deficit schizophrenia, non-deficit schizophrenia, and healthy controls.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Schizophrenia is categorized into deficit and non-deficit subtypes, potentially representing distinct pathophysiological entities.
- Matrix metalloproteinase-9 (MMP-9) is implicated in synaptic plasticity, learning, and memory.
- The MMP-9 -1562C/T gene polymorphism is a functional variant potentially influencing MMP-9 activity.
Purpose of the Study:
- To investigate the association between the MMP-9 -1562C/T gene polymorphism and the deficit and non-deficit subtypes of schizophrenia.
- To determine if this genetic polymorphism differentiates schizophrenia subtypes from each other and from healthy controls.
Main Methods:
- A case-control study involving 468 schizophrenia patients (189 non-deficit, 279 deficit) and 532 healthy controls of Polish descent.
- Diagnosis of deficit schizophrenia was confirmed using the SDS (Symptomالدلالة Scale).
- MMP-9 -1562C/T gene polymorphism was genotyped using the fluorescence resonance energy transfer (FRET) method on the Light Cycler System 2.0.
Main Results:
- No significant differences in genotype or allele frequencies of the MMP-9 -1562C/T polymorphism were observed between schizophrenia patients and the control group.
- The deficit and non-deficit schizophrenia subgroups did not differ in their genotype or allele frequencies for this polymorphism.
- No significant differences were found when comparing deficit patients to controls, or non-deficit patients to controls.
Conclusions:
- The study found no evidence to support an association between the functional MMP-9 -1562C/T gene polymorphism and the deficit or non-deficit subtypes of schizophrenia.
- These findings suggest that the investigated MMP-9 polymorphism is unlikely to be a genetic marker for schizophrenia subtypes in the studied population.
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