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A SOD2 Polymorphism is Associated with Abnormal Quantitative Sensory Testing in Type 2 Diabetic Patients
Ali Işikli1, Ayşe Kubat-Üzüm2, İlhan Satman2
1Department of Neuroscience, Aziz Sancar Institute for Experimental Medicine, İstanbul University, İstanbul, Turkey.
Diabetic polyneuropathy (DPN) is linked to oxidative stress. A specific superoxide dismutase 2 (SOD2) gene variant (TT) was more common in patients with DPN and correlated with higher sensory thresholds.
Area of Science:
- Neurology
- Genetics
- Metabolic Disorders
Background:
- Diabetes mellitus (DM) frequently leads to peripheral nerve damage, known as diabetic polyneuropathy (DPN).
- Mitochondrial dysfunction and increased oxidative stress are implicated as key contributors to DPN pathogenesis.
Purpose of the Study:
- To investigate the association between a specific superoxide dismutase 2 (SOD2) gene single nucleotide polymorphism (SNP) and diabetic polyneuropathy (DPN).
- To evaluate the role of oxidative stress markers in DPN development and progression.
Main Methods:
- Nerve conduction studies and quantitative sensory testing (QST) were conducted on 20 type 2 diabetes mellitus (DM) patients (11 with DPN) and 15 healthy controls.
- Genotyping for the SOD2 SNP (rs5746136) was performed using polymerase chain reaction (PCR).
- Perception thresholds for cold, warm, and vibration were assessed using QST.
Main Results:
- DPN patients exhibited significantly elevated sensory perception thresholds compared to controls and DM patients without DPN.
- The TT genotype of the SOD2 SNP (rs5746136) was found to be more prevalent in patients with DM and DPN.
- DM patients carrying the TT variant demonstrated higher sensory threshold values, suggesting a functional impact.
Conclusions:
- The SOD2 SNP (rs5746136) is associated with increased sensory thresholds in diabetic patients, reinforcing the link between oxidative stress and DPN.
- Quantitative sensory testing and standard nerve conduction studies are valuable diagnostic tools for DPN.
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