Key result
PDE4D SNP 41 shows no significant association with noncardiogenic ischemic stroke risk.
Why the study?
Conflicting evidence exists on the association between the PDE4D gene and ischemic stroke across different populations.
Does the PDE4D SNP 41 genotype increase the risk of noncardiogenic ischemic stroke in a Korean population?
Case-Control (n=308)
No
Does the PDE4D SNP 41 genotype increase the risk of noncardiogenic ischemic stroke in a Korean population?
Odds Ratio: 1.427 (95% CI 0.848–2.403)
p-value: p=0.18
The PDE4D SNP 41 genotype is not a major risk factor for noncardiogenic ischemic stroke in the Korean population, suggesting that causative genetic variants for stroke may differ across populations.
Does not warrant PDE4D SNP 41 genotyping for stroke risk in Koreans; leaves open population-specific genetic determinants.
Recently published studies from different populations provide apparently conflicting evidence on the association between the phosphodiesterase 4D (PDE4D) gene and ischemic stroke. The relationship between a representative PDE4D genotype and ischemic stroke was explored in a case-control study of 205 consecutive Korean patients with noncardiogenic ischemic stroke and 103 healthy controls who were neurologically and radiologically proven to be stroke-free. We selected and genotyped a PDE4D single nucleotide polymorphism (SNP 41, rs152312) as a candidate marker for susceptibility to ischemic stroke because SNP 41 has shown the most significant association with stroke in both a meta-analysis and the original Icelandic study of the PDE4D gene. No significant difference was observed between the cases and controls in the distribution of the PDE4D SNP 41 genotypes. The results from the adjusted conditional logistic regression analysis (adjusted for age, hypertension, diabetes and smoking status) showed no significant association between PDE4D SNP 41 genotypes and an increased risk of noncardiogenic ischemic stroke. The PDE4D gene is not a major risk factor for noncardiogenic ischemic stroke in a Korean population, which supports the recent evidence suggesting that the causative genetic variants of ischemic stroke may differ across populations.
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Kim et al. (2009) conducted a case-control in Noncardiogenic ischemic stroke (n=308). PDE4D SNP 41 (rs152312) genotype vs. Stroke-free controls was evaluated on Risk of noncardiogenic ischemic stroke (OR 1.427, 95% CI 0.848-2.403, p=0.18). The PDE4D SNP 41 genotype was not significantly associated with an increased risk of noncardiogenic ischemic stroke in a Korean population (adjusted OR 1.427).
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