Key result
The ADA gene rs452159 polymorphism was significantly associated with an increased risk of chronic heart failure under a dominant model (OR 1.537; 95% CI 1.10-2.16; p=0.013).
Why the study?
Is the adenosine deaminase (ADA) gene polymorphism associated with an increased risk of chronic heart failure in a northern Chinese Han population?
Case-Control (n=700)
Is the adenosine deaminase (ADA) gene polymorphism associated with an increased risk of chronic heart failure in a northern Chinese Han population?
Odds Ratio: 1.537 (95% CI 1.1–2.16)
p-value: p=0.013
The ADA gene polymorphism rs452159 is associated with an increased risk of chronic heart failure in the northern Chinese Han population, suggesting a potential genetic role in CHF pathogenesis.
Should not change CHF risk assessment; hypothesis-generating in northern Chinese Han, needs prospective validation.
Adenosine (Ado) is an important cardioprotective agent. Since endogenous Ado levels are affected by the enzyme Ado deaminase (ADA), polymorphisms within the ADA gene may exert some effect on chronic heart failure (CHF). This study applied a case-control investigation to 300 northern Chinese Han CHF patients and 400 ethnicity-matched healthy controls in which nine single-nucleotide polymorphisms (SNPs) of ADA were genotyped and association analyses were performed. Odds ratios (ORs) with 95% confidence intervals (CI) were used to assess the association. Overall, rs452159 polymorphism in ADA gene was significantly associated with susceptibility to CHF under the dominant model (p = 0.013, OR = 1.537, 95% CI = 1.10-2.16), after adjustment for age, sex, and traditional cardiovascular risk factors. No difference in genotype distribution and allele frequency for the rs452159 according to the functional New York Heart Association class was found. Furthermore, the values of left ventricular ejection fraction, left-ventricle end-diastolic diameter or left-ventricle end-systolic diameter did not differ significantly among the different rs452159 genotype CHF patients. Although further studies with larger cohorts and other ethnicities are required to validate the conclusions, the findings of this study potentially provide novel insight into the pathogenesis of CHF.
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He et al. (2014) conducted a case-control in Chronic heart failure (n=700). ADA gene rs452159 polymorphism vs. Healthy controls was evaluated on Susceptibility to chronic heart failure (OR 1.537, 95% CI 1.10-2.16, p=0.013). The ADA gene rs452159 polymorphism was significantly associated with an increased risk of chronic heart failure under a dominant model (OR 1.537; 95% CI 1.10-2.16; p=0.013).
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