Key result
The ACE D allele and DD genotype were not significantly associated with steroid-resistant nephrotic syndrome susceptibility (OR 1.60) and cannot serve as predictive markers for steroid responsiveness in Asian children.
Why the study?
Does ACE I/D gene polymorphism predict steroid responsiveness in Asian children with idiopathic nephrotic syndrome?
Meta-Analysis (n=1,269)
Does ACE I/D gene polymorphism predict steroid responsiveness in Asian children with idiopathic nephrotic syndrome?
Odds Ratio: 1.6 (95% CI 0.71–3.61)
p-value: p=0.26
The ACE I/D gene polymorphism (D allele or DD homozygous) cannot serve as a significant genetic marker to predict steroid responsiveness in Asian children with idiopathic nephrotic syndrome.
ACE I/D polymorphism lacks predictive value for steroid responsiveness; challenges prior candidate-gene associations in Asian children.
BACKGROUND: The results from the published studies on the association between angiotensin-converting enzyme (ACE) insertion/deletion (I/D) gene polymorphism and the treatment response to steroid in Asian children with idiopathic nephrotic syndrome (INS) is still conflicting. This meta-analysis was performed to evaluate the relation between ACE I/D gene polymorphism and treatment response to steroid in Asian children and to explore whether ACE D allele or DD genotype could become a predictive marker for steroid responsiveness. METHODOLOGY/PRINCIPAL FINDINGS: Association studies were identified from the databases of PubMed, Embase, Cochrane Library and CBM-disc (China Biological Medicine Database) as of September 1, 2010, and eligible investigations were synthesized using meta-analysis method. Five investigations were identified for the analysis of association between ACE I/D gene polymorphism and steroid-resistant nephrotic syndrome (SRNS) risk in Asian children and seven studies were included to explore the relationship between ACE I/D gene polymorphism and steroid-sensitive nephrotic syndrome (SSNS) susceptibility. Five investigations were recruited to explore the difference of ACE I/D gene distribution between SRNS and SSNS. There was no a markedly association between D allele or DD genotype and SRNS susceptibility or SSNS risk, and the gene distribution differences of ACE between SRNS and SSNS were not statistically significant. II genotype might play a positive role against SRNS onset but not for SSNS (OR = 0.51, P = 0.02; OR = 0.95, P = 0.85; respectively), however, the result for the association of II genotype with SRNS risk was not stable. CONCLUSIONS/SIGNIFICANCE: Our results indicate that D allele or DD homozygous can't become a significant genetic molecular marker to predict the treatment response to steroid in Asian children with INS.
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Zhou et al. (2011) conducted a meta-analysis in Idiopathic Nephrotic Syndrome (n=1,269). ACE I/D gene polymorphism (D allele) vs. I allele was evaluated on Association of ACE D allele with steroid-resistant nephrotic syndrome (SRNS) risk (OR 1.60, 95% CI 0.71-3.61, p=0.26). The ACE D allele and DD genotype were not significantly associated with steroid-resistant nephrotic syndrome susceptibility (OR 1.60) and cannot serve as predictive markers for steroid responsiveness in Asian children.
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