Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
To examine a potential association between the response to the phosphodiesterase-5 inhibitor sildenafil and angiotensin-converting enzyme (
ACE), as well as
NOS3 G894T genotypes in patients with erectile dysfunction (ED). An insertion/deletion (I/D) polymorphism in the gene encoding the
ACE and a single nucleotide exchange polymorphism (G894T) in the gene
NOS3 encoding endothelial nitric oxide synthase have been associated with cardiovascular disorders.
The response to sildenafil in 113 men with ED was monitored according to the patients’ diaries.
ACE and
NOS3 genotypes were determined in patients with ED and in 108 healthy male blood donors.
Genotype distributions of
ACE and
NOS3 polymorphisms in the patient group were similar to those of the healthy control group. Analysis of the response to sildenafil revealed that 15 of 20 individuals homozygous for the
ACE II genotype showed a positive erectile response after sildenafil use and only 46 of 93 D allele (combined DD and DI genotypes) carriers had a positive response (positive erectile response, odds ratio 3.07, 95% confidence interval 1.03 to 9.13,
P = 0.04; chi-square test). Analysis of
NOS3 genotypes revealed that 30 of 52 individuals homozygous for the G894 allele had a sufficient response to sildenafil and only 4 of 12 patients homozygous for the 894T allele had a sufficient erection.
It appears that patients with elevated ACE serum concentrations, as associated with the D allele of the
ACE I/D polymorphism, are less likely to respond to sildenafil.