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Clin Chem Lab Med ; 44(7): 807-12, 2006.
Article in English | MEDLINE | ID: mdl-16776624

ABSTRACT

BACKGROUND: A genetic association/prospective follow-up study was conducted to investigate whether genetic variation of the alpha(2B)-adrenergic receptor gene was associated with the risk of restenosis in 96 Greek coronary artery disease patients undergoing coronary angioplasty and stent implantation. METHODS: For comparison of genotype frequency, a control group of 83 asymptomatic individuals was also studied. The end-point of the current study was the incidence of restenosis at 7 months of clinical follow-up. RESULTS: The majority of patients (70/96) had the insertion/insertion genotype, fewer patients (23/96) had the insertion/deletion genotype and only 3/96 had the deletion/deletion genotype; overall the frequency distribution was not different from that of the control subjects. Restenosis occurred in 15 of the 96 patients. CONCLUSIONS: In the population studied, alpha(2B)-adrenoreceptor polymorphisms were not found to predispose patients to an increased incidence of restenosis. Nevertheless, these findings should be considered as preliminary, taking into account the small number of patients that were studied and the rarity of the deletion/deletion genotype.


Subject(s)
Angioplasty , Coronary Disease/genetics , Coronary Disease/surgery , Polymorphism, Genetic/genetics , Receptors, Adrenergic, alpha-2/genetics , Stents/adverse effects , Adult , Aged , Coronary Disease/complications , Coronary Disease/pathology , Female , Genotype , Humans , Male , Middle Aged , Risk Factors
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