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Submitted on July 23, 2003
Accepted on September 18, 2003
Polymorphisms and Angiographic Outcome After Coronary Artery Stenting
From the Division of Cardiology, Universita del Piemonte Orientale, Ospedale Maggiore della Carita (V.F., F.R., C.V.), Novara, Italy; Department of Genetics, Biology and Biochemistry (G.M., S.G., S.C., A.P.), Universita di Torino, Italy; I.S.I. Foundation (G.M.), Villa Gualino, Torino, Italy; Department of Cardiovascular Diseases (A.V., E.U.), Ospedale Santa Croce e Carle, Cuneo, Italy; and Cardiovascular Center (W.W.), OLV Hospital, Aalst, Belgium.
* To whom correspondence should be addressed. E-mail: uslenghi.e{at}scroce.sanitacn.it.
Objective--Because of the receptor-mediated antiproliferative effects of estradiol on vascular smooth muscle cells, our study aimed at identifying a role of PvuII and XbaI polymorphisms of the
-estrogen receptor (
ER) gene in the occurrence of restenosis after coronary stent implantation (in-stent restenosis [ISR]).
Methods and Results--In 858 patients (148 women), 955 lesions were treated with stent implantation, and the PvuII C/T and XbaI G/A polymorphisms of the
ER gene were determined. Quantitative angiography was performed before and after stenting and at 6-month follow-up. The allelic frequencies were similar between sexes (C/T allele, 0.43/0.57 and 0.44/0.56; P=0.9; G/A allele, 0.35/0.65 and 0.38/0.62; P=0.8; in women and men, respectively). A significantly higher ISR rate in women than in men homozygous for the T-allele of the PvuII polymorphism (42.6% versus 26.9%, P=0.03) or the G-allele of the XbaI polymorphism (41.2% versus 19.4%, P=0.04) was observed. At multivariate analysis, T/T genotype was the only independent predictor of ISR in women but not in men (odds ratio, 1.5; 95% CI, 1.0 to 2.1; P=0.03). XbaI polymorphism was no longer associated with ISR in both sexes.
Conclusions--Women homozygous for the T-allele of the PvuII polymorphism of the
ER gene treated with coronary stent implantation have a higher risk of ISR than men.
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