Heme Oxygenase-1 Gene Promoter Microsatellite Polymorphism Is Associated With Progressive Atherosclerosis and Incident Cardiovascular Disease

OBJECTIVE—The enzyme heme oxygenase-1 (HO-1) exerts cytoprotective effects in response to various cellular stressors. A variable number tandem repeat polymorphism in the HO-1 gene promoter region has previously been linked to cardiovascular disease. We examined this association prospectively in the...

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Veröffentlicht in:Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 2015-01, Vol.35 (1), p.229-236
Hauptverfasser: Pechlaner, Raimund, Willeit, Peter, Summerer, Monika, Santer, Peter, Egger, Georg, Kronenberg, Florian, Demetz, Egon, Weiss, Günter, Tsimikas, Sotirios, Witztum, Joseph L, Willeit, Karin, Iglseder, Bernhard, Paulweber, Bernhard, Kedenko, Lyudmyla, Haun, Margot, Meisinger, Christa, Gieger, Christian, Müller-Nurasyid, Martina, Peters, Annette, Willeit, Johann, Kiechl, Stefan
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Sprache:eng
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Zusammenfassung:OBJECTIVE—The enzyme heme oxygenase-1 (HO-1) exerts cytoprotective effects in response to various cellular stressors. A variable number tandem repeat polymorphism in the HO-1 gene promoter region has previously been linked to cardiovascular disease. We examined this association prospectively in the general population. APPROACH AND RESULTS—Incidence of stroke, myocardial infarction, or vascular death was registered between 1995 and 2010 in 812 participants of the Bruneck Study aged 45 to 84 years (49.4% males). Carotid atherosclerosis progression was quantified by high-resolution ultrasound. HO-1 variable number tandem repeat length was determined by polymerase chain reaction. Subjects with ≥32 tandem repeats on both HO-1 alleles compared with the rest of the population (recessive trait) featured substantially increased cardiovascular disease risk (hazard ratio [95% confidence interval], 5.45 [2.39, 12.42]; P
ISSN:1079-5642
1524-4636
DOI:10.1161/ATVBAHA.114.304729