Sex-specific effect of the α-adducin (G460W) and AGTR1 (A1166C) polymorphism on carotid intima–media thickness

OBJECTIVEIn a primary care population covering a broad spectrum of cardiovascular risk (HIPPOCRATES project) the relationship between carotid intima–media thickness (CIMT) and six cardiovascular polymorphisms were analyzed in a cross-sectional study. METHODSCIMT was assessed in 618 participants, who...

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Veröffentlicht in:Journal of hypertension 2009-11, Vol.27 (11), p.2165-2173
Hauptverfasser: Plat, Arian W, Stoffers, Henri EJH, de Leeuw, Peter W, van Schayck, Constant P, Soomers, Frank L, Kester, Arnold DM, Aretz, Karin, Kroon, Abraham A
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Sprache:eng
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Zusammenfassung:OBJECTIVEIn a primary care population covering a broad spectrum of cardiovascular risk (HIPPOCRATES project) the relationship between carotid intima–media thickness (CIMT) and six cardiovascular polymorphisms were analyzed in a cross-sectional study. METHODSCIMT was assessed in 618 participants, who were genotyped for the AGTR1 (A1166C), AGT (M235T), ACE (4656rpt), NOS3 (E298D), GNB3 (C825T) and ADD1 (G460W) polymorphisms. Linear regression analyses were performed to assess the relationship between CIMT and the polymorphisms. RESULTSThe study population included 289 men (46.8%) and 329 (53.2%) women of whom 52.3% were treated with cardiovascular medication. CIMT was significantly associated with age, female sex, use of cardiovascular medication, waist circumference and dyslipidemia. After correction for these covariates, multivariate linear regression analyses showed that only in women the C-allele of AGTR1 was associated with a thicker CIMT (P = 0.03). The T-allele of ADD1 was associated with a smaller CIMT in both men and women, but this only reached statistical significance in women (P = 0.03). CONCLUSIONAlthough the effect of both genetic variants on CIMT was small, this study showed a statistically significant effect of AGTR1 and ADD1 in women. However, our findings should be viewed as hypothesis-generating and require further confirmation in prospective epidemiological primary care studies.
ISSN:0263-6352
1473-5598
DOI:10.1097/HJH.0b013e3283300506