2007
DOI: 10.1111/j.1365-2796.2007.01894.x
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Renin–angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study

Abstract: Abstract. Conen D, Glynn RJ, Buring JE, Ridker PM, Zee RY (Harvard Medical School, Boston, MA, USA). Renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study. J Intern Med 2008; 263: 376-385.Objective. The renin-angiotensin system and endothelial function have both been implicated in the pathogenesis of type 2 diabetes. The aim of this study was to assess the relationship between a set of well-ch… Show more

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Cited by 13 publications
(9 citation statements)
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“…Another potential explanation is that high BP levels cause microvascular dysfunction that precede islet cell failure as shown in animal models 14; in epidemiological studies, biomarkers of endothelial dysfunction independently predict T2DM 15,16. Alternatively BP and T2DM could share a common gene polymorphism; for example, the renin-angiotensin system gene polymorphism associated with essential hypertension 17 has also been associated with increased risk for T2DM 18,19, although these results were not replicated in other studies20,21.…”
Section: Discussionmentioning
confidence: 99%
“…Another potential explanation is that high BP levels cause microvascular dysfunction that precede islet cell failure as shown in animal models 14; in epidemiological studies, biomarkers of endothelial dysfunction independently predict T2DM 15,16. Alternatively BP and T2DM could share a common gene polymorphism; for example, the renin-angiotensin system gene polymorphism associated with essential hypertension 17 has also been associated with increased risk for T2DM 18,19, although these results were not replicated in other studies20,21.…”
Section: Discussionmentioning
confidence: 99%
“…The genetic marker selection of 42 candidate genes was based on previous evidence of their potential functionality in pathways of inflammation, thrombosis, homeostasis, neurohormonal activation and endothelial dysfunction (8, 9). Further, a validated allele frequency and heterozygosity, and sequence-proven allelic variation were considered for this current analysis.…”
Section: Methodsmentioning
confidence: 99%
“…Genetic variants in pathways related to inflammation, thrombosis, homeostasis, neurohormonal activation and endothelial dysfunction may represent potential risk factors for the MetS (810). Although previous studies have shown genetic associations for many of the components of the MetS, few genome wide linkage studies have examined the full MetS (913). Recent candidate-gene association studies have studied polymorphisms in candidate genes for CVD in the context of the MetS and its components;(1417) however, no polymorphisms have been consistently replicated.…”
Section: Introductionmentioning
confidence: 99%
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“…However, Conen et al (38) identified no association between NOS3 rs1800779 and NOS3 rs3918226 polymorphisms and occurrence of T2D on a total of 24,309 Caucasian women free of diabetes at baseline in a prospective cohort study (37). In a meta-analysis performed by Zintzaras et al (39), a significant association was revealed between endothelial NO synthase gene polymorphisms (G894T) and diabetic nephropathy on 7,401 cases and 8,046 controls.…”
Section: Discussionmentioning
confidence: 97%