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Association of Toll-like receptor 4 polymorphism with age-dependent systolic blood pressure increase in patients with coronary artery disease.


ABSTRACT: BACKGROUND:Systolic blood pressure (SBP) increases steadily with age and bears an independent continuous relationship with the incidence of cardiovascular events. Low-grade inflammation is a suspected pathomechanism causing vascular aging and promote coronary artery disease (CAD). Recent animal studies give evidence that Toll-like receptor 4 (TLR4) modulate inflammation and contribute to age-dependent SBP increase. However, there are no data about TLR4 and age-dependent blood pressure increase in human. METHODS AND RESULTS:We therefor investigate a human cohort of 2679 patients with CAD aged between 50-80 years. Genotypes were determined for the TLR4 single nucleotide polymorphism rs4986790 (TLR4 896A/G). Patients were stratified according to tertiles of age and the upper tertile was compared to lower tertiles. In this cohort we show that older patients with the TLR4 896 G allele had significantly lower SBP (TLR4 G allele carriers: 148.2?±?30.4 mmHg versus A/A allele carrier: 154.9?±?27.2 mmHg; P?

SUBMITTER: Schneider S 

PROVIDER: S-EPMC4443624 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Association of Toll-like receptor 4 polymorphism with age-dependent systolic blood pressure increase in patients with coronary artery disease.

Schneider Simon S   Koch Werner W   Hoppmann Petra P   Ubrich Romy R   Kemmner Stephan S   Steinlechner Eva E   Heemann Uwe U   Laugwitz Karl-Ludwig KL   Kastrati Adnan A   Baumann Marcus M  

Immunity & ageing : I & A 20150520


<h4>Background</h4>Systolic blood pressure (SBP) increases steadily with age and bears an independent continuous relationship with the incidence of cardiovascular events. Low-grade inflammation is a suspected pathomechanism causing vascular aging and promote coronary artery disease (CAD). Recent animal studies give evidence that Toll-like receptor 4 (TLR4) modulate inflammation and contribute to age-dependent SBP increase. However, there are no data about TLR4 and age-dependent blood pressure in  ...[more]

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