coronary artery disease/hypoxia

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Endothelial Cell-Derived Microparticles from Patients with Obstructive Sleep Apnea Hypoxia Syndrome and Coronary Artery Disease Increase Aortic Endothelial Cell Dysfunction.

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OBJECTIVE Obstructive sleep apnea hypoxia syndrome (OSAHS) is an independent risk factor for coronary artery disease (CAD). Treatment of OSAHS improves clinical outcome in some CAD patients, but the relationship between OSAHS and CAD is complex. Microparticles (MPs) are shed by the plasma membrane

The effect of acute hypoxemia on coronary arterial dimensions in patients with coronary artery disease.

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OBJECTIVE To assess the influence of acute hypoxemia on the dimensions of diseased and nondiseased coronary arterial segments in humans. METHODS In 18 subjects (age 53 +/- 8 years) with known or suspected coronary artery disease, quantitative coronary angiography was performed before and after being

[Nocturnal hypoxia--its relevance with reference to sleep structure in patients with coronary heart disease].

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A disorder in the physiological structure of the sleep cycles (macrostructure) is known to occur both in patients with sleep apnoea (SA) and coronary heart disease (CHD). The study presented here was concerned with the problem whether the sleep structure in patients suffering from CHD and

Hypoxia-inducible factor-1α polymorphisms link to coronary artery collateral development and clinical presentation of coronary artery disease.

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OBJECTIVE This study aimed to investigate the association of Hypoxia-inducible factor-1α (HIF-1α) C1772T and G1790A single nucleotide polymorphisms (SNPs) with: incidence, clinical type, severity of coronary atherosclerosis and coronary collaterals of coronary artery disease (CAD). METHODS The

Hypoxia-inducible factor 1alpha polymorphism and coronary collaterals in patients with ischemic heart disease.

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OBJECTIVE Marked variability exists in coronary artery collaterals in patients with ischemic heart disease. Although multiple factors are thought to play a role in collateral development, the contribution of genetic factors is largely unknown. Hypoxia inducible factor 1 (HIF-1), a transcriptional

Disordered breathing and hypoxia during sleep in coronary artery disease.

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The occurrence of breathing disorders and hypoxia during sleep was studied in 17 male patients with coronary artery disease, demonstrated by coronary angiography, who did not have symptomatic pulmonary disease. Thirteen patients (76 percent) experienced disordered breathing during sleep; of these,

Regulatory systems for hypoxia-inducible gene expression in ischemic heart disease gene therapy.

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Ischemic heart diseases are caused by narrowed coronary arteries that decrease the blood supply to the myocardium. In the ischemic myocardium, hypoxia-responsive genes are up-regulated by hypoxia-inducible factor-1 (HIF-1). Gene therapy for ischemic heart diseases uses genes encoding angiogenic

Nocturnal intermittent hypoxia and short sleep duration are independently associated with elevated C-reactive protein levels in patients with coronary artery disease.

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Sleep-disordered breathing (SDB) or short sleep duration and coronary artery disease (CAD) are related, yet, the prevalence of SDB and short sleep duration as well as their mechanism remain unknown. Enhanced vascular inflammation is also implicated as one of the pathophysiologic mechanisms in CAD.

Hypoxia-inducible factor-1alpha induces the coronary collaterals for coronary artery disease.

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BACKGROUND Marked variability exists in coronary artery collaterals in patients with ischemic heart disease. Multiple factors are thought to play a role in collateral development; however, the contribution of hypoxia inducible factor-1alpha (HIF-1alpha), which is a transcriptional activator that

Things get broken: the hypoxia-inducible factor prolyl hydroxylases in ischemic heart disease.

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A major challenge in developing new treatments for myocardial infarction (MI) is an improved understanding of the pathophysiology of hypoxic tissue damage and the activation of endogenous adaptive programs to hypoxia. Due to the relevance of oxygen in metabolism, molecular adaptation to hypoxia

Expression of heme oxygenase-1, hypoxia inducible factor-1alpha, and ubiquitin in peripheral inflammatory cells from patients with coronary heart disease.

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BACKGROUND The increased expression of heme oxygenase-1 content, a stress-response protein, directly correlates with the incidence of coronary heart disease. Down-regulation of hypoxia inducible factor-1alpha activity, a major downstream effector of the signaling pathways activated by hypoxia,

Effects of intermittent hypobaric hypoxia on blood lipid concentrations in male coronary heart disease patients.

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The objective of the study was to evaluate the effects of intermittent hypobaric hypoxia (IHH) on plasma lipid concentrations of male coronary heart disease (CHD) patients. Forty-six male coronary patients were enrolled in the study. Thirty had a history of myocardial infarction and 16 had ischemic

Adaptations following an intermittent hypoxia-hyperoxia training in coronary artery disease patients: a controlled study.

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BACKGROUND Repeated exposure to intermittent normobaric hypoxia improves exercise tolerance in cardiac patients. Little is known on the effects of intermittent normobaric hypoxia-hyperoxia exposure in coronary artery disease (CAD) patients (New York Heart Association II-III). OBJECTIVE IHHT improves

MiR-145-5p alleviates hypoxia/reoxygenation- induced cardiac microvascular endothelial cell injury in coronary heart disease by inhibiting Smad4 expression

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Objective: To investigate the effects and mechanism of miR-145-5p on hypoxia/reoxygenation (H/R)-induced cardiac microvascular endothelial cell (CMEC) injury in coronary heart disease (CHD). Patients and

Intermittent hypoxia increases exercise tolerance in elderly men with and without coronary artery disease.
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BACKGROUND Intermittent hypoxia has been suggested to increase exercise tolerance by enhancing stress resistance and improving oxygen delivery. Because the improvement of exercise tolerance reduces mortality in the elderly with and without coronary artery disease intermittent hypoxia might be a

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coronary artery disease/hypoxia

Endothelial Cell-Derived Microparticles from Patients with Obstructive Sleep Apnea Hypoxia Syndrome and Coronary Artery Disease Increase Aortic Endothelial Cell Dysfunction.

The effect of acute hypoxemia on coronary arterial dimensions in patients with coronary artery disease.

[Nocturnal hypoxia--its relevance with reference to sleep structure in patients with coronary heart disease].

Hypoxia-inducible factor-1α polymorphisms link to coronary artery collateral development and clinical presentation of coronary artery disease.

Hypoxia-inducible factor 1alpha polymorphism and coronary collaterals in patients with ischemic heart disease.

Disordered breathing and hypoxia during sleep in coronary artery disease.

Regulatory systems for hypoxia-inducible gene expression in ischemic heart disease gene therapy.

Nocturnal intermittent hypoxia and short sleep duration are independently associated with elevated C-reactive protein levels in patients with coronary artery disease.

Hypoxia-inducible factor-1alpha induces the coronary collaterals for coronary artery disease.

Things get broken: the hypoxia-inducible factor prolyl hydroxylases in ischemic heart disease.

Expression of heme oxygenase-1, hypoxia inducible factor-1alpha, and ubiquitin in peripheral inflammatory cells from patients with coronary heart disease.

Effects of intermittent hypobaric hypoxia on blood lipid concentrations in male coronary heart disease patients.

Adaptations following an intermittent hypoxia-hyperoxia training in coronary artery disease patients: a controlled study.

MiR-145-5p alleviates hypoxia/reoxygenation- induced cardiac microvascular endothelial cell injury in coronary heart disease by inhibiting Smad4 expression

Intermittent hypoxia increases exercise tolerance in elderly men with and without coronary artery disease.

Cơ sở dữ liệu đầy đủ nhất về dược liệu được hỗ trợ bởi khoa học