Inflammatory markers and cardiovascular risk in the metabolic syndrome

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Inflammatory markers and cardiovascular risk in the metabolic syndrome. / Espinola-Klein, Christine; Gori, Tommaso; Blankenberg, Stefan; Munzel, Thomas.

In: FRONT BIOSCI-LANDMRK, Vol. 16, 01.01.2011, p. 1663-1674.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

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@article{112a19f701cc43c59c8e6ca006971ef6,
title = "Inflammatory markers and cardiovascular risk in the metabolic syndrome",
abstract = "Elevated blood glucose, obesity, high blood pressure, elevated triglycerides and low high density lipoprotein (HDL) cholesterol are well accepted risk factors in the development of coronary artery disease. Clustering of at least three of these factors in an individual is defined as metabolic syndrome (MetS). Obesity is a central pathological mechanism in the disease and it is expected that the incidence of this condition will increase dramatically within the next years. The visceral adipose tissue is not only an energy depot but also an endocrine organ which produces a large number of bioactive molecules, the so called adipokines. In the setting of obesity, the over-production of proinflammatory and pro-thrombotic adipokines is associated with insulin resistance. This mechanism represents the pathophysiological basis for the development of MetS. Inflammation has a central role in the pathogenesis of MetS and in mediating its impact on the development of cardiovascular disease. Knowledge of these mechanisms has relevance in the context of preventive and therapeutic strategies.",
keywords = "Adiponectin/blood, Adolescent, Adult, Angiotensinogen/blood, Atherosclerosis/blood, Biomarkers/blood, Cardiovascular Diseases/etiology, Chemokine CCL2/blood, Endothelium, Vascular/physiopathology, Humans, Inflammation/complications, Insulin Resistance, Interleukin-6/blood, Intra-Abdominal Fat/physiopathology, Leptin/blood, Life Style, Metabolic Syndrome/blood, Obesity/complications, Plaque, Atherosclerotic/pathology, Plasminogen Activator Inhibitor 1/blood, Prognosis, Resistin/blood, Risk, Tumor Necrosis Factor-alpha/blood",
author = "Christine Espinola-Klein and Tommaso Gori and Stefan Blankenberg and Thomas Munzel",
year = "2011",
month = jan,
day = "1",
doi = "10.2741/3812",
language = "English",
volume = "16",
pages = "1663--1674",
journal = "FRONT BIOSCI-LANDMRK",
issn = "2768-6701",
publisher = "Frontiers in Bioscience",

}

RIS

TY - JOUR

T1 - Inflammatory markers and cardiovascular risk in the metabolic syndrome

AU - Espinola-Klein, Christine

AU - Gori, Tommaso

AU - Blankenberg, Stefan

AU - Munzel, Thomas

PY - 2011/1/1

Y1 - 2011/1/1

N2 - Elevated blood glucose, obesity, high blood pressure, elevated triglycerides and low high density lipoprotein (HDL) cholesterol are well accepted risk factors in the development of coronary artery disease. Clustering of at least three of these factors in an individual is defined as metabolic syndrome (MetS). Obesity is a central pathological mechanism in the disease and it is expected that the incidence of this condition will increase dramatically within the next years. The visceral adipose tissue is not only an energy depot but also an endocrine organ which produces a large number of bioactive molecules, the so called adipokines. In the setting of obesity, the over-production of proinflammatory and pro-thrombotic adipokines is associated with insulin resistance. This mechanism represents the pathophysiological basis for the development of MetS. Inflammation has a central role in the pathogenesis of MetS and in mediating its impact on the development of cardiovascular disease. Knowledge of these mechanisms has relevance in the context of preventive and therapeutic strategies.

AB - Elevated blood glucose, obesity, high blood pressure, elevated triglycerides and low high density lipoprotein (HDL) cholesterol are well accepted risk factors in the development of coronary artery disease. Clustering of at least three of these factors in an individual is defined as metabolic syndrome (MetS). Obesity is a central pathological mechanism in the disease and it is expected that the incidence of this condition will increase dramatically within the next years. The visceral adipose tissue is not only an energy depot but also an endocrine organ which produces a large number of bioactive molecules, the so called adipokines. In the setting of obesity, the over-production of proinflammatory and pro-thrombotic adipokines is associated with insulin resistance. This mechanism represents the pathophysiological basis for the development of MetS. Inflammation has a central role in the pathogenesis of MetS and in mediating its impact on the development of cardiovascular disease. Knowledge of these mechanisms has relevance in the context of preventive and therapeutic strategies.

KW - Adiponectin/blood

KW - Adolescent

KW - Adult

KW - Angiotensinogen/blood

KW - Atherosclerosis/blood

KW - Biomarkers/blood

KW - Cardiovascular Diseases/etiology

KW - Chemokine CCL2/blood

KW - Endothelium, Vascular/physiopathology

KW - Humans

KW - Inflammation/complications

KW - Insulin Resistance

KW - Interleukin-6/blood

KW - Intra-Abdominal Fat/physiopathology

KW - Leptin/blood

KW - Life Style

KW - Metabolic Syndrome/blood

KW - Obesity/complications

KW - Plaque, Atherosclerotic/pathology

KW - Plasminogen Activator Inhibitor 1/blood

KW - Prognosis

KW - Resistin/blood

KW - Risk

KW - Tumor Necrosis Factor-alpha/blood

U2 - 10.2741/3812

DO - 10.2741/3812

M3 - SCORING: Review article

C2 - 21196255

VL - 16

SP - 1663

EP - 1674

JO - FRONT BIOSCI-LANDMRK

JF - FRONT BIOSCI-LANDMRK

SN - 2768-6701

ER -