• Sonuç bulunamadı

METABOLIC SYNDROME

N/A
N/A
Protected

Academic year: 2021

Share "METABOLIC SYNDROME"

Copied!
14
0
0

Yükleniyor.... (view fulltext now)

Tam metin

(1)

METABOLIC SYNDROME

(2)

Visc Med.

2016 , 32(5):336-341. Epub 2016 Sep 19.

Clinical Scenario of the Metabolic Syndrome.

Brede S,

Serfling G,

Klement J,

Schmid SM,

Lehnert H.

Abstract

The term metabolic syndrome (MeS) refers to a cluster of associated symptoms

composed of impaired fasting glucose, abdominal obesity, hypertension, and

dyslipidemia. MeS is associated with an increased risk of cardiovascular and

diabetes-associated morbidity and mortality. The increased amount of visceral fat together

with a chronic inflammatory state predisposes to the development of arteriosclerosis.

Furthermore, insulin resistance (IR) and dyslipidemia are associated with fatty liver

disease. In addition, MeS is linked to non-cardiovascular diseases such as cancer as

well as psychiatric or endocrine disorders. Here, we discuss the clinical impact of MeS

in cardiovascular and non-cardiovascular diseases to highlight the importance of

prevention, early diagnosis, and multifactorial treatment of high-r

(3)

Pathogenesis of elevated cardiovascular risk in the MeS.

Visc Med.

2016 Oct;32(5):336-341. Epub 2016 . Clinical Scenario of the Metabolic

(4)

The whole-body glucose homeostasis

.

(5)

Insulin actions on many tissues.

(6)

Visc Med.2016 Oct;32(5):319-326. Epub 2016 Oct 7.

Metabolic Vascular Syndrome: New Insights into a Multidimensional Network of

Risk Factors and Diseases.

Scholz GH, Hanefeld M.

Abstract

BACKGROUND:

Since 1981, we have used the term metabolic syndrome to describe an association of a dysregulation in lipid metabolism (high triglycerides, low high-density lipoprotein cholesterol, disturbed glucose homeostasis (enhanced fasting and/or prandial glucose), gout, and hypertension), with android obesity being based on a common soil (overnutrition, reduced physical activity, sociocultural factors, and genetic predisposition). We hypothesized that main traits of the syndrome occur early and are tightly connected with hyperinsulinemia/insulin resistance, procoagulation, and cardiovascular diseases.

METHODS:

To establish a close link between the traits of the metabolic vascular syndrome, we focused our literature search on recent original work and comprehensive reviews dealing with the topics metabolic syndrome, visceral obesity, fatty liver, fat tissue inflammation, insulin resistance, atherogenic dyslipidemia, arterial hypertension, and type 2 diabetes mellitus.

RESULTS:

Recent research supports the concept that the metabolic vascular syndrome is a multidimensional and interactive network of risk factors and diseases based on individual genetic susceptibility and epigenetic changes where metabolic dysregulation/metabolic inflexibility in different organs and vascular dysfunction are early interconnected.

CONCLUSION:

The metabolic vascular syndrome is not only a risk factor constellation but rather a life-long abnormality of a closely connected interactive cluster of developing diseases which escalate each other and should continuously attract the attention of every clinician.

(7)

Historic description of the metabolic syndrome

.

Visc Med. 2016 Oct;32(5):319-326. Epub 2016 Oct 7. Metabolic Vascular Syndrome: New Insights into a Multidimensional Network of Risk

(8)

The multidimensional network of the metabolic vascular syndrome

Visc Med. 2016 32(5):319-326. Epub 2016 Oct 7. Metabolic Vascular Syndrome: New Insights into a Multidimensional Network of Risk

(9)

Effects of visceral obesity and ectopic fat depots on liver, vasculature, and muscle.

Visc Med.2016 32(5):319-326. Epub 2016 Oct 7. Metabolic Vascular Syndrome: New Insights into a Multidimensional Network of Risk Factors and Diseases. Scholz GH andHanefeld M.

(10)

Dysfunctional adipose tissue

Early central obesity is associated with a low-grade chronic inflammatory state characterized by slow infiltration of macrophages which are an important source of inflammation of this adipose tissue

World J Diabetes. 2016 Nov 15;7(19):483-514. Nutrition, insulin resistance and dysfunctional adipose

(11)

Coordinated influence of obesity, insulin resistance, activation of the RAAS and the SNS in

the pathophysiology of hypertension in the CMS.

Med Clin North Am.

2017 Jan;101(1):129-137. doi: 10.1016/j.mcna.2016.08.009. The Renin

Angiotensin Aldosterone System in Obesity and Hypertension: Roles in the Cardiorenal

(12)

Insulin

Signaling and Insulin Resistance (IR) in the Heart.

Trends Endocr Metab.,

Volume 28, Issue 6

, June 2017, Pages 416-427 Insulin and β

Adrenergic Receptor Signaling: Crosstalk in Heart.

QinFu

et al.

(13)

Structure of insulin receptor.

Insulin receptor is a heterotetrameric receptor that contains two α subunits, which is

extracellular and has the ligand-binding domain, and two β subunits, which consist of

extracellular, transmembrane and intracellular domains. The tyrosine kinase domain of the

receptor is present at the intracellular β subunits.

(14)

Insulin signaling pathway.

Biomol Ther (Seoul). 2017 Jan; 25(1): 44–56. Mangmool S

et al

Referanslar

Benzer Belgeler

(2014) conducted a parametric study of a well- monitored pile–slab-supported embankment for a high-speed railway to investigate the settlement, the load distribution

The salient findings of our study are that metabolic syndrome prevalence and uric acid levels were higher in psoriasis patients compared with those in healthy control group, and

If 1 of the diagnostic criteria defined by ACE-ACCE (i.e. hypertension, obesity, diabetes mellitus, dyslipid- emia) was present, presence of at least another metabolic syn-

patients without atrial arrhythmia displayed an in- creased PWD and significant intra- and inter-atrial electromechanical delay which was assessed by tissue

paraoxonase-1 (PON-1) activity with coronary artery dis- ease (CAD) in patients with metabolic syndrome (MetS).. Demographic and clinical characteristics, insulin levels,

Metabolic syndrome (3.6 fold) and increased levels of fasting blood glucose (1.1 fold), uric acid (2.2 fold), gamma-glutamyl transferase (1 fold), high-sensitivity CRP (1.1

SF-36 Yaşam Kalitesi Ölçeği alt birim değerleri karşılaştırıldığında, fiziksel güçlük ve ağrı alt birim puanlarındaki artış çalışma grubunda kontrol grubu- na

In our study, the mean gestational week at birth was significantly lower in the GDM group than in the control group, but there was no significant difference between the two groups