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Journal ArticleDOI

Elevated Levels of Macrophage Migration Inhibitory Factor in Women with Metabolic Syndrome

TLDR
Circulating MIF concentrations showed a gender disparity between healthy and metabolic syndrome subjects, and an elevation of systemic MIF in women with metabolic syndrome may contribute to pathogenesis of metabolic syndrome or to the development of metabolic Syndrome-related diseases, such as atherosclerosis and type 2 diabetes mellitus.
Abstract
Metabolic syndrome is a complex clinical disorder characterized by obesity, a disturbance of glucose metabolism, dyslipidemia, and hypertension, leading to increased cardiovascular risk. Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine produced both by innate immune cells and by adipocytes, and it plays an important role in inflammatory and cardiovascular diseases. The goal of this study was to evaluate the expression of circulating MIF in patients with metabolic syndrome. A study was conducted involving 172 persons who attended the Jeju National University Hospital Health Promotion Center. Among the 172 subjects, 88 patients with metabolic syndrome and 84 healthy control subjects were included. Serum MIF levels were considerably higher in patients with metabolic syndrome than in healthy subjects (mean±SEM, 1413.0-pg/ml±102.6 vs. 1077.0-pg/ml±-91.3, p=0.016). Among the metabolic syndrome patients, MIF levels were significantly increased in women (1403.0-pg/ml±114.2 vs. 921.3pg/ml±117.3, p=0.005), but not in men. Even after further linear regression adjustment for age and body mass index, the expression of MIF for women with metabolic syndrome was still clearly elevated when compared to healthy subjects (p=0.011). Circulating MIF concentrations showed a gender disparity between healthy and metabolic syndrome subjects. An elevation of systemic MIF in women with metabolic syndrome may contribute to pathogenesis of metabolic syndrome or to the development of metabolic syndrome-related diseases, such as atherosclerosis and type 2 diabetes mellitus.

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Journal ArticleDOI

Role of Macrophage Migration Inhibitory Factor in Obesity, Insulin Resistance, Type 2 Diabetes, and Associated Hepatic Co-Morbidities: A Comprehensive Review of Human and Rodent Studies.

TL;DR: A comprehensive summary of current knowledge on the role of MIF in obesity, its production by adipose tissue, and its involvement in the development of insulin resistance, type 2 diabetes, and NAFLD is provided.
Journal ArticleDOI

Macrophage migration inhibitory factor in myocardial ischaemia/reperfusion injury

TL;DR: Co-ordinating several pathways in the ischaemic heart, MIF contributes to receptor-mediated regulation of cardioprotective AMP-activated protein kinase signalling, inhibition of pro-apoptotic cascades, and the reduction of oxidative stress in the post-ischaemicheart.
Journal ArticleDOI

The Role of MIF in Type 1 and Type 2 Diabetes Mellitus

TL;DR: This review highlights the current knowledge about the involvement of MIF in both types of diabetes in the clinical environment and in experimental disease models and examines its role in autoimmune or inflammatory responses that influence diabetic pathology.
Journal ArticleDOI

Macrophage migration inhibitory factor involvement in breast cancer (Review)

TL;DR: This set of experimental and clinical data shows the involvement of MIF pathways in breast carcinogenesis and several anti-MIF targeted strategies are being explored in therapeutic goals and should merit further investigations.
Journal ArticleDOI

The macrophage migration inhibitory factor protein superfamily in obesity and wound repair

TL;DR: The macrophage migration inhibitory factor (MIF) superfamily consists of MIF and the recently identified homolog D-dopachrome tautomerase (D-DT or MIF-2), which positively correlates with obesity as well as insulin resistance and contributes to adipose tissue inflammation by modulating ATM functions.
References
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Journal ArticleDOI

Role of Insulin Resistance in Human Disease

TL;DR: The possibility is raised that resistance to insulin-stimulated glucose uptake and hyperinsulinemia are involved in the etiology and clinical course of three major related diseases— NIDDM, hypertension, and CAD.
Journal ArticleDOI

Macrophage migration inhibitory factor: a regulator of innate immunity.

TL;DR: A rapidly increasing amount of literature indicates that Mif is implicated in the pathogenesis of sepsis, and inflammatory and autoimmune diseases, suggesting that MIF-directed therapies might offer new treatment opportunities for human diseases in the future.
Journal ArticleDOI

Gender differences in the metabolic syndrome and their role for cardiovascular disease

TL;DR: The presently available data suggest that the pathophysiology of the metabolic syndrome and its contribution to the relative risk of cardiovascular events and heart failure show gender differences, which might be of potential relevance for prevention, diagnostics, and therapy of the syndrome.
Journal ArticleDOI

Hormonal changes in the menopause transition.

TL;DR: Symptoms of the menopause can be interpreted as resulting primarily from the profound fall in estradiol, occurring over a 3- to 4-year period around final menses, a fall that presumably contributes importantly to the beginning, in the late perimenopause, of loss of bone mineral density.
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