scholarly journals Perivascular adipose tissue of the descending thoracic aorta is associated with systemic lupus erythematosus and vascular calcification in women

2013 ◽  
Vol 231 (1) ◽  
pp. 129-135 ◽  
Author(s):  
Kelly J. Shields ◽  
Emma Barinas-Mitchell ◽  
Matthew R. Gingo ◽  
Ping Tepper ◽  
Bret H. Goodpaster ◽  
...  
2011 ◽  
Vol 11 ◽  
pp. 1932-1947 ◽  
Author(s):  
Morena Scotece ◽  
Javier Conde ◽  
Rodolfo Gómez ◽  
Veronica López ◽  
Francisca Lago ◽  
...  

The cloning of leptin in 1994 by Zhang et al. introduced a novel concept about white adipose tissue (WAT) as a very dynamic organ that releases a plethora of immune and inflammatory mediators, such as adipokines and cytokines, which are involved in multiple diseases. Actually, adipokines exert potent modulatory actions on target tissues involved in rheumatic diseases including cartilage, synovial, bone and immune cells. The goal of this paper is to elucidate the recent findings concerning the involvement of adipokines in rheumatic diseases, such as rheumatoid arthritis (RA), osteoarthritis (OA), and systemic lupus erythematosus (SLE).


2012 ◽  
Vol 303 (11) ◽  
pp. E1313-E1324 ◽  
Author(s):  
Curtis L. Gabriel ◽  
Patricia B. Smith ◽  
Yanice V. Mendez-Fernandez ◽  
Ashley J. Wilhelm ◽  
Audrey Musi Ye ◽  
...  

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by the production of autoantibodies against self-antigens such as double-stranded DNA and phospholipids. Classical comorbidities of SLE include glomerulonephritis, infection, cardiovascular disease, arthritis, skin disorders, and neurological disease. In addition to these classical comorbidities, there is emerging evidence that SLE patients are at higher risk of developing insulin resistance and other components of the metabolic syndrome. Visceral adipose tissue inflammation is a central mediator of insulin resistance in the obese setting, but the mechanism behind the pathogenesis of metabolic disease in the SLE patient population is unclear. We hypothesize that lupus-associated changes in the adaptive immune system are associated with disruption in glucose homeostasis in the context of SLE. To test this hypothesis, we assessed the metabolic and immunological phenotype of SLE-prone B6.SLE mice. B6.SLE mice fed a low-fat diet had significantly worsened glucose tolerance, increased adipose tissue insulin resistance, increased β-cell insulin secretion, and increased adipocyte size compared with their respective B6 controls. Independently of diet, B cells isolated from the white adipose tissue of B6.SLE mice were skewed toward IgG production, and the level of IgG1 was elevated in the serum of SLE-prone mice. These data show that B6.SLE mice develop defects in glucose homeostasis even when fed a low-fat diet and suggest that B cells may play a role in this metabolic dysfunction.


2020 ◽  
Vol 14 (1) ◽  
pp. 20-25
Author(s):  
L. V. Kondratyeva ◽  
T. A. Panafidina ◽  
T. V. Popkova ◽  
Yu. R. Varaeva ◽  
A. V. Starodubova

Objective: to determine body composition (BC) in women with systemic lupus erythematosus (SLE), by using bioimpedance analysis.Patients and methods. The investigation enrolled 12 women with a reliable diagnosis of SLE, who were followed up at the Clinic of the V.A. Nasonova Research Institute of Rheumatology. Their median age was 46.5 [38.5; 54.7] years. All the patients underwent estimation of waist circumference (WC) and body mass index (BMI). BC was analyzed using an InBody 770 multi-frequency bioimpedance analyzer (Biospace Co. Ltd, South Korea) at the Clinical Nutrition Clinic, Federal Research Institute of Nutrition and Biotechnology.Results and discussion. BMI corresponding to overweight or obesity was observed in 67% of patients; abdominal obesity (AO) was seen in 83%. BC study showed that in most patients, adipose tissue mass was greater than the normal values (75%), lean body mass, skeletal muscle mass, and the amount of body water were within normal limits (83%), and the basal metabolic rate was reduced (67%). There were positive correlations between the percentage of adipose tissue and BMI (r=0.9; p<0.01), WC (r=0.7; p<0.01), C-reactive protein (CRP) levels (r=0.6; p<0.05), and complement C3 concentrations (r=0.9; p<0.01). Similar results were obtained when assessing the relationship between visceral fat area and BMI (r=0.9; p<0.01), WC (r=0.78; p<0.01), CRP (r=0.6; p<0.05), complement component C3 (r=0.8; p<0.01). There was an inverse correlation between visceral fat area and the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) (r=-0.6; p<0.05).Conclusion. Most women with SLE have AO, increased adipose tissue mass, normal lean body mass, and decreased basal metabolism. There is a direct correlation of visceral fat content and inflammatory markers (CRP, complement component C3) and an inverse correlation of those with the SLEDAI-2K. 


2012 ◽  
Vol 223 (2) ◽  
pp. 389-393 ◽  
Author(s):  
Aliza Lipson ◽  
Nikolaos Alexopoulos ◽  
Gregory Randell Hartlage ◽  
Chesnal Arepalli ◽  
Annette Oeser ◽  
...  

2002 ◽  
Vol 35 (4) ◽  
pp. 801-804 ◽  
Author(s):  
Hisato Takagi ◽  
Yoshio Mori ◽  
Hisashi Iwata ◽  
Masaki Kimura ◽  
Mansyo Itokazu ◽  
...  

2013 ◽  
Vol 228 (2) ◽  
pp. 515
Author(s):  
Aliza Lipson ◽  
Nikolaos Alexopoulos ◽  
Gregory Randell Hartlage ◽  
Chesnal Arepalli ◽  
Annette Oeser ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document