The mineralocorticoid receptor blocker spironolactone lowers plasma interferon-γ and interleukin-6 in patients with type 2 diabetes and treatment-resistant hypertension

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Sai Sindhu Thangaraj ◽  
Christina Stolzenburg Oxlund ◽  
Micaella Pereira Da Fonseca ◽  
Per Svenningsen ◽  
Jane Stubbe ◽  
...  
2014 ◽  
Vol 32 (8) ◽  
pp. 1672-1677 ◽  
Author(s):  
Kristian B. Buhl ◽  
Christina S. Oxlund ◽  
Ulla G. Friis ◽  
Per Svenningsen ◽  
Claus Bistrup ◽  
...  

Author(s):  
Yangyang Cheng ◽  
Xiaohui Du ◽  
Bilin Zhang ◽  
Junxia Zhang

Abstract Background Serum wnt1-induced signaling pathway protein 1 (WISP1) levels are increased with obesity, which is a common complication associated with lower extremity atherosclerotic disease (LEAD). However, to date, the relationship between elevated WISP1 levels and the incidence of lower extremity atherosclerotic disease (LEAD) in type 2 diabetes mellitus (T2DM) remains unclear. Methods 174 newly diagnosed type 2 diabetic patients were enrolled in our study. Patients were divided into two groups, LEAD group (n=100) and control group (n=74). Anthropometric parameters, blood pressure and some biochemical parameters were obtained. Body composition was detected by bioelectrical impedance analysis (BIA). Levels of serum insulin were determined by radioimmunoassay. Serum WISP1 and interleukin 6 (IL-6) levels were determined using an enzyme-linked immunosorbent assay. Results It was shown that serum WISP1 levels in diabetic patients with LEAD were higher than those without LEAD (P<0.001). Serum WISP1 levels were positively related with waist circumference (r=0.237, P=0.003), waist-hip ratio (r=0.22, P=0.006), visceral fat area (r=0.354, P<0.001), serum creatinine (r=0.192, P=0.012), interleukin 6 (r=0.182, P=0.032), c-reactive protein (r=0.681, P<0.001), triglycerides (r=0.119, P<0.001), fasting glucose (r=0.196, P=0.011), glycated hemoglobin (r=0.284, P<0.001), and HOMA-IR (r=0.285, P<0.026). Compared with the lowest tertile, the odds ratio of the middle tertile for LEAD incidence was 3.27 (95% CI, 1.24–8.64) and 4.46 (95% CI, 1.62–12.29) for the highest tertile after adjusting confounding factors. Conclusion The results suggest that increased serum WISP1 levels independently contribute to the incidence of LEAD in patients with newly diagnosed T2DM.


2019 ◽  
Vol 56 (6) ◽  
pp. e13334 ◽  
Author(s):  
Laura Panagi ◽  
Lydia Poole ◽  
Ruth A. Hackett ◽  
Andrew Steptoe

Diabetes ◽  
2004 ◽  
Vol 53 (12) ◽  
pp. 3342-3345 ◽  
Author(s):  
Y. H. Hamid ◽  
S. A. Urhammer ◽  
D. P. Jensen ◽  
C. Glumer ◽  
K. Borch-Johnsen ◽  
...  

2000 ◽  
Vol 50 ◽  
pp. 130
Author(s):  
Olga Kolcowa ◽  
Elzbieta Orłowska-Kunikowska ◽  
Krzystof Narkiewicz ◽  
Anna Owczarzak ◽  
Wiesława Łysiak-Szydłowska

2016 ◽  
Vol 5 (1) ◽  
pp. 18 ◽  
Author(s):  
Mohammadreza Sharifi ◽  
Reza Ghavimi ◽  
MohammadAli Mohaghegh ◽  
Hossein Mohammadian ◽  
Saedeh Khadempar ◽  
...  

2020 ◽  
Author(s):  
Ada Admin ◽  
Marie Louise Johansen ◽  
Jaime Ibarrola ◽  
Amaya Fernández-Celis ◽  
Morten Schou ◽  
...  

Activation of the mineralocorticoid receptor (MR) may promote dysfunctional adipose tissue in patients with type 2 diabetes, where increased pericellular fibrosis has emerged as a major contributor. The knowledge of the association between the MR, fibrosis and the effects of an MR antagonist (MRA) in human adipocytes remains very limited. The present sub-study including 30 participants was prespecified as part of the Mineralocorticoid Receptor Antagonist in type 2 Diabetes (MIRAD) trial, randomizing patients to either high dose eplerenone or placebo for 26 weeks. In adipose tissue biopsies, changes in fibrosis were evaluated by immunohistological examinations and by the expression of mRNA and protein markers of fibrosis. Treatment with an MRA reduced pericellular fibrosis, synthesis of the major subunits of collagen type I and VI, and the profibrotic factor α-smooth muscle actin, as compared to placebo in subcutaneous adipose tissue. Furthermore, we found decreased expression of the MR and downstream molecules neutrophil gelatinase–associated lipocalin, galectin-3, and lipocalin-like prostaglandin D2 synthase with an MRA. In conclusions, we present original data demonstrating reduced fibrosis in adipose tissue with inhibition of the MR, which could be a potential therapeutic approach to prevent the extracellular matrix remodeling of adipose tissue in type 2 diabetes.


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