Excess of visceral adipose tissue with or without aortic elongation leads to a steeper heart position

2021 ◽  
pp. 028418512110340
Author(s):  
S Petteri Kauhanen ◽  
Petri Saari ◽  
Tarmo Korpela ◽  
Timo Liimatainen ◽  
Ritva Vanninen ◽  
...  

Background The heart’s position determined as the heart–aorta angle (HAA) has been demonstrated to associate with ascending aortic (AA) dilatation. Visceral adipose tissue (VAT) and aortic elongation may shift the heart to the steeper position. Purpose To investigate whether VAT and aortic length influence the HAA. Material and Methods We examined 346 consecutive patients (58.4% men; mean age = 67.0 ± 14.1 years) who underwent aortic computed tomography angiography (CTA). HAA was measured as the angle between the long axis of the heart and AA midline. The amount of VAT was measured at the level of middle L4 vertebra from a single axial CT slice. Aortic length was measured by combining four anatomical segments in different CTA images. The amount of VAT and aortic length were determined as mild with values in the lowest quartile and as excessive with values in the other three quartiles. Results A total of 191 patients (55.2%) had no history of aortic diseases, 134 (38.7%) displayed AA dilatation, 8 (2.3%) had abdominal aortic aneurysm (AAA), and 13 (3.8%) had both AA dilatation and AAA. There was a strong nonlinear regression between smaller HAA and VAT/height, and HAA and aortic length/height. Median HAA was 124.2° (interquartile range 119.0°–130.8°) in patients with a mild amount of VAT versus 120.5° (interquartile range 115.4°–124.7°) in patients with excessive VAT ( P < 0.001). Conclusion An excessive amount of VAT and aortic elongation led to a steeper heart position. These aspects may possess clinical value when evaluating aortic diseases in obese patients.

2017 ◽  
Vol 69 (11) ◽  
pp. 1436
Author(s):  
Koutagiar Peter Iosif ◽  
Konstantinos Toutouzas ◽  
Georgios Benetos ◽  
Nikoletta Piannou ◽  
Alexios Antonopoulos ◽  
...  

Metabolism ◽  
2011 ◽  
Vol 60 (12) ◽  
pp. 1775-1780 ◽  
Author(s):  
René Baudrand ◽  
José Miguel Domínguez ◽  
Cristian A. Carvajal ◽  
Arnoldo Riquelme ◽  
Carmen Campino ◽  
...  

2009 ◽  
Vol 104 (4) ◽  
pp. 543-547 ◽  
Author(s):  
Caroline S. Fox ◽  
Shih-Jen Hwang ◽  
Joseph M. Massaro ◽  
Kathrin Lieb ◽  
Ramachandran S. Vasan ◽  
...  

2019 ◽  
Vol 91 (3) ◽  
pp. 400-410 ◽  
Author(s):  
Judith Brock ◽  
Andreas Schmid ◽  
Thomas Karrasch ◽  
Petra Pfefferle ◽  
Jutta Schlegel ◽  
...  

2010 ◽  
Vol 20 (6) ◽  
pp. 831-831
Author(s):  
Cíntia dos Santos Costa ◽  
Thais Ortiz Hammes ◽  
Francieli Rohden ◽  
Rogério Margis ◽  
Josiane Woutheres Bortolotto ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Nicolas Linder ◽  
Alexander Schaudinn ◽  
Nikita Garnov ◽  
Matthias Blüher ◽  
Arne Dietrich ◽  
...  

2014 ◽  
Vol 46 ◽  
pp. 627-628
Author(s):  
Tamara E. Carver ◽  
Robert Bracewell ◽  
Olivier Babineau ◽  
Olivier Court ◽  
Ross E. Andersen

Author(s):  
Mark Colin Gissler ◽  
Nathaly Anto-Michel ◽  
Jan Pennig ◽  
Philipp Scherrer ◽  
Xiaowei Li ◽  
...  

Objective: The accumulation of inflammatory leukocytes is a prerequisite of adipose tissue inflammation during cardiometabolic disease. We previously reported that a genetic deficiency of the intracellular signaling adaptor TRAF5 (TNF [tumor necrosis factor] receptor–associated factor 5) accelerates atherosclerosis in mice by increasing inflammatory cell recruitment. Here, we tested the hypothesis that an impairment of TRAF5 signaling modulates adipose tissue inflammation and its metabolic complications in a model of diet-induced obesity in mice. Approach and Results: To induce diet-induced obesity and adipose tissue inflammation, wild-type or Traf5 −/− mice consumed a high-fat diet for 18 weeks. Traf5 −/− mice showed an increased weight gain, impaired insulin tolerance, and increased fasting blood glucose. Weight of livers and peripheral fat pads was increased in Traf5 −/− mice, whereas lean tissue weight and growth were not affected. Flow cytometry of the stromal vascular fraction of visceral adipose tissue from Traf5 −/− mice revealed an increase in cytotoxic T cells, CD11c + macrophages, and increased gene expression of proinflammatory cytokines and chemokines. At the level of cell types, expression of TNFα, MIP (macrophage inflammatory protein)-1α, MCP (monocyte chemoattractant protein)-1, and RANTES (regulated on activation, normal T-cell expressed and secreted) was significantly upregulated in Traf5 -deficient adipocytes but not in Traf5 -deficient leukocytes from visceral adipose tissue. Finally, Traf5 expression was lower in adipocytes from obese patients and mice and recovered in adipose tissue of obese patients one year after bariatric surgery. Conclusions: We show that a genetic deficiency of TRAF5 in mice diet-induced obesity and its metabolic derangements by a proinflammatory response in adipocytes. Our data indicate that TRAF5 may promote anti-inflammatory and obesity-preventing signaling events in adipose tissue.


2009 ◽  
Vol 20 (5) ◽  
pp. 633-639 ◽  
Author(s):  
Cíntia dos Santos Costa ◽  
Thais Ortiz Hammes ◽  
Francieli Rohden ◽  
Rogério Margis ◽  
Josiane Woutheres Bortolotto ◽  
...  

2007 ◽  
Vol 17 (7) ◽  
pp. 934-940 ◽  
Author(s):  
Josiane Woutheres Bortolotto ◽  
Rogério Margis ◽  
Ângela Cristine Bersch Ferreira ◽  
Alexandre Vontobel Padoin ◽  
Cláudio Cora Mottin ◽  
...  

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