scholarly journals P1690Diminished macrophage cholesterol efflux mediated by HDL and coronary artery disease in young male anabolic androgenic steroid users

2018 ◽  
Vol 39 (suppl_1) ◽  
Author(s):  
F R Souza ◽  
M R Santos ◽  
R A Porello ◽  
G W P Fonseca ◽  
A L C Sayegh ◽  
...  
2019 ◽  
Vol 283 ◽  
pp. 100-105 ◽  
Author(s):  
Francis Ribeiro de Souza ◽  
Marcelo Rodrigues Dos Santos ◽  
Rafael Armani Porello ◽  
Guilherme Wesley Peixoto da Fonseca ◽  
Ana Luiza Carrari Sayegh ◽  
...  

Heart ◽  
2012 ◽  
Vol 98 (Suppl 2) ◽  
pp. E152.1-E152
Author(s):  
Wei Song ◽  
Li-Yang Dou ◽  
Wei Wang ◽  
Yu Wang ◽  
Lian-Feng Chen ◽  
...  

The Lancet ◽  
1996 ◽  
Vol 347 (9005) ◽  
pp. 849-853 ◽  
Author(s):  
C-G Ericsson ◽  
U de Faire ◽  
L Grip ◽  
B Svane ◽  
A Hamsten ◽  
...  

Author(s):  
Luciana Uint ◽  
Andrei Sposito ◽  
Laura Ines Ventura Brandizzi ◽  
Vanda Mitie Yoshida ◽  
Raul Cavalcante Maranhão ◽  
...  

Circulation ◽  
2015 ◽  
Vol 131 (suppl_1) ◽  
Author(s):  
Tina Costacou ◽  
Jay W Heinecke ◽  
Tomas Vaisar ◽  
Trevor J Orchard

Background: The Hp 2-2 genotype has been associated with increased cardiovascular risk in type 2 diabetes, potentially relating to dysfunctional HDL mediated cholesterol efflux. We have shown that the Hp 2 allele predicts the development of both coronary artery disease (CAD) and kidney dysfunction also in childhood onset type 1 diabetes over 18 years of follow-up in the Epidemiology of Diabetes Complications (EDC) study. We now present results on the Hp-CAD association after an additional 7 year follow-up and Hp’s relation to impaired sterol efflux capacity, a proposed cardioprotective effect of HDL. Methods: Participants free of CAD at baseline and with Hp determined were studied (n=565; mean age, 27 and duration, 19 years; 11.5% Hp 1-1, 42.5% Hp 2-2). CAD was defined as EDC physician diagnosed angina, ischemic ECG changes (MC 1.3, 4.1-4.3, 5.1-5.3, 7.1), confirmed MI (MC 1.1, 1.2 or validated medical records), stenosis >50%, revascularization or CAD death. In a pilot study, serum HDL sterol efflux was assessed in Mifepristone stimulated ABCA1-BHK cells among 20 individuals (6 Hp 1-1; 7 Hp 2-1; 7 Hp 2-2) attending the 25 year exam. Results: During follow-up, 186 (32.9%) developed CAD. Incidence increased with the number of Hp 2 alleles (24.6% in Hp 1-1, 31.1% in Hp 2-1 and 37.1% in Hp 2-2, p-trend=0.04; Fig. 1). Multivariably, Hp 2-2 significantly increased risk by almost 80% (HR=1.79, 1.03-3.09). The risk associated with Hp 2-1 did not reach significance (HR=1.46, 0.85-2.53). In the pilot study, serum HDL sterol efflux was lower in Hp 2 allele carriers: 14.0% in Hp 1-1, 12.5% in Hp 2-1, 12.4% in Hp 2-2, p-trend=0.06, p-value Hp 1-1 vs Hp 2-1/2-2 =0.04. Conclusion: These results extend our previous findings of increased CAD risk associated with the Hp 2 allele in type 1 diabetes and further suggest that this allele associates with impaired sterol efflux capacity. These results support the hypothesis that sterol efflux explains the increased Hp 2 risk for CAD and should be confirmed prospectively. Figure 1. CAD-free survival curves by Hp genotype


2016 ◽  
Vol 117 (4) ◽  
pp. 508-514 ◽  
Author(s):  
Jianhua Zhang ◽  
Jia Xu ◽  
Jingfeng Wang ◽  
Changhao Wu ◽  
Yan Xu ◽  
...  

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