Pattern of coronary artery disease in patients with ventricular tachycardia and fibrillation exposed by exercise-induced ischemia

1995 ◽  
Vol 129 (4) ◽  
pp. 733-738 ◽  
Author(s):  
Rolf Franck Berntsen ◽  
Pål Gunnes ◽  
Knut Rasmussen
1986 ◽  
Vol 27 (4) ◽  
pp. 443-460 ◽  
Author(s):  
Mitsuhiro YOKOTA ◽  
Shoji NODA ◽  
Masafumi KOIDE ◽  
Naoki KAWAI ◽  
Reiki YOSHIDA ◽  
...  

1993 ◽  
Vol 95 (1) ◽  
pp. 23-28 ◽  
Author(s):  
Robert M. Carney ◽  
Kenneth E. Freedland ◽  
Michael W. Rich ◽  
Laurie J. Smith ◽  
Allan S. Jaffe

1992 ◽  
Vol 123 (1) ◽  
pp. 82-89 ◽  
Author(s):  
Teresa Kus ◽  
Maria Aurora Campa ◽  
Réginald Nadeau ◽  
Marc Dubuc ◽  
Wilhelm Kaltenbrunner ◽  
...  

Author(s):  
Barbara Mayr ◽  
Edith E. Müller ◽  
Christine Schäfer ◽  
Silke Droese ◽  
Martin Schönfelder ◽  
...  

Abstract Objectives Micro ribonucleic acids (miRNAs) are small non-coding RNA molecules that control gene expression by translational inhibition. Exercise has been shown to affect several miRNAs’ expression in healthy subjects, but this has not yet been studied in patients with coronary artery disease (CAD). Since exercise training confers beneficial long-term effects and may also trigger acute coronary events, it is of utmost interest to be able to identify those who are risk for untoward effects. Therefore, we set out to assess miRNA expression in response to maximal ergospirometry in patients with CAD. Methods Total RNA was extracted from blood drawn immediately before and 5 min after maximal cycle-ergospirometry (10 male and 10 female CAD patients). A qRT-PCR was performed for 187 target miRNAs associated with endothelial function/dysfunction, cardiovascular disease, myocardial infarction, and sudden cardiac death. Results In response to a maximal ergospirometry, 33 miRNAs significantly changed their expression levels. Of these miRNAs 16 were significantly differently expressed between gender. Using multi-variance analysis, nine miRNAs (let-7e-5p; miR-1; miR-19b-1-5p; miR-103a-3p; miR-148b-3p; miR-181b-5p; miR-188-5p; miR-423-5p; miR-874-3p) showed significantly different responses to maximal ergospirometry between genders. Conclusions We report for the first time that in patients with CAD, miRNA expression is amenable to maximal ergospirometry and that the extent of changes differs between genders. Affected by exercise and gender were miRNAs that are associated, among others, with pathways for glucose metabolism, oxidative stress, and angiogenesis. Future studies should assess whether disease-specific miRNA expression in response to maximal exercise might serve as a marker for patient outcome.


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