Literature DB >> 26475583

Plasma levels of microRNA in chronic kidney disease: patterns in acute and chronic exercise.

Amaryllis H Van Craenenbroeck1, Kristien J Ledeganck2, Katrijn Van Ackeren3, Angelika Jürgens2, Vicky Y Hoymans4, Erik Fransen5, Volker Adams6, Benedicte Y De Winter2, Gert A Verpooten2, Christiaan J Vrints4, Marie M Couttenye7, Emeline M Van Craenenbroeck4.   

Abstract

Exercise training is an effective way to improve exercise capacity in chronic kidney disease (CKD), but the underlying mechanisms are only partly understood. In healthy subjects (HS), microRNA (miRNA or miR) are dynamically regulated following exercise and have, therefore, been suggested as regulators of cardiovascular adaptation to exercise. However, these effects were not studied in CKD before. The effect of acute exercise (i.e., an acute exercise bout) was assessed in 32 patients with CKD and 12 age- and sex-matched HS (study 1). miRNA expression in response to chronic exercise (i.e., a 3-mo exercise training program) was evaluated in 40 CKD patients (study 2). In a subgroup of study 2, the acute-exercise induced effect was evaluated at baseline and at follow-up. Plasma levels of a preselected panel miRNA, involved in exercise adaptation processes such as angiogenesis (miR-126, miR-210), inflammation (miR-21, miR-146a), hypoxia/ischemia (miR-21, miR-210), and progenitor cells (miR-150), were quantified by RT-PCR. Additionally, seven miRNA involved in similar biological processes were quantified in the subgroup of study 2. Baseline, studied miRNA were comparable in CKD and HS. Following acute exercise, miR-150 levels increased in both CKD (fold change 2.12 ± 0.39, P = 0.002; and HS: fold change 2.41 ± 0.48 P = 0.018, P for interaction > 0.05). miR-146a acutely decreased in CKD (fold change 0.92 ± 0.13, P = 0.024), whereas it remained unchanged in HS. Levels of miR-21, miR-126, and miR-210 remained unaltered. Chronic exercise did not elicit a significant change in the studied miRNA levels. However, an acute exercise-induced decrease in miR-210 was observed in CKD patients, only after training (fold change 0.76 ± 0.15). The differential expression in circulating miRNA in response to acute and chronic exercise may point toward a physiological role in cardiovascular adaptation to exercise, also in CKD.
Copyright © 2015 the American Physiological Society.

Entities:  

Keywords:  acute exercise; chronic kidney disease; exercise training; microRNA

Mesh:

Substances:

Year:  2015        PMID: 26475583      PMCID: PMC4698424          DOI: 10.1152/ajpheart.00346.2015

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  50 in total

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Review 7.  Heart Failure With Preserved Ejection Fraction: A Review of Cardiac and Noncardiac Pathophysiology.

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