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Extreme exercise enhances chromogranin A levels correlating with stress levels but not with cardiac burden
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4399376
Author(s) Nickel, T.; Vogeser, M.; Emslander, I.; David, R.; Heilmeier, B.; op den Winkel, M.; Schmidt-Trucksäss, A.; Wilbert-Lampen, U.; Hanssen, Henner; Halle, M.
Author(s) at UniBasel Hanssen, Henner
Year 2012
Title Extreme exercise enhances chromogranin A levels correlating with stress levels but not with cardiac burden
Journal Atherosclerosis
Volume 220
Number 1
Pages / Article-Number 219-222
Mesh terms Adiposity; Biomarkers, blood; Chromogranin A, blood; Enzyme-Linked Immunosorbent Assay; Germany; Heart Rate; Humans; Natriuretic Peptide, Brain, blood; Obesity, physiopathology; Physical Endurance; Physical Fitness; Running; Stress, Physiological; Time Factors; Troponin T, blood; Up-Regulation
Abstract OBJECTIVE: Stress and heart failure are associated with increased systemic levels of chromogranin A (CGA). Here we analyzed the effects of marathon running on systemic CGA levels and the association with cardiac burden and stress. METHODS: We recruited 47 lean and obese runners for a 10week training program aiming at running a marathon. Heart rates, individual fitness and marathon finishing times were monitored. CGA, proBNP and troponin T levels were analyzed by ELISA. RESULTS: We found a significant increase of CGA (+51%; p<0.01) in lean runners after marathon. The obese group showed the highest troponin T (0.22ng/ml; p<0.01) and proBNP (176.6ng/ml; p<0.01) levels. There were no correlations between proBNP, troponin T and CGA. An inverse correlation (r=-0.45; p<0.01) was found between CGA and finishing times. CONCLUSION: Marathon running is associated with increased CGA levels. However, this does not seem to reflect cardiac burden but rather marathon induced stress.
Publisher Elsevier
ISSN/ISBN 0021-9150 ; 1879-1484
edoc-URL https://edoc.unibas.ch/62272/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.atherosclerosis.2011.09.036
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/22035982
ISI-Number WOS:000298374800037
Document type (ISI) Article
 
   

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