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Soluble urokinase plasminogen activator receptor, C ‐reactive protein and triglyceride are associated with heart rate variability in non‐diabetic Danes
Author(s) -
Intzilakis Theodoros,
Hartmann Gro,
Mouridsen Mette R.,
EugenOlsen Jesper,
Kumarathurai Preman,
Madsbad Sten,
Almdal Thomas P.,
Haugaard Steen B.,
Sajadieh Ahmed
Publication year - 2013
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1111/eci.12070
Subject(s) - medicine , heart rate variability , endocrinology , insulin resistance , triglyceride , diabetes mellitus , plasminogen activator , inflammation , c reactive protein , type 2 diabetes , plasminogen activator inhibitor 1 , heart rate , blood pressure , cholesterol
Background Heart rate variability ( HRV ) is associated with an increased risk of cardiovascular morbidity and mortality. HRV is in part a function of the activity of the autonomic nervous system and has been associated with low‐grade inflammation. In patients with type 2 diabetes, HRV is decreased and is a predictor of poor outcome. As HRV and its determinants in non‐diabetic individuals have not been studied properly, the aim of this observational study was to evaluate possible associations between HRV vs. impaired fasting glucose, insulin resistance, lipidaemia and markers of inflammation and immune activation in these individuals. Materials and methods Healthy individuals ( n = 596, 55–75 years) from the community were evaluated with ambulant 48‐h continuous electrocardiogram monitoring and fasting markers of lipidaemia, inflammation and immune activation, respectively. Insulin resistance was estimated by HOMA ‐ IR . Time domain components of HRV were calculated. Results Heart rate and HRV were not associated with glucose metabolic parameters but were inversely associated with soluble urokinase plasminogen activator receptor (su PAR ), high‐sensitive CRP and leucocyte number ( P < 0·001), respectively. Both 24‐h and night‐time HRV were inversely associated with plasma triglyceride, whereas HDL , LDL and total cholesterol were not. A model including su PAR , CRP , gender, triglyceride, age, systolic blood pressure, physical activity and smoking status explained 12·2% ( P < 0·0001) of the 24‐h HRV and 7·3% ( P < 0·0001) of the night‐time HRV . The single strongest factor to explain 24‐h and night‐time HRV appeared to be su PAR ( P = 0·001 and P = 0·0067, respectively). Conclusion A low HRV is not related to prediabetes, that is, insulin resistance and impaired fasting glucose, but is related to the immune and inflammatory markers su PAR and CRP and plasma triglyceride.