Premium
Relationship between heart rate variability and carotid intima‐media thickness in the Brazilian Longitudinal Study of Adult Health – ELSA‐Brasil
Author(s) -
Hoshi Rosangela A.,
Santos Itamar S.,
Dantas Eduardo M.,
Andreão Rodrigo V.,
Mill José G.,
Goulart Alessandra C.,
Lotufo Paulo A.,
Bensenor Isabela
Publication year - 2020
Publication title -
clinical physiology and functional imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.608
H-Index - 67
eISSN - 1475-097X
pISSN - 1475-0961
DOI - 10.1111/cpf.12613
Subject(s) - medicine , heart rate variability , quartile , percentile , cardiology , intima media thickness , anthropometry , subclinical infection , logistic regression , heart rate , carotid arteries , blood pressure , confidence interval , statistics , mathematics
Summary Background Both increased carotid intima‐media thickness (cIMT) and low heart rate variability (HRV) have been associated with cardiovascular mortality and morbidity. Thus, the aim of this study was to investigate whether cardio autonomic alterations are accompanied or not by subclinical atherosclerosis in participants of the Brazilian Longitudinal Study of Adult Health (ELSA‐Brasil). Methods cIMT measures and 5‐min HRV analyses were performed in apparently healthy adults. Heart rate variability was evaluated by linear time and frequency domain analyses. cIMT was defined as the average between the mean left and mean right cIMT values and was analysed as continuous and categorized variables ( P ≥75 or P <75). Multiple linear models using continuous variables and multivariate logistic regression with categorized cIMT and HRV quartiles were performed. Results Out of 7256 participants eligible for analyses, 23·4% presented cIMT ≥ 75th percentile. Heart rate variability variables were reduced in cIMT ≥ P75 in comparison with cIMT < P75: SDNN 33·0 versus 37·0 ms, P <0·001; RMSSD 22·0 versus 26·0 ms, P <0·001; LF 191·0 versus 260·0 ms 2 , P <0·001; HF 164·0 versus 238·5 ms 2 , P <0·001. In crude analysis, an increased odds ratio for cIMT ≥ P75 was verified within the lowest two quartiles of LF and HF, but significances did not remain after adjustments for anthropometric and clinical variables. Conclusions Considering the entire sample, subjects with cIMT ≥ P75 presented lower HRV values, but no independent relationships were detected between cIMT and HRV after multivariate adjustment.