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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Age and Sex Differences in Heart Rate Variability and Vagal Specific Patterns - Baependi Heart Study

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Author(s):
Geovanini, Glaucylara Reis [1] ; Vasques, Enio Rodrigues [2] ; Alvim, Rafael de Oliveira [3] ; Mill, Jose Geraldo [4] ; Andreao, Rodrigo Varejao [5] ; Vasques, Bruna Kim [6] ; Pereira, Alexandre Costa [1] ; Krieger, Jose Eduardo [1]
Total Authors: 8
Affiliation:
[1] Univ Sao Paulo, Med Sch, InCor Heart Inst, Lab Genet & Mol Cardiol, Sao Paulo - Brazil
[2] Univ Sao Paulo, Med Sch, Lab Med Invest LIM 37, Sao Paulo - Brazil
[3] Univ Fed Espirito Santo, Postgrad Program Publ Hlth, Vitoria, ES - Brazil
[4] Univ Fed Espirito Santo, Hlth Sci Ctr, Dept Physiol Sci, Vitoria, ES - Brazil
[5] Fed Inst Espirito Santo, Dept Elect Engn, Vitoria, ES - Brazil
[6] Univ Anhembi Morumbi, Med Sch, Sao Paulo - Brazil
Total Affiliations: 6
Document type: Journal article
Source: GLOBAL HEART; v. 15, n. 1 2020.
Web of Science Citations: 0
Abstract

Background: Heart rate variability (HRV) is a noninvasive method for assessing autonomic function. Age, sex, and chronic conditions influence HRV. Objectives: Our aim was to evaluate HRV measures exploring differences by age, sex, and race in a sample from a rural area. Methods: Analytical sample (n = 1,287) included participants from the 2010 to 2016 evaluation period of the Baependi Heart Study, a family-based cohort in Brazil. Participants underwent 24-hour Holter-ECG (Holter) monitoring. To derive population reference values, we restricted our analysis to a `healthy' subset (i.e. absence of medical comorbidities). A confirmatory analysis was conducted with a subgroup sample that also had HRV derived from a resting ECG 10'-protocol obtained during the same time period. Results: The `healthy' subset included 543 participants. Mean age was 40 +/- 14y, 41% were male, 74% self-referred as white and mean body-mass-index was 24 +/- 3kg/m(2). Time domain HRV measures showed significant differences by age-decade and by sex. Higher values were observed for males across almost all age-groups. Parasympathetic associated variables (rMSSD and pNN50) showed a U-shaped distribution and reversal increase above 60y. Sympathetic-parasympathetic balance variables (SDNN, SDANN) decreased linearly by age. Race differences were no significant. We compared time domain variables with complete data (Holter and resting ECG) between `healthy' versus `unhealthy' groups. Higher HRV values were shown for the `healthy' subset compared with the `unhealthy' group. Conclusion: HRV measures vary across age and sex. A U-shaped pattern and a reversal increase in parasympathetic variables may reflect an age-related autonomic dysfunction even in healthy individuals that could be used as a predictor of disease development. (AU)

FAPESP's process: 13/17368-0 - Cardiovascular genomics: mechanisms & novel therapeutics - CVGen mech2ther
Grantee:José Eduardo Krieger
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 11/05804-5 - Phenotypic characterization of circadian rhythms in different genotype individuals for clock gene polymorphisms in different regions in Brazil: an emphasis on the effect of the gene PER3 and latitude
Grantee:Mario Pedrazzoli Neto
Support Opportunities: Regular Research Grants