Cargando…

Diminution of Heart Rate Variability in Bipolar Depression

Autonomic nervous system (ANS) dysregulation in depression is associated with symptoms associated with the ANS. The beat-to-beat pattern of heart rate defined as heart rate variability (HRV) provides a noninvasive portal to ANS function and has been proposed to represent a means of quantifying resti...

Descripción completa

Detalles Bibliográficos
Autores principales: Hage, Brandon, Britton, Briana, Daniels, David, Heilman, Keri, Porges, Stephen W., Halaris, Angelos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723669/
https://www.ncbi.nlm.nih.gov/pubmed/29270399
http://dx.doi.org/10.3389/fpubh.2017.00312
_version_ 1783285253667815424
author Hage, Brandon
Britton, Briana
Daniels, David
Heilman, Keri
Porges, Stephen W.
Halaris, Angelos
author_facet Hage, Brandon
Britton, Briana
Daniels, David
Heilman, Keri
Porges, Stephen W.
Halaris, Angelos
author_sort Hage, Brandon
collection PubMed
description Autonomic nervous system (ANS) dysregulation in depression is associated with symptoms associated with the ANS. The beat-to-beat pattern of heart rate defined as heart rate variability (HRV) provides a noninvasive portal to ANS function and has been proposed to represent a means of quantifying resting vagal tone. We quantified HRV in bipolar depressed (BDD) patients as a measure of ANS dysregulation seeking to establish HRV as a potential diagnostic and prognostic biomarker for treatment outcome. Forty-seven BDD patients were enrolled. They were randomized to receive either escitalopram–celecoxib or escitalopram-placebo over 8 weeks in a double-blind study design. Thirty-five patients completed the HRV studies. Thirty-six healthy subjects served as controls. HRV was assessed at pretreatment and end of study and compared with that of controls. HRV was quantified and corrected for artifacts using an algorithm that incorporates time and frequency domains to address non-stationarity of the beat-to-beat heart rate pattern. Baseline high frequency-HRV (i.e., respiratory sinus arrhythmia) was lower in BDD patients than controls, although the difference did not reach significance. Baseline low-frequency HRV was significantly lower in BDD patients (ln4.20) than controls (ln = 5.50) (p < 0.01). Baseline heart period was significantly shorter (i.e., faster heart rate) in BDD patients than controls. No significant change in HRV parameters were detected over the course of the study with either treatment. These findings suggest that components of HRV may be diminished in BDD patients.
format Online
Article
Text
id pubmed-5723669
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57236692017-12-21 Diminution of Heart Rate Variability in Bipolar Depression Hage, Brandon Britton, Briana Daniels, David Heilman, Keri Porges, Stephen W. Halaris, Angelos Front Public Health Public Health Autonomic nervous system (ANS) dysregulation in depression is associated with symptoms associated with the ANS. The beat-to-beat pattern of heart rate defined as heart rate variability (HRV) provides a noninvasive portal to ANS function and has been proposed to represent a means of quantifying resting vagal tone. We quantified HRV in bipolar depressed (BDD) patients as a measure of ANS dysregulation seeking to establish HRV as a potential diagnostic and prognostic biomarker for treatment outcome. Forty-seven BDD patients were enrolled. They were randomized to receive either escitalopram–celecoxib or escitalopram-placebo over 8 weeks in a double-blind study design. Thirty-five patients completed the HRV studies. Thirty-six healthy subjects served as controls. HRV was assessed at pretreatment and end of study and compared with that of controls. HRV was quantified and corrected for artifacts using an algorithm that incorporates time and frequency domains to address non-stationarity of the beat-to-beat heart rate pattern. Baseline high frequency-HRV (i.e., respiratory sinus arrhythmia) was lower in BDD patients than controls, although the difference did not reach significance. Baseline low-frequency HRV was significantly lower in BDD patients (ln4.20) than controls (ln = 5.50) (p < 0.01). Baseline heart period was significantly shorter (i.e., faster heart rate) in BDD patients than controls. No significant change in HRV parameters were detected over the course of the study with either treatment. These findings suggest that components of HRV may be diminished in BDD patients. Frontiers Media S.A. 2017-12-06 /pmc/articles/PMC5723669/ /pubmed/29270399 http://dx.doi.org/10.3389/fpubh.2017.00312 Text en Copyright © 2017 Hage, Britton, Daniels, Heilman, Porges and Halaris. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Hage, Brandon
Britton, Briana
Daniels, David
Heilman, Keri
Porges, Stephen W.
Halaris, Angelos
Diminution of Heart Rate Variability in Bipolar Depression
title Diminution of Heart Rate Variability in Bipolar Depression
title_full Diminution of Heart Rate Variability in Bipolar Depression
title_fullStr Diminution of Heart Rate Variability in Bipolar Depression
title_full_unstemmed Diminution of Heart Rate Variability in Bipolar Depression
title_short Diminution of Heart Rate Variability in Bipolar Depression
title_sort diminution of heart rate variability in bipolar depression
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723669/
https://www.ncbi.nlm.nih.gov/pubmed/29270399
http://dx.doi.org/10.3389/fpubh.2017.00312
work_keys_str_mv AT hagebrandon diminutionofheartratevariabilityinbipolardepression
AT brittonbriana diminutionofheartratevariabilityinbipolardepression
AT danielsdavid diminutionofheartratevariabilityinbipolardepression
AT heilmankeri diminutionofheartratevariabilityinbipolardepression
AT porgesstephenw diminutionofheartratevariabilityinbipolardepression
AT halarisangelos diminutionofheartratevariabilityinbipolardepression