Cargando…
Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury
Background: Heart rate variability (HRV), the physiological variance in the heart's R-R interval length, can be analyzed to produce various parameters reflective of one's autonomic balance. HRV analysis may be used to capture those autonomic aberrations associated with chronic neuropathic...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513934/ https://www.ncbi.nlm.nih.gov/pubmed/28769815 http://dx.doi.org/10.3389/fphys.2017.00495 |
_version_ | 1783250741469642752 |
---|---|
author | Karri, Jay Zhang, Larry Li, Shengai Chen, Yen-Ting Stampas, Argyrios Li, Sheng |
author_facet | Karri, Jay Zhang, Larry Li, Shengai Chen, Yen-Ting Stampas, Argyrios Li, Sheng |
author_sort | Karri, Jay |
collection | PubMed |
description | Background: Heart rate variability (HRV), the physiological variance in the heart's R-R interval length, can be analyzed to produce various parameters reflective of one's autonomic balance. HRV analysis may be used to capture those autonomic aberrations associated with chronic neuropathic pain (NP) in spinal cord injury (SCI). This study assesses the capacity of HRV parameters to diagnose NP in an SCI cohort. Methods: An electrocardiogram (ECG) was collected at rest from able bodied participants (AB, n = 15), participants with SCI only (SCI-NP, n = 11), and those with SCI and NP (SCI+NP, n = 20). HRV parameters were analyzed using conventional time and frequency analysis. Results: At rest, there were no heart rate differences amongst groups. However, SCI+NP participants demonstrated lower overall HRV, as determined by the SDNN time domain parameter, compared to either AB (p < 0.01) or SCI-NP (p < 0.05) groups. Moreover, AB and SCI-NP participants were statistically comparable for all HRV time and frequency domain parameters. Additional analyses demonstrated no differences in HRV parameters between T4, above vs. T5, below SCI groups (for all parameters: p > 0.15) or between C8, above vs. T1, below SCI groups (p > 0.30). Conclusions: Participants with SCI and NP exhibit a lower overall HRV, which can be determined by HRV time domain parameter SDNN. HRV analysis is an innovative modality with the capacity for objective quantification of chronic NP in participants with SCI. |
format | Online Article Text |
id | pubmed-5513934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55139342017-08-02 Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury Karri, Jay Zhang, Larry Li, Shengai Chen, Yen-Ting Stampas, Argyrios Li, Sheng Front Physiol Physiology Background: Heart rate variability (HRV), the physiological variance in the heart's R-R interval length, can be analyzed to produce various parameters reflective of one's autonomic balance. HRV analysis may be used to capture those autonomic aberrations associated with chronic neuropathic pain (NP) in spinal cord injury (SCI). This study assesses the capacity of HRV parameters to diagnose NP in an SCI cohort. Methods: An electrocardiogram (ECG) was collected at rest from able bodied participants (AB, n = 15), participants with SCI only (SCI-NP, n = 11), and those with SCI and NP (SCI+NP, n = 20). HRV parameters were analyzed using conventional time and frequency analysis. Results: At rest, there were no heart rate differences amongst groups. However, SCI+NP participants demonstrated lower overall HRV, as determined by the SDNN time domain parameter, compared to either AB (p < 0.01) or SCI-NP (p < 0.05) groups. Moreover, AB and SCI-NP participants were statistically comparable for all HRV time and frequency domain parameters. Additional analyses demonstrated no differences in HRV parameters between T4, above vs. T5, below SCI groups (for all parameters: p > 0.15) or between C8, above vs. T1, below SCI groups (p > 0.30). Conclusions: Participants with SCI and NP exhibit a lower overall HRV, which can be determined by HRV time domain parameter SDNN. HRV analysis is an innovative modality with the capacity for objective quantification of chronic NP in participants with SCI. Frontiers Media S.A. 2017-07-18 /pmc/articles/PMC5513934/ /pubmed/28769815 http://dx.doi.org/10.3389/fphys.2017.00495 Text en Copyright © 2017 Karri, Zhang, Li, Chen, Stampas and Li. 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 | Physiology Karri, Jay Zhang, Larry Li, Shengai Chen, Yen-Ting Stampas, Argyrios Li, Sheng Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury |
title | Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury |
title_full | Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury |
title_fullStr | Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury |
title_full_unstemmed | Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury |
title_short | Heart Rate Variability: A Novel Modality for Diagnosing Neuropathic Pain after Spinal Cord Injury |
title_sort | heart rate variability: a novel modality for diagnosing neuropathic pain after spinal cord injury |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513934/ https://www.ncbi.nlm.nih.gov/pubmed/28769815 http://dx.doi.org/10.3389/fphys.2017.00495 |
work_keys_str_mv | AT karrijay heartratevariabilityanovelmodalityfordiagnosingneuropathicpainafterspinalcordinjury AT zhanglarry heartratevariabilityanovelmodalityfordiagnosingneuropathicpainafterspinalcordinjury AT lishengai heartratevariabilityanovelmodalityfordiagnosingneuropathicpainafterspinalcordinjury AT chenyenting heartratevariabilityanovelmodalityfordiagnosingneuropathicpainafterspinalcordinjury AT stampasargyrios heartratevariabilityanovelmodalityfordiagnosingneuropathicpainafterspinalcordinjury AT lisheng heartratevariabilityanovelmodalityfordiagnosingneuropathicpainafterspinalcordinjury |