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Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population

BACKGROUND: Heart rate variability (HRV) and baroreflex sensitivity (BRS) measurements provide means for the objective assessment of cardiovascular autonomic function. As previous studies have associated chronic pain with abnormal autonomic function, we aimed to characterize the relationship between...

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Autores principales: Oura, Petteri, Hautala, Arto, Kiviniemi, Antti, Auvinen, Juha, Puukka, Katri, Tulppo, Mikko, Huikuri, Heikki, Seppänen, Tapio, Karppinen, Jaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357438/
https://www.ncbi.nlm.nih.gov/pubmed/30704437
http://dx.doi.org/10.1186/s12891-019-2426-2
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author Oura, Petteri
Hautala, Arto
Kiviniemi, Antti
Auvinen, Juha
Puukka, Katri
Tulppo, Mikko
Huikuri, Heikki
Seppänen, Tapio
Karppinen, Jaro
author_facet Oura, Petteri
Hautala, Arto
Kiviniemi, Antti
Auvinen, Juha
Puukka, Katri
Tulppo, Mikko
Huikuri, Heikki
Seppänen, Tapio
Karppinen, Jaro
author_sort Oura, Petteri
collection PubMed
description BACKGROUND: Heart rate variability (HRV) and baroreflex sensitivity (BRS) measurements provide means for the objective assessment of cardiovascular autonomic function. As previous studies have associated chronic pain with abnormal autonomic function, we aimed to characterize the relationship between the number of musculoskeletal pain sites (NPS), pain intensity, and cardiovascular autonomic function among the population-based Northern Finland Birth Cohort 1966. METHODS: At the age of 46, cohort members self-reported their musculoskeletal pains (enabling the determination of NPS [0–8] and pain intensity [Numerical Rating Scale, NRS, 0–10]) and underwent clinical assessments of cardiovascular autonomic function in seated and standing positions (HRV variables: heart rate [HR] and root mean square of successive differences in beat-to-beat intervals [rMSSD] for the entire cohort; BRS variables: low-frequency systolic blood pressure variability [SBPV] and cross-spectral baroreflex sensitivity [BRS] for those attending the examination in Oulu, Finland). Extensive confounder data were also collected (body mass index, physical activity, smoking, Hopkins Symptom Checklist-25, comorbidities, and medications). The full samples included 4186 and 2031 individuals (HRV and BRS samples, respectively). Three subanalyses focused on individuals with intense and frequent pain, individuals with symptoms of depression and anxiety, and the relationship between pain intensity and autonomic parameters. RESULTS: Linear regression models showed varying associations between NPS, pain intensity, and cardiovascular autonomic parameters. However, after all adjustments NPS was only associated with one outcome among women (BRS, standing: beta = − 0.015, p = 0.048) and two among men (HR, seated: beta = − 0.902, p = 0.003; HR, standing: beta = − 0.843, p = 0.014). Pain intensity was not associated with any outcome after full adjustments. Significant sex*pain interactions were found in the data. CONCLUSIONS: Our data suggest that musculoskeletal pain has, at most, a limited independent association with cardiovascular autonomic function. Future studies should carefully account for the potential confounders and sex interactions that this study revealed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12891-019-2426-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-63574382019-02-07 Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population Oura, Petteri Hautala, Arto Kiviniemi, Antti Auvinen, Juha Puukka, Katri Tulppo, Mikko Huikuri, Heikki Seppänen, Tapio Karppinen, Jaro BMC Musculoskelet Disord Research Article BACKGROUND: Heart rate variability (HRV) and baroreflex sensitivity (BRS) measurements provide means for the objective assessment of cardiovascular autonomic function. As previous studies have associated chronic pain with abnormal autonomic function, we aimed to characterize the relationship between the number of musculoskeletal pain sites (NPS), pain intensity, and cardiovascular autonomic function among the population-based Northern Finland Birth Cohort 1966. METHODS: At the age of 46, cohort members self-reported their musculoskeletal pains (enabling the determination of NPS [0–8] and pain intensity [Numerical Rating Scale, NRS, 0–10]) and underwent clinical assessments of cardiovascular autonomic function in seated and standing positions (HRV variables: heart rate [HR] and root mean square of successive differences in beat-to-beat intervals [rMSSD] for the entire cohort; BRS variables: low-frequency systolic blood pressure variability [SBPV] and cross-spectral baroreflex sensitivity [BRS] for those attending the examination in Oulu, Finland). Extensive confounder data were also collected (body mass index, physical activity, smoking, Hopkins Symptom Checklist-25, comorbidities, and medications). The full samples included 4186 and 2031 individuals (HRV and BRS samples, respectively). Three subanalyses focused on individuals with intense and frequent pain, individuals with symptoms of depression and anxiety, and the relationship between pain intensity and autonomic parameters. RESULTS: Linear regression models showed varying associations between NPS, pain intensity, and cardiovascular autonomic parameters. However, after all adjustments NPS was only associated with one outcome among women (BRS, standing: beta = − 0.015, p = 0.048) and two among men (HR, seated: beta = − 0.902, p = 0.003; HR, standing: beta = − 0.843, p = 0.014). Pain intensity was not associated with any outcome after full adjustments. Significant sex*pain interactions were found in the data. CONCLUSIONS: Our data suggest that musculoskeletal pain has, at most, a limited independent association with cardiovascular autonomic function. Future studies should carefully account for the potential confounders and sex interactions that this study revealed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12891-019-2426-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-31 /pmc/articles/PMC6357438/ /pubmed/30704437 http://dx.doi.org/10.1186/s12891-019-2426-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Oura, Petteri
Hautala, Arto
Kiviniemi, Antti
Auvinen, Juha
Puukka, Katri
Tulppo, Mikko
Huikuri, Heikki
Seppänen, Tapio
Karppinen, Jaro
Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population
title Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population
title_full Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population
title_fullStr Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population
title_full_unstemmed Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population
title_short Musculoskeletal pains and cardiovascular autonomic function in the general Northern Finnish population
title_sort musculoskeletal pains and cardiovascular autonomic function in the general northern finnish population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357438/
https://www.ncbi.nlm.nih.gov/pubmed/30704437
http://dx.doi.org/10.1186/s12891-019-2426-2
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