Conditioned pain modulation and pain sensitivity in functional somatic disorders: The DanFunD study

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Standard

Conditioned pain modulation and pain sensitivity in functional somatic disorders : The DanFunD study. / Petersen, Marie Weinreich; Skovbjerg, Sine; Jensen, Jens Søndergaard; Carstensen, Tina Birgitte Wisbech; Dantoft, Thomas Meinertz; Fink, Per; Benros, Michael Eriksen; Mortensen, Erik Lykke; Jørgensen, Torben; Gormsen, Lise Kirstine.

In: European Journal of Pain, Vol. 26, No. 1, 2021, p. 154-166.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Petersen, MW, Skovbjerg, S, Jensen, JS, Carstensen, TBW, Dantoft, TM, Fink, P, Benros, ME, Mortensen, EL, Jørgensen, T & Gormsen, LK 2021, 'Conditioned pain modulation and pain sensitivity in functional somatic disorders: The DanFunD study', European Journal of Pain, vol. 26, no. 1, pp. 154-166. https://doi.org/10.1002/ejp.1847

APA

Petersen, M. W., Skovbjerg, S., Jensen, J. S., Carstensen, T. B. W., Dantoft, T. M., Fink, P., Benros, M. E., Mortensen, E. L., Jørgensen, T., & Gormsen, L. K. (2021). Conditioned pain modulation and pain sensitivity in functional somatic disorders: The DanFunD study. European Journal of Pain, 26(1), 154-166. https://doi.org/10.1002/ejp.1847

Vancouver

Petersen MW, Skovbjerg S, Jensen JS, Carstensen TBW, Dantoft TM, Fink P et al. Conditioned pain modulation and pain sensitivity in functional somatic disorders: The DanFunD study. European Journal of Pain. 2021;26(1): 154-166. https://doi.org/10.1002/ejp.1847

Author

Petersen, Marie Weinreich ; Skovbjerg, Sine ; Jensen, Jens Søndergaard ; Carstensen, Tina Birgitte Wisbech ; Dantoft, Thomas Meinertz ; Fink, Per ; Benros, Michael Eriksen ; Mortensen, Erik Lykke ; Jørgensen, Torben ; Gormsen, Lise Kirstine. / Conditioned pain modulation and pain sensitivity in functional somatic disorders : The DanFunD study. In: European Journal of Pain. 2021 ; Vol. 26, No. 1. pp. 154-166.

Bibtex

@article{aa8f2d3a287b4edc8e3093f50c498bb3,
title = "Conditioned pain modulation and pain sensitivity in functional somatic disorders: The DanFunD study",
abstract = "Background Disrupted pain regulation has been proposed as a component in functional somatic disorders (FSD). The objective of this study was to examine a general population sample, encompassing three delimitations of FSD while assessing pain sensitivity and conditioning pain modulation (CPM). Methods Pressure pain thresholds (PPTs) at the tibialis and trapezius muscles were recorded at baseline. During cold pressor stimulation of the hand, the tibialis PPTs were re-assessed and the difference from baseline measures defined the CPM effect. Participants (n = 2,198, 53% females) were randomly selected from the adult Danish population. FSD was established by self-reported symptom questionnaires. Results With a few exceptions, only weak associations were seen between PPTs and CPM in cases with FSD (p > .1). A high PPT was associated with lower odds of having multi-organ bodily distress syndrome (ORPPT trapezius: 0.66, 95% CI: 0.49-0.88, p = .005), with the symptom profile characterized by all symptoms (ORPPT trapezius: 0.72, 95% CI: 0.58-0.90, p = .003 and ORPPT tibialis: 0.75, 95% CI: 0.62-0.91, p = .004), and with multiple chemical sensitivity (ORPPT trapezius: 0.81, 95% CI: 0.67-0.97, p = .022). High CPM was associated with high odds of having irritable bowel (ORCPM relative: 1.22, 95% CI: 1.04-1.43, p = .013 and ORCPM absolute = 2.66, 95% CI: 1.07-6.45, p = .033). Conclusion However, only PPT measured over the trapezius muscle were still significant after correction for multiple testing for the symptom profile characterized by all symptoms. Findings from this study do not support altered pain regulation in questionnaire-based FSD which is in contrast with the existing presumption. Further epidemiological studies in this field are needed. Significance Disrupted pain regulation as measured by abnormal pain thresholds has been hypothesized as a central mechanism in Functional Somatic Disorders (FSD). The hypothesis has been raised in clinical setting where patients presented subjective and objective features of hypersensitivity. The present population-based study does not support this notion. This points to the importance of further studies into the underlying pathophysiology mechanisms of FSD.",
keywords = "IRRITABLE-BOWEL-SYNDROME, CHRONIC-FATIGUE-SYNDROME, WHIPLASH-ASSOCIATED DISORDERS, CENTRAL SENSITIZATION, GENERAL-POPULATION, PRESSURE ALGOMETRY, BACK-PAIN, FIBROMYALGIA, HYPERSENSITIVITY, INHIBITION",
author = "Petersen, {Marie Weinreich} and Sine Skovbjerg and Jensen, {Jens S{\o}ndergaard} and Carstensen, {Tina Birgitte Wisbech} and Dantoft, {Thomas Meinertz} and Per Fink and Benros, {Michael Eriksen} and Mortensen, {Erik Lykke} and Torben J{\o}rgensen and Gormsen, {Lise Kirstine}",
year = "2021",
doi = "10.1002/ejp.1847",
language = "English",
volume = "26",
pages = " 154--166",
journal = "European Journal of Pain",
issn = "1090-3801",
publisher = "JohnWiley & Sons Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - Conditioned pain modulation and pain sensitivity in functional somatic disorders

T2 - The DanFunD study

AU - Petersen, Marie Weinreich

AU - Skovbjerg, Sine

AU - Jensen, Jens Søndergaard

AU - Carstensen, Tina Birgitte Wisbech

AU - Dantoft, Thomas Meinertz

AU - Fink, Per

AU - Benros, Michael Eriksen

AU - Mortensen, Erik Lykke

AU - Jørgensen, Torben

AU - Gormsen, Lise Kirstine

PY - 2021

Y1 - 2021

N2 - Background Disrupted pain regulation has been proposed as a component in functional somatic disorders (FSD). The objective of this study was to examine a general population sample, encompassing three delimitations of FSD while assessing pain sensitivity and conditioning pain modulation (CPM). Methods Pressure pain thresholds (PPTs) at the tibialis and trapezius muscles were recorded at baseline. During cold pressor stimulation of the hand, the tibialis PPTs were re-assessed and the difference from baseline measures defined the CPM effect. Participants (n = 2,198, 53% females) were randomly selected from the adult Danish population. FSD was established by self-reported symptom questionnaires. Results With a few exceptions, only weak associations were seen between PPTs and CPM in cases with FSD (p > .1). A high PPT was associated with lower odds of having multi-organ bodily distress syndrome (ORPPT trapezius: 0.66, 95% CI: 0.49-0.88, p = .005), with the symptom profile characterized by all symptoms (ORPPT trapezius: 0.72, 95% CI: 0.58-0.90, p = .003 and ORPPT tibialis: 0.75, 95% CI: 0.62-0.91, p = .004), and with multiple chemical sensitivity (ORPPT trapezius: 0.81, 95% CI: 0.67-0.97, p = .022). High CPM was associated with high odds of having irritable bowel (ORCPM relative: 1.22, 95% CI: 1.04-1.43, p = .013 and ORCPM absolute = 2.66, 95% CI: 1.07-6.45, p = .033). Conclusion However, only PPT measured over the trapezius muscle were still significant after correction for multiple testing for the symptom profile characterized by all symptoms. Findings from this study do not support altered pain regulation in questionnaire-based FSD which is in contrast with the existing presumption. Further epidemiological studies in this field are needed. Significance Disrupted pain regulation as measured by abnormal pain thresholds has been hypothesized as a central mechanism in Functional Somatic Disorders (FSD). The hypothesis has been raised in clinical setting where patients presented subjective and objective features of hypersensitivity. The present population-based study does not support this notion. This points to the importance of further studies into the underlying pathophysiology mechanisms of FSD.

AB - Background Disrupted pain regulation has been proposed as a component in functional somatic disorders (FSD). The objective of this study was to examine a general population sample, encompassing three delimitations of FSD while assessing pain sensitivity and conditioning pain modulation (CPM). Methods Pressure pain thresholds (PPTs) at the tibialis and trapezius muscles were recorded at baseline. During cold pressor stimulation of the hand, the tibialis PPTs were re-assessed and the difference from baseline measures defined the CPM effect. Participants (n = 2,198, 53% females) were randomly selected from the adult Danish population. FSD was established by self-reported symptom questionnaires. Results With a few exceptions, only weak associations were seen between PPTs and CPM in cases with FSD (p > .1). A high PPT was associated with lower odds of having multi-organ bodily distress syndrome (ORPPT trapezius: 0.66, 95% CI: 0.49-0.88, p = .005), with the symptom profile characterized by all symptoms (ORPPT trapezius: 0.72, 95% CI: 0.58-0.90, p = .003 and ORPPT tibialis: 0.75, 95% CI: 0.62-0.91, p = .004), and with multiple chemical sensitivity (ORPPT trapezius: 0.81, 95% CI: 0.67-0.97, p = .022). High CPM was associated with high odds of having irritable bowel (ORCPM relative: 1.22, 95% CI: 1.04-1.43, p = .013 and ORCPM absolute = 2.66, 95% CI: 1.07-6.45, p = .033). Conclusion However, only PPT measured over the trapezius muscle were still significant after correction for multiple testing for the symptom profile characterized by all symptoms. Findings from this study do not support altered pain regulation in questionnaire-based FSD which is in contrast with the existing presumption. Further epidemiological studies in this field are needed. Significance Disrupted pain regulation as measured by abnormal pain thresholds has been hypothesized as a central mechanism in Functional Somatic Disorders (FSD). The hypothesis has been raised in clinical setting where patients presented subjective and objective features of hypersensitivity. The present population-based study does not support this notion. This points to the importance of further studies into the underlying pathophysiology mechanisms of FSD.

KW - IRRITABLE-BOWEL-SYNDROME

KW - CHRONIC-FATIGUE-SYNDROME

KW - WHIPLASH-ASSOCIATED DISORDERS

KW - CENTRAL SENSITIZATION

KW - GENERAL-POPULATION

KW - PRESSURE ALGOMETRY

KW - BACK-PAIN

KW - FIBROMYALGIA

KW - HYPERSENSITIVITY

KW - INHIBITION

U2 - 10.1002/ejp.1847

DO - 10.1002/ejp.1847

M3 - Journal article

C2 - 34309927

VL - 26

SP - 154

EP - 166

JO - European Journal of Pain

JF - European Journal of Pain

SN - 1090-3801

IS - 1

ER -

ID: 276155716