Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome

Standard

Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome. / Kumowski, N; Hegelmaier, T; Kolbenschlag, Jonas; Maier, C; Mainka, T; Vollert, Jörn; Enax-Krumova, Elena K.

In: EUR J PAIN, Vol. 21, No. 5, 05.2017, p. 855-865.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Kumowski, N, Hegelmaier, T, Kolbenschlag, J, Maier, C, Mainka, T, Vollert, J & Enax-Krumova, EK 2017, 'Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome', EUR J PAIN, vol. 21, no. 5, pp. 855-865. https://doi.org/10.1002/ejp.988

APA

Kumowski, N., Hegelmaier, T., Kolbenschlag, J., Maier, C., Mainka, T., Vollert, J., & Enax-Krumova, E. K. (2017). Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome. EUR J PAIN, 21(5), 855-865. https://doi.org/10.1002/ejp.988

Vancouver

Kumowski N, Hegelmaier T, Kolbenschlag J, Maier C, Mainka T, Vollert J et al. Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome. EUR J PAIN. 2017 May;21(5):855-865. https://doi.org/10.1002/ejp.988

Bibtex

@article{6d5e56ae02eb458888439ff4245dc783,
title = "Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome",
abstract = "BACKGROUND: The complex regional pain syndrome (CRPS) is characterized by distal generalisation of pain beyond the initial trauma. This might be the result of impaired endogenous pain inhibition.METHOD: We compared Conditioned Pain Modulation (CPM) between patients with CRPS (n = 24; pain: 4.5 ± 2.2, NRS 0-10; disease duration <1 year), neuralgia (n = 17; pain: 5.5 ± 1.1) and healthy subjects (n = 23) and its correlation with loss and gain of function as assessed by Quantitative Sensory Testing (QST). CPM was assessed with heat as test stimulus (TS) and cold water as conditioning stimulus (CS). The early CPM-effect was calculated as difference between heat pain during and before conditioning, the late CPM-effect, 5 minutes after and before conditioning, respectively.RESULTS: Heat pain decreased comparably after CS in all groups, resulting in a significant CPM-effect (healthy: -12.5 ± 12.4, NRS 0-100; CRPS: -14.7 ± 15.7; neuralgia: -7.9 ± 9.8; p < 0.001). When compared to healthy subjects, heat pain declined significantly steeper in CRPS patients (healthy: -2.0 ± 5.5, NRS 0-100/10 s; CRPS: -6.3 ± 8.1; p < 0.05). Only CRPS patients demonstrated a late CPM effect (-6.0 ± 9.0, p < 0.005). Neither spontaneous pain nor any QST parameter correlated with CPM, with the exception of a decreased cold pain threshold, which correlated with an enhanced CPM in CRPS patients only (r = -0.456, p < 0.05).CONCLUSION: An impairment of endogenous pain inhibition does not explain the extent of pain in the early stage of CRPS or in neuralgia. The unexpectedly high CPM in CRPS patients might result from activation of the intact descending pathways in response to central sensitization, as cold hyperalgesia correlated with the CPM-effect.SIGNIFICANCE: Conditioned pain modulation (CPM) is not impaired in the early phase of complex regional pain syndrome (CRPS) and neuralgia. Only in CRPS higher CPM was associated with lower cold pain thresholds.",
keywords = "Journal Article",
author = "N Kumowski and T Hegelmaier and Jonas Kolbenschlag and C Maier and T Mainka and J{\"o}rn Vollert and Enax-Krumova, {Elena K}",
note = "{\textcopyright} 2017 European Pain Federation - EFIC{\textregistered}.",
year = "2017",
month = may,
doi = "10.1002/ejp.988",
language = "English",
volume = "21",
pages = "855--865",
journal = "EUR J PAIN",
issn = "1090-3801",
publisher = "W.B. Saunders Ltd",
number = "5",

}

RIS

TY - JOUR

T1 - Unimpaired endogenous pain inhibition in the early phase of complex regional pain syndrome

AU - Kumowski, N

AU - Hegelmaier, T

AU - Kolbenschlag, Jonas

AU - Maier, C

AU - Mainka, T

AU - Vollert, Jörn

AU - Enax-Krumova, Elena K

N1 - © 2017 European Pain Federation - EFIC®.

PY - 2017/5

Y1 - 2017/5

N2 - BACKGROUND: The complex regional pain syndrome (CRPS) is characterized by distal generalisation of pain beyond the initial trauma. This might be the result of impaired endogenous pain inhibition.METHOD: We compared Conditioned Pain Modulation (CPM) between patients with CRPS (n = 24; pain: 4.5 ± 2.2, NRS 0-10; disease duration <1 year), neuralgia (n = 17; pain: 5.5 ± 1.1) and healthy subjects (n = 23) and its correlation with loss and gain of function as assessed by Quantitative Sensory Testing (QST). CPM was assessed with heat as test stimulus (TS) and cold water as conditioning stimulus (CS). The early CPM-effect was calculated as difference between heat pain during and before conditioning, the late CPM-effect, 5 minutes after and before conditioning, respectively.RESULTS: Heat pain decreased comparably after CS in all groups, resulting in a significant CPM-effect (healthy: -12.5 ± 12.4, NRS 0-100; CRPS: -14.7 ± 15.7; neuralgia: -7.9 ± 9.8; p < 0.001). When compared to healthy subjects, heat pain declined significantly steeper in CRPS patients (healthy: -2.0 ± 5.5, NRS 0-100/10 s; CRPS: -6.3 ± 8.1; p < 0.05). Only CRPS patients demonstrated a late CPM effect (-6.0 ± 9.0, p < 0.005). Neither spontaneous pain nor any QST parameter correlated with CPM, with the exception of a decreased cold pain threshold, which correlated with an enhanced CPM in CRPS patients only (r = -0.456, p < 0.05).CONCLUSION: An impairment of endogenous pain inhibition does not explain the extent of pain in the early stage of CRPS or in neuralgia. The unexpectedly high CPM in CRPS patients might result from activation of the intact descending pathways in response to central sensitization, as cold hyperalgesia correlated with the CPM-effect.SIGNIFICANCE: Conditioned pain modulation (CPM) is not impaired in the early phase of complex regional pain syndrome (CRPS) and neuralgia. Only in CRPS higher CPM was associated with lower cold pain thresholds.

AB - BACKGROUND: The complex regional pain syndrome (CRPS) is characterized by distal generalisation of pain beyond the initial trauma. This might be the result of impaired endogenous pain inhibition.METHOD: We compared Conditioned Pain Modulation (CPM) between patients with CRPS (n = 24; pain: 4.5 ± 2.2, NRS 0-10; disease duration <1 year), neuralgia (n = 17; pain: 5.5 ± 1.1) and healthy subjects (n = 23) and its correlation with loss and gain of function as assessed by Quantitative Sensory Testing (QST). CPM was assessed with heat as test stimulus (TS) and cold water as conditioning stimulus (CS). The early CPM-effect was calculated as difference between heat pain during and before conditioning, the late CPM-effect, 5 minutes after and before conditioning, respectively.RESULTS: Heat pain decreased comparably after CS in all groups, resulting in a significant CPM-effect (healthy: -12.5 ± 12.4, NRS 0-100; CRPS: -14.7 ± 15.7; neuralgia: -7.9 ± 9.8; p < 0.001). When compared to healthy subjects, heat pain declined significantly steeper in CRPS patients (healthy: -2.0 ± 5.5, NRS 0-100/10 s; CRPS: -6.3 ± 8.1; p < 0.05). Only CRPS patients demonstrated a late CPM effect (-6.0 ± 9.0, p < 0.005). Neither spontaneous pain nor any QST parameter correlated with CPM, with the exception of a decreased cold pain threshold, which correlated with an enhanced CPM in CRPS patients only (r = -0.456, p < 0.05).CONCLUSION: An impairment of endogenous pain inhibition does not explain the extent of pain in the early stage of CRPS or in neuralgia. The unexpectedly high CPM in CRPS patients might result from activation of the intact descending pathways in response to central sensitization, as cold hyperalgesia correlated with the CPM-effect.SIGNIFICANCE: Conditioned pain modulation (CPM) is not impaired in the early phase of complex regional pain syndrome (CRPS) and neuralgia. Only in CRPS higher CPM was associated with lower cold pain thresholds.

KW - Journal Article

U2 - 10.1002/ejp.988

DO - 10.1002/ejp.988

M3 - SCORING: Journal article

C2 - 28146319

VL - 21

SP - 855

EP - 865

JO - EUR J PAIN

JF - EUR J PAIN

SN - 1090-3801

IS - 5

ER -