Is the Conditioned Pain Modulation Paradigm Reliable? A Test-Retest Assessment Using the Nociceptive Withdrawal Reflex

被引:57
|
作者
Manresa, Jose A. Biurrun [1 ]
Fritsche, Raphael [2 ]
Vuilleumier, Pascal H. [3 ]
Oehler, Carmen [2 ]
Morch, Carsten D. [1 ]
Arendt-Nielsen, Lars [1 ]
Andersen, Ole K. [1 ]
Curatolo, Michele [1 ,3 ]
机构
[1] Aalborg Univ, Dept Hlth Sci & Technol, Ctr Sensory Motor Interact, Aalborg, Denmark
[2] Univ Bern, Inselspital, Univ Dept Anaesthesiol & Pain Therapy, CH-3010 Bern, Switzerland
[3] Univ Washington, Dept Anaesthesiol & Pain Med, Seattle, WA 98195 USA
来源
PLOS ONE | 2014年 / 9卷 / 06期
基金
瑞士国家科学基金会;
关键词
NOXIOUS INHIBITORY CONTROLS; TENSION-TYPE HEADACHE; TEMPORAL SUMMATION; RELIABILITY; STIMULI; FIBROMYALGIA; COEFFICIENT; ERROR;
D O I
10.1371/journal.pone.0100241
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The aim of this study was to determine the reliability of the conditioned pain modulation (CPM) paradigm assessed by an objective electrophysiological method, the nociceptive withdrawal reflex (NWR), and psychophysical measures, using hypothetical sample sizes for future studies as analytical goals. Thirty-four healthy volunteers participated in two identical experimental sessions, separated by 1 to 3 weeks. In each session, the cold pressor test (CPT) was used to induce CPM, and the NWR thresholds, electrical pain detection thresholds and pain intensity ratings after suprathreshold electrical stimulation were assessed before and during CPT. CPM was consistently detected by all methods, and the electrophysiological measures did not introduce additional variation to the assessment. In particular, 99% of the trials resulted in higher NWR thresholds during CPT, with an average increase of 3.4 mA (p<0.001). Similarly, 96% of the trials resulted in higher electrical pain detection thresholds during CPT, with an average increase of 2.2 mA (p<0.001). Pain intensity ratings after suprathreshold electrical stimulation were reduced during CPT in 84% of the trials, displaying an average decrease of 1.5 points in a numeric rating scale (p<0.001). Under these experimental conditions, CPM reliability was acceptable for all assessment methods in terms of sample sizes for potential experiments. The presented results are encouraging with regards to the use of the CPM as an assessment tool in experimental and clinical pain.
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页数:9
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