Ratings of experimental pain and pain-related negative affect predict clinical pain in patients with fibromyalgia syndrome

被引:112
作者
Staud, R
Robinson, ME
Vierck, CJ
Cannon, RC
Mauderli, AP
Price, DD
机构
[1] Univ Florida, Coll Med, Dept Med, McKnight Brain Inst, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Clin & Hlth Psychol, McKnight Brain Inst, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Med, Dept Neurosci, McKnight Brain Inst, Gainesville, FL 32610 USA
[4] Univ Florida, Coll Med, Dept Prosthodont, McKnight Brain Inst, Gainesville, FL 32610 USA
关键词
fibromyalgia; muscle; predictor; chronic pain intensity; temporal summation;
D O I
10.1016/S0304-3959(03)00208-2
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Patients with fibromyalgia syndrome (FMS) report chronic pain related to abnormal sensitivity of muscles that is reflected by so-called tender points (TP). TP represent areas of abnormal mechanical pain thresholds that have only shown a minor correlation with clinical pain of FMS patients and seem to be better suited for predicting distress. Pain-related negative affect (PRNA), abnormal temporal summation of second pain (termed wind-up or WU), and abnormal WU decay are frequently present in FMS patients. WU and WU decay call provide measures of central sensitization, which may contribute to clinical FMS pain. We therefore investigated the role of WU, WU decay, TP count, and PRNA as predictors of clinical pain in FMS subjects. Fifty-five FMS subjects rated their clinical pain at entry into the study using a visual analogue scale (VAS). After a TP evaluation, all subjects received two trials of thermal WU and WU decay testing. Hierarchical regression analysis demonstrated that the combination of PRNA ratings, TP count, and WU decay ratings predicted 49.7% of the variance of clinical pain in FMS. This model demonstrates independent relationships of biological and psychological factors to clinical pain and underscores the important role of abnormal peripheral and central pain mechanisms for FMS. Therefore, the combination of PRNA, TP count, and WU decay may provide an excellent measure to]future clinical studies of FMS patients. (C) 2003 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 222
页数:8
相关论文
共 71 条
[11]   More pain, more tender points: Is fibromyalgia just one end of a continuous spectrum? [J].
Croft, P ;
Burt, J ;
Schollum, J ;
Thomas, E ;
Macfarlane, G ;
Silman, A .
ANNALS OF THE RHEUMATIC DISEASES, 1996, 55 (07) :482-485
[12]   POPULATION STUDY OF TENDER POINT COUNTS AND PAIN AS EVIDENCE OF FIBROMYALGIA [J].
CROFT, P ;
SCHOLLUM, J ;
SILMAN, A .
BRITISH MEDICAL JOURNAL, 1994, 309 (6956) :696-699
[13]   NMDA RECEPTORS AND CENTRAL HYPERALGESIC STATES [J].
DICKENSON, AH ;
SULLIVAN, AF .
PAIN, 1991, 46 (03) :344-345
[14]   EVIDENCE FOR A ROLE OF THE NMDA RECEPTOR IN THE FREQUENCY-DEPENDENT POTENTIATION OF DEEP RAT DORSAL HORN NOCICEPTIVE NEURONS FOLLOWING C-FIBER STIMULATION [J].
DICKENSON, AH ;
SULLIVAN, AF .
NEUROPHARMACOLOGY, 1987, 26 (08) :1235-1238
[15]   IDIOPATHIC TRIGEMINAL NEURALGIA - SENSORY FEATURES AND PAIN MECHANISMS [J].
DUBNER, R ;
SHARAV, Y ;
GRACELY, RH ;
PRICE, DD .
PAIN, 1987, 31 (01) :23-33
[16]   NEGATIVE AFFECT AND THE EXPERIENCE OF CHRONIC PAIN [J].
GASKIN, ME ;
GREENE, AF ;
ROBINSON, ME ;
GEISSER, ME .
JOURNAL OF PSYCHOSOMATIC RESEARCH, 1992, 36 (08) :707-713
[17]   CATASTROPHIZING, DEPRESSION AND THE SENSORY, AFFECTIVE AND EVALUATIVE ASPECTS OF CHRONIC PAIN [J].
GEISSER, ME ;
ROBINSON, ME ;
KEEFE, FJ ;
WEINER, ML .
PAIN, 1994, 59 (01) :79-83
[18]   PRESSURE PAIN THRESHOLD IN PAIN-FREE SUBJECTS, IN PATIENTS WITH CHRONIC REGIONAL PAIN SYNDROMES, AND IN PATIENTS WITH FIBROMYALGIA SYNDROME [J].
GRANGES, G ;
LITTLEJOHN, G .
ARTHRITIS AND RHEUMATISM, 1993, 36 (05) :642-646
[19]   Ketamine reduces muscle pain, temporal summation, and referred pain in fibromyalgia patients [J].
Graven-Nielsen, T ;
Kendall, SA ;
Henriksson, KG ;
Bengtsson, M ;
Sörensen, J ;
Johnson, A ;
Gerdle, B ;
Arendt-Nielsen, L .
PAIN, 2000, 85 (03) :483-491
[20]  
HEWETT JE, 1995, J RHEUMATOL, V22, P2307