期刊论文详细信息
JOURNAL OF PAIN 卷:19
Individual Variation in Pain Sensitivity and Conditioned Pain Modulation in Acute Low Back Pain: Effect of Stimulus Type, Sleep, and Psychological and Lifestyle Factors
Article
Klyne, David M.1  Moseley, G. Lorimer2,3  Sterling, Michele4  Barbe, Mary F.5  Hodges, Paul W.1 
[1] Univ Queensland, NHMRC Ctr Clin Res Excellence Spinal Pain Injury, Sch Hlth & Rehabil Sci, Brisbane, Qld, Australia
[2] Univ South Australia, Sansom Inst Hlth Res, Adelaide, SA, Australia
[3] Neurosci Res Australia, Sydney, NSW, Australia
[4] Griffith Univ, NHMRC CRE Recovery Rd Traff Injury, Recover Injury Res Ctr, Southport, Qld, Australia
[5] Temple Univ, Dept Anat & Cell Biol, Sch Med, Philadelphia, PA 19122 USA
关键词: Generalized hyperalgesia;    localized hyperalgesia;    conditioned pain modulation;    central;    sensitization;    peripheral sensitization;    low back pain.;   
DOI  :  10.1016/j.jpain.2018.02.017
来源: Elsevier
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【 摘 要 】

Generalized hyperalgesia and impaired pain modulation are reported in chronic low back pain (LBP). Few studies have tested whether these features are present in the acute phase. This study aimed to test for differences in pain presentation in early-acute LBP and evaluate the potential contribution of other factors to variation in sensitivity. Individuals within 2 weeks of onset of acute LBP (n = 126) and pain-free controls (n = 74) completed questionnaires related to their pain, disability, behavior, and psychological status before undergoing conditioned pain modulation (CPM) and pain threshold (heat, cold, and pressure) testing at the back and forearm/thumb. LBP participants were more sensitive to heat and cold at both sites and pressure at the back than controls, without differences in CPM. Only those with high-pain (numeric rating scale =4) were more sensitive to heat at the forearm and pressure at the back. Four subgroups with distinct features were identified: high sensitivity, low CPM efficacy, high sensitivity/low CPM efficacy, and low sensitivity/high CPM efficacy. Various factors such as sleep and alcohol were associated with each pain measure. Results provide evidence for generalized hyperalgesia in many, but not all, individuals during acute LBP, with variation accounted for by several factors. Specific pain phenotypes provide candidate features to test in longitudinal studies of LBP outcome. Perspective: Sensory changes indicative of increased/decreased central processing of pain and nociceptive input presented differently between individuals with acute LBP and were related to factors such as sleep and alcohol. This may underlie variation in outcome and suggest potential for early identification of individuals with poor long-term outcome.

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