Pain modulatory phenotypes differentiate subgroups with different clinical and experimental pain sensitivity

被引:98
作者
Vaegter, Henrik B. [1 ,2 ]
Graven-Nielsen, Thomas [3 ]
机构
[1] Odense Univ Hosp, Dept Anesthesiol & Intens Care Med, Pain Res Grp, Pain Ctr South, Odense, Denmark
[2] Univ Southern Denmark, Fac Hlth Sci, Dept Clin Res, DK-5000 Odense C, Denmark
[3] Aalborg Univ, Fac Med, Dept Hlth Sci & Technol, SMI,Ctr Neuroplast & Pain, Aalborg, Denmark
基金
新加坡国家研究基金会;
关键词
Chronic pain; Temporal summation of pain; Conditioned pain modulation; Pain sensitivity; Pain biomarkers; Cuff algometry; CHRONIC POSTOPERATIVE PAIN; TEMPORAL SUMMATION; DOUBLE-BLIND; KETAMINE; STIMULATION; PREDICTS; SENSITIZATION; HYPERALGESIA; HYPOALGESIA; INHIBITION;
D O I
10.1097/j.pain.0000000000000543
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Pain biomarkers are warranted for individualized pain management. Based on different pain modulatory phenotypes, the objectives of this study were to explore the existence of subgroups within patients with nonmalignant chronic pain and to investigate differences in clinical pain and pain hypersensitivity between subgroups. Cuff algometry was performed on lower legs in 400 patients with chronic pain to assess pressure pain threshold, pressure pain tolerance, temporal summation of pain (TSP: increase in pain scores to 10 repeated stimulations), and conditioned pain modulation (CPM: increase in cuff pressure pain threshold during cuff pain conditioning on the contralateral leg). Heat detection and heat pain thresholds at clinical painful and nonpainful body areas were assessed. Based on TSP and CPM, 4 distinct groups were formed: group 1 (n=85) had impaired CPM and facilitated TSP; group 2 (n = 148) had impaired CPM and normal TSP; group 3 (n = 45) had normal CPM and facilitated TSP; and group 4 (n = 122) had normal CPM and normal TSP. Group 1 showed more pain regions than the other 3 groups (P<0.001), indicating that impaired CPM and facilitated TSP play an important role in widespread pain. Groups 1 and 2 compared with group 4 had lower heat pain threshold at nonpainful areas and lower cuff pressure pain tolerance (P<0.02), indicating that CPM plays a role for widespread hyperalgesia. Moreover, group 1 demonstrated higher clinical pain scores than group 4 (P<0.05). Although not different between subgroups, patients were profiled on demographics, disability, pain catastrophizing, and fear of movement. Future research should investigate interventions tailored towards these subgroups.
引用
收藏
页码:1480 / 1488
页数:9
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