Peripheral neuropathic pain: a mechanism-related organizing principle based on sensory profiles

被引:470
作者
Baron, Ralf [1 ]
Maier, Christoph [2 ]
Attal, Nadine [3 ,4 ]
Binder, Andreas
Bouhassira, Didier [3 ,4 ]
Cruccu, Giorgio [5 ]
Finnerup, Nanna B. [6 ]
Haanpaa, Maija [7 ,8 ]
Hansson, Per [9 ,10 ]
Huellemann, Philipp [1 ]
Jensen, Troels S. [6 ]
Freynhagen, Rainer [11 ,12 ]
Kennedy, Jeffrey D. [13 ]
Magerl, Walter [14 ]
Mainka, Tina [2 ,15 ]
Reimer, Maren [1 ]
Rice, Andrew S. C. [16 ]
Segerdahl, Marta [17 ,18 ]
Serra, Jordi [19 ]
Sindrup, Soren [20 ]
Sommer, Claudia [21 ]
Toelle, Thomas [22 ]
Vollert, Jan [2 ,14 ]
Treede, Rolf-Detlef [14 ]
机构
[1] Univ klinikum Schleswig Holstein, Dept Neurol, Div Neurol Pain Res & Therapy, Campus Kiel,House 41,Arnold Heller Strasse 3, D-24105 Kiel, Germany
[2] Ruhr Univ Bochum, BG Univ Hosp Bergmannsheil GmbH, Dept Pain Med, Bochum, Germany
[3] CHU Ambroise Pare, Ctr Evaluat & Traitement Douleur, INSERM, U 987, Boulogne, France
[4] Univ Versailles Saint Quentin, Versailles, France
[5] Sapienza Univ, Dept Neurol & Psychiat, Rome, Italy
[6] Aarhus Univ Hosp, Danish Pain Res Ctr, Dept Neurol, Aarhus, Denmark
[7] Univ Helsinki, Cent Hosp, Helsinki, Finland
[8] Etera Mutual Pens Insurance, Helsinki, Finland
[9] Oslo Univ Hosp, Dept Pain Management & Res, Div Emergencies & Crit, Oslo, Norway
[10] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[11] Benedictus Hosp Tutzing, Pain Ctr Lake Starnberg, Dept Anaesthesiol, Crit CareMedicine Pain Therapy & Palliat Care, Tutzing, Germany
[12] Tech Univ Munich, Klin Anasthesie, Munich, Germany
[13] Eli Lilly & Co, Neuroscience Discovery Res, Indianapolis, IN USA
[14] Heidelberg Univ, Med Fac Mannheim, Ctr Biomed & Med Technol Mannheim CBTM, Dept Neurophysiol, Mannheim, Germany
[15] Univ Med Ctr Hamburg Eppendorf, Dept Neurol, Hamburg, Germany
[16] Imperial Coll, Dept Surg & Canc, Pain Res, London, England
[17] Clin R&D Neurol, Lundbeck A-S, Copenhagen, Denmark
[18] Karolinska Inst, Dept Physiol & Pharmacol, Stockholm, Sweden
[19] Neurosci Technol SLP, Barcelona, Spain
[20] Odense Univ Hosp, Dept Neurol, Odense, Denmark
[21] Univ Hosp Wurzburg, Dept Neurol, Wurzburg, Germany
[22] Tech Univ Munich, Klinikum Rechts Isar, Dept Neurol, Munich, Germany
关键词
Neuropathic pain; Sensory signs; Clinical trials; QST; Epidemiology; LONG-TERM POTENTIATION; GERMAN RESEARCH NETWORK; DOUBLE-BLIND; NEUROGENIC HYPERALGESIA; POSTHERPETIC NEURALGIA; SYSTEMIC LIDOCAINE; GRADING SYSTEM; VALIDATION; PHENOTYPE; FIBERS;
D O I
10.1097/j.pain.0000000000000753
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Patients with neuropathic pain are heterogeneous in etiology, pathophysiology, and clinical appearance. They exhibit a variety of painrelated sensory symptoms and signs (sensory profile). Different sensory profiles might indicate different classes of neurobiological mechanisms, and hence subgroups with different sensory profilesmight respond differently to treatment. The aim of the investigation was to identify subgroups in a large sample of patients with neuropathic pain using hypothesis-free statistical methods on the database of 3 large multinational research networks (German Research Network on Neuropathic Pain (DFNS), IMI-Europain, and Neuropain). Standardized quantitative sensory testing was used in 902 (test cohort) and 233 (validation cohort) patients with peripheral neuropathic pain of different etiologies. For subgrouping, we performed a cluster analysis using 13 quantitative sensory testing parameters. Three distinct subgroupswith characteristic sensory profileswere identified and replicated. Cluster 1 (sensory loss, 42%) showed a loss of small and large fiber function in combination with paradoxical heat sensations. Cluster 2 (thermal hyperalgesia, 33%) was characterized by preserved sensory functions in combination with heat and cold hyperalgesia and mild dynamic mechanical allodynia. Cluster 3 (mechanical hyperalgesia, 24%) was characterized by a loss of small fiber function in combinationwith pinprick hyperalgesia and dynamic mechanical allodynia. All clusters occurred across etiologies but frequencies differed. We present a new approach of subgrouping patients with peripheral neuropathic pain of different etiologies according to intrinsic sensory profiles. These 3 profiles may be related to pathophysiological mechanisms and may be useful in clinical trial design to enrich the study population for treatment responders.
引用
收藏
页码:261 / 272
页数:12
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