Central sensitization in CRPS patients with widespread pain: a cross-sectional study

Author:

De Schoenmacker Iara1ORCID,Mollo Anna1,Scheuren Paulina Simonne1ORCID,Sirucek Laura2ORCID,Brunner Florian3ORCID,Schweinhardt Petra24,Curt Armin1,Rosner Jan156,Hubli Michèle1

Affiliation:

1. Spinal Cord Injury Center, Balgrist University Hospital, University of Zurich , 8008 Zurich, Switzerland

2. Integrative Spinal Research, Department of Chiropractic Medicine, University Hospital Balgrist, University of Zurich , 8008 Zurich, Switzerland

3. Physical Medicine and Rheumatology, Balgrist University Hospital , 8008 Zurich, Switzerland

4. Alan Edward Center for Research on Pain, McGill University , Montreal, Quebec, Canada

5. Department of Neurology, University Hospital Bern, Inselspital, University of Bern , Bern, Switzerland

6. Danish Pain Research Center, Department of Clinical Medicine, Aarhus University , Aarhus, Denmark

Abstract

Abstract Objective Widespread pain hypersensitivity and enhanced temporal summation of pain (TSP) are commonly reported in patients with complex regional pain syndrome (CRPS) and discussed as proxies for central sensitization. This study aimed to directly relate such signs of neuronal hyperexcitability to the pain phenotype of CRPS patients. Methods Twenty-one CRPS patients and 20 healthy controls (HC) were recruited. The pain phenotype including spatial pain extent (assessed in % body surface) and intensity were assessed and related to widespread pain hypersensitivity, TSP, and psychological factors. Quantitative sensory testing (QST) was performed in the affected, the contralateral and a remote (control) area. Results CRPS patients showed decreased pressure pain thresholds in all tested areas (affected: t(34)  = 4.98, P < .001, contralateral: t(35) = 3.19, P = .005, control: t(31) = 2.65, P = .012). Additionally, patients showed increased TSP in the affected area (F(3,111) = 4.57, P = .009) compared to HC. TSP was even more enhanced in patients with a high compared to a low spatial pain extent (F(3,51) = 5.67, P = .008), suggesting pronounced spinal sensitization in patients with extended pain patterns. Furthermore, the spatial pain extent positively correlated with the Bath Body Perception Disturbance Scale (ρ = 0.491; P = .048). Conclusions Overall, we provide evidence that the pain phenotype in CRPS, that is, spatial pain extent, might be related to sensitization mechanism within the central nociceptive system. This study points towards central neuronal excitability as a potential therapeutic target in patients with more widespread CRPS.

Funder

Clinical Research Priority Program (CRPP) Pain of the University of Zurich

Publisher

Oxford University Press (OUP)

Subject

Anesthesiology and Pain Medicine,Neurology (clinical),General Medicine

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