TY - JOUR
T1 - Central sensitisation in chronis pain
T2 - Latest discoveries and their potential for precision medicine
AU - Nijs, Jo
AU - George, S.Z.
AU - Clauw, Daniel J
AU - Fernandez-de-las-Penas, César
AU - Kosek, Eva
AU - Ickmans, Kelly
AU - Fernandez-Carnero, Josue
AU - Polli, Andrea
AU - Kapreli, Eleni
AU - Huysmans, Eva
AU - Cuesta-Vargas, Antonio
AU - Mani, R
AU - Lundberg, Mari
AU - Leysen, Laurence
AU - Rice, David
AU - Sterling, M
AU - Curatolo, M.
N1 - Funding Information:
KI, EH, and AP are research fellows funded by the Research Foundation Flanders (FWO), Belgium. SZG received salary support from the US National Institutes of Health (grant AR055899) while writing this manuscript. There was no funding source for this Review.
Funding Information:
EK reports personal fees from Eli Lilly and personal fees from Lundbeck, outside the submitted work. DC reports grants and personal fees from Aptinyx, Eli Lilly, Samumed, Tonix, Nix Patterson on behalf of State of OK, and Lundbeck Pharmaceuticals, and Pfizer, outside the submitted work. JN and the Vrije Universiteit Brussel received lecturing and teaching fees from various professional associations and educational organisations. SG reports grants from NIH, and personal fees from Rehab Essentials and Med Risk, outside the submitted work. All other authors declare no competing interests.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/3/30
Y1 - 2021/3/30
N2 - Chronic pain is a leading cause of disability globally and associated with enormous health-care costs. The discrepancy between the extent of tissue damage and the magnitude of pain, disability, and associated symptoms represents a diagnostic challenge for rheumatology specialists. Central sensitisation, defined as an amplification of neural signalling within the CNS that elicits pain hypersensitivity, has been investigated as a reason for this discrepancy. Features of central sensitisation have been documented in various pain conditions common in rheumatology practice, including fibromyalgia, osteoarthritis, rheumatoid arthritis, Ehlers-Danlos syndrome, upper extremity tendinopathies, headache, and spinal pain. Within individual pain conditions, there is substantial variation among patients in terms of presence and magnitude of central sensitisation, stressing the importance of individual assessment. Central sensitisation predicts poor treatment outcomes in multiple patient populations. The available evidence supports various pharmacological and non-pharmacological strategies to reduce central sensitisation and to improve patient outcomes in several conditions commonly seen in rheumatology practice. These data open up new treatment perspectives, with the possibility for precision pain medicine treatment according to pain phenotyping as a logical next step. With this view, studies suggest the possibility of matching non-pharmacological approaches, or medications, or both to the central sensitisation pain phenotypes.
AB - Chronic pain is a leading cause of disability globally and associated with enormous health-care costs. The discrepancy between the extent of tissue damage and the magnitude of pain, disability, and associated symptoms represents a diagnostic challenge for rheumatology specialists. Central sensitisation, defined as an amplification of neural signalling within the CNS that elicits pain hypersensitivity, has been investigated as a reason for this discrepancy. Features of central sensitisation have been documented in various pain conditions common in rheumatology practice, including fibromyalgia, osteoarthritis, rheumatoid arthritis, Ehlers-Danlos syndrome, upper extremity tendinopathies, headache, and spinal pain. Within individual pain conditions, there is substantial variation among patients in terms of presence and magnitude of central sensitisation, stressing the importance of individual assessment. Central sensitisation predicts poor treatment outcomes in multiple patient populations. The available evidence supports various pharmacological and non-pharmacological strategies to reduce central sensitisation and to improve patient outcomes in several conditions commonly seen in rheumatology practice. These data open up new treatment perspectives, with the possibility for precision pain medicine treatment according to pain phenotyping as a logical next step. With this view, studies suggest the possibility of matching non-pharmacological approaches, or medications, or both to the central sensitisation pain phenotypes.
UR - http://www.scopus.com/inward/record.url?scp=85111225797&partnerID=8YFLogxK
U2 - 10.1016/S2665-9913(21)00032-1
DO - 10.1016/S2665-9913(21)00032-1
M3 - Article
SN - 2665-9913
VL - 3
SP - 383
EP - 392
JO - The Lancet Rheumatology
JF - The Lancet Rheumatology
ER -