Association of sensory phenotype with quality of life, functionality, and emotional well-being in patients suffering from neuropathic pain.


Journal

Pain
ISSN: 1872-6623
Titre abrégé: Pain
Pays: United States
ID NLM: 7508686

Informations de publication

Date de publication:
01 07 2022
Historique:
received: 30 04 2021
accepted: 15 09 2021
pubmed: 26 9 2021
medline: 22 6 2022
entrez: 25 9 2021
Statut: ppublish

Résumé

Neuropathic pain highly affects quality of life, well-being, and function. It has recently been shown based on cluster analysis studies that most patients with neuropathic pain may be categorized into 1 of 3 sensory phenotypes: sensory loss, mechanical hyperalgesia, and thermal hyperalgesia. If these phenotypes reflect underlying pathophysiological mechanisms, they may be more relevant for patient management than underlying neurological diagnosis or pain intensity. The aim of this study was thus to examine the impact of these sensory phenotypes on mental health, functionality, and quality of life. Data of 433 patients from the IMI/EuroPain network database were analyzed, and results of HADS-D/A, Pain Catastrophizing Scale, Euro Quality of Life 5D/-VAS, Brief Pain Inventory, and Graded Chronic Pain Scale between the sensory phenotypes were compared using multiple regression analysis. There was no difference in chronic pain grade, pain intensity, depression, or anxiety scores between phenotypes. Pain interference (Brief Pain Inventory) was higher (P = 0.002); self-reported health state lower (Euro Quality of Life 5D VAS, P = 0.02); and problems regarding mobility (P = 0.008), usual activities (P = 0.004), and self-care (P = 0.039) more prominent (EQ5-D) in the sensory loss compared with the thermal hyperalgesia phenotype. Patients with sensory loss also showed higher pain catastrophizing scores (P = 0.006 and 0.022, respectively) compared with the 2 other groups. Sensory phenotype is associated with the impact of neuropathic pain conditions on well-being, daily functionality, and quality of life but is less associated with pain intensity. These results suggest that the somatosensory phenotype should be considered for personalized pain management.

Identifiants

pubmed: 34561391
doi: 10.1097/j.pain.0000000000002501
pii: 00006396-202207000-00016
pmc: PMC9199110
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1378-1387

Informations de copyright

Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain.

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Auteurs

Janne Gierthmühlen (J)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Johann Böhmer (J)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Nadine Attal (N)

Inserm U987, APHP, UVSQ, Paris-Saclay University, CHU Ambroise Pare, Boulogne-Billancourt, France.

Didier Bouhassira (D)

Inserm U987, APHP, UVSQ, Paris-Saclay University, CHU Ambroise Pare, Boulogne-Billancourt, France.

Rainer Freynhagen (R)

Department of Anaesthesiology, Critical Care Medicine, Pain Therapy & Palliative Care, Pain Center Lake Starnberg, Benedictus Hospital Feldafing, Germany.
Department of Anaesthesiology, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany.

Maija Haanpää (M)

Department of Neurosurgery, Helsinki University Central Hospital (HUCH), Helsinki, Finland.

Per Hansson (P)

Department of Pain Management and Research, Norwegian National Advisory Unit on Neuropathic Pain, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Troels Staehelin Jensen (TS)

Department of Clinical Medicine, Neurological Research and Dansih Pain Research Center, Aarhus University Hospital, Aarhus, Denmark.

Jeffrey Kennedy (J)

Eli Lilly and Company, Indianapolis, IN, United States.

Christoph Maier (C)

University Hospital of Pediatrics and Adolescent Medicine, Ruhr-University Bochum, Germany.

Andrew S C Rice (ASC)

Pain Research, Department of Surgery and Cancer, Faculty of Medicine, Imperial College, London, United Kingdom.

Juliane Sachau (J)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Märta Segerdahl (M)

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden and MS Medical Consulting, Stockholm, Sweden.

Sören Sindrup (S)

Department of Neurology, Odense University Hospital OUH, Odense, Denmark.

Thomas Tölle (T)

Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Rolf-Detlef Treede (RD)

Neurophysiology, Mannheim Center for Translational Neurosciences (MCTN), Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Lise Ventzel (L)

Department of Pain Management and Research, Norwegian National Advisory Unit on Neuropathic Pain, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

Jan Vollert (J)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.
Neurophysiology, Mannheim Center for Translational Neurosciences (MCTN), Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Ralf Baron (R)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

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