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Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations
For genetic research to contribute more fully to furthering our knowledge of neuropathic pain, we require an agreed, valid, and feasible approach to phenotyping, to allow collaboration and replication in samples of sufficient size. Results from genetic studies on neuropathic pain have been inconsist...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747983/ https://www.ncbi.nlm.nih.gov/pubmed/26469320 http://dx.doi.org/10.1097/j.pain.0000000000000335 |
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author | van Hecke, Oliver Kamerman, Peter R. Attal, Nadine Baron, Ralf Bjornsdottir, Gyda Bennett, David L.H. Bennett, Michael I. Bouhassira, Didier Diatchenko, Luda Freeman, Roy Freynhagen, Rainer Haanpää, Maija Jensen, Troels S. Raja, Srinivasa N. Rice, Andrew S.C. Seltzer, Ze'ev Thorgeirsson, Thorgeir E. Yarnitsky, David Smith, Blair H. |
author_facet | van Hecke, Oliver Kamerman, Peter R. Attal, Nadine Baron, Ralf Bjornsdottir, Gyda Bennett, David L.H. Bennett, Michael I. Bouhassira, Didier Diatchenko, Luda Freeman, Roy Freynhagen, Rainer Haanpää, Maija Jensen, Troels S. Raja, Srinivasa N. Rice, Andrew S.C. Seltzer, Ze'ev Thorgeirsson, Thorgeir E. Yarnitsky, David Smith, Blair H. |
author_sort | van Hecke, Oliver |
collection | PubMed |
description | For genetic research to contribute more fully to furthering our knowledge of neuropathic pain, we require an agreed, valid, and feasible approach to phenotyping, to allow collaboration and replication in samples of sufficient size. Results from genetic studies on neuropathic pain have been inconsistent and have met with replication difficulties, in part because of differences in phenotypes used for case ascertainment. Because there is no consensus on the nature of these phenotypes, nor on the methods of collecting them, this study aimed to provide guidelines on collecting and reporting phenotypes in cases and controls for genetic studies. Consensus was achieved through a staged approach: (1) systematic literature review to identify all neuropathic pain phenotypes used in previous genetic studies; (2) Delphi survey to identify the most useful neuropathic pain phenotypes and their validity and feasibility; and (3) meeting of experts to reach consensus on the optimal phenotype(s) to be collected from patients with neuropathic pain for genetic studies. A basic “entry level” set of phenotypes was identified for any genetic study of neuropathic pain. This set identifies cases of “possible” neuropathic pain, and controls, and includes: (1) a validated symptom-based questionnaire to determine whether any pain is likely to be neuropathic; (2) body chart or checklist to identify whether the area of pain distribution is neuroanatomically logical; and (3) details of pain history (intensity, duration, any formal diagnosis). This NeuroPPIC “entry level” set of phenotypes can be expanded by more extensive and specific measures, as determined by scientific requirements and resource availability. |
format | Online Article Text |
id | pubmed-4747983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-47479832016-02-17 Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations van Hecke, Oliver Kamerman, Peter R. Attal, Nadine Baron, Ralf Bjornsdottir, Gyda Bennett, David L.H. Bennett, Michael I. Bouhassira, Didier Diatchenko, Luda Freeman, Roy Freynhagen, Rainer Haanpää, Maija Jensen, Troels S. Raja, Srinivasa N. Rice, Andrew S.C. Seltzer, Ze'ev Thorgeirsson, Thorgeir E. Yarnitsky, David Smith, Blair H. Pain Research Paper For genetic research to contribute more fully to furthering our knowledge of neuropathic pain, we require an agreed, valid, and feasible approach to phenotyping, to allow collaboration and replication in samples of sufficient size. Results from genetic studies on neuropathic pain have been inconsistent and have met with replication difficulties, in part because of differences in phenotypes used for case ascertainment. Because there is no consensus on the nature of these phenotypes, nor on the methods of collecting them, this study aimed to provide guidelines on collecting and reporting phenotypes in cases and controls for genetic studies. Consensus was achieved through a staged approach: (1) systematic literature review to identify all neuropathic pain phenotypes used in previous genetic studies; (2) Delphi survey to identify the most useful neuropathic pain phenotypes and their validity and feasibility; and (3) meeting of experts to reach consensus on the optimal phenotype(s) to be collected from patients with neuropathic pain for genetic studies. A basic “entry level” set of phenotypes was identified for any genetic study of neuropathic pain. This set identifies cases of “possible” neuropathic pain, and controls, and includes: (1) a validated symptom-based questionnaire to determine whether any pain is likely to be neuropathic; (2) body chart or checklist to identify whether the area of pain distribution is neuroanatomically logical; and (3) details of pain history (intensity, duration, any formal diagnosis). This NeuroPPIC “entry level” set of phenotypes can be expanded by more extensive and specific measures, as determined by scientific requirements and resource availability. Wolters Kluwer 2015-11 2015-10-22 /pmc/articles/PMC4747983/ /pubmed/26469320 http://dx.doi.org/10.1097/j.pain.0000000000000335 Text en Copyright © 2015 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper van Hecke, Oliver Kamerman, Peter R. Attal, Nadine Baron, Ralf Bjornsdottir, Gyda Bennett, David L.H. Bennett, Michael I. Bouhassira, Didier Diatchenko, Luda Freeman, Roy Freynhagen, Rainer Haanpää, Maija Jensen, Troels S. Raja, Srinivasa N. Rice, Andrew S.C. Seltzer, Ze'ev Thorgeirsson, Thorgeir E. Yarnitsky, David Smith, Blair H. Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
title | Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
title_full | Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
title_fullStr | Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
title_full_unstemmed | Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
title_short | Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
title_sort | neuropathic pain phenotyping by international consensus (neuroppic) for genetic studies: a neupsig systematic review, delphi survey, and expert panel recommendations |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747983/ https://www.ncbi.nlm.nih.gov/pubmed/26469320 http://dx.doi.org/10.1097/j.pain.0000000000000335 |
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