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. 2016 Sep;32(9):737-46.
doi: 10.1097/AJP.0000000000000354.

Fibromyalgia and Chronic Pain Syndromes: A White Paper Detailing Current Challenges in the Field

Affiliations

Fibromyalgia and Chronic Pain Syndromes: A White Paper Detailing Current Challenges in the Field

Lesley M Arnold et al. Clin J Pain. 2016 Sep.

Abstract

This manuscript, developed by a group of chronic pain researchers and clinicians from around the world, aims to address the state of knowledge about fibromyalgia (FM) and identify ongoing challenges in the field of FM and other chronic pain syndromes that may be characterized by pain centralization/amplification/hypersensitivity. There have been many exciting developments in research studies of the pathophysiology and treatment of FM and related syndromes that have the potential to improve the recognition and management of patients with FM and other conditions with FM-like pain. However, much of the new information has not reached all clinicians, especially primary care clinicians, who have the greatest potential to use this new knowledge to positively impact their patients' lives. Furthermore, there are persistent misconceptions about FM and a lack of consensus regarding the diagnosis and treatment of FM. This paper presents a framework for future global efforts to improve the understanding and treatment of FM and other associated chronic pain syndromes, disseminate research findings, identify ways to enhance advocacy for these patients, and improve global efforts to collaborate and reach consensus about key issues related to FM and chronic pain in general.

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Conflict of interest statement

Editorial support was provided by SuEllen Farrell at Health and Wellness Partners of New Jersey LLC, and was funded by Pfizer Inc., New York, NY. L.M.A.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; she did not receive an honorarium for serving as an author. She currently is a consultant for Pfizer Inc., New York, NY; Daiichi Sankyo, Tokyo, Japan; Forest Laboratories, New York, NY; and Zynerba Pharmaceuticals, Devon, PA; and has received past consultancy fees from Dainippon Sumitomo Pharma, Tokyo, Japan; Innovative Med Concepts LLC (IMC), Tuscaloosa, AL; Ironwood Pharmaceuticals, Cambridge, MA; Purdue Pharma, Stamford, CT; Shire, Lexington, MA; Theravance Biopharma, South San Francisco, CA; and Toray, Tokyo, Japan. She has grants pending with Pfizer Inc., New York, NY; Eli Lilly and Company, Indianapolis, IN; Forest Laboratories, New York, NY; and Tonix Pharmaceuticals, New York, NY (money to institution); and has received past grants from Cerephex Corporation, Los Altos, CA, and Theravance Biopharma, South San Francisco, CA (money to institution). She also has received payment for lectures on behalf of Pfizer Inc., New York, NY. E.C.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. Currently he is receiving consultancy fees and payment for lectures from Pfizer Inc., New York, NY. In addition, he is involved in Pfizer clinical trials for which fees are paid to his institution. D.J.C.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. He is a consultant for Tonix Pharmaceuticals, New York, NY; Theravance Biopharma, South San Francisco, CA; Pfizer Inc., New York, NY; Abbott Laboratories, Abbott Park, Illinois; Samumed, San Diego, CA; Merck, Kenilworth, NJ; Eli Lilly and Company, Indianapolis, IN; UCB Pharma, Smyrna, GA; Johnson & Johnson, New Brunswick, NJ; Forest Laboratories, New York, NY; Purdue Pharma, Stamford, CT; and Zynerba Pharmaceuticals, Devon, PA. He has received grants from the National Institutes of Health, Bethesda, MD, and Eli Lilly and Company, Indianapolis, IN, and has several grants pending with the National Institutes of Health. D.L.G.: is a consultant to Pfizer Inc., New York, NY, and received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. R.E.H.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. He also has received funding including grants (past; money to institution), consulting fees or honoraria (ongoing), support for travel to meetings (past), and fees for participating in review activities (past) from Pfizer Inc., New York, NY. M.H.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. He also has received consultancy fees (past), payment for lectures including service on speakers bureaus (current), and payment for development of educational presentations (current) from Pfizer Inc., New York, NY. T.S.J.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript (money to institution); he did not receive an honorarium for serving as an author. He also has received consultancy fees from Grünenthal, Aachen Germany (ongoing); Orion Pharma, Espoo, Finland (ongoing); and Pfizer Inc., New York, NY (past). K.N.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. He received consulting fees or honoraria and support for travel to meetings from Pfizer Inc., New York, NY (past). He also has received consultancy fees (ongoing), grants (ongoing), and speaker fees (past) from Pfizer Japan, Tokyo, Japan. S.L.S.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. In addition, he is receiving board membership fees from Pfizer Inc., New York, NY (current). T.U.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. He has received expert testimony fees (past), and grants (ongoing), from Pfizer Inc., New York, NY, and payment for lectures from other pharmaceutical companies. G.W.: received an honorarium and support for travel to a meeting to discuss the development of this manuscript; he did not receive an honorarium for serving as an author. He also has received payment for lectures, development of educational presentations, and meeting expenses, and has patents planned, pending, or issued with Pfizer Inc., New York, NY. S.F. has reported no conflicts of interest related to the content of this manuscript.

Figures

FIGURE 1
FIGURE 1
The pain continuum. Fibromyalgia (FM) is part of a larger continuum that comprises a number of clinical syndromes, some examples of which are shown here. This continuum ranges from predominantly nociceptive (peripheral), to predominantly neuropathic, to predominantly centralized pain conditions. Many experts agree that FM rests at the end of the continuum of pain processing. IBS indicates irritable bowel syndrome; TMJD, temporomandibular joint disorder. Courtesy of Don L. Goldenberg, MD.
FIGURE 2
FIGURE 2
The prevalence of fibromyalgia (FM) in other chronic pain conditions. A number of chronic pain conditions can overlap or coexist with FM. It is useful to keep this in mind so that proper diagnosis and management can be undertaken. The percentages in this graphic are for illustrative purposes and are based upon the medical literature. CRPS indicates complex regional pain syndrome; IBS, irritable bowel syndrome; TMJD, temporomandibular joint disorder. Courtesy of Daniel J. Clauw, MD.
FIGURE 3
FIGURE 3
Objective evidence shows augmented pain sensitivity in individuals with fibromyalgia (FM) versus matched controls. A, The graph depicts mean pain ratings plotted against stimulus intensity. In FM patients, a low stimulus pressure (2.4 kg/cm2) produced a much higher pain level (mean±SD, 11.30±0.90) than in controls. However, in control subjects, a much higher stimulus pressure elicited a pain response similar to that in FM patients. B, The scan is a functional magnetic resonance image (fMRI) of the brain of a patient with FM from the same study. The imaging study demonstrated that, in patients with FM, pain processing areas of the brain are activated at a much lower level of stimulus than in control subjects. There is overlap (as indicated by the yellow area on the fMRI) between the areas activated with a low-intensity stimulus in FM patients (red area) and a high-intensity stimulus in control subjects (green area). In other words, the overlap between brain activation in FM patients receiving a low stimulus pressure and controls receiving almost twice as much pressure (ie, the amount required to cause the same amount of pain) suggests a mechanism involving central amplification of pain in the patients with FM. Because regions of brain activation in FM patients and healthy controls overlap, the pain experienced by both sets of subjects is real. Objective evidence such as this would be a valuable component of the educational framework proposed in this publication. Gracely et al. Reprinted with permission from John Wiley and Sons. Copyright [John Wiley and Sons, New York, NY]. All permission requests for this image should be made to the copyright holder.

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