Advertisement
Research Article| Volume 19, ISSUE 8, P897-909, August 2018

Pain Adaptability in Individuals With Chronic Musculoskeletal Pain Is Not Associated With Conditioned Pain Modulation

      Highlights

      • The dichotomy of pain adaptability existed in chronic musculoskeletal pain patients.
      • Pain adaptability was dissociated with the potency of conditioned pain modulation.
      • Pain adaptability could reflect the temporal aspect of pain inhibition.

      Abstract

      Healthy humans can be divided into the pain adaptive (PA) and the pain nonadaptive (PNA) groups; PA showed a greater decrease in pain rating to a cold pressor test (CPT) than PNA. This study examined if the dichotomy of pain adaptability existed in individuals with chronic musculoskeletal pain. CPTs at 2°C and 7°C were used to assess the status of pain adaptability in participants with either chronic nonspecific low back pain or knee osteoarthritis. The participants' potency of conditioned pain modulation (CPM) and local inhibition were measured. The strengths of pain adaptability at both CPTs were highly correlated. PA and PNA did not differ in their demographic characteristics, pain thresholds from thermal and pressure stimuli, or potency of local inhibition or CPM. PA reached their maximum pain faster than PNA (t41 = −2.76, P < .01), and had a gradual reduction of pain unpleasantness over 7 days whereas PNA did not (F6,246 = 3.01, P = .01). The dichotomy of pain adaptability exists in musculoskeletal pain patients. Consistent with the healthy human study, the strength of pain adaptability and potency of CPM are not related. Pain adaptability could be another form of endogenous pain inhibition of which clinical implication is yet to be understood.

      Perspective

      The dichotomy of pain adaptability was identified in healthy humans. The current study confirms that this dichotomy also exists in individuals with chronic musculoskeletal pain, and could be reliably assessed with CPTs at 2°C and 7°C. Similar to the healthy human study, pain adaptability is not associated with CPM, and may reflect the temporal aspect of pain inhibition.

      Key words

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to The Journal of Pain
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Ahles T.A.
        • Blanchard E.B.
        • Leventhal H.
        Cognitive control of pain: Attention to the sensory aspects of the cold pressor stimulus.
        Cognit Ther Res. 1983; 7: 159-177
        • Allen K.D.
        • Golightly Y.M.
        Epidemiology of osteoarthritis: State of the evidence.
        Curr Opin Rheumatol. 2015; 27: 276-283
        • Altman R.
        • Asch E.
        • Bloch D.
        • Bole G.
        • Borenstein D.
        • Brandt K.
        • Christy W.
        • Cooke T.D.
        • Greenwald R.
        • Hochberg M.
        • Howell D.
        • Kaplan D.
        • Koopman W.
        • Longley S.
        • Mankin H.
        • McShane D.
        • Medsger T.
        • Meenan R.
        • Mikkelsen W.
        • Moskowitz R.
        • Murphy W.
        • Rothschild B.
        • Segal M.
        • Sokoloff L.
        • Wolfe F.
        Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association.
        Arthritis Rheum. 1986; 29: 1039-1049
        • Arendt-Nielsen L.
        • Egsgaard L.L.
        • Petersen K.K.
        • Eskehave T.N.
        • Graven-Nielsen T.
        • Hoeck H.C.
        • Simonsen O.
        A mechanism-based pain sensitivity index to characterize knee osteoarthritis patients with different disease stages and pain levels.
        Eur J Pain. 2015; 19: 1406-1417
        • Arendt-Nielsen L.
        • Nie H.
        • Laursen M.B.
        • Laursen B.S.
        • Madeleine P.
        • Simonsen O.H.
        • Graven-Nielsen T.
        Sensitization in patients with painful knee osteoarthritis.
        Pain. 2010; 149: 573-581
        • Asghari A.
        • Nicholas M.K.
        Pain self-efficacy beliefs and pain behaviour. A prospective study.
        Pain. 2001; 94: 85-100
        • Blumenstiel K.
        • Gerhardt A.
        • Rolke R.
        • Bieber C.
        • Tesarz J.
        • Friederich H.C.
        • Eich W.
        • Treede R.D.
        Quantitative sensory testing profiles in chronic back pain are distinct from those in fibromyalgia.
        Clin J Pain. 2011; 27: 682-690
        • Brown T.A.
        • Chorpita B.F.
        • Korotitsch W.
        • Barlow D.H.
        Psychometric properties of the Depression Anxiety Stress Scales (DASS) in clinical samples.
        Behav Res Ther. 1997; 35: 79-89
        • Buysse D.J.
        • Reynolds 3rd, C.F.
        • Monk T.H.
        • Berman S.R.
        • Kupfer D.J.
        The Pittsburgh Sleep Quality Index: A new instrument for psychiatric practice and research.
        Psychiatry Res. 1989; 28: 193-213
        • Cardoso J.S.
        • Riley 3rd, J.L.
        • Glover T.
        • Sibille K.T.
        • Bartley E.J.
        • Goodin B.R.
        • Bulls H.W.
        • Herbert M.
        • Addison A.S.
        • Staud R.
        • Redden D.T.
        • Bradley L.A.
        • Fillingim R.B.
        • Cruz-Almeida Y.
        Experimental pain phenotyping in community-dwelling individuals with knee osteoarthritis.
        Pain. 2016; 157: 2104-2114
        • Chou R.
        • Qaseem A.
        • Snow V.
        • Casey D.
        • Cross Jr, J.T.
        • Shekelle P.
        • Owens D.K.
        Diagnosis and treatment of low back pain: A joint clinical practice guideline from the American College of Physicians and the American Pain Society.
        Ann Intern Med. 2007; 147: 478-491
        • Coghill R.C.
        • McHaffie J.G.
        • Yen Y.F.
        Neural correlates of interindividual differences in the subjective experience of pain.
        Proc Natl Acad Sci. 2003; 100: 8538-8542
        • Correa J.B.
        • Costa L.O.
        • de Oliveira N.T.
        • Sluka K.A.
        • Liebano R.E.
        Central sensitization and changes in conditioned pain modulation in people with chronic nonspecific low back pain: A case-control study.
        Exp Brain Res. 2015; 233: 2391-2399
        • Cruz-Almeida Y.
        • King C.D.
        • Goodin B.R.
        • Sibille K.T.
        • Glover T.L.
        • Riley J.L.
        • Sotolongo A.
        • Herbert M.S.
        • Schmidt J.
        • Fessler B.J.
        • Redden D.T.
        • Staud R.
        • Bradley L.A.
        • Fillingim R.B.
        Psychological profiles and pain characteristics of older adults with knee osteoarthritis.
        Arthritis Care Res. 2013; 65: 1786-1794
        • Devoize L.
        • Chalaye P.
        • Lafrenaye S.
        • Marchand S.
        • Dallel R.
        Relationship between adaptation and cardiovascular response to tonic cold and heat pain Adaptability to tonic pain and cardiovascular responses.
        Eur J Pain. 2015; 20: 731-741
        • Edwards R.R.
        • Dolman A.J.
        • Martel M.O.
        • Finan P.H.
        • Lazaridou A.
        • Cornelius M.
        • Wasan A.D.
        Variability in conditioned pain modulation predicts response to NSAID treatment in patients with knee osteoarthritis.
        BMC Musculoskelet Disord. 2016; 17: 284
        • Egsgaard L.L.
        • Eskehave T.N.
        • Bay-Jensen A.C.
        • Hoeck H.C.
        • Arendt-Nielsen L.
        Identifying specific profiles in patients with different degrees of painful knee osteoarthritis based on serological biochemical and mechanistic pain biomarkers: A diagnostic approach based on cluster analysis.
        Pain. 2015; 156: 96-107
        • Finan P.H.
        • Buenaver L.F.
        • Bounds S.C.
        • Hussain S.
        • Park R.J.
        • Haque U.J.
        • Campbell C.M.
        • Haythornthwaite J.A.
        • Edwards R.R.
        • Smith M.T.
        Discordance between pain and radiographic severity in knee osteoarthritis: findings from quantitative sensory testing of central sensitization.
        Arthritis Rheum. 2013; 65: 363-372
        • Fujii K.
        • Motohashi K.
        • Umino M.
        Heterotopic ischemic pain attenuates somatosensory evoked potentials induced by electrical tooth stimulation: diffuse noxious inhibitory controls in the trigeminal nerve territory.
        Eur J Pain. 2006; 10: 495-504
        • Gerhardt A.
        • Eich W.
        • Treede R.D.
        • Tesarz J.
        Conditioned pain modulation in patients with nonspecific chronic back pain with chronic local pain, chronic widespread pain, and fibromyalgia.
        Pain. 2017; 158: 430-439
        • Grandner M.A.
        • Kripke D.F.
        • Yoon I.Y.
        • Youngstedt S.D.
        Criterion validity of the Pittsburgh Sleep Quality Index: Investigation in a non-clinical sample.
        Sleep Biol Rhythms. 2006; 4: 129-139
        • Granovsky Y.
        • Nahman-Averbuch H.
        • Khamaisi M.
        • Granot M.
        Efficient conditioned pain modulation despite pain persistence in painful diabetic neuropathy.
        Pain Rep. 2017; 2: e592
        • Graven-Nielsen T.
        • Babenko V.
        • Svensson P.
        • Arendt-Nielsen L.
        Experimentally induced muscle pain induces hypoalgesia in heterotopic deep tissues, but not in homotopic deep tissues.
        Brain Res. 1998; 787: 203-210
        • Hagander L.G.
        • Midani H.A.
        • Kuskowski M.A.
        • Parry G.J.
        Quantitative sensory testing: effect of site and skin temperature on thermal thresholds.
        Clin Neurophysiol. 2000; 111: 17-22
        • Harkness E.F.
        • Macfarlane G.J.
        • Silman A.J.
        • McBeth J.
        Is musculoskeletal pain more common now than 40 years ago?: Two population-based cross-sectional studies.
        Rheumatology (Oxford). 2005; 44: 890-895
        • Heldestad V.
        • Linder J.
        • Sellersjo L.
        • Nordh E.
        Reproducibility and influence of test modality order on thermal perception and thermal pain thresholds in quantitative sensory testing.
        Clin Neurophysiol. 2010; 121: 1878-1885
        • Holm S.
        A simple sequentially rejective multiple test procedure.
        Scand J Stat. 1979; 6: 65-70
        • Houle T.T.
        • Miller S.
        • Lang J.E.
        • Booth J.L.
        • Curry R.S.
        • Harris L.
        • Aschenbrenner C.A.
        • Eisenach J.C.
        Day-to-day experience in resolution of pain after surgery.
        Pain. 2017; 158: 2147-2154
        • Hudon C.
        • Fortin M.
        • Vanasse A.
        Cumulative Illness Rating Scale was a reliable and valid index in a family practice context.
        J Clin Epidemiol. 2005; 58: 603-608
        • Jensen M.P.
        • Strom S.E.
        • Turner J.A.
        • Romano J.M.
        Validity of the Sickness Impact Profile Roland scale as a measure of dysfunction in chronic pain patients.
        Pain. 1992; 50: 157-162
        • Kashima K.
        • Rahman O.I.
        • Sakoda S.
        • Shiba R.
        Increased pain sensitivity of the upper extremities of TMD patients with myalgia to experimentally-evoked noxious stimulation: possibility of worsened endogenous opioid systems.
        Cranio. 1999; 17: 241-246
        • King C.D.
        • Sibille K.T.
        • Goodin B.R.
        • Cruz-Almeida Y.
        • Glover T.L.
        • Bartley E.
        • Riley J.L.
        • Herbert M.S.
        • Sotolongo A.
        • Schmidt J.
        • Fessler B.J.
        • Redden D.T.
        • Staud R.
        • Bradley L.A.
        • Fillingim R.B.
        Experimental pain sensitivity differs as a function of clinical pain severity in symptomatic knee osteoarthritis.
        Osteoarthritis Cartilage. 2013; 21: 1243-1252
        • Kittelson A.J.
        • Stevens-Lapsley J.E.
        • Schmiege S.J.
        Determination of pain phenotypes in knee osteoarthritis: A latent class analysis using data from the osteoarthritis initiative.
        Arthritis Care Res. 2016; 68: 612-620
        • Koes B.W.
        • van Tulder M.W.
        • Thomas S.
        Diagnosis and treatment of low back pain.
        BMJ. 2006; 332: 1430-1434
        • Kosek E.
        • Ordeberg G.
        Lack of pressure pain modulation by heterotopic noxious conditioning stimulation in patients with painful osteoarthritis before, but not following, surgical pain relief.
        Pain. 2000; 88: 69-78
        • Lewis G.N.
        • Heales L.
        • Rice D.A.
        • Rome K.
        • McNair P.J.
        Reliability of the conditioned pain modulation paradigm to assess endogenous inhibitory pain pathways.
        Pain Res Manag. 2012; 17: 98-102
        • Lewis G.N.
        • Rice D.A.
        • McNair P.J.
        Conditioned pain modulation in populations with chronic pain: A systematic review and meta-analysis.
        J Pain. 2012; 13: 936-944
        • Linn B.S.
        • Linn M.W.
        • Gurel L.
        Cumulative illness rating scale.
        J Am Geriatr Soc. 1968; 16: 622-626
        • Lovibond S.H.
        • Lovibond P.F.
        Manual for the Depression Anxiety Stress Scales. Sydney: Psychology Foundation.
        1995
        • Meucci R.D.
        • Fassa A.G.
        • Faria N.M.
        Prevalence of chronic low back pain: Systematic review.
        Rev Saude Publica. 2015; 49: 1
        • Mollayeva T.
        • Thurairajah P.
        • Burton K.
        • Mollayeva S.
        • Shapiro C.M.
        • Colantonio A.
        The Pittsburgh Sleep Quality Index as a screening tool for sleep dysfunction in clinical and non-clinical samples: A systematic review and meta-analysis.
        Sleep Med Rev. 2016; 25: 52-73
        • Neziri A.Y.
        • Curatolo M.
        • Limacher A.
        • Nuesch E.
        • Radanov B.
        • Andersen O.K.
        • Arendt-Nielsen L.
        • Juni P.
        Ranking of parameters of pain hypersensitivity according to their discriminative ability in chronic low back pain.
        Pain. 2012; 153: 2083-2091
        • Nielsen C.S.
        • Stubhaug A.
        • Price D.D.
        • Vassend O.
        • Czajkowski N.
        • Harris J.R.
        Individual differences in pain sensitivity: Genetic and environmental contributions.
        Pain. 2008; 136: 21-29
        • Nir R.R.
        • Yarnitsky D.
        • Honigman L.
        • Granot M.
        Cognitive manipulation targeted at decreasing the conditioning pain perception reduces the efficacy of conditioned pain modulation.
        Pain. 2012; 153: 170-176
        • Nouwen A.
        • Cloutier C.
        • Kappas A.
        • Warbrick T.
        • Sheffield D.
        Effects of focusing and distraction on cold pressor-induced pain in chronic back pain patients and control subjects.
        J Pain. 2006; 7: 62-71
        • Osman A.
        • Barrios F.X.
        • Gutierrez P.M.
        • Kopper B.A.
        • Merrifield T.
        • Grittmann L.
        The Pain Catastrophizing Scale: Further psychometric evaluation with adult samples.
        J Behav Med. 2000; 23: 351-365
        • Osman A.
        • Barrios F.X.
        • Kopper B.A.
        • Hauptmann W.
        • Jones J.
        • O'Neill E.
        Factor structure, reliability, and validity of the Pain Catastrophizing Scale.
        J Behav Med. 1997; 20: 589-605
        • Pickering G.
        • Pereira B.
        • Dufour E.
        • Soule S.
        • Dubray C.
        Impaired modulation of pain in patients with postherpetic neuralgia.
        Pain Res Manag. 2014; 19: e19-e23
        • Potvin S.
        • Larouche A.
        • Normand E.
        • de Souza J.B.
        • Gaumond I.
        • Marchand S.
        • Grignon S.
        No relationship between the ins del polymorphism of the serotonin transporter promoter and pain perception in fibromyalgia patients and healthy controls.
        Eur J Pain. 2010; 14: 742-746
        • Roland M.
        • Morris R.
        A study of the natural history of back pain. Part I: Development of a reliable and sensitive measure of disability in low-back pain.
        Spine. 1983; 8: 141-144
        • Rolke R.
        • Baron R.
        • Maier C.
        • Tolle T.R.
        • Treede R.D.
        • Beyer A.
        • Binder A.
        • Birbaumer N.
        • Birklein F.
        • Botefur I.C.
        • Braune S.
        • Flor H.
        • Huge V.
        • Klug R.
        • Landwehrmeyer G.B.
        • Magerl W.
        • Maihofner C.
        • Rolko C.
        • Schaub C.
        • Scherens A.
        • Sprenger T.
        • Valet M.
        • Wasserka B.
        Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Standardized protocol and reference values.
        Pain. 2006; 123: 231-243
        • Staud R.
        Evidence for shared pain mechanisms in osteoarthritis, low back pain, and fibromyalgia.
        Curr Rheumatol Rep. 2011; 13: 513-520
        • Staud R.
        • Robinson M.E.
        • Vierck Jr, C.J.
        • Price D.D.
        Diffuse noxious inhibitory controls (DNIC) attenuate temporal summation of second pain in normal males but not in normal females or fibromyalgia patients.
        Pain. 2003; 101: 167-174
        • Sullivan M.J.
        • Bishop S.R.
        • Pivik J.
        The pain catastrophizing scale: Development and validation.
        Psychol Assess. 1995; 7: 524-532
        • Svensson P.
        • Hashikawa C.H.
        • Casey K.L.
        Site- and modality-specific modulation of experimental muscle pain in humans.
        Brain Res. 1999; 851: 32-38
        • Tesarz J.
        • Gerhardt A.
        • Schommer K.
        • Treede R.D.
        • Eich W.
        Alterations in endogenous pain modulation in endurance athletes: An experimental study using quantitative sensory testing and the cold-pressor task.
        Pain. 2013; 154: 1022-1029
        • Tuveson B.
        • Leffler A.S.
        • Hansson P.
        Time dependent differences in pain sensitivity during unilateral ischemic pain provocation in healthy volunteers.
        Eur J Pain. 2006; 10: 225-232
        • Vos T.
        • Flaxman A.D.
        • Naghavi M.
        • Lozano R.
        • Michaud C.
        • Ezzati M.
        • Shibuya K.
        • Salomon J.A.
        • Abdalla S.
        • Aboyans V.
        • Abraham J.
        • Ackerman I.
        • Aggarwal R.
        • Ahn S.Y.
        • Ali M.K.
        • AlMazroa M.A.
        • Alvarado M.
        • Anderson H.R.
        • Anderson L.M.
        • Andrews K.G.
        • Atkinson C.
        • Baddour L.M.
        • Bahalim A.N.
        • Barker-Collo S.
        • Barrero L.H.
        • Bartels D.H.
        • Basáñez M.G.
        • Baxter A.
        • Bell M.L.
        • Benjamin E.J.
        • Bennett D.
        • Bernabé E.
        • Bhalla K.
        • Bhandari B.
        • Bikbov B.
        • Abdulhak A.B.
        • Birbeck G.
        • Black J.A.
        • Blencowe H.
        • Blore J.D.
        • Blyth F.
        • Bolliger I.
        • Bonaventure A.
        • Boufous S.
        • Bourne R.
        • Boussinesq M.
        • Braithwaite T.
        • Brayne C.
        • Bridgett L.
        • Brooker S.
        • Brooks P.
        • Brugha T.S.
        • Bryan-Hancock C.
        • Bucello C.
        • Buchbinder R.
        • Buckle G.
        • Budke C.M.
        • Burch M.
        • Burney P.
        • Burstein R.
        • Calabria B.
        • Campbell B.
        • Canter C.E.
        • Carabin H.
        • Carapetis J.
        • Carmona L.
        • Cella C.
        • Charlson F.
        • Chen H.
        • Cheng A.T.
        • Chou D.
        • Chugh S.S.
        • Coffeng L.E.
        • Colan S.D.
        • Colquhoun S.
        • Colson K.E.
        • Condon J.
        • Connor M.D.
        • Cooper L.T.
        • Corriere M.
        • Cortinovis M.
        • de Vaccaro K.C.
        • Couser W.
        • Cowie B.C.
        • Criqui M.H.
        • Cross M.
        • Dabhadkar K.C.
        • Dahiya M.
        • Dahodwala N.
        • Damsere-Derry J.
        • Danaei G.
        • Davis A.
        • De Leo D.
        • Degenhardt L.
        • Dellavalle R.
        • Delossantos A.
        • Denenberg J.
        • Derrett S.
        • Des Jarlais D.C.
        • Dharmaratne S.D.
        • Dherani M.
        • Diaz-Torne C.
        • Dolk H.
        • Dorsey E.R.
        • Driscoll T.
        • Duber H.
        • Ebel B.
        • Edmond K.
        • Elbaz A.
        • Ali S.E.
        • Erskine H.
        • Erwin P.J.
        • Espindola P.
        • Ewoigbokhan S.E.
        • Farzadfar F.
        • Feigin V.
        • Felson D.T.
        • Ferrari A.
        • Ferri C.P.
        • Fèvre E.M.
        • Finucane M.M.
        • Flaxman S.
        • Flood L.
        • Foreman K.
        • Forouzanfar M.H.
        • Fowkes F.G.
        • Franklin R.
        • Fransen M.
        • Freeman M.K.
        • Gabbe B.J.
        • Gabriel S.E.
        • Gakidou E.
        • Ganatra H.A.
        • Garcia B.
        • Gaspari F.
        • Gillum R.F.
        • Gmel G.
        • Gosselin R.
        • Grainger R.
        • Groeger J.
        • Guillemin F.
        • Gunnell D.
        • Gupta R.
        • Haagsma J.
        • Hagan H.
        • Halasa Y.A.
        • Hall W.
        • Haring D.
        • Haro J.M.
        • Harrison J.E.
        • Havmoeller R.
        • Hay R.J.
        • Higashi H.
        • Hill C.
        • Hoen B.
        • Hoffman H.
        • Hotez P.J.
        • Hoy D.
        • Huang J.J.
        • Ibeanusi S.E.
        • Jacobsen K.H.
        • James S.L.
        • Jarvis D.
        • Jasrasaria R.
        • Jayaraman S.
        • Johns N.
        • Jonas J.B.
        • Karthikeyan G.
        • Kassebaum N.
        • Kawakami N.
        • Keren A.
        • Khoo J.P.
        • King C.H.
        • Knowlton L.M.
        • Kobusingye O.
        • Koranteng A.
        • Krishnamurthi R.
        • Lalloo R.
        • Laslett L.L.
        • Lathlean T.
        • Leasher J.L.
        • Lee Y.Y.
        • Leigh J.
        • Lim S.S.
        • Limb E.
        • Lin J.K.
        • Lipnick M.
        • Lipshultz S.E.
        • Liu W.
        • Loane M.
        • Ohno S.L.
        • Lyons R.
        • Ma J.
        • Mabweijano J.
        • MacIntyre M.F.
        • Malekzadeh R.
        • Mallinger L.
        • Manivannan S.
        • Marcenes W.
        • March L.
        • Margolis D.J.
        • Marks G.B.
        • Marks R.
        • Matsumori A.
        • Matzopoulos R.
        • Mayosi B.M.
        • McAnulty J.H.
        • McDermott M.M.
        • McGill N.
        • McGrath J.
        • Medina-Mora M.E.
        • Meltzer M.
        • Memish Z.A.
        • Mensah G.A.
        • Merriman T.R.
        • Meyer A.C.
        • Miglioli V.
        • Miller M.
        • Miller T.R.
        • Mitchell P.B.
        • Mocumbi A.O.
        • Moffitt T.E.
        • Mokdad A.A.
        • Monasta L.
        • Montico M.
        • Moradi-Lakeh M.
        • Moran A.
        • Morawska L.
        • Mori R.
        • Murdoch M.E.
        • Mwaniki M.K.
        • Naidoo K.
        • Nair M.N.
        • Naldi L.
        • Narayan K.M.
        • Nelson P.K.
        • Nelson R.G.
        • Nevitt M.C.
        • Newton C.R.
        • Nolte S.
        • Norman P.
        • Norman R.
        • O'Donnell M.
        • O'Hanlon S.
        • Olives C.
        • Omer S.B.
        • Ortblad K.
        • Osborne R.
        • Ozgediz D.
        • Page A.
        • Pahari B.
        • Pandian J.D.
        • Rivero A.P.
        • Patten S.B.
        • Pearce N.
        • Padilla R.P.
        • Perez-Ruiz F.
        • Perico N.
        • Pesudovs K.
        • Phillips D.
        • Phillips M.R.
        • Pierce K.
        • Pion S.
        • Polanczyk G.V.
        • Polinder S.
        • Pope 3rd, C.A.
        • Popova S.
        • Porrini E.
        • Pourmalek F.
        • Prince M.
        • Pullan R.L.
        • Ramaiah K.D.
        • Ranganathan D.
        • Razavi H.
        • Regan M.
        • Rehm J.T.
        • Rein D.B.
        • Remuzzi G.
        • Richardson K.
        • Rivara F.P.
        • Roberts T.
        • Robinson C.
        • De Leòn F.R.
        • Ronfani L.
        • Room R.
        • Rosenfeld L.C.
        • Rushton L.
        • Sacco R.L.
        • Saha S.
        • Sampson U.
        • Sanchez-Riera L.
        • Sanman E.
        • Schwebel D.C.
        • Scott J.G.
        • Segui-Gomez M.
        • Shahraz S.
        • Shepard D.S.
        • Shin H.
        • Shivakoti R.
        • Singh D.
        • Singh G.M.
        • Singh J.A.
        • Singleton J.
        • Sleet D.A.
        • Sliwa K.
        • Smith E.
        • Smith J.L.
        • Stapelberg N.J.
        • Steer A.
        • Steiner T.
        • Stolk W.A.
        • Stovner L.J.
        • Sudfeld C.
        • Syed S.
        • Tamburlini G.
        • Tavakkoli M.
        • Taylor H.R.
        • Taylor J.A.
        • Taylor W.J.
        • Thomas B.
        • Thomson W.M.
        • Thurston G.D.
        • Tleyjeh I.M.
        • Tonelli M.
        • Towbin J.A.
        • Truelsen T.
        • Tsilimbaris M.K.
        • Ubeda C.
        • Undurraga E.A.
        • van der Werf M.J.
        • van Os J.
        • Vavilala M.S.
        • Venketasubramanian N.
        • Wang M.
        • Wang W.
        • Watt K.
        • Weatherall D.J.
        • Weinstock M.A.
        • Weintraub R.
        • Weisskopf M.G.
        • Weissman M.M.
        • White R.A.
        • Whiteford H.
        • Wiersma S.T.
        • Wilkinson J.D.
        • Williams H.C.
        • Williams S.R.
        • Witt E.
        • Wolfe F.
        • Woolf A.D.
        • Wulf S.
        • Yeh P.H.
        • Zaidi A.K.
        • Zheng Z.J.
        • Zonies D.
        • Lopez A.D.
        • Murray C.J.
        Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: A systematic analysis for the Global Burden of Disease Study 2010.
        Lancet. 2012; 380: 2163-2196
        • Wager T.D.
        • Rilling J.K.
        • Smith E.E.
        • Sokolik A.
        • Casey K.L.
        • Davidson R.J.
        • Kosslyn S.M.
        • Rose R.M.
        • Cohen J.D.
        Placebo-induced changes in fMRI in the anticipation and experience of pain.
        Science. 2004; 303: 1162
        • Wilder-Smith C.H.
        • Robert-Yap J.
        Abnormal endogenous pain modulation and somatic and visceral hypersensitivity in female patients with irritable bowel syndrome.
        World J Gastroenterol. 2007; 13: 3699-3704
        • Wolf S.
        • Hardy J.D.
        Studies on pain. Observations on pain due to local cooling and on factors involved in the “cold pressor” effect.
        J Clin Invest. 1941; 20: 521-533
        • Yarnitsky D.
        Role of endogenous pain modulation in chronic pain mechanisms and treatment.
        Pain. 2015; 156: S24-S31
        • Yarnitsky D.
        • Arendt-Nielsen L.
        • Bouhassira D.
        • Edwards R.R.
        • Fillingim R.B.
        • Granot M.
        • Hansson P.
        • Lautenbacher S.
        • Marchand S.
        • Wilder-Smith O.
        Recommendations on terminology and practice of psychophysical DNIC testing.
        Eur J Pain. 2010; 14: 339
        • Yarnitsky D.
        • Crispel Y.
        • Eisenberg E.
        • Granovsky Y.
        • Ben-Nun A.
        • Sprecher E.
        • Best L.A.
        • Granot M.
        Prediction of chronic post-operative pain: Pre-operative DNIC testing identifies patients at risk.
        Pain. 2008; 138: 22-28
        • Yarnitsky D.
        • Granot M.
        • Nahman-Averbuch H.
        • Khamaisi M.
        • Granovsky Y.
        Conditioned pain modulation predicts duloxetine efficacy in painful diabetic neuropathy.
        Pain. 2012; 153: 1193-1198
        • Zheng Z.
        • Gibson S.J.
        • Helme R.D.
        • McMeeken J.M.
        The effect of local anaesthetic on age-related capsaicin-induced mechanical hyperalgesia–a randomised, controlled study.
        Pain. 2009; 144: 101-109
        • Zheng Z.
        • Wang K.
        • Yao D.
        • Xue C.C.
        • Arendt-Nielsen L.
        Adaptability to pain is associated with potency of local pain inhibition, but not conditioned pain modulation: A healthy human study.
        Pain. 2014; 155: 968-976