The Association Between Conditioned Pain Modulation and Manipulation-induced Analgesia in People With Lateral Epicondylalgia

Ahmad Muhsen, Penny Moss, William Gibson, Bruce Walker, Angela Jacques, Stephan Schug, Anthony Wright, Ahmad Muhsen, Penny Moss, William Gibson, Bruce Walker, Angela Jacques, Stephan Schug, Anthony Wright

Abstract

Objectives: Conditioned pain modulation (CPM) and manipulation-induced analgesia (MIA) may activate similar neurophysiological mechanisms to mediate their analgesic effects. This study assessed the association between CPM and MIA responses in people with lateral epicondylalgia.

Materials and methods: Seventy participants with lateral epicondylalgia were assessed for CPM followed by MIA. A single assessor measured pressure pain thresholds (PPT) before, during, and after cold water immersion (10°C) of the asymptomatic hand and contralateral lateral glide (CLG) mobilization of the neck. For analyses, linear mixed models evaluated differences in CPM and MIA responses. Pearson partial correlations and regression analyses evaluated the association between CPM and MIA PPT.

Results: There was a significant increase (CPM and MIA, P<0.001) in PPT from baseline during the interventions (CPM mean: 195.84 kPa for elbow and 201.87 kPa for wrist, MIA mean: 123.01 kPa for elbow and 126.06 kPa for wrist) and after the interventions (CPM mean: 126.06 kPa for elbow, 114.24 kPa for wrist, MIA mean: 123.50 kPa for elbow and 122.16 kPa for wrist). There were also significant moderate and positive partial linear correlations (r: 0.40 to 0.54, P<0.001) between CPM and MIA measures, controlling for baseline measures. Regression analyses showed that CPM PPT was a significant predictor of MIA PPT (P<0.001) and the models explained between 73% and 85% of the variance in MIA PPT.

Discussion: This study showed that CPM and MIA responses were significantly correlated and that the CPM response was a significant predictor of MIA response.

Figures

FIGURE 1
FIGURE 1
Test session timeline. CLG indicates cervical lateral glide mobilization; CPM, conditioned pain modulation; CPT, cold pressor test; MIA, manipulation-induced analgesia; PFG, pain-free grip; PPT, pressure pain threshold; PRTEE, Patient-rated Tennis Elbow Evaluation; ULNDT-RN, upper limb neurodynamic test-radial nerve.
FIGURE 2
FIGURE 2
Consort diagram. Flow of participants during the recruitment process. CPM indicates conditioned pain modulation; MIA, manipulation-induced analgesia.
FIGURE 3
FIGURE 3
Differences in pressure pain threshold values between CPM and MIA over time (mean±SEM). CPM indicates conditioned pain modulation; MIA, manipulation-induced analgesia.

References

    1. Yarnitsky D, Arendt-Nielsen L, Bouhassira D, et al. Recommendations on terminology and practice of psychophysical DNIC testing. Eur J Pain. 2010;14:339.
    1. Le Bars HD, Dickenson HA, Besson HJ-M. Diffuse noxious inhibitory controls (DNIC). I. Effects on dorsal horn convergent neurones in the rat. Pain. 1979;6:283–304.
    1. Reinert A, Treede R-D, Bromm B. The pain inhibiting pain effect: an electrophysiological study in humans. Brain Res. 2000;862:103–110.
    1. Kennedy LD, Kemp IH, Ridout SCD, et al. Reliability of conditioned pain modulation: a systematic review. Pain. 2016;157:2410–2419.
    1. Yarnitsky D. Role of endogenous pain modulation in chronic pain mechanisms and treatment. Pain. 2015;156(suppl 1):S24–S31.
    1. Wright A. Hypoalgesia post-manipulative therapy: a review of a potential neurophysiological mechanism. Man Ther. 1995;1:11–16.
    1. Wright A, Vicenzino B.Shacklock M. Cervical mobilisation techniques, sympathetic nervous system effects and their relationship to analgesia. Moving in on Pain. Melbourne: Butterworth-Heinemann; 1995:164–173.
    1. Voogt L, de Vries J, Meeus M, et al. Analgesic effects of manual therapy in patients with musculoskeletal pain: a systematic review. Man Ther. 2015;20:250–256.
    1. Vicenzino B, Collins D, Benson HAE, et al. An investigation of the interrelationship between manipulative therapy-induced hypoalgesia and sympathoexcitation. J Manipulative Physiol Therap. 1998;21:448–453.
    1. Chalaye P, Devoize L, Lafrenaye S, et al. Cardiovascular influences on conditioned pain modulation. Pain. 2013;154:1377–1382.
    1. Chalaye P, Lafrenaye S, Goffaux P, et al. The role of cardiovascular activity in fibromyalgia and conditioned pain modulation. Pain. 2014;155:1064–1069.
    1. Sanada T, Kohase H, Makino K, et al. Effects of alpha-adrenergic agonists on pain modulation in diffuse noxious inhibitory control. JMed Dental Sci. 2009;56:17–24.
    1. Makino K, Kohase H, Sanada T, et al. Phenylephrine suppresses the pain modulation of diffuse noxious inhibitory control in rats. Anesth Analg. 2010;110:1215–1221.
    1. Bannister K, Lockwood S, Goncalves L, et al. An investigation into the inhibitory function of serotonin in diffuse noxious inhibitory controls in the neuropathic rat. Eur J Pain. 2017;21:750–760.
    1. Skyba DA, Radhakrishnan R, Rohlwing JJ, et al. Joint manipulation reduces hyperalgesia by activation of monoamine receptors but not opioid or GABA receptors in the spinal cord. Pain. 2003;106:159–168.
    1. Lemley JK, Hunter KS, Bement HMK. Conditioned pain modulation predicts exercise-induced hypoalgesia in healthy adults. Med Sci Sports Exerc. 2015;47:176–184.
    1. Vaegter HB, Handberg G, Jørgensen MN, et al. Aerobic exercise and cold pressor test induce hypoalgesia in active and inactive men and women. Pain Med. 2015;16:923–933.
    1. Haker E, Lundeberg T. Acupuncture treatment in epicondylalgia: a comparative study of two acupuncture techniques. Clin J Pain. 1990;6:221–226.
    1. Waller R, Straker L, O’Sullivan P, et al. Reliability of pressure pain threshold testing in healthy pain free young adults. Scand J Pain. 2015;9:38–41.
    1. Fernández-Carnero J, Fernández-De-Las-Peñas C, De La Llave-Rincón A, et al. Widespread mechanical pain hypersensitivity as sign of central sensitization in unilateral epicondylalgia: a blinded, controlled study. Clin J Pain. 2009;25:555–561.
    1. Locke D, Gibson W, Moss P, et al. Analysis of meaningful conditioned pain modulation effect in a pain-free adult population. J Pain. 2014;15:1190–1198.
    1. Vicenzino B, Collins D, Wright A. The initial effects of a cervical spine manipulative physiotherapy treatment on the pain and dysfunction of lateral epicondylalgia. Pain. 1996;68:69–74.
    1. Paungmali A, O’Leary S, Souvlis T, et al. Hypoalgesic and sympathoexcitatory effects of mobilization with movement for lateral epicondylalgia. Phys Ther. 2003;83:374–383.
    1. Smidt N, van Der Windt DA, Assendelft WJ, et al. Interobserver reproducibility of the assessment of severity of complaints, grip strength, and pressure pain threshold in patients with lateral epicondylitis. Arch Phys Med Rehabil. 2002;83:1145–1150.
    1. Butler DS. The Sensitive Nervous System. Adelaide: Noigroup Publications; 2000.
    1. Yaxley GA, Jull GA. Adverse tension in the neural system. A preliminary study of tennis elbow. Aust J Physiother. 1993;39:15–22.
    1. Hoffken O, Ozgul O, Enax-Krumova E, et al. Evoked potentials after painful cutaneous electrical stimulation depict pain relief during a conditioned pain modulation. BMC Neurol. 2017;17:167.
    1. Vicenzino B, Neal R, Collins D, et al. The displacement, velocity and frequency profile of the frontal plane motion produced by the cervical lateral glide treatment technique. Clin Biomech (Bristol, Avon). 1999;14:515–521.
    1. Vicenzino B, Cartwright T, Collins D, et al. An investigation of stress and pain perception during manual therapy in asymptomatic subjects. Eur J Pain. 1999;3:13–18.
    1. Macdermid J. Update: the Patient-Rated Forearm Evaluation Questionnaire is now the Patient-Rated Tennis Elbow. Evaluation. 2005;18:407–410.
    1. Overend TJ, Wuori-Fearn JL, Kramer JF, et al. Reliability of a Patient-rated Forearm Evaluation Questionnaire for patients with lateral epicondylitis. J Hand Ther. 1999;12:31–37.
    1. Rompe JD, Overend TJ, Macdermid JC. Validation of the Patient-rated Tennis Elbow Evaluation Questionnaire. J Hand Ther. 2007;20:3–11.
    1. Vincent JI, Macdermid JC, King GJ, et al. Validity and sensitivity to change of patient-reported pain and disability measures for elbow pathologies. J Orthop Sports Phys Ther. 2013;43:263–274.
    1. Gerhardt A, Eich W, Treede R-D, et al. Conditioned pain modulation in patients with nonspecific chronic back pain with chronic local pain, chronic widespread pain, and fibromyalgia. Pain. 2017;158:430–439.
    1. Rathleff M, Stephenson A, Mellor R, et al. Adults with patellofemoral pain do not exhibit manifestations of peripheral and central sensitization when compared to healthy pain-free age and sex matched controls—An assessor blinded cross-sectional study. PLoS One. 2017;12:e0188930.
    1. Leffler A-S, Hansson P, Kosek E. Somatosensory perception in a remote pain-free area and function of diffuse noxious inhibitory controls (DNIC) in patients suffering from long-term trapezius myalgia. Eur J Pain. 2002;6:149–159.
    1. Pud D, Sprecher E, Yarnitsky D. Homotopic and heterotopic effects of endogenous analgesia in healthy volunteers. Neurosci Lett. 2005;380:209–213.
    1. Lim WEC, Sterling M, Vicenzino B. Chronic lateral epicondylalgia does not exhibit mechanical pain modulation in response to noxious conditioning heat stimulus. Clin J Pain. 2017;33:932–938.
    1. Oono Y, Nie H, Matos RL, et al. The inter- and intra-individual variance in descending pain modulation evoked by different conditioning stimuli in healthy men. Scand J Pain. 2011;2:162–169.
    1. Fernández-Carnero J, Fernández-de-Las-Peñas C, Cleland JA. Immediate hypoalgesic and motor effects after a single cervical spine manipulation in subjects with lateral epicondylalgia. J Manipulative Physiol Ther. 2008;31:675–681.
    1. Maduro de Camargo V, Alburquerque-Sendín F, Bérzin F, et al. Immediate effects on electromyographic activity and pressure pain thresholds after a cervical manipulation in mechanical neck pain: a randomized controlled trial. J Manipulative Physiol Ther. 2011;34:211–220.
    1. Moss P, Sluka K, Wright A. The initial effects of knee joint mobilization on osteoarthritic hyperalgesia. Man Ther. 2007;12:109–118.
    1. Courtney CA, Steffen AD, Fernández-De-Las-Peñas C, et al. Joint mobilization enhances mechanisms of conditioned pain modulation in individuals with osteoarthritis of the knee. J Orthop Sports Phys Ther. 2016;46:168–176.
    1. La Cesa S, Tinelli E, Toschi N, et al. fMRI pain activation in the periaqueductal gray in healthy volunteers during the cold pressor test. Magn Reson Imaging. 2014;32:236–240.
    1. Sprenger C, Bingel U, Büchel C. Treating pain with pain: supraspinal mechanisms of endogenous analgesia elicited by heterotopic noxious conditioning stimulation. Pain. 2011;152:428–439.
    1. Piché M, Arsenault M, Rainville P. Cerebral and cerebrospinal processes underlying counterirritation analgesia. J Neurosci. 2009;29:14236–14246.
    1. Gay CW, Robinson ME, George SZ, et al. Immediate changes following manual therapy in resting state functional connectivity as measured by magnetic resonance imaging (fMRI) In subjects with induced low back pain. J Manipulative Physiol Ther. 2014;37:614–627.
    1. Sparks C, Cleland JA, Elliott JM, et al. Using functional magnetic resonance imaging to determine if cerebral hemodynamic responses to pain change following thoracic spine thrust manipulation in healthy individuals. J Orthop Sports Phys Therapy. 2013;43:340–348.
    1. Boendermaker B, Meier ML, Luechinger R, et al. The cortical and cerebellar representation of the lumbar spine. Hum Brain Mapp. 2014;35:3962–3971.
    1. Yarnitsky D, Granot M, Nahman-Averbuch H, et al. Conditioned pain modulation predicts duloxetine efficacy in painful diabetic neuropathy. Pain. 2012;153:1193–1198.
    1. Bannister K, Patel R, Goncalves L, et al. Diffuse noxious inhibitory controls and nerve injury: restoring an imbalance between descending monoamine inhibitions and facilitations. Pain. 2015;156:1803–1811.
    1. Edwards RR, Ness TJ, Fillingim RB. Endogenous opioids, blood pressure, and diffuse noxious inhibitory controls: a preliminary study. Percept Mot Skills. 2004;99:679–687.
    1. Hermans L, Nijs J, Calders P, et al. Influence of morphine and naloxone on pain modulation in rheumatoid arthritis, chronic fatigue syndrome/fibromyalgia, and controls: a double‐blind, randomized, placebo‐controlled, cross‐over study. Pain Pract. 2018;18:418–430.
    1. Peters LM, Schmidt JMA, Van Den Hout AM, et al. Chronic back pain, acute postoperative pain and the activation of diffuse noxious inhibitory controls (DNIC). Pain. 1992;50:177–187.
    1. Pertovaara A, Kemppainen P, Johansson G, et al. Ischemic pain nonsegmentally produces a predominant reduction of pain and thermal sensitivity in man: a selective role for endogenous opioids. Brain Res. 1982;251:83–92.
    1. Willer JC, Le Bars D, De Broucker T. Diffuse noxious inhibitory controls in man: involvement of an opioidergic link. Eur J Pharmacol. 1990;182:347–355.
    1. Vicenzino B, O’Callaghan J, Kermode F, et al. No influence of naloxone on the initial hypoalgesic effect of spinal manual therapy. Proceedings of the 9th World Congress on Pain. Prog Pain Res Manag. 2000;16:1039–1044.
    1. Zusman M, Edwards BC, Donaghy A. Investigation of a proposed mechanism for the relief of spinal pain with passive joint movement. J Man Med. 1989;4:58–61.
    1. Paungmali A, O’Leary S, Souvlis T, et al. Naloxone fails to antagonize initial hypoalgesic effect of a manual therapy treatment for lateral epicondylalgia. J Manipulative Physiol Ther. 2004;27:180–185.
    1. Sluka KA, Wright A. Knee joint mobilization reduces secondary mechanical hyperalgesia induced by capsaicin injection into the ankle joint. Eur J Pain. 2001;5:81–87.

Source: PubMed

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