Cited by 29Fibromyalgia and Chronic Fatigue Syndrome ResearchPain Mechanisms and TreatmentsMyofascial pain diagnosis and treatment

Hyperbaric oxygen and aerobic exercise in the long-term treatment of fibromyalgia: A narrative review

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El-Shewy, Kholoud M., Kunbaz, Ahmad, Gad, Mohamed M., Al-Husseini, Muneer J., Saad, Anas M., Sammour, Yasser M., Abdel-Daim, Mohamed M.·2019·Biomedicine & Pharmacotherapy

Abstract

Chronic pain is one of the most common clinical presentations in the primary care settings. In the US, Fibromyalgia (FM) affects about 1-3% of adults and commonly occurs in adults between the ages of 40-50 years. FM causes widespread muscular pain and tenderness with hyperalgesia and allodynia and may be associated with other somatic complaints. Hyperbaric oxygen therapy (HBOT) has been utilized and has recently shown promising effects in the management of FM and other chronic pain disorders. In HBOT, the intermittent breathing of 100% oxygen in a pressurized chamber where the pressure is higher than 1 atmosphere absolute (ATA) has been utilized. HBOT exhibits a significant anti-inflammatory effect through reducing production of glial cells and inflammatory mediators which results in pain alleviation in different chronic pain conditions. HBOT can also influence neuroplasticity and affects the mitochondrial mechanisms resulting in functional brain changes. In addition to that, HBOT stimulates nitric oxide (NO) synthesis which helps in alleviating hyperalgesia and NO-dependent release of endogenous opioids which seemed to be the primary HBOT mechanism of antinociception. Moreover, aerobic exercise and meditative movement therapies (MMT) have gained attention for their role in pain alleviation through different anti-inflammatory and antioxidant mechanisms. In this review, we aim to elucidate the different mechanisms of HBOT and aerobic exercise in attenuating pain as adjuvant therapy in the multidisciplinary treatment strategy of chronic pain, and more particularly fibromyalgia.

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  • FM patients have symptoms of central sensitization, characterized by hypersensitivity to bright light, touch, noise, temperature, and mechanical pressure.

    “as have symptoms of central sensitization, characterized by hypersensitivity to bright light, touch, noise, temperature, and mechanical pressure.4,7,16”

    From A Review of Movement and Functional Impairments in Fibromyalgia: Implications for Targeted Treatment (2025) · cites this paper as [7]

    The Introduction describes fibromyalgia-related sensitivity to touch, mechanical stimuli, and heat or cold. Section 2 discusses increased sensitivity to a wide range of stimuli and central sensitization, but does not specifically identify hypersensitivity to bright light or noise in FM patients. (LLM, conf=0.87)

    Experimental — accuracy not yet measured
  • Fibromyalgia is a disabling chronic pain syndrome characterized by multiple symptoms, including medically unexplained widespread pain, fatigue, cognitive, mood and sleep disorders.

    “Fibromyalgia (FM) is a disabling chronic pain syndrome characterized by multiple symptoms, including medically unexplained widespread pain, fatigue, cognitive, mood and sleep disorders.1–11”

    From A Review of Movement and Functional Impairments in Fibromyalgia: Implications for Targeted Treatment (2025) · cites this paper as [7]

    The Introduction describes fibromyalgia as chronic and reports widespread pain, sleep disturbances, anxiety, cognitive dysfunction, and depressive symptoms; section 3 also mentions fatigue. Section 2 notes a lack of evidence for structural abnormalities, but the paper does not clearly characterize the pain as medically unexplained or fibromyalgia as disabling. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • FM has an unknown aetiology but has been described as a complex hyperalgesic pain syndrome in which abnormalities of central sensory processing interact with peripheral pain generators.

    “FM has an unknown aetiology but has been described as a complex hyperalgesic pain syndrome in which abnormalities of central sensory processing interact with peripheral pain generators.1,5,7”

    From A Review of Movement and Functional Impairments in Fibromyalgia: Implications for Targeted Treatment (2025) · cites this paper as [7]

    The Introduction describes fibromyalgia as involving hyperalgesia, and Section 2 discusses possible abnormalities in central pain processing and says nociceptive input can maintain central sensitization. Section 3 also describes hypothesized muscle abnormalities. The review does not clearly establish the claimed interaction between central abnormalities and peripheral pain generators; it presents these mechanisms as possibilities. (LLM, conf=0.82)

    Experimental — accuracy not yet measured
  • Understanding the underlying disease process will provide insights for targeted therapeutic approaches.

    “Understanding the underlying disease process will provide insights for targeted therapeutic approaches.7,10”
  • Fibromyalgia patients exhibit reduced blood flow and degenerative changes in the muscles.

    “FM patients exhibit reduced blood flow and degenerative changes in the muscles, presumably due to local hypoxia, creating higher levels of free radicals that induce apoptosis, reduce ATP and increase lactate concentrations in muscle cells, leading to muscle weakness and pain.7,15”

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Research works printed but not linked: 76

  1. A.M. Elliott, B.H. Smith, K.I. Penny, W.C. Smith, W.A. Chambers, The epide- miology of chronic pain in the community, Lancet (London, England) 354 (9186) (1999) 1248-1252, https://doi.org/10.1016/S0140-6736(99)03057-3. · DOI
  2. H. Merskey, N. Bogduk (Eds.), Classification of Chronic Pain. Descriptions of Chronic Pain Syndromes and Definitions of Pain Terms, IASP Press, 1994, , https://doi.org/10.1002/ana.20394 i-xvi. · DOI
  3. P. Mease, Fibromyalgia syndrome: review of clinical presentation, pathogenesis, outcome measures, and treatment, J. Rheumatol. 32 (2005) 6-21 http://search. ebscohost.com/login.aspx?direct=true&db=cin20&AN=2009041318&site= ehost-live.
  4. E.N. Thomas, F. Blotman, Aerobic exercise in fibromyalgia: a practical review, Rheumatol. Int. 30 (9) (2010) 1143-1150, https://doi.org/10.1007/s00296-010- 1369-6. · DOI
  5. G.A. Kelley, K.S. Kelley, D.L. Jones, Efficacy and effectiveness of exercise on tender points in adults with fibromyalgia: a meta-analysis of randomized controlled trials, Arthritis 2011 (2011) 1-10, https://doi.org/10.1155/2011/125485. · DOI
  6. C. Gouvinhas, D. Veiga, L. Mendonça, R. Sampaio, L.F. Azevedo, J.M. Castro- Lopes, Interventional pain management in multidisciplinary chronic pain clinics: a prospective multicenter cohort study with one-year follow-up, Pain Res. Treat. 2017 (2017) 1-11, https://doi.org/10.1155/2017/8402413. · DOI
  7. B.H. Smith, A.M. Elliott, W.A. Chambers, W.C. Smith, P.C. Hannaford, K. Penny, The impact of chronic pain in the community, Fam. Pract. 18 (3) (2001) 292-299, https://doi.org/10.1093/FAMPRA/18.3.292. · DOI · Paper page
  8. F. Di Sabato, M. Rocco, P. Martelletti, M. Giacovazzo, Hyperbaric oxygen in chronic cluster headaches: influence on serotonergic pathways, Undersea Hyperb. Med. 24 (2) (1997) 117-122 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=9171470.
  9. M.H. Bennett, C. French, A. Schnabel, J. Wasiak, P. Kranke, Normobaric and hy- perbaric oxygen therapy for migraine and cluster headache, Cochrane Database Syst. Rev. (3) (2008), https://doi.org/10.1002/14651858.CD005219.pub2. · DOI
  10. S. Yildiz, M.Z. Kiralp, A. Akin, et al., A new treatment modality for fibromyalgia syndrome: hyperbaric oxygen therapy, J. Int. Med. Res. 32 (3) (2004) 263-267, https://doi.org/10.1177/147323000403200305. · DOI
  11. M.Z. Kiralp, Ş Yildiz, D. Vural, I. Keskin, H. Ay, H. Dursun, Effectiveness of hy- perbaric oxygen therapy in the treatment of complex regional pain syndrome, J. Int. Med. Res. 32 (3) (2004) 258-262, https://doi.org/10.1177/ 147323000403200304. · DOI
  12. N. Gu, J.Y. Niu, W.T. Liu, et al., Hyperbaric oxygen therapy attenuates neuropathic hyperalgesia in rats and idiopathic trigeminal neuralgia in patients, Eur. J. Pain (United Kingdom) 16 (8) (2012) 1094-1105, https://doi.org/10.1002/j.1532- 2149.2012.00113.x. · DOI
  13. S. Yildiz, G. Uzun, M.Z. Kiralp, Hyperbaric oxygen therapy in chronic pain man- agement, Curr. Pain Headache Rep. 10 (2) (2006) 95-100, https://doi.org/10. 1007/s11916-006-0019-x. · DOI
  14. J. Hui, Z.J. Zhang, X. Zhang, Y. Shen, Y.J. Gao, Repetitive hyperbaric oxygen treatment attenuates complete Freund's adjuvant-induced pain and reduces glia- mediated neuroinflammation in the spinal cord, J. Pain 14 (7) (2013) 747-758, https://doi.org/10.1016/j.jpain.2013.02.003. · DOI
  15. S. Efrati, G. Fishlev, Y. Bechor, et al., Hyperbaric oxygen induces late neuroplas- ticity in post stroke patients-randomized, prospective trial, PLoS One 8 (1) (2013), https://doi.org/10.1371/journal.pone.0053716 e53716. · DOI
  16. S. Efrati, H. Golan, Y. Bechor, et al., Hyperbaric oxygen therapy can diminish fibromyalgia syndrome -prospective clinical trial, PLoS One 10 (5) (2015), https://doi.org/10.1371/journal.pone.0127012. · DOI
  17. B. Van Houdenhove, E. Neerinckx, P. Onghena, R. Lysens, H. Vertommen, Premorbid "overactive" lifestyle in chronic fatigue syndrome and fibromyalgia: an etiological factor or proof of good citizenship? J. Psychosom. Res. 51 (4) (2001) 571-576, https://doi.org/10.1016/S0022-3999(01)00247-1. · DOI
  18. M. Meeus, J. Nijs, L. Hermans, D. Goubert, P. Calders, The role of mitochondrial dysfunctions due to oxidative and nitrosative stress in the chronic pain or chronic fatigue syndromes and fibromyalgia patients: peripheral and central mechanisms as therapeutic targets? Expert Opin. Ther. Targets 17 (9) (2013) 1081-1089, https://doi.org/10.1517/14728222.2013.818657. · DOI
  19. J.H. Park, P. Phothimat, C.T. Oates, M. Hernanz-Schulman, N.J. Olsen, Use of P-31 magnetic resonance spectroscopy to detect metabolic abnormalities in muscles of patients with fibromyalgia, Arthritis Rheum. 41 (3) (1998) 406-413, https://doi. org/10.1002/1529-0131(199803)41:3<406::AID-ART5>3.0.CO;2-L. · DOI
  20. N. Lund, A. Bengtsson, P. Thorborg, Muscle tissue oxygen pressure in primary fibromyalgia, Scand. J. Rheumatol. 15 (2) (1986) 165-173, https://doi.org/10. 3109/03009748609102084. · DOI
  21. G. Yu, T. Durduran, G. Lech, et al., Time-dependent blood flow and oxygenation in human skeletal muscles measured with noninvasive near-infrared diffuse optical spectroscopies, J. Biomed. Opt. 10 (2) (2005) 24027, https://doi.org/10.1117/1. 1884603. · DOI
  22. S.A. Detmer, D.C. Chan, Functions and dysfunctions of mitochondrial dynamics, Nat. Rev. Mol. Cell Biol. 8 (11) (2007) 870-879, https://doi.org/10.1038/ nrm2275. · DOI · Paper page
  23. E.P. Kindwall, L.J. Gottlieb, D.L. Larson, Hyperbaric oxygen therapy in plastic surgery: a review article, Plast. Reconstr. Surg. 88 (5) (1991) 898-908.
  24. J. Hink, E. Jansen, Are superoxide and/or hydrogen peroxide responsible for some of the beneficial effects of hyperbaric oxygen therapy? Med. Hypotheses 57 (6) (2001) 764-769, https://doi.org/10.1054/mehy.2001.1488. · DOI
  25. S. Oter, A. Korkmaz, T. Topal, et al., Correlation between hyperbaric oxygen ex- posure pressures and oxidative parameters in rat lung, brain, and erythrocytes, Clin. Biochem. 38 (8) (2005) 706-711, https://doi.org/10.1016/j.clinbiochem. 2005.04.005. · DOI
  26. A. Korkmaz, S. Öter, S. Sadir, et al., Exposure time related oxidative action of hyperbaric oxygen in rat brain, Neurochem. Res. 33 (1) (2008) 160-166, https:// doi.org/10.1007/s11064-007-9428-4. · DOI
  27. H. Ay, T. Topal, M. Özler, et al., Persistence of hyperbaric oxygen-induced oxi- dative effects after exposure in rat brain cortex tissue, Life Sci. 80 (22) (2007) 2025-2029, https://doi.org/10.1016/J.LFS.2007.03.002. · DOI
  28. E. Palzur, M. Zaaroor, E. Vlodavsky, F. Milman, J.F. Soustiel, Neuroprotective effect of hyperbaric oxygen therapy in brain injury is mediated by preservation of mitochondrial membrane properties, Brain Res. 1221 (2008) 126-133, https:// doi.org/10.1016/j.brainres.2008.04.078. · DOI
  29. M. Brentnall, L. Rodriguez-Menocal, R.L. De Guevara, E. Cepero, L.H. Boise, Caspase-9, caspase-3 and caspase-7 have distinct roles during intrinsic apoptosis, BMC Cell Biol. 14 (2013) 32, https://doi.org/10.1186/1471-2121-14-32. · DOI
  30. E. Vlodavsky, E. Palzur, M. Feinsod, J.F. Soustiel, Evaluation of the apoptosis- related proteins of the BCL-2 family in the traumatic penumbra area of the rat model of cerebral contusion, treated by hyperbaric oxygen therapy: a quantitative immunohistochemical study, Acta Neuropathol. 110 (2) (2005) 120-126, https:// doi.org/10.1007/s00401-004-0946-8. · DOI
  31. T.S. Jensen, R. Baron, M. Haanpää, et al., A new definition of neuropathic pain, Pain 152 (10) (2011) 2204-2205, https://doi.org/10.1016/j.pain.2011.06.017. · DOI
  32. G. Moalem, D.J. Tracey, Immune and inflammatory mechanisms in neuropathic pain, Brain Res. Rev. 51 (2) (2006) 240-264, https://doi.org/10.1016/j. brainresrev.2005.11.004. · DOI
  33. J.-M. Zhang, J. An, Cytokines, inflammation, and pain, Int. Anesthesiol. Clin. 45 (2) (2007) 27-37, https://doi.org/10.1097/AIA.0b013e318034194e. · DOI
  34. Y.-Q. Zhou, Z. Liu, Z.-H. Liu, et al., Interleukin-6: an emerging regulator of pa- thological pain, J. Neuroinflammation 13 (1) (2016) 141, https://doi.org/10. 1186/s12974-016-0607-6. · DOI
  35. K. Ren, R. Torres, Role of interleukin-1beta during pain and inflammation, Brain Res. Rev. 60 (1) (2009) 57-64, https://doi.org/10.1016/j.brainresrev.2008.12. 020. · DOI
  36. A. Latremoliere, C.J. Woolf, Central sensitization: a generator of pain hy- persensitivity by central neural plasticity, J. Pain 10 (9) (2009) 895-926, https:// doi.org/10.1016/j.jpain.2009.06.012. · DOI · Paper page
  37. C.D. Thompson, M.L. Uhelski, J.R. Wilson, P.N. Fuchs, Hyperbaric oxygen treat- ment decreases pain in two nerve injury models, Neurosci. Res. 66 (3) (2010) 279-283, https://doi.org/10.1016/j.neures.2009.11.010. · DOI
  38. B.S. Zhao, L.X. Meng, Y.Y. Ding, Y.Y. Cao, Hyperbaric oxygen treatment produces an antinociceptive response phase and inhibits astrocyte activation and in- flammatory response in a rat model of neuropathic pain, J. Mol. Neurosci. 53 (2) (2014) 251-261, https://doi.org/10.1007/s12031-013-0213-3. · DOI
  39. Y. Inamoto, F. Okuno, K. Saito, et al., Effect of hyperbaric oxigenation on mac- rophage function in mice, Biochem. Biophys. Res. Commun. 31 (2) (1991) 1-19, https://doi.org/10.1016/0006-291X(91)91901-N. · DOI
  40. F. Li, L. Fang, S. Huang, et al., Hyperbaric oxygenation therapy alleviates chronic constrictive injury-induced neuropathic pain and reduces tumor necrosis factor- alpha production, Anesth. Analg. 113 (3) (2011) 626-633, https://doi.org/10. 1213/ANE.0b013e31821f9544. · DOI
  41. W.-S. Gui, X. Wei, C.-L. Mai, et al., Interleukin-1β overproduction is a common cause for neuropathic pain, memory deficit, and depression following peripheral nerve injury in rodents, Mol. Pain 12 (2016), https://doi.org/10.1177/ 1744806916646784 174480691664678. · DOI
  42. L. Leung, C.M. Cahill, TNF-alpha and neuropathic pain-a review, J. Neuroinflammation 7 (2010) 27, https://doi.org/10.1186/1742-2094-7-27. · DOI
  43. N. Kobayashi, S.-i. Mita, K. Yoshida, et al., Celiprolol activates eNOS through the PI3K-Akt pathway and inhibits VCAM-1 via NF-B induced by oxidative stress, Hypertension 42 (5) (2003) 1004-1013, https://doi.org/10.1161/01.HYP. 0000097547.35570.70. · DOI
  44. A.A. Larson, S.L. Giovengo, I.J. Russell, J.E. Michalek, Changes in the concentra- tions of amino acids in the cerebrospinal fluid that correlate with pain in patients with fibromyalgia: implications for nitric oxide pathways, Pain 87 (2) (2000) 201-211, https://doi.org/10.1016/S0304-3959(00)00284-0. · DOI
  45. G. Laumet, S.-R. Chen, H.-L. Pan, NMDA receptors and signaling in chronic neu- ropathic pain, The NMDA Receptors, Springer International Publishing, Cham, 2017, pp. 103-119, https://doi.org/10.1007/978-3-319-49795-2_6. · DOI
  46. M.A. Sackner, E.M. Gummels, J.A. Adams, Say NO to fibromyalgia and chronic fatigue syndrome: an alternative and complementary therapy to aerobic exercise, Med. Hypotheses 63 (1) (2004) 118-123, https://doi.org/10.1016/j.mehy.2004. 01.025. · DOI
  47. Y. Ohgami, C.C. Zylstra, L.P. Quock, E. Chung, D.Y. Shirachi, R.M. Quock, Nitric oxide in hyperbaric oxygen-induced acute antinociception in mice, Neuroreport 20 (15) (2009) 1325-1329, https://doi.org/10.1097/WNR.0b013e3283305a49. · DOI
  48. J.H. Heeman, Y. Zhang, D.Y. Shirachi, R.M. Quock, Involvement of spinal cord opioid mechanisms in the acute antinociceptive effect of hyperbaric oxygen in mice, Brain Res. 1540 (2013) 42-47, https://doi.org/10.1016/j.brainres.2013.09. 050. · DOI
  49. L.M. Zelinski, Y. Ohgami, E. Chung, D.Y. Shirachi, R.M. Quock, A prolonged nitric oxide-dependent, opioid-mediated antinociceptive effect of hyperbaric oxygen in mice, J. Pain 10 (2) (2009) 167-172, https://doi.org/10.1016/j.jpain.2008.08. 003. · DOI
  50. M. Tanabe, Y. Nagatani, K. Saitoh, K. Takasu, H. Ono, Pharmacological assess- ments of nitric oxide synthase isoforms and downstream diversity of NO signaling in the maintenance of thermal and mechanical hypersensitivity after peripheral nerve injury in mice, Neuropharmacology 56 (3) (2009) 702-708, https://doi.org/ 10.1016/j.neuropharm.2008.12.003. · DOI
  51. G. Han, L. Li, Meng L-XX, Effects of hyperbaric oxygen on pain-related behaviors and nitric oxide synthase in a rat model of neuropathic pain, Pain Res. Manag. 18 (3) (2013) 137-141, https://doi.org/10.1155/2013/147043. · DOI
  52. V.A. Straub, J. Grant, M. O'Shea, P.R. Benjamin, Modulation of serotonergic neurotransmission by nitric oxide, J. Neurophysiol. 97 (2) (2007) 1088-1099, https://doi.org/10.1152/jn.01048.2006. · DOI
  53. N.T. Sandor, A. Brassai, A. Pliskas, B. Lendvai, Role of nitric oxide in modulating neurotransmitter release from rat striatum, Brain Res. Bull. 36 (5) (1995) 483-486, https://doi.org/10.1016/0361-9230(94)00229-T. · DOI
  54. H.D. Wilson, J.R. Wilson, P.N. Fuchs, Hyperbaric oxygen treatment decreases in- flammation and mechanical hypersensitivity in an animal model of inflammatory pain, Brain Res. 1098 (1) (2006) 126-128, https://doi.org/10.1016/j.brainres. 2006.04.088. · DOI
  55. G. Sumen, M. Cimsit, L. Eroglu, Hyperbaric oxygen treatment reduces carra- geenan-induced acute inflammation in rats, Eur. J. Pharmacol. 431 (2) (2001) 265-268, https://doi.org/10.1016/S0014-2999(01)01446-7. · DOI
  56. Medicine AC of S. ACSM's Guidelines for Exercise Testing and Prescription, Lippincott Williams & Wilkins, 2013 books.google.com VN -readcube.com.
  57. J. Bidonde, A.J. Busch, C.L. Schachter, et al., Aerobic exercise training for adults with fibromyalgia, Cochrane Database Syst. Rev. 2017 (6) (2017), https://doi.org/ 10.1002/14651858.CD012700. · DOI
  58. J. Henriksson, J.S. Reitman, Time course of changes in human skeletal muscle succinate dehydrogenase and cytochrome oxidase activities and maximal oxygen uptake with physical activity and inactivity, Acta Physiol. Scand. 99 (1) (1977) 91-97, https://doi.org/10.1111/j.1748-1716.1977.tb10356.x. · DOI · Paper page
  59. B. Egan, P. Dowling, P.L. O'Connor, et al., 2-D DIGE analysis of the mitochondrial proteome from human skeletal muscle reveals time course-dependent remodelling in response to 14 consecutive days of endurance exercise training, Proteomics 11 (8) (2011) 1413-1428, https://doi.org/10.1002/pmic.201000597. · DOI
  60. T.P. Gavin, R.S. Ruster, J.A. Carrithers, et al., No difference in the skeletal muscle angiogenic response to aerobic exercise training between young and aged men, J. Physiol. (Paris) 585 (1) (2007) 231-239, https://doi.org/10.1113/jphysiol.2007. 143198. · DOI
  61. T. Schmidt-Wilcke, D.J. Clauw, Fibromyalgia: from pathophysiology to therapy, Nat. Rev. Rheumatol. 7 (9) (2011) 518-527, https://doi.org/10.1038/nrrheum. 2011.98. · DOI
  62. L. Scheef, J. Jankowski, M. Daamen, et al., An fMRI study on the acute effects of exercise on pain processing in trained athletes, Pain 153 (8) (2012) 1702-1714, https://doi.org/10.1016/j.pain.2012.05.008. · DOI
  63. A.L. Lopresti, S.D. Hood, P.D. Drummond, A review of lifestyle factors that con- tribute to important pathways associated with major depression: diet, sleep and exercise, J. Affect. Disord. 148 (1) (2013) 12-27, https://doi.org/10.1016/j.jad. 2013.01.014. · DOI
  64. N.K.Y. Tang, A.N. Sanborn, Better quality sleep promotes daytime physical activity in patients with chronic pain? A multilevel analysis of the within-person re- lationship, PLoS One 9 (3) (2014), https://doi.org/10.1371/journal.pone. 0092158. · DOI
  65. A.J. Busch, C.L. Schachter, T.J. Overend, P.M. Peloso, K.A. Barber, Exercise for fibromyalgia: a systematic review, J. Rheumatol. 35 (June (6)) (2008) 1130-1144.
  66. H. Wahbeh, S.M. Elsas, B.S. Oken, Mind-body interventions: applications in neu- rology, Neurology 70 (24) (2008) 2321-2328, https://doi.org/10.1212/01.wnl. 0000314667.16386.5e. · DOI · Paper page
  67. K. Beri, Breathing to younger skin: "reversing the molecular mechanism of skin aging with yoga.", Fut. Sci. OA 2 (2) (2016), https://doi.org/10.4155/fsoa-2016- 0015 fsoa-2016-0015. · DOI
  68. F. Saatcioglu, Regulation of gene expression by yoga, meditation and related practices: a review of recent studies, Asian J. Psychiatr. 6 (1) (2013) 74-77, https://doi.org/10.1016/j.ajp.2012.10.002. · DOI
  69. J.D. Creswell, E.K. Lindsay, How does mindfulness training affect health? A mindfulness stress buffering account, Curr. Dir. Psychol. Sci. 23 (6) (2014) 401-407, https://doi.org/10.1177/0963721414547415. · DOI · Paper page
  70. A. Vijayaraghava, V. Doreswamy, O.S. Narasipur, R. Kunnavil, N. Srinivasamurthy, Effect of yoga practice on levels of inflammatory markers after moderate and strenuous exercise, J. Clin. Diagn. Res. 9 (6) (2015), https:// doi.org/10.7860/JCDR/2015/12851.6021 CC08-12. · DOI
  71. M.R. Irwin, R. Olmstead, E.C. Breen, et al., Cognitive behavioral therapy and tai chi reverse cellular and genomic markers of inflammation in late-life insomnia: a randomized controlled trial, Biol. Psychiatry 78 (10) (2015) 721-729, https://doi. org/10.1016/j.biopsych.2015.01.010. · DOI · Paper page
  72. S. Opasanon, W. Pongsapich, S. Taweepraditpol, B. Suktitipat, A. Chuangsuwanich, Clinical effectiveness of hyperbaric oxygen therapy in com- plex wounds, J. Am. Coll. Clin. Wound Spec. 6 (1-2) (2014) 9-13, https://doi.org/ 10.1016/j.jccw.2015.03.003. · DOI
  73. D.J. Clauw, L.M. Arnold, B.H. McCarberg, The science of fibromyalgia, Mayo Clin. Proc. 86 (9) (2011) 907-911, https://doi.org/10.4065/mcp.2011.0206. · DOI
  74. R. Boussi-Gross, H. Golan, G. Fishlev, et al., Hyperbaric oxygen therapy can im- prove post concussion syndrome years after mild traumatic brain injury -rando- mized prospective trial, PLoS One 8 (11) (2013), https://doi.org/10.1371/journal. pone.0079995. · DOI
  75. N. Üçeyler, D. Zeller, A.-K. Kahn, et al., Small fibre pathology in patients with fibromyalgia syndrome, Brain 136 (Pt 6) (2013) 1857-1867, https://doi.org/10. 1093/brain/awt053. · DOI · Paper page
  76. E. Guedj, S. Cammilleri, J. Niboyet, et al., Clinical correlate of brain SPECT per- fusion abnormalities in fibromyalgia, J. Nucl. Med. 49 (11) (2008) 1798-1803, https://doi.org/10.2967/jnumed.108.053264. · DOI

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Authors
El-Shewy, K. M., Kunbaz, A., Gad, M. M., Al-Husseini, M. J., Saad, A. M., Sammour, Y. M., & Abdel-Daim, M. M.
Affiliations
  • Ain Shams University (EG)
  • Istanbul University-Cerrahpaşa (TR)
  • Cleveland Clinic (US)
Corresponding author
Saad, Anas M.
Venue
Biomedicine & Pharmacotherapy
Publisher
Elsevier BV
Published
2019-01
Volume
109
Pages
629-638
ISSN
0753-3322 (ISSN-L)
OpenAlex
W2899377289
Cited by
29
References
8
Citations by year
2026: 3 · 2025: 2 · 2024: 5 · 2023: 6 · 2022: 1 · 2021: 5 · 2020: 3 · 2019: 2 · 2018: 2
FWCI
0.46
Type
journal article
Language
en
Open access
Locations
  • Biomedicine & Pharmacotherapy (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Fibromyalgia and Chronic Fatigue Syndrome Research
  • Health Sciences › Medicine › Physiology › Pain Mechanisms and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Myofascial pain diagnosis and treatment
Keywords
fibromyalgia, hyperbaric oxygen therapy, aerobic exercise, chronic pain, hyperalgesia, allodynia, anti-inflammatory mechanism, neuroplasticity, nitric oxide, endogenous opioids, adjuvant therapy
MeSH terms
Clinical Trials as Topic, Combined Modality Therapy, Fibromyalgia, Humans, Hyperbaric Oxygenation, Time Factors, Exercise, Treatment Outcome, Pain Management

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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