615: Analysis of research hotspots and emerging trends in mitochondria and pain from 2004 to 2024
Topic: Education, Societal Impact, and Others
Subtopic: Methodology (SLRs, Meta analysis)
Background and Aims: Background: Mitochondria play a crucial role in various cellular processes, and their dysfunction has been increasingly recognized as a significant factor in the pathophysiology of chronic pain. Despite growing interest in this area, a comprehensive bibliometric analysis of the research trends, key themes, and influential contributions in the study of mitochondria and pain has not been conducted. This study aims to fill this gap by providing a detailed overview of the research landscape from 2004 to 2024.
Methods: Methods: A comprehensive literature search was performed using the Web of Science Core Collection database to identify relevant studies published between January 1, 2004, and June 24, 2024. A total of 1,995 articles were identified and included in the analysis. Bibliometric tools, including CiteSpace, VOSviewer, and RStudio, were employed to analyze and visualize data related to co-citation networks, keyword co-occurrence, and clustering patterns. The analysis focused on identifying research trends, key authors, influential journals, and emerging themes within the field.
Results: Results: The analysis revealed a significant increase in research activity on mitochondria and pain, particularly after 2011, with a marked surge between 2015 and 2020. Key themes identified include mitochondrial dysfunction, oxidative stress, neuroinflammation, autophagy, and mitochondrial biogenesis. The United States, China, Germany, and the United Kingdom emerged as leading contributors to the field, with prominent institutions such as Harvard University and the University of California playing central roles in collaborative networks. Influential authors and foundational studies were identified through co-citation analysis, highlighting the interdisciplinary nature of the research.
Conclusions: Conclusion: This bibliometric analysis provides a comprehensive overview of the evolving research landscape in mitochondria and pain, highlighting key trends, influential contributions, and emerging research directions. The findings underscore the growing recognition of mitochondrial dysfunction as a critical factor in pain mechanisms and suggest that future research should focus on translating basic findings into clinical practice while expanding global collaborations.
References: [1] S. Xu, H. Li, Z. Ai, R. Guo, H. Cheng, Y. Wang, Exploring viral neuropathic pain: Molecular mechanisms and therapeutic implications, PLoS Pathog 20(8) (2024) e1012397.
[2] E. Hazrati, S.P. Eftekhar, R. Mosaed, S. Shiralizadeh Dini, M. Namazi, Understanding the kynurenine pathway: A narrative review on its impact across chronic pain conditions, Mol Pain 20 (2024) 17448069241275097.
[3] S.P. Cohen, L. Vase, W.M. Hooten, Chronic pain: an update on burden, best practices, and new advances, Lancet 397(10289) (2021) 2082-2097.
[4] N. Bakshi, A.L. Hart, M.C. Lee, A.C.C. Williams, J.M. Lackner, C. Norton, P. Croft, Chronic pain in patients with inflammatory bowel disease, Pain 162(10) (2021) 2466-2471.
[5] A.P.A. Dagnino, M.M. Campos, Chronic Pain in the Elderly: Mechanisms and Perspectives, Front Hum Neurosci 16 (2022) 736688.
[6] M. Parisien, L.V. Lima, C. Dagostino, N. El-Hachem, G.L. Drury, A.V. Grant, J. Huising, V. Verma, C.B. Meloto, J.R. Silva, G.G.S. Dutra, T. Markova, H. Dang, P.A. Tessier, G.D. Slade, A.G. Nackley, N. Ghasemlou, J.S. Mogil, M. Allegri, L. Diatchenko, Acute inflammatory response via neutrophil activation protects against the development of chronic pain, Sci Transl Med 14(644) (2022) eabj9954.
[7] T.J. Schwedt, J.G. Hentz, S. Sahai-Srivastava, N.M. Spare, V.T. Martin, C. Treppendahl, K. Digre, N.L. Bennett, M. Birlea, D. Watson, N. Murinova, T. Robert, D.W. Dodick, M. Investigators, Headache characteristics and burden from chronic migraine with medication overuse headache: Cross-sectional observations from the Medication Overuse Treatment Strategy trial, Headache 61(2) (2021) 351-362.
[8] J.S. Harrington, S.W. Ryter, M. Plataki, D.R. Price, A.M.K. Choi, Mitochondria in health, disease, and aging, Physiol Rev 103(4) (2023) 2349-2422.
[9] S. Javadov, A.V. Kozlov, A.K.S. Camara, Mitochondria in Health and Diseases, Cells 9(5) (2020).
[10] T.M. Doyle, D. Salvemini, Mini-Review: Mitochondrial dysfunction and chemotherapy-induced neuropathic pain, Neurosci Lett 760 (2021) 136087.
[11] P.M. Grace, V.L. Tawfik, C.I. Svensson, M.D. Burton, M.L. Loggia, M.R. Hutchinson, The Neuroimmunology of Chronic Pain: From Rodents to Humans, J Neurosci 41(5) (2021) 855-865.
[12] J. van den Ameele, J. Fuge, R.D.S. Pitceathly, S. Berry, Z. McIntyre, M.G. Hanna, M. Lee, P.F. Chinnery, Chronic pain is common in mitochondrial disease, Neuromuscul Disord 30(5) (2020) 413-419.
[13] C.Q. Dai, Y. Guo, X.Y. Chu, Neuropathic Pain: the Dysfunction of Drp1, Mitochondria, and ROS Homeostasis, Neurotox Res 38(3) (2020) 553-563.
[14] P. Silva Santos Ribeiro, H. Willemen, N. Eijkelkamp, Mitochondria and sensory processing in inflammatory and neuropathic pain, Front Pain Res (Lausanne) 3 (2022) 1013577.
[15] M.S. Yousuf, A.D. Maguire, T. Simmen, B.J. Kerr, Endoplasmic reticulum-mitochondria interplay in chronic pain: The calcium connection, Mol Pain 16 (2020) 1744806920946889.
[16] M.K. L., R.J. George, A. P.S., Bibliometric Analysis for Medical Research, Indian Journal of Psychological Medicine 45(3) (2023) 277-282.
[17] D. D'Amico, M. Olmer, A.M. Fouassier, P. Valdes, P.A. Andreux, C. Rinsch, M. Lotz, Urolithin A improves mitochondrial health, reduces cartilage degeneration, and alleviates pain in osteoarthritis, Aging Cell 21(8) (2022) e13662.
[18] J. Jiang, L. Xu, L. Yang, S. Liu, Z. Wang, Mitochondrial-Derived Peptide MOTS-c Ameliorates Spared Nerve Injury-Induced Neuropathic Pain in Mice by Inhibiting Microglia Activation and Neuronal Oxidative Damage in the Spinal Cord via the AMPK Pathway, ACS Chem Neurosci 14(12) (2023) 2362-2374.
[19] E. Eftekharpour, P. Fernyhough, Oxidative Stress and Mitochondrial Dysfunction Associated with Peripheral Neuropathy in Type 1 Diabetes, Antioxid Redox Signal 37(7-9) (2022) 578-596.
[20] C. Khuankaew, P. Sawaddiruk, P. Surinkaew, N. Chattipakorn, S.C. Chattipakorn, Possible roles of mitochondrial dysfunction in neuropathy, Int J Neurosci 131(10) (2021) 1019-1041.
[21] Y. Chen, Y. Li, C. Li, D. Zhu, O. Cheng, J. Cui, Dexmedetomidine alleviates pain in MPTP-treated mice by activating the AMPK/mTOR/NF-kappaB pathways in astrocytes, Neurosci Lett 791 (2022) 136933.
[22] L. Degrugillier, K.M. Prautsch, D.J. Schaefer, R. Guzman, D.F. Kalbermatten, S. Scharen, S. Madduri, Systematic investigation and comparison of US FDA-approved immunosuppressive drugs FK506, cyclosporine and rapamycin for neuromuscular regeneration following chronic nerve compression injury, Regen Med 16(11) (2021) 989-1003.
[23] S. Ilari, L.A. Giancotti, F. Lauro, M. Gliozzi, V. Malafoglia, E. Palma, M. Tafani, M.A. Russo, C. Tomino, M. Fini, D. Salvemini, V. Mollace, C. Muscoli, Natural Antioxidant Control of Neuropathic Pain-Exploring the Role of Mitochondrial SIRT3 Pathway, Antioxidants (Basel) 9(11) (2020).
[24] P. Gupta, T.K. Makkar, L. Goel, M. Pahuja, Role of inflammation and oxidative stress in chemotherapy-induced neurotoxicity, Immunol Res 70(6) (2022) 725-741.
[25] G. Raghu, M. Berk, P.A. Campochiaro, H. Jaeschke, G. Marenzi, L. Richeldi, F.Q. Wen, F. Nicoletti, P.M.A. Calverley, The Multifaceted Therapeutic Role of N-Acetylcysteine (NAC) in Disorders Characterized by Oxidative Stress, Curr Neuropharmacol 19(8) (2021) 1202-1224.
[26] L. Kang, S. Liu, J. Li, Y. Tian, Y. Xue, X. Liu, The mitochondria-targeted anti-oxidant MitoQ protects against intervertebral disc degeneration by ameliorating mitochondrial dysfunction and redox imbalance, Cell Prolif 53(3) (2020) e12779.
[27] L. Li, T. Li, X. Qu, G. Sun, Q. Fu, G. Han, Stress/cell death pathways, neuroinflammation, and neuropathic pain, Immunol Rev 321(1) (2024) 33-51.
[28] S. Licht-Mayer, G.R. Campbell, M. Canizares, A.R. Mehta, A.B. Gane, K. McGill, A. Ghosh, A. Fullerton, N. Menezes, J. Dean, J. Dunham, S. Al-Azki, G. Pryce, S. Zandee, C. Zhao, M. Kipp, K.J. Smith, D. Baker, D. Altmann, S.M. Anderton, Y.S. Kap, J.D. Laman, B.A. Hart, M. Rodriguez, R. Watzlawick, J.M. Schwab, R. Carter, N. Morton, M. Zagnoni, R.J.M. Franklin, R. Mitchell, S. Fleetwood-Walker, D.A. Lyons, S. Chandran, H. Lassmann, B.D. Trapp, D.J. Mahad, Enhanced axonal response of mitochondria to demyelination offers neuroprotection: implications for multiple sclerosis, Acta Neuropathol 140(2) (2020) 143-167.
[29] S.J. Park, J.W. Choi, Brain energy metabolism and multiple sclerosis: progress and prospects, Arch Pharm Res 43(10) (2020) 1017-1030.
[30] S.R. Gilstrap, J.M. Hobson, M.A. Owens, D.M. White, M.J. Sammy, S. Ballinger, R.E. Sorge, B.R. Goodin, Mitochondrial reactivity following acute exposure to experimental pain testing in people with HIV and chronic pain, Mol Pain 19 (2023) 17448069231195975.
[31] D. Liu, Z.J. Cai, Y.T. Yang, W.H. Lu, L.Y. Pan, W.F. Xiao, Y.S. Li, Mitochondrial quality control in cartilage damage and osteoarthritis: new insights and potential therapeutic targets, Osteoarthritis Cartilage 30(3) (2022) 395-405.
[32] T. Zhang, J. Li, G. Zhao, Quality Control Mechanisms of Mitochondria: Another Important Target for Treatment of Peripheral Neuropathy, DNA Cell Biol 40(12) (2021) 1513-1527.
[33] V.K. Arruri, C. Gundu, A.K. Kalvala, B. Sherkhane, D.K. Khatri, S.B. Singh, Carvacrol abates NLRP3 inflammasome activation by augmenting Keap1/Nrf-2/p62 directed autophagy and mitochondrial quality control in neuropathic pain, Nutr Neurosci 25(8) (2022) 1731-1746.
[34] M.F. Liao, K.T. Lu, J.L. Hsu, C.H. Lee, M.Y. Cheng, L.S. Ro, The Role of Autophagy and Apoptosis in Neuropathic Pain Formation, Int J Mol Sci 23(5) (2022).
[35] J. Li, M. Tian, T. Hua, H. Wang, M. Yang, W. Li, X. Zhang, H. Yuan, Combination of autophagy and NFE2L2/NRF2 activation as a treatment approach for neuropathic pain, Autophagy 17(12) (2021) 4062-4082.
[36] X.J. Chen, L. Wang, X.Y. Song, Mitoquinone alleviates vincristine-induced neuropathic pain through inhibiting oxidative stress and apoptosis via the improvement of mitochondrial dysfunction, Biomed Pharmacother 125 (2020) 110003.
[37] L. Kang, S. Liu, J. Li, Y. Tian, Y. Xue, X. Liu, Parkin and Nrf2 prevent oxidative stress-induced apoptosis in intervertebral endplate chondrocytes via inducing mitophagy and anti-oxidant defenses, Life Sci 243 (2020) 117244.
[38] M. Alotaibi, F. Al-Aqil, F. Alqahtani, M. Alanazi, A. Nadeem, S.F. Ahmad, R. Lapresa, M. Alharbi, A. Alshammari, M. Alotaibi, T. Saleh, R. Alrowis, Alleviation of cisplatin-induced neuropathic pain, neuronal apoptosis, and systemic inflammation in mice by rapamycin, Front Aging Neurosci 14 (2022) 891593.
[39] J. Sun, F.H. Song, J.Y. Wu, L.Q. Zhang, D.Y. Li, S.J. Gao, D.Q. Liu, Y.Q. Zhou, W. Mei, Sestrin2 overexpression attenuates osteoarthritis pain via induction of AMPK/PGC-1alpha-mediated mitochondrial biogenesis and suppression of neuroinflammation, Brain Behav Immun 102 (2022) 53-70.
[40] J. Sun, J.Y. Li, L.Q. Zhang, D.Y. Li, J.Y. Wu, S.J. Gao, D.Q. Liu, Y.Q. Zhou, W. Mei, Nrf2 Activation Attenuates Chronic Constriction Injury-Induced Neuropathic Pain via Induction of PGC-1alpha-Mediated Mitochondrial Biogenesis in the Spinal Cord, Oxid Med Cell Longev 2021 (2021) 9577874.
Presenting Author: Yimeng Xia
Submitting Author: Yimeng Xia
Senior Author: Yimeng Xia
IASP 2026 Global Year theme of Neuropathic Pain: Yes
Co-Authors:
- Ming Hu: MD - Department of Anesthesiology and Pain, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China
- Yan Luo: MD, PhD - Department of Anesthesiology and Pain, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China
Analysis of research hotspots and emerging trends in mitochondria and pain from 2004 to 2024
Category
Poster
Description
Session Type: Posters
Room: Exhibit Hall EH102-103
28/10/2026
03:15 PM - 04:45 PM