Muscle Atrophy Secondary to Spinal Cord Injury: A Global Understanding

Autores/as

DOI:

https://doi.org/10.36105/psrua.2025v5n10.03

Palabras clave:

atrofia muscular, lesión medular, tratamiento

Resumen

Introducción: en el presente estudio se aborda una introducción al tema en cuestión. Las lesiones de la médula espinal se caracterizan por su repercusión en la calidad de vida de los pacientes, por lo tanto, resulta de particular interés comprender los mecanismos patológicos moleculares y genéticos fuertemente asociados al desarrollo de complicaciones musculares, tales como la atrofia. Estas complicaciones son características esenciales de las lesiones medulares, ocasionando restricciones adicionales en la movilidad y alteraciones sistémicas en el equilibrio celular. Objetivos: El propósito de la presente revisión es esclarecer los mecanismos moleculares e inflamatorios implicados en la atrofia muscular, contribuyendo así a la degeneración de las personas afectadas por lesiones de la médula espinal. En este estudio, se explorarán las opciones terapéuticas actuales con el objetivo de proporcionar un enfoque integral al estudio de la atrofia muscular en la lesión de la médula espinal y de identificar potenciales dianas terapéuticas. Métodos y materiales empleados: Este estudio constituye una revisión narrativa de la literatura, llevada a cabo mediante una exhaustiva investigación en línea en las bases de datos PubMed, SciELO y Web of Science, entre los meses de octubre de 2023 y enero de 2024. Se emplearon palabras clave como “lesión de la médula espinal”, “atrofia muscular”, “estrés oxidativo” y “músculo esquelético”, utilizando operadores booleanos para refinar la búsqueda. El presente estudio aborda un total de 48 estudios seleccionados mediante criterios específicos. Conclusiones: La atrofia muscular posterior a la lesión medular se caracteriza por la interrupción de las señales motoras, lo que resulta en la afectación de las uniones neuromusculares, un desequilibrio en el calcio y la activación de vías de muerte celular y degradación de proteínas. El incremento de los factores inflamatorios estimula el catabolismo a través de la inhibición de la síntesis de proteínas y la activación de los genes reguladores de la degradación muscular, tales como MuRF1 y MAFbx. Las enzimas dependientes de calcio contribuyen a la degradación de las proteínas, lo que resulta en una pérdida progresiva de la masa muscular. Los hallazgos subrayan la relevancia de las intervenciones multidisciplinarias tempranas, que integran estrategias farmacológicas, de rehabilitación y moleculares, con el propósito de preservar la función muscular y optimizar los resultados en individuos con lesión medular.

Descargas

Los datos de descarga aún no están disponibles.

Biografía del autor/a

  • Ivan Ignacio-Mejia , Secretaría de la Defensa Nacional, Escuela Militar de Graduados en Sanidad, Ciudad de México.

     

     

     

     

     

     

  • Humberto Carrasco-Vargas, Secretaría de la Defensa Nacional, Escuela Militar de Graduados en Sanidad, Ciudad de México.  

     

     

     

     

  • Marco Antonio Vargas-Hernández, Secretaría de la Defensa Nacional, Escuela Militar de Graduados en Sanidad, Ciudad de México.

     

     

     

     

     

  • Antonio Ibarra, Universidad Anáhuac México, Centro de Investigación en Ciencias de la Salud (CICSA), Estado de México.

     

     

     

     

Referencias

1. James SL, Bannick MS, Montjoy-Venning WC, Lucchesi LR, Dandona L, Dandona R, et al. Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990-2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2019 Jan 1;18[1]:56–87. DOI: https://doi.org/10.1016/S1474-4422(18)30415-0 DOI: https://doi.org/10.1016/S1474-4422(18)30415-0

2. Badhiwala JH, Wilson JR, Fehlings MG. Global burden of traumatic brain and spinal cord injury. Vol. 18, The Lancet Neurology. Lancet Publishing Group; 2019. p. 24–5. DOI: https://doi.org/10.1016/s1474-4422(18)30444-7 DOI: https://doi.org/10.1016/S1474-4422(18)30444-7

3. Liu Y, Yang X, He Z, Li J, Li Y, Wu Y, et al. Spinal cord injury: global burden from 1990 to 2019 and projections up to 2030 using Bayesian age-period-cohort analysis. Vol. 14, Frontiers in Neurology. Frontiers Media SA; 2023. DOI: https://doi.org/10.3389/fneur.2023.1304153 DOI: https://doi.org/10.3389/fneur.2023.1304153

4. Ding W, Hu S, Wang P, Kang H, Peng R, Dong Y, et al. Spinal Cord Injury: The Global Incidence, Prevalence, and Disability From the Global Burden of Disease Study 2019. Spine [Phila Pa 1976]. 2022 Nov 1;47[21]:1532–40. DOI: https://doi.org/10.1097/brs.0000000000004417 DOI: https://doi.org/10.1097/BRS.0000000000004417

5. Ahuja CS, Wilson JR, Nori S, Kotter MRN, Druschel C, Curt A, et al. Traumatic spinal cord injury. Vol. 3, Nature Reviews Disease Primers. Nature Publishing Group; 2017. DOI: https://doi.org/10.1038/nrdp.2017.18 DOI: https://doi.org/10.1038/nrdp.2017.18

6. Yin L, Li N, Jia W, Wang N, Liang M, Yang X, et al. Skeletal muscle atrophy: From mechanisms to treatments. Vol. 172, Pharmacological Research. Academic Press; 2021. DOI: https://doi.org/10.1016/j.phrs.2021.105807 DOI: https://doi.org/10.1016/j.phrs.2021.105807

7. Friese A, Kaltschmidt JA, Ladle DR, Sigrist M, Jessell TM, Arber S. Gamma and alpha motor neurons distinguished by expression of transcription factor Err3 [Internet]. 2009 Jun. Available from: www.pnas.org/cgi/content/full/ DOI: https://doi.org/10.1073/pnas.0906809106 DOI: https://doi.org/10.1073/pnas.0906809106

8. Ninfali C, Siles L, Darling DS, Postigo A. Regulation of muscle atrophy-related genes by the opposing transcriptional activities of ZEB1/CtBP and FOXO3. Nucleic Acids Res. 2018;46[20]:10697–708. DOI: https://doi.org/10.1093/nar/gky835 DOI: https://doi.org/10.1093/nar/gky835

9. Tong T, Marino JS, Li JJ, Yang DG, C-j Z, Y-z P, et al. OPEN ACCESS EDITED BY Mechanism of skeletal muscle atrophy after spinal cord injury: A narrative review. 2023; 3; 10; 1099143. DOI: https://doi.org/10.3389/fnut.2023.1099143 DOI: https://doi.org/10.3389/fnut.2023.1099143

10. Torrie A. Crabbs. Skeletal Muscle - Atrophy [Internet]. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25035576

11. Cohen S. Role of calpains in promoting desmin filaments depolymerization and muscle atrophy. Vol. 1867, Biochimica et Biophysica Acta - Molecular Cell Research. Elsevier B.V.; 2020. DOI: https://doi.org/10.1016/j.bbamcr.2020.118788 DOI: https://doi.org/10.1016/j.bbamcr.2020.118788

12. Singh A, Yadav A, Phogat J, Dabur R. Dynamics and Interplay between Autophagy and Ubiquitin-proteasome system Coordination in Skeletal Muscle Atrophy. Curr Mol Pharmacol. 2021 Aug 9;15[3]:475–86. DOI: https://doi.org/10.2174/1874467214666210806163851 DOI: https://doi.org/10.2174/1874467214666210806163851

13. Franco-Romero A, Sandri M. Role of autophagy in muscle disease. Mol Aspects Med. 2021 Dec 1;82. DOI: https://doi.org/10.1016/j.mam.2021.101041 DOI: https://doi.org/10.1016/j.mam.2021.101041

14. Ji Y, Li M, Chang M, Liu R, Qiu J, Wang K, et al. Inflammation: Roles in Skeletal Muscle Atrophy. Vol. 11, Antioxidants. MDPI; 2022. DOI: https://doi.org/10.3390/antiox11091686 DOI: https://doi.org/10.3390/antiox11091686

15. Otzel DM, Lee J, Ye F, Borst SE, Yarrow JF. Activity-based physical rehabilitation with adjuvant testosterone to promote neuromuscular recovery after spinal cord injury. Vol. 19, International Journal of Molecular Sciences. MDPI AG; 2018. DOI: https://doi.org/10.3390/ijms19061701 DOI: https://doi.org/10.3390/ijms19061701

16. Otzel DM, Kok HJ, Graham ZA, Barton ER, Yarrow JF. Pharmacologic approaches to prevent skeletal muscle atrophy after spinal cord injury. Vol. 60, Current Opinion in Pharmacology. Elsevier Ltd; 2021. p. 193–9. DOI: https://doi.org/10.1016/j.coph.2021.07.023 DOI: https://doi.org/10.1016/j.coph.2021.07.023

17. Idriss HT, Naismith JH. TNFα and the TNF receptor superfamily: Structure-function relationship[s]. Microsc Res Tech. 2000 Aug 1;50[3]:184–95. DOI: https://doi.org/10.1002/1097-0029(20000801)50:3%3C184::aid-jemt2%3E3.0.co;2-h DOI: https://doi.org/10.1002/1097-0029(20000801)50:3<184::AID-JEMT2>3.0.CO;2-H

18. Drasites KP, Shams R, Zaman V, Matzelle D, Shields DC, Garner DP, et al. Review pathophysiology, biomarkers, and therapeutic modalities associated with skeletal muscle loss following spinal cord injury. Vol. 10, Brain Sciences. MDPI AG; 2020. p. 1–13. DOI: https://doi.org/10.3390/brainsci10120933 DOI: https://doi.org/10.3390/brainsci10120933

19. Abati E, Manini A, Comi G Pietro, Corti S. Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseases. Vol. 79, Cellular and Molecular Life Sciences. Springer Science and Business Media Deutschland GmbH; 2022. DOI: https://doi.org/10.1007/s00018-022-04408-w DOI: https://doi.org/10.1007/s00018-022-04408-w

20. Zhang Y, Zeng W, Xia Y. TWEAK/Fn14 axis is an important player in fibrosis. Vol. 236, Journal of Cellular Physiology. Wiley-Liss Inc.; 2021. p. 3304–16. DOI: https://doi.org/10.1002/jcp.30089 DOI: https://doi.org/10.1002/jcp.30089

21. Rius-Pérez S, Torres-Cuevas I, Millán I, Ortega ÁL, Pérez S, Sandhu MA. PGC-1 α, Inflammation, and Oxidative Stress: An Integrative View in Metabolism. Oxid Med Cell Longev. 2020;2020. DOI: https://doi.org/10.1155/2020/1452696 DOI: https://doi.org/10.1155/2020/1452696

22. Zhang B, Pan C, Feng C, Yan C, Yu Y, Chen Z, et al. Role of mitochondrial reactive oxygen species in homeostasis regulation. Vol. 27, Redox Report. Taylor and Francis Ltd.; 2022. p. 45–52. DOI: https://doi.org/10.1080/13510002.2022.2046423 DOI: https://doi.org/10.1080/13510002.2022.2046423

23. Savikj M, Kostovski E, Lundell LS, Iversen PO, Massart J, Widegren U. Altered oxidative stress and antioxidant defence in skeletal muscle during the first year following spinal cord injury. Physiol Rep. 2019;7[16]. DOI: https://doi.org/10.14814/phy2.14218 DOI: https://doi.org/10.14814/phy2.14218

24. Abdelrahman S, Ireland A, Winter EM, Purcell M, Coupaud S. Osteoporosis after spinal cord injury: aetiology, effects and therapeutic approaches [Internet]. Available from: http://www.ismni.org.

25. Shams R, Drasites KP, Zaman V, Matzelle D, Shields DC, Garner DP, et al. The pathophysiology of osteoporosis after spinal cord injury. Vol. 22, International Journal of Molecular Sciences. MDPI AG; 2021. p. 1–17. DOI: https://doi.org/10.3390/ijms22063057 DOI: https://doi.org/10.3390/ijms22063057

26. Choi H, Chang SY, Yoo J, Lim SH, Hong BY, Kim JS. Correlation Between Duration From Injury and Bone Mineral Density in Individuals With Spinal Cord Injury. Ann Rehabil Med. 2021 Feb 1;45[1]:1–6. DOI: https://doi.org/10.5535/arm.20169 DOI: https://doi.org/10.5535/arm.20169

27. Peterson MD, Berri M, Lin P, Kamdar N, Rodriguez G, Mahmoudi E, et al. Cardiovascular and metabolic morbidity following spinal cord injury. Spine Journal. 2021 Sep 1;21[9]:1520–7. DOI: https://doi.org/10.1016/j.spinee.2021.05.014 DOI: https://doi.org/10.1016/j.spinee.2021.05.014

28. Smith DL, Yarar-Fisher C. Contributors to Metabolic Disease Risk Following Spinal Cord Injury. Vol. 4, Current Physical Medicine and Rehabilitation Reports. Springer; 2016. p. 190–9. DOI: https://doi.org/10.1007/s40141-016-0124-7 DOI: https://doi.org/10.1007/s40141-016-0124-7

29. Gibbs JC, Gagnon DH, Bergquist AJ, Arel J, Cervinka T, El-Kotob R, et al. Rehabilitation Interventions to modify endocrine-metabolic disease risk in Individuals with chronic Spinal cord injury living in the Community [RIISC]: A systematic review and scoping perspective. Journal of Spinal Cord Medicine. 2017 Nov 2;40[6]:733–47. DOI: https://doi.org/10.1080/10790268.2017.1350341 DOI: https://doi.org/10.1080/10790268.2017.1350341

30. Holman ME, Gorgey AS. Testosterone and Resistance Training Improve Muscle Quality in Spinal Cord Injury. Med Sci Sports Exerc. 2019 Aug 1;51[8]:1591–8. DOI: https://doi.org/10.1249/mss.0000000000001975 DOI: https://doi.org/10.1249/MSS.0000000000001975

31. Gorgey AS, Lester RM, Ghatas MP, Sisturn SN, Lavis T. Dietary manipulation and testosterone replacement therapy may explain changes in body composition after spinal cord injury: A retrospective case report. World J Clin Cases. 2019 Sep 1;7[17]:2427–37. DOI: https://doi.org/10.12998/wjcc.v7.i17.2427 https://doi.org/10.12998/wjcc.v7.i17.2427 DOI: https://doi.org/10.12998/wjcc.v7.i17.2427

32. Sengelaub DR, Han Q, Liu NK, MacZuga MA, Szalavari V, Valencia SA, et al. Protective Effects of Estradiol and Dihydrotestosterone following Spinal Cord Injury. J Neurotrauma. 2018 Mar 15;35[6]:825–41. DOI: https://doi.org/10.1089/neu.2017.5329 DOI: https://doi.org/10.1089/neu.2017.5329

33. Huang L, Li M, Deng C, Qiu J, Wang K, Chang M, et al. Potential Therapeutic Strategies for Skeletal Muscle Atrophy. Vol. 12, Antioxidants. MDPI; 2023. DOI: https://doi.org/10.3390/antiox12010044

34. Scholpa NE, Simmons EC, Tilley DG, Schnellmann RG. β2-adrenergic receptor-mediated mitochondrial biogenesis improves skeletal muscle recovery following spinal cord injury. Exp Neurol. 2019 Dec 1;322. DOI: https://doi.org/10.3390/antiox12010044 DOI: https://doi.org/10.1016/j.expneurol.2019.113064

35. Kutschenko A, Manig A, Mönnich A, Bryl B, Alexander CS, Deutschland M, et al. Intramuscular tetanus neurotoxin reverses muscle atrophy: a randomized controlled trial in dogs with spinal cord injury. J Cachexia Sarcopenia Muscle. 2022 Feb 1;13[1]:443–53. DOI: https://doi.org/10.1002/jcsm.12836 DOI: https://doi.org/10.1002/jcsm.12836

36. Megighian A, Pirazzini M, Fabris F, Rossetto O, Montecucco C. Tetanus and tetanus neurotoxin: From peripheral uptake to central nervous tissue targets. Vol. 158, Journal of Neurochemistry. John Wiley and Sons Inc; 2021. p. 1244–53. DOI: https://doi.org/10.1111/jnc.15330 DOI: https://doi.org/10.1111/jnc.15330

37. Chandrasekaran S, Davis J, Bersch I, Goldberg G, Gorgey AS. Electrical stimulation and denervated muscles after spinal cord injury. Vol. 15, Neural Regeneration Research. Wolters Kluwer Medknow Publications; 2020. p. 1397–407. DOI: https://doi.org/10.4103/1673-5374.274326 DOI: https://doi.org/10.4103/1673-5374.274326

38. Atkins KD, Bickel CS. Effects of functional electrical stimulation on muscle health after spinal cord injury. Vol. 60, Current Opinion in Pharmacology. Elsevier Ltd; 2021. p. 226–31. DOI: https://doi.org/10.1016/j.coph.2021.07.025 DOI: https://doi.org/10.1016/j.coph.2021.07.025

39. Thomaz SR, Cipriano G, Formiga MF, Fachin-Martins E, Cipriano GFB, Martins WR, et al. Effect of electrical stimulation on muscle atrophy and spasticity in patients with spinal cord injury – a systematic review with meta-analysis. Vol. 57, Spinal Cord. Nature Publishing Group; 2019. p. 258–66. DOI: https://doi.org/10.1038/s41393-019-0250-z DOI: https://doi.org/10.1038/s41393-019-0250-z

40. Gorgey AS, Khalil RE, Davis JC, Carter W, Gill R, Rivers J, et al. Skeletal muscle hypertrophy and attenuation of cardio-metabolic risk factors [SHARC] using functional electrical stimulation-lower extremity cycling in persons with spinal cord injury: Study protocol for a randomized clinical trial. Trials. 2019 Aug 23;20[1]. DOI: https://doi.org/10.1186/s13063-019-3560-8 DOI: https://doi.org/10.1186/s13063-019-3560-8

41. Skiba GH, Andrade SF, Rodacki AF. Effects of functional electro-stimulation combined with blood flow restriction in affected muscles by spinal cord injury. Neurological Sciences. 2022 Jan 1;43[1]:603–13. DOI: https://doi.org/10.1007/s10072-021-05307-x DOI: https://doi.org/10.1007/s10072-021-05307-x

42. Pizzolato C, Saxby DJ, Palipana D, Diamond LE, Barrett RS, Teng YD, et al. Neuromusculoskeletal modeling-based prostheses for recovery after spinal cord injury. Front Neurorobot. 2019;13. DOI: https://doi.org/10.3389/fnbot.2019.00097 DOI: https://doi.org/10.3389/fnbot.2019.00097

43. Nistor-Cseppento CD, Gherle A, Negrut N, Bungau SG, Sabau AM, Radu AF, et al. The Outcomes of Robotic Rehabilitation Assisted Devices Following Spinal Cord Injury and the Prevention of Secondary Associated Complications. Vol. 58, Medicina [Lithuania]. MDPI; 2022. DOI: https://doi.org/10.3390/medicina58101447 DOI: https://doi.org/10.3390/medicina58101447

44. de Sire A, Moggio L, Marotta N, Curci C, Lippi L, Invernizzi M, et al. Impact of rehabilitation on volumetric muscle loss in subjects with traumatic spinal cord injury: A systematic review. Vol. 52, NeuroRehabilitation. IOS Press BV; 2023. p. 365–86. DOI: https://doi.org/10.3233/nre-220277 DOI: https://doi.org/10.3233/NRE-220277

45. Hurst C, Robinson SM, Witham MD, Dodds RM, Granic A, Buckland C, et al. Resistance exercise as a treatment for sarcopenia: Prescription and delivery. Vol. 51, Age and Ageing. Oxford University Press; 2022. DOI: https://doi.org/10.1093/ageing/afac003 DOI: https://doi.org/10.1093/ageing/afac003

46. Mirea A, Leanca MC, Onose G, Sporea C, Padure L, Shelby ES, et al. Physical Therapy and Nusinersen Impact on Spinal Muscular Atrophy Rehabilitative Outcome. Frontiers in Bioscience - Landmark. 2022 Jun 1;27[6]. DOI: https://doi.org/10.31083/j.fbl2706179 DOI: https://doi.org/10.31083/j.fbl2706179

47. Lu L, Mao L, Feng Y, Ainsworth BE, Liu Y, Chen N. Effects of different exercise training modes on muscle strength and physical performance in older people with sarcopenia: a systematic review and meta-analysis. BMC Geriatr. 2021 Dec 1;21[1]. DOI: https://doi.org/10.1186/s12877-021-02642-8 DOI: https://doi.org/10.1186/s12877-021-02642-8

48. Jones MA, McEwen IR, Hansen L. Use of Power Mobility for a Young Child With Spinal Muscular Atrophy. 2003. DOI: https://doi.org/10.1093/ptj/83.3.253

Descargas

Publicado

2026-05-14

Cómo citar

Muscle Atrophy Secondary to Spinal Cord Injury: A Global Understanding. (2026). Proceedings of Scientific Research Universidad Anáhuac. Multidisciplinary Journal of Healthcare, 5(10), 27-38. https://doi.org/10.36105/psrua.2025v5n10.03

Artículos más leídos del mismo autor/a