Singapur un camino interrumpido hacia la regulación de las técnicas de reemplazo mitocondrial

Autores/as

DOI:

https://doi.org/10.12795/IESTSCIENTIA.2023.i01.08

Palabras clave:

Enfermedades mitocondriales, Leyes, Técnicas de reproducción asistida, Reemplazo mitocondrial, Singapur

Resumen

Las técnicas de reemplazo mitocondrial pueden reducir significativamente el riesgo de transmisión de enfermedades mitocondriales a la descendencia. Singapur estaba analizando la posibilidad de realizar cambios legislativos históricos que permitirían a las parejas afectadas por enfermedades mitocondriales hereditarias maternas la oportunidad de tener hijos genéticamente no afectados. Sin embargo, tras el informe del BAC, parece que la República de Singapur, no se convertirá en el tercer país a nivel internacional en autorizar el uso de las técnicas de reemplazo mitocondrial.

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Citas

BAC. (2018). Consultation Paper on Ethical, Legal and Social Issues Arising from Mitochondrial Genome Replacement Technology (p. 49). Bioethics Advisory Committe. https://www.bioethics-singapore.org/publications/press-releases/bac-mgrt-press-release

Border, P., & Barber, S. (2015). Mitochondrial donation. Standard Note: SN/ SC/6833. (London: House of Commons Library). United Kingdom Parliament. https://commonslibrary.parliament.uk/research-briefings/sn06833/

Bredenoord, A. L., & Appleby, J. B. (2017). Mitochondrial Replacement Techniques: Remaining Ethical Challenges. Cell Stem Cell, 21(3), 301-304. https://doi.org/10.1016/j.stem.2017.08.009

Cohen, G. (2018). Circumvention Medical Tourism and Cutting Edge Medicine: The Case of Mitochondrial Replacement Therapy. Indiana Journal of Global Legal Studies, 25(1), 439-462. https://doi.org/10.2979/indjglolegstu.25.1.0439

Cohen, I. G., Adashi, E. Y., Gerke, S., Palacios-González, C., & Ravitsky, V. (2020). The Regulation of Mitochondrial Replacement Techniques Around the World. Annual Review of Genomics and Human Genetics, 21(1), 565-586. https://doi.org/10.1146/annurev-genom-111119-101815

Craven, L., Murphy, J. L., & Turnbull, D. M. (2020). Mitochondrial donation—Hope for families with mitochondrial DNA disease. Emerging Topics in Life Sciences, 4(2), 151-154. https://doi.org/10.1042/ETLS20190196

Cristina, M. (2022). ¿Alquiler o sustitución del embarazo? Sobre la importancia de los significantes en la construcción de sentido. Revista de Bioética y Derecho, 54, 5-22. https://doi.org/10.1344/rbd2021.54.34891

Davis, R. L., Liang, C., & Sue, C. M. (2018). Mitochondrial diseases. Handbook of Clinical Neurology, 147, 125-141. https://doi.org/10.1016/B978-0-444-63233-3.00010-5

De Miguel Beriain, I., Atienza Macías, E., & Armaza Armaza, E. J. (2016). Algunas consideraciones sobre la transferencia mitocondrial: ¿un nuevo problema para la bioética? Acta bioethica, 22(2), 203-211. https://doi.org/10.4067/S1726-569X2016000200007

Dziadek, M. A., & Sue, C. M. (2022). Mitochondrial donation: Is Australia ready? Medical Journal of Australia, 216(3), 118-121. https://doi.org/10.5694/mja2.51309

Farnezi, H. C. M., Goulart, A. C. X., Santos, A. D., Ramos, M. G., & Penna, M. L. F. (2020). Three-parent babies: Mitochondrial replacement therapies. JBRA Assisted Reproduction, 24(2), 189-196. https://doi.org/10.5935/1518-0557.20190086

Grady, J. P., Pickett, S. J., Ng, Y. S., Alston, C. L., Blakely, E. L., Hardy, S. A., Feeney, C. L., Bright, A. A., Schaefer, A. M., Gorman, G. S., McNally, R. J., Taylor, R. W., Turnbull, D. M., & McFarland, R. (2018). MtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease. EMBO Molecular Medicine, 10(6), e8262. https://doi.org/10.15252/emmm.201708262

Kirillova, A., & Mazunin, I. (2022). Operation «mitochondrial wipeout»—Clearing recipient mitochondria DNA during the cytoplasmic replacement therapy. Journal of Assisted Reproduction and Genetics, 39(10), 2205-2207. https://doi.org/10.1007/s10815-022-02561-6

Newson, A. J., de Lacey, S., Dowling, D. K., Murray, S., Sue, C. M., Thorburn, D. R., Gillam, L., & Degeling, C. (2019). Public attitudes towards novel reproductive technologies: A citizens’ jury on mitochondrial donation. Human Reproduction (Oxford, England), 34(4), 751-757. https://doi.org/10.1093/humrep/dez021

Noohi, F., Ravitsky, V., Knoppers, B. M., & Joly, Y. (2022). Mitochondrial Replacement Therapy: In Whose Interests? The Journal of Law, Medicine & Ethics: A Journal of the American Society of Law, Medicine & Ethics, 50(3), 597-602. https://doi.org/10.1017/jme.2022.98

Palacios-González, C., & Medina-Arellano, M. de J. (2017). Mitochondrial replacement techniques and Mexico’s rule of law: On the legality of the first maternal spindle transfer case. Journal of Law and the Biosciences, 4(1), 50-69. https://doi.org/10.1093/jlb/lsw065

Pfeffer, G., Majamaa, K., Turnbull, D. M., Thorburn, D., & Chinnery, P. F. (2012). Treatment for mitochondrial disorders. The Cochrane Database of Systematic Reviews, 4. https://doi.org/10.1002/14651858.CD004426.pub3

Richardson, J., Irving, L., Hyslop, L. A., Choudhary, M., Murdoch, A., Turnbull, D. M., & Herbert, M. (2015). Concise reviews: Assisted reproductive technologies to prevent transmission of mitochondrial DNA disease. Stem Cells (Dayton, Ohio), 33(3), 639-645. https://doi.org/10.1002/stem.1887

Schaefer, & Labude, M. K. (2017). Genetic affinity and the right to «three-parent IVF». Journal of Assisted Reproduction and Genetics, 34(12), 1577-1580. https://doi.org/10.1007/s10815-017-1046-8

Sheldon, K. (2015). Crossing the Germline Barrier: The Three Genome Baby. Ethics in Biology, Engineering and Medicine: An International Journal, 6(3-4), 237-261. https://doi.org/10.1615/EthicsBiologyEngMed.2016016331

Tachibana, M., Amato, P., Sparman, M., Woodward, J., Sanchis, D. M., Ma, H., Gutierrez, N. M., Tippner-Hedges, R., Kang, E., Lee, H.-S., Ramsey, C., Masterson, K., Battaglia, D., Lee, D., Wu, D., Jensen, J., Patton, P., Gokhale, S., Stouffer, R., & Mitalipov, S. (2013). Towards germline gene therapy of inherited mitochondrial diseases. Nature, 493(7434), 627-631. https://doi.org/10.1038/nature11647

Wei, W., & Chinnery, P. F. (2020). Inheritance of mitochondrial DNA in humans: Implications for rare and common diseases. Journal of Internal Medicine, 287(6), 634-644. https://doi.org/10.1111/joim.13047

Yamada, M., Akashi, K., Ooka, R., Miyado, K., & Akutsu, H. (2020). Mitochondrial Genetic Drift after Nuclear Transfer in Oocytes. International Journal of Molecular Sciences, 21(16), 5880. https://doi.org/10.3390/ijms21165880

Zhang, J., Liu, H., Luo, S., Lu, Z., Chávez-Badiola, A., Liu, Z., Yang, M., Merhi, Z., Silber, S. J., Munné, S., Konstantinidis, M., Wells, D., Tang, J. J., & Huang, T. (2017). Live birth derived from oocyte spindle transfer to prevent mitochondrial disease. Reproductive Biomedicine Online, 34(4), 361-368. https://doi.org/10.1016/j.rbmo.2017.01.013

Zinkant, K. (2016). Da traut sich niemand ran. Süddeutsche.de. https://www.sueddeutsche.de/wissen/bioethik-da-traut-sich-niemand-ran-1.2850609

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Publicado

2023-06-29

Cómo citar

Reguera Cabezas, M. (2023). Singapur un camino interrumpido hacia la regulación de las técnicas de reemplazo mitocondrial. IUS ET SCIENTIA, 9(1), 116–128. https://doi.org/10.12795/IESTSCIENTIA.2023.i01.08
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