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Live birth derived from oocyte spindle transfer to prevent mitochondrial disease.
Reprod Biomed Online. 2017 04; 34(4):361-368.RB

Abstract

Mutations in mitochondrial DNA (mtDNA) are maternally inherited and can cause fatal or debilitating mitochondrial disorders. The severity of clinical symptoms is often associated with the level of mtDNA mutation load or degree of heteroplasmy. Current clinical options to prevent transmission of mtDNA mutations to offspring are limited. Experimental spindle transfer in metaphase II oocytes, also called mitochondrial replacement therapy, is a novel technology for preventing mtDNA transmission from oocytes to pre-implantation embryos. Here, we report a female carrier of Leigh syndrome (mtDNA mutation 8993T > G), with a long history of multiple undiagnosed pregnancy losses and deaths of offspring as a result of this disease, who underwent IVF after reconstitution of her oocytes by spindle transfer into the cytoplasm of enucleated donor oocytes. A male euploid blastocyst wasobtained from the reconstituted oocytes, which had only a 5.7% mtDNA mutation load. Transfer of the embryo resulted in a pregnancy with delivery of a boy with neonatal mtDNA mutation load of 2.36-9.23% in his tested tissues. The boy is currently healthy at 7 months of age, although long-term follow-up of the child's longitudinal development remains crucial.

Authors+Show Affiliations

New Hope Fertility Center, Punto Sao Paulo, Lobby Corporativo, Américas 1545 Providencia, Guadalajara, Mexico; New Hope Fertility Center, 4 Columbus Circle, New York, NY 10019, USA. Electronic address: johnzhang211@gmail.com.New Hope Fertility Center, 4 Columbus Circle, New York, NY 10019, USA.Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.New Hope Fertility Center, 4 Columbus Circle, New York, NY 10019, USA.New Hope Fertility Center, Punto Sao Paulo, Lobby Corporativo, Américas 1545 Providencia, Guadalajara, Mexico.New Hope Fertility Center, 4 Columbus Circle, New York, NY 10019, USA.New Hope Fertility Center, 4 Columbus Circle, New York, NY 10019, USA.Department of Obstetrics and Gynecology, Division of Reproductive Biology, NYU School of Medicine, 180 Varick Street, New York, NY 10014, USA.Infertility Center of St Louis, St Luke's Hospital, St Louis, MO 63017, USA.Reprogenetics, 3 Regent Street, Livingston, NJ 07078, USA.Reprogenetics, 3 Regent Street, Livingston, NJ 07078, USA.Reprogenetics, 3 Regent Street, Livingston, NJ 07078, USA.Department of Obstetrics and Gynecology, The Mount Sinai Hospital, E 101(st) Street, New York, NY 10029, USA.Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA. Electronic address: Taosheng.Huang@cchmc.org.

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

28385334

Citation

Zhang, John, et al. "Live Birth Derived From Oocyte Spindle Transfer to Prevent Mitochondrial Disease." Reproductive Biomedicine Online, vol. 34, no. 4, 2017, pp. 361-368.
Zhang J, Liu H, Luo S, et al. Live birth derived from oocyte spindle transfer to prevent mitochondrial disease. Reprod Biomed Online. 2017;34(4):361-368.
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
Zhang J, et al. Live Birth Derived From Oocyte Spindle Transfer to Prevent Mitochondrial Disease. Reprod Biomed Online. 2017;34(4):361-368. PubMed PMID: 28385334.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Live birth derived from oocyte spindle transfer to prevent mitochondrial disease. AU - Zhang,John, AU - Liu,Hui, AU - Luo,Shiyu, AU - Lu,Zhuo, AU - Chávez-Badiola,Alejandro, AU - Liu,Zitao, AU - Yang,Mingxue, AU - Merhi,Zaher, AU - Silber,Sherman J, AU - Munné,Santiago, AU - Konstantinidis,Michalis, AU - Wells,Dagan, AU - Tang,Jian J, AU - Huang,Taosheng, PY - 2016/11/12/received PY - 2017/01/23/revised PY - 2017/01/31/accepted PY - 2017/4/8/entrez PY - 2017/4/8/pubmed PY - 2017/10/11/medline KW - Cytoplasm KW - Leigh syndrome KW - Meiotic spindle KW - Mitochondria KW - Nuclear transfer KW - Oocyte SP - 361 EP - 368 JF - Reproductive biomedicine online JO - Reprod. Biomed. Online VL - 34 IS - 4 N2 - Mutations in mitochondrial DNA (mtDNA) are maternally inherited and can cause fatal or debilitating mitochondrial disorders. The severity of clinical symptoms is often associated with the level of mtDNA mutation load or degree of heteroplasmy. Current clinical options to prevent transmission of mtDNA mutations to offspring are limited. Experimental spindle transfer in metaphase II oocytes, also called mitochondrial replacement therapy, is a novel technology for preventing mtDNA transmission from oocytes to pre-implantation embryos. Here, we report a female carrier of Leigh syndrome (mtDNA mutation 8993T > G), with a long history of multiple undiagnosed pregnancy losses and deaths of offspring as a result of this disease, who underwent IVF after reconstitution of her oocytes by spindle transfer into the cytoplasm of enucleated donor oocytes. A male euploid blastocyst wasobtained from the reconstituted oocytes, which had only a 5.7% mtDNA mutation load. Transfer of the embryo resulted in a pregnancy with delivery of a boy with neonatal mtDNA mutation load of 2.36-9.23% in his tested tissues. The boy is currently healthy at 7 months of age, although long-term follow-up of the child's longitudinal development remains crucial. SN - 1472-6491 UR - https://www.unboundmedicine.com/medline/citation/28385334/Live_birth_derived_from_oocyte_spindle_transfer_to_prevent_mitochondrial_disease_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S1472-6483(17)30041-X DB - PRIME DP - Unbound Medicine ER -