Literature DB >> 29872942

Compensating human subjects providing oocytes for stem cell research: 9-year experience and outcomes.

L Zakarin Safier1, A Gumer1, M Kline1, D Egli2,3, M V Sauer1,4,5.   

Abstract

PURPOSE: Human oocytes are arguably one of the most important cell types in humans, yet they are one of the least investigated cells. Because oocytes are limited in number, the use of high-quality oocytes is almost entirely in reproduction. Furthermore, regulatory hurdles for research on gametes and regulations on funding related to research on gametes present significant obstacles to research and the advancement of reproductive treatments. Here we report the outcomes of the largest compensated oocyte donation program for research in the USA to date, and probably worldwide.
METHODS: Women who participated in oocyte donation for research between 2008 and 2017 were contacted in a phone interview and completed a standardized questionnaire.
RESULTS: Of 114 participants, 98 oocyte donors completed donation, donating 1787 mature MII oocytes and a total of 86 skin biopsies. Complication rate, including minor complications, of oocyte donation was 8/98, or 8.1%, for which two involved follow-up. Fifty-seven donors answered questions about their experience. Participants were incentivized primarily by money and a desire to help others and reported an overall favorable experience. Most, but not all, human subjects recalled that they had donated for research, and approximately half recalled that their oocytes were being used specifically for stem cell research.
CONCLUSIONS: Compensated oocyte donation provides a reliable path to obtaining high-quality oocytes for research and is reviewed favorably by oocyte donors. The continuation of programs that offer compensation for oocyte donation is invaluable to continued progress and advancements in stem cell research and human embryology, and for the advancement of novel reproductive treatments.

Entities:  

Keywords:  Mitochondrial replacement; Nuclear transfer; Oocyte donation; Stem cells; Survey

Mesh:

Year:  2018        PMID: 29872942      PMCID: PMC6063839          DOI: 10.1007/s10815-018-1171-z

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  25 in total

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Journal:  Cell Stem Cell       Date:  2016-11-10       Impact factor: 24.633

10.  Towards germline gene therapy of inherited mitochondrial diseases.

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Journal:  Nature       Date:  2012-10-24       Impact factor: 49.962

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