4.7 Article

Sperm deoxyribonucleic acid fragmentation (by terminal deoxynucleotidyl transferase biotin dUTP nick end labeling assay) does not impair reproductive success measured as cumulative live birth rates per donor metaphase II oocyte used

Journal

FERTILITY AND STERILITY
Volume 118, Issue 1, Pages 79-89

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2022.04.002

Keywords

Cumulative live birth rates; donated oocytes; male factor infertility; sperm DNA fragmentation; TUNEL assay

Funding

  1. Conselleria de Educacion, Investigacion, Cultura y Deporte, Generalitat de Valencia [ACIF/2019/261]
  2. European Social Fund
  3. Contrato Predoctoral de Formacion en Investigacion en Salud from the Instituto de Salud Carlos III [2019/0172]
  4. Ministerio de Ciencia, Innovacion y Universidades (Spain)
  5. Fundacion para la Investigacion Hospital La Fe (Valencia, Spain)

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This study found that elevated sperm DNA fragmentation does not reduce the live birth rate or cumulative probability of having a child in couples undergoing intracytoplasmic sperm injection (ICSI) cycles, when calculated per embryo transfer, per replaced embryo, and per donated metaphase II oocyte.
Objective: To better study the effect of sperm deoxyribonucleic acid fragmentation (SDF) on intracytoplasmic sperm injection (ICSI) outcomes from an ovum donation program by assessing the cumulative live birth rates (CLBRs) per number of embryo transfers (ETs), embryos replaced (EmbR), and metaphase II (MII) oocytes required in consecutive treatments to achieve the first newborn. Design: A multicenter retrospective cohort study was conducted, and the Kaplan-Meier survival curves were generated to calculate the CLBR with regard to the SDF degree. Setting: Private university-affiliated in vitro fertilization centers. Patient(s): Data from 864 couples using donated eggs and undergoing ICSI from 2000 to 2019 were analyzed. Sperm deoxyribonucleic acid fragmentation was measured using terminal deoxynucleotidyl transferase biotin dUTP nick end labeling assay on their ejaculated sperm. Intervention(s): None. Main Outcome Measure(s): Live birth rate (LBR) per first ET and per all consecutive ETs within the same patient and CLBR per ET, per EmbR, and per MII oocyte used considering the SDF level. Result(s): A total of 1,903 ICSI cycles were considered, encompassing 6,340 donated oocytes, 2,543 embryos, and 1,145 ETs. Comparing <= 15% SDF (low) with >15% SDF (high) or by 10% SDF ranges, the LBRs per first ET and per all ETs did not significantly differ. The Kaplan-Meier curves of the CLBR per ET, per EmbR, and per donor oocyte consumed were similar between the SDF groups evaluated. Conclusion(s): Elevated SDF does not reduce the LBR or cumulative probability to obtain a child when calculated per ET, per EmbR, and per donated MII oocyte used in couples undergoing ICSI cycles. ((C) 2022 by American Society for Reproductive Medicine.)

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