Evidence map›Paper›PMID 29785530›Full record

ArticleJournal of assisted reproduction and genetics2018

Azoospermia and embryo morphokinetics: testicular sperm-derived embryos exhibit delays in early cell cycle events and increased arrest prior to compaction.

Nina Desai, Pavinder Gill, Nicholas N Tadros, Jeffrey M Goldberg, Edmund Sabanegh, Tommaso Falcone

Abstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Review
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  14. The clinical use of time-lapse in human-assisted reproduction.Therapeutic advances in reproductive health
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Nina DesaiCleveland Clinic, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, 26900 Cedar Road, Beachwood, OH, 44122, USA. Desain@ccf.org.
Pavinder GillCleveland Clinic, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, 26900 Cedar Road, Beachwood, OH, 44122, USA.
Nicholas N TadrosDivision of Urology, Southern Illinois University, PO Box 19665, Springfield, IL, 62794, USA.
Jeffrey M GoldbergCleveland Clinic, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, 26900 Cedar Road, Beachwood, OH, 44122, USA.
Edmund SabaneghCleveland Clinic, Department of Urology, Glickman Urological and Kidney Institute, 26900 Cedar Road, Beachwood, OH, 44122, USA.
Tommaso FalconeCleveland Clinic, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, 26900 Cedar Road, Beachwood, OH, 44122, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSperm play an essential role in embryonic genome activation and embryonic progression to blastocyst. In the present work, we focus on development of embryos created as a result of ICSI with testicular or epididymal sperm from azoospermic males and compare this to outcomes from normospermic males. The objective of this study was to determine if sperm origin influences clinical outcomes, the kinetics of embryo development, or the incidence of cleavage anomalies and multinucleation.

methodsA total of 93 consecutive intracytoplasmic sperm injection cycles (ICSI) performed for 83 couples were included in this study. Observations were made on 594 fertilized oocytes cultured in the EmbryoScope using time-lapse microscopy (TLM). Epididymal sperm (n = 29) cycles or surgically retrieved sperm from the testis (TESE; n = 37 cycles) of men with either obstructive (OA) or non-obstructive azoospermia (NOA) were used to inject oocytes. A further 27 ICSI cycles were performed using ejaculated sperm from normospermic males, designated as our control sperm (CS) group. Kinetic data and cycle outcomes were retrospectively analyzed.

resultsThe clinical pregnancy rate was not different between the three groups (TESE 51.4%, PESA 57.7%, and CS 59.3%). A non-significant decrease was observed in both implantation (30.9%) and live birth rate (43%) with TESE as compared to PESA (35.3%, 58%, respectively) and CS groups (45.1%, 56%, respectively). Failure to compact was significantly higher amongst TESE-NOA embryos (35.2%; P < 0.001) as compared to TESE-OA (4%), PESA (9%), and CS (3.8%) embryos. The two points at which TESE-derived embryos (both NOA and OA) behaved most differently from PESA and CS embryos was at cc2 (t3-t2; time to initiation of the second cell cycle) and tSB (time to start of blastulation). A significantly lower percentage of TESE embryos exhibited kinetics typically ascribed to high quality embryos with the greatest developmental potential. Finally, the incidence of direct uneven cleavage (DUC) was observed to be significantly higher after ICSI with sperm retrieved from azoospermic males.

conclusionsTLM allowed a more in depth comparison of paternal influence on embryo morphokinetics and helped to identify specific differences in cell cycle kinetics. TESE-NOA embryos exhibited a higher incidence of compaction failure.

Indexed as

AdultAzoospermiaBirth RateBlastocystCell CycleFemaleHumansInfertility, MaleMalePregnancyPregnancy RateRetrospective StudiesSpermatozoaSperm Injections, IntracytoplasmicSperm RetrievalTestisAzoospermiaBlastocystEpidiymal spermGenome activation, compactionTesticular spermTime-lapse, morphokinetics

Identifiers

PMID29785530
PMCPMC6063819

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.