Evidence map›Paper›PMID 30604135›Full record

ReviewJournal of assisted reproduction and genetics2019

Male infertility: establishing sperm aneuploidy thresholds in the laboratory.

Elena García-Mengual, Juan Carlos Triviño, Alba Sáez-Cuevas, Juan Bataller, Miguel Ruíz-Jorro, Xavier Vendrell

Abstract readReview
In one paragraph

Review in Journal of assisted reproduction and genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Rediscovering FISH in the midst of a sperm chromatin conundrum.Journal of assisted reproduction and genetics · 2019
    Article
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.

Elena García-MengualReproductive Genetics Unit, Sistemas Genómicos S.L, Ronda G. Marconi 6, Parque Tecnológico, 46980, Paterna, Valencia, Spain. elena.garcia@sistemasgenomicos.com.ORCID http://orcid.org/0000-0002-4492-3144
Juan Carlos TriviñoBioinformatics Department, Sistemas Genómicos S.L, Ronda G. Marconi 6, Parque Tecnológico, 46980, Paterna, Valencia, Spain.
Alba Sáez-CuevasReproductive Genetics Unit, Sistemas Genómicos S.L, Ronda G. Marconi 6, Parque Tecnológico, 46980, Paterna, Valencia, Spain.
Juan BatallerCREA, Assisted Reproduction Medical Center, Carrer de Sant Martí 4, 46003, Valencia, Spain.
Miguel Ruíz-JorroCREA, Assisted Reproduction Medical Center, Carrer de Sant Martí 4, 46003, Valencia, Spain.
Xavier VendrellReproductive Genetics Unit, Sistemas Genómicos S.L, Ronda G. Marconi 6, Parque Tecnológico, 46980, Paterna, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeFluorescence in situ hybridization (FISH) in spermatozoa provides an estimate of the frequency of chromosomal abnormalities, but there is not a clinical consensus on how to statistically analyze sperm FISH results. We therefore propose a statistical approach to establish sperm aneuploidy thresholds in a fertile population.

methodsWe have determined the distribution and variation of the frequency of nullisomy, disomy, and diploidy for a set of 13 chromosomes (1, 2, 9, 13, 15, 16, 17, 18, 19, 21, 22, X, and Y) in sperm nuclei from 14 fertile men by means of automatized FISH. The dispersion of data has been analyzed by the non-parametric Wilcoxon Rank Sum test. We have established the threshold values for each chromosome and aneuploidy type on the basis of the confidence interval values (99.9%).

resultsNullisomy thresholds ranged from 0.49% for chromosome 19 to 3.09% for chromosome 22; disomy thresholds ranged from 0.30% for chromosome 21 to 1.47% for chromosome 15; diploidy thresholds ranged from 0.24% for the 9/19 chromosome set to 1.21% for the 13/21 chromosome set.

conclusionsApplying this approach with clinical purposes will enable us to categorize the patient as altered or normal regarding his sperm aneuploidy. Any result surpassing the cited threshold values indicates a 99.9% probability of being significantly different from fertile controls.

Indexed as

Chromosome AberrationsAneuploidyCell NucleusDiploidyHumansInfertility, MaleIn Situ Hybridization, FluorescenceMaleSpermatozoaAneuploidy thresholdsAutomatized analysisDiploidyDisomyFertile donorsFluorescence in situ hybridization (FISH)Human sperm aneuploidyNullisomy

Identifiers

PMID30604135
PMCPMC6439035

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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.