Evidence map›Paper›PMID 34975072›Full record

ArticleAsian journal of andrology

MACS-annexin V cell sorting of semen samples with high TUNEL values decreases the concentration of cells with abnormal chromosomal content: a pilot study.

Sahar El Fekih, Nadia Gueganic, Corinne Tous, Habib Ben Ali, Mounir Ajina, Nathalie Douet-Guilbert, Hortense Drapier, Damien Beauvillard, Frédéric Morel, Aurore Perrin

Open access · goldAbstract read
In one paragraph

Article in Asian journal of andrology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 38% of its field
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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
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

10 authors at 3 institutions in 2 countries.

Sahar El FekihUniversity of Brest, Inserm, UMR U1078, Faculty of Medicine and Health Sciences, Brest 29238, France.
Nadia GueganicUniversity of Brest, Inserm, UMR U1078, Faculty of Medicine and Health Sciences, Brest 29238, France.
Corinne TousDepartement of Medical Genetics and Reproductive Biology, Brest University Regional Hospital, Brest 29609, France.
Habib Ben AliLaboratory of Human Cytogenetics, Molecular Genetics and Reproductive Biology, Farhat Hached University Hospital, Sousse 4031, Tunisia.
Mounir AjinaDepartment of Reproductive Medicine, Farhat Hached Teaching Hospital, Sousse 4031, Tunisia.
Nathalie Douet-GuilbertUniversity of Brest, Inserm, UMR U1078, Faculty of Medicine and Health Sciences, Brest 29238, France.
Hortense DrapierDepartement of Medical Genetics and Reproductive Biology, Brest University Regional Hospital, Brest 29609, France.
Damien BeauvillardDepartement of Medical Genetics and Reproductive Biology, Brest University Regional Hospital, Brest 29609, France.
Frédéric MorelUniversity of Brest, Inserm, UMR U1078, Faculty of Medicine and Health Sciences, Brest 29238, France.
Aurore PerrinUniversity of Brest, Inserm, UMR U1078, Faculty of Medicine and Health Sciences, Brest 29238, France.
Inserm · FRUniversité de Bretagne Occidentale · FRLaboratoire des Sciences et Techniques de l’Information de la Communication et de la Connaissance · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We question whether, in men with an abnormal rate of sperm DNA fragmentation, the magnetic-activated cell sorting (MACS) could select spermatozoa with lower rates of DNA fragmentation as well as spermatozoa with unbalanced chromosome content. Cryopreserved spermatozoa from six males were separated into nonapoptotic and apoptotic populations. We determined the percentages of spermatozoa with (i) externalization of phosphatidylserine (EPS) by annexin V-Fluorescein isothiocyanate (FITC) labeling, (ii) DNA fragmentation by TdT-mediated-dUTP nick-end labeling (TUNEL), and (iii) numerical abnormalities for chromosomes X, Y, 13, 18, and 21 by fluorescence in situ hybridization (FISH), on the whole ejaculate and selected spermatozoa in the same patient. Compared to the nonapoptotic fraction, the apoptotic fraction statistically showed a higher number of spermatozoa with EPS, with DNA fragmentation, and with numerical chromosomal abnormalities. Compared to the whole ejaculate, we found a significant decrease in the percentage of spermatozoa with EPS and decrease tendencies of the DNA fragmentation rate and the sum of disomy levels in the nonapoptotic fraction. Conversely, we observed statistically significant higher rates of these three parameters in the apoptotic fraction. MACS may help to select spermatozoa with lower rates of DNA fragmentation and unbalanced chromosome content in men with abnormal rates of sperm DNA fragmentation.

Indexed as

SemenSpermatozoaAnnexin A5Chromosome AberrationsDNA FragmentationHumansIn Situ Hybridization, FluorescenceIn Situ Nick-End LabelingMalePilot ProjectsAnnexin A5chromosomal abnormalitiesDNA fragmentationexternalization of phosphatidylserinemagnetic-activated cell separationspermatozoa

Identifiers

PMID34975072
PMCPMC9491034
OpenAlexW4205530672

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.