Evidence map›Paper›PMID 35328464›Full record

ArticleInternational journal of molecular sciences2022

Cryoprotectants-Free Vitrification and Conventional Freezing of Human Spermatozoa: A Comparative Transcript Profiling.

Mengying Wang, Plamen Todorov, Wanxue Wang, Evgenia Isachenko, Gohar Rahimi, Peter Mallmann, Vladimir Isachenko

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. A Pilot Analysis of Whole Transcriptome of Human Cryopreserved Sperm.International journal of molecular sciences · 2024
    Article
  7. Article
  8. Review
  9. Molecular Markers: A New Paradigm in the Prediction of Sperm Freezability.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Article
  12. Review
  13. 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

7 authors.

Mengying WangDepartment of Obstetrics and Gynaecology, Medical Faculty, Cologne University, 50931 Cologne, Germany.
Plamen TodorovInstitute of Biology and Immunology of Reproduction of Bulgarian Academy of Sciences, Tsarigradsko Highway 73A, 1113 Sofia, Bulgaria.ORCID 0000-0003-3731-6116
Wanxue WangDepartment of Obstetrics and Gynaecology, Medical Faculty, Cologne University, 50931 Cologne, Germany.ORCID 0000-0003-0606-6628
Evgenia IsachenkoDepartment of Obstetrics and Gynaecology, Medical Faculty, Cologne University, 50931 Cologne, Germany.
Gohar RahimiDepartment of Obstetrics and Gynaecology, Medical Faculty, Cologne University, 50931 Cologne, Germany.
Peter MallmannDepartment of Obstetrics and Gynaecology, Medical Faculty, Cologne University, 50931 Cologne, Germany.
Vladimir IsachenkoDepartment of Obstetrics and Gynaecology, Medical Faculty, Cologne University, 50931 Cologne, Germany.ORCID 0000-0002-3674-543X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSpermatozoa cryopreservation is an important technique to preserve fertility for males. This study aimed at exploring the stability of epigenetics information in human spermatozoa, manipulated by two different technologies, freezing and vitrification.

methodsSpermatozoa samples were distributed into three groups: 1. Fresh spermatozoa (control group), 2. Frozen spermatozoa, 3. Vitrified spermatozoa. Epigenetic differences of fresh and cryopreserved spermatozoa were evaluated using high-throughput RNA sequencing.

resultsDifferentially expressed genes (DEGs) in frozen (1103 genes) and vitrified (333 genes) spermatozoa were evaluated. The bioinformatical analysis identified 8 and 15 significant pathways in groups of frozen and vitrified spermatozoa, respectively. The majority of these pathways are most relevant to immune and infectious diseases. The DEGs of the fertilization process are not detected during vitrification. The freezing process induces more down-regulation of genes and is relevant to apoptosis changes and immune response.

conclusionCryopreservation of human spermatozoa is an epigenetically safe method for male fertility preservation. Cryoprotectant-free vitrification can induce more minor biological changes in human spermatozoa, in comparison with conventional freezing.

Indexed as

Semen PreservationVitrificationCryopreservationCryoprotective AgentsFreezingHumansMaleSpermatozoaSperm MotilityCryoprotective AgentscryopreservationDEGdifferentially expressed genesfreezinghuman spermatozoatranscriptome stabilityvitrification

Identifiers

PMID35328464
PMCPMC8956043

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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.