Evidence map›Paper›PMID 40342881›Full record

ArticleJournal of human reproductive sciences

Novel Genetic Variants of CDC25A Significantly Increase Risk of Spermatogenesis Arrest in Men from Bengali Population, India: A Cross-Sectional Study.

Samudra Pal, Pranab Paladhi, Saurav Dutta, Ratna Chattopadhyay, Sujay Ghosh

Abstract read
In one paragraph

Article in Journal of human reproductive sciences. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Samudra PalDepartment of Zoology, Cytogenetics and Genomics Research Unit, University of Calcutta, Taraknath Palit Siksha Prangan, Ballygunge Science College Campus, Kolkata, India.
Pranab PaladhiDepartment of Zoology, Cytogenetics and Genomics Research Unit, University of Calcutta, Taraknath Palit Siksha Prangan, Ballygunge Science College Campus, Kolkata, India.
Saurav DuttaDepartment of Zoology, Cytogenetics and Genomics Research Unit, University of Calcutta, Taraknath Palit Siksha Prangan, Ballygunge Science College Campus, Kolkata, India.
Ratna ChattopadhyayDepartment of Embryology, Institute of Reproductive Medicine, Kolkata, India.
Sujay GhoshDepartment of Zoology, Cytogenetics and Genomics Research Unit, University of Calcutta, Taraknath Palit Siksha Prangan, Ballygunge Science College Campus, Kolkata, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Idiopathic azoospermia is one of the most common reasons for male infertility, but little is known about its genetic origins. The CDC25A gene, a meiotic core regulator, encodes a phosphatase that triggers the G1/S transition of meiosis. It dephosphorylates and activates CDK2, as well as enhances CDC2-cyclin E, CDK2-cyclin A and CDK1-cyclin B complex formation, which is crucial for chromosome condensation and progression of meiosis. Aim: The aim of this study was to identify individual variants of the CDC25A gene that make men susceptible to idiopathic azoospermia. Setting and Design: Genetic association study comparing the CDC25A gene in men with idiopathic azoospermia. Materials and Methods: The coding sequence of the entire CDC25A gene was sequenced in a population of azoospermic men. Recently discovered heterozygous mutations were assessed using Statistical Analysis Used: Bioinformatics software such as SIFT, PolyPhen-2 and MutationTaster were applied to forecast the functional consequence of detected variants. Results: Novel heterozygous mutations were found in CDC25A. Variants present only in azoospermic men were evaluated for their pathogenicity, indicating their potential involvement in infertility. Conclusion: This work identifies new CDC25A gene variants that may be linked with idiopathic azoospermia. These discoveries add to the knowledge of the genetic aetiology of male infertility and could contribute to the development of future diagnostics and treatments.

Indexed as

AzoopermiaCDC25Agenetic variants

Identifiers

PMID40342881
PMCPMC12057834

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.