Evidence map›Paper›PMID 40188177›Full record

SynthesisCommunications biology2025

Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndrome.

Sara González-Muñoz, Yichen Long, Andrea Guzmán-Jiménez, Miriam Cerván-Martín, Inmaculada Higueras-Serrano, José A Castilla, Ana Clavero, Nicolás Garrido, Saturnino Luján, Xiaoyu Yang and 12 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

22 authors.

Sara González-Muñoz *Departamento de Genética e Instituto de Biotecnología, Centro de Investigación Biomédica (CIBM), Universidad de Granada, Granada, Spain.ORCID http://orcid.org/0000-0001-7519-8320
Yichen Long *State Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China.
Andrea Guzmán-Jiménez *Departamento de Genética e Instituto de Biotecnología, Centro de Investigación Biomédica (CIBM), Universidad de Granada, Granada, Spain.ORCID http://orcid.org/0000-0002-2091-0568
Miriam Cerván-MartínInstitute of Parasitology and Biomedicine Lopez-Neyra (IPBLN), CSIC, Granada, Spain.
Inmaculada Higueras-SerranoDepartamento de Genética e Instituto de Biotecnología, Centro de Investigación Biomédica (CIBM), Universidad de Granada, Granada, Spain.
José A CastillaInstituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.ORCID http://orcid.org/0000-0003-2185-565X
Ana ClaveroInstituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
Nicolás GarridoIVIRMA Global Research Alliance. IVI Foundation, Health Research Institute La Fe, Valencia, Spain.ORCID http://orcid.org/0000-0001-8271-5218
Saturnino LujánServicio de Urología. Hospital Universitari i Politecnic La Fe e Instituto de Investigación Sanitaria La Fe (IIS La Fe), Valencia, Spain.ORCID http://orcid.org/0000-0002-5005-3325
Xiaoyu YangState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China.
Xuejiang GuoState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China.ORCID http://orcid.org/0000-0002-0475-5705
Jiayin LiuState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China.
Lluís BassasLaboratory of Seminology and Embryology, Andrology Service-Fundació Puigvert, Barcelona, Spain.
Susana SeixasInstituto de Investigação e Inovação em Saúde, Universidade do Porto (I3S), Porto, Portugal.
João GonçalvesDepartamento de Genética Humana, Instituto Nacional de Saúde Dr. Ricardo Jorge, Lisbon, Portugal.
Alexandra M LopesInstituto de Investigação e Inovação em Saúde, Universidade do Porto (I3S), Porto, Portugal.
Sara LarribaImmune-Inflammatory Processes and Gene Therapeutics Group, Genes, Disease and Therapy Program, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Lara Bossini-CastilloDepartamento de Genética e Instituto de Biotecnología, Centro de Investigación Biomédica (CIBM), Universidad de Granada, Granada, Spain.ORCID http://orcid.org/0000-0002-5471-5824
Rogelio J Palomino-MoralesInstituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
Cheng WangState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China.ORCID http://orcid.org/0000-0002-8193-9276
Zhibin HuState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China. zhibin_hu@njmu.edu.cn.ORCID http://orcid.org/0000-0002-8277-5234
F David CarmonaDepartamento de Genética e Instituto de Biotecnología, Centro de Investigación Biomédica (CIBM), Universidad de Granada, Granada, Spain. dcarmona@ugr.es.ORCID http://orcid.org/0000-0002-1427-7639

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-obstructive azoospermia, a severe form of male infertility caused by spermatogenic failure (SPGF), has a largely unknown genetic basis across ancestries. To our knowledge, this is the first trans-ethnic meta-analysis of genome-wide association studies on SPGF, involving 2255 men with idiopathic SPGF and 3608 controls from European and Asian populations. Using logistic regression and inverse variance methods, we identify two significant genetic associations with Sertoli cell-only (SCO) syndrome, the most extreme SPGF phenotype. The G allele of rs34915133, in the major histocompatibility complex class II region, significantly increases SCO risk (P = 5.25E-10, OR = 1.57), supporting a potential immune-related cause. Additionally, the rs10842262 variant in the SOX5 gene region is also a genetic marker of SCO (P = 5.29E-09, OR = 0.72), highlighting the key role of this gene in the male reproductive function. Our findings reveal shared genetic factors in male infertility across ancestries and provide insights into the molecular mechanisms underlying SCO.

Indexed as

AzoospermiaGenome-Wide Association StudySertoli Cell-Only SyndromeSpermatogenesisAsian PeopleEuropean PeopleGenetic Predisposition to DiseaseHumansInfertility, MaleMalePolymorphism, Single NucleotideSOXD Transcription FactorsSOX5 protein, humanSOXD Transcription Factors

Identifiers

PMID40188177
PMCPMC11972312

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.