Evidence map›Paper›PMID 38540177›Full record

ArticleBiomedicines2024

Telomere Dysfunction in Pediatric Patients with Differences/Disorders of Sexual Development.

Haifaou Younoussa, Macoura Gadji, Mamadou Soumboundou, Bruno Colicchio, Ahmed Said, Ndeye Aby Ndoye, Steffen Junker, Andreas Plesch, Leonhard Heidingsfelder, Ndeye Rama Diagne and 5 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

15 authors at 7 institutions in 3 countries.

Haifaou YounoussaCell Environment DNA Damage R&D, Genopole, 91000 Evry-Courcouronnes, France.
Macoura GadjiService of Biological Hematology & Oncology-Hematology (BHOH), National Centre of Blood Transfusion (NCBT), Faculty of Medicine, Pharmacy and Odonto-Stomatology (FMPO), Cheikh Anta Diop University of Dakar (UCAD), Dakar BP 5002, Senegal.ORCID 0000-0003-0252-3772
Mamadou SoumboundouMedical Diagnostic Laboratory, Diamniadjo Hospital, UFR-Santé de Thiès, Iba Der Thiam University of Thies, Thiès BP A967, Senegal.
Bruno ColicchioIRIMAS, Institut de Recherche en Informatique, Mathématiques, Automatique et Signal, Université de Haute-Alsace, 68093 Mulhouse, France.ORCID 0000-0002-1742-8631
Ahmed SaidCell Environment DNA Damage R&D, Genopole, 91000 Evry-Courcouronnes, France.
Ndeye Aby NdoyeService de Chirurgie Pédiatrique de L'hôpital Albert Royer, Cheikh Anta Diop Ave, Dakar BP 25755, Senegal.
Steffen JunkerInstitute of Biomedicine, University of Aarhus, DK-8000 Aarhus, Denmark.
Andreas PleschMetaSystems GmbH, D-68804 Altlussheim, Germany.
Leonhard HeidingsfelderMetaSystems GmbH, D-68804 Altlussheim, Germany.
Ndeye Rama DiagneMedical Diagnostic Laboratory, Diamniadjo Hospital, UFR-Santé de Thiès, Iba Der Thiam University of Thies, Thiès BP A967, Senegal.
Alain DieterlenIRIMAS, Institut de Recherche en Informatique, Mathématiques, Automatique et Signal, Université de Haute-Alsace, 68093 Mulhouse, France.
Philippe VoisinCell Environment DNA Damage R&D, Genopole, 91000 Evry-Courcouronnes, France.
Patrice CardeDepartment of Hematology, Gustave Roussy Cancer Campus, 94805 Villejuif, France.
Eric JeandidierService de Génétique, Groupe Hospitalier de la Région de Mulhouse Sud-Alsace, 68100 Mulhouse, France.ORCID 0000-0002-2757-0770
Radhia M'kacherCell Environment DNA Damage R&D, Genopole, 91000 Evry-Courcouronnes, France.ORCID 0000-0003-0639-4760
Genopole (France) · FRUniversité de Haute-Alsace · FRUniversité de Thiès · SNAarhus University · DKCheikh Anta Diop University · SNGroupe Hospitalier de la Région de Mulhouse et Sud Alsace · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differences/Disorders of sex development (DSDs) are conditions in which the development of chromosomal, gonadal, and anatomical sexes is atypical. DSDs are relatively rare, but their incidence is becoming alarmingly common in sub-Saharan Africa (SSA). Their etiologies and mechanisms are poorly understood. Therefore, we have investigated cytogenetic profiles, including telomere dysfunction, in a retrospective cohort of Senegalese DSD patients. MATERIALS AND

methodsPeripheral blood lymphocytes were sampled from 35 DSD patients (mean age: 3.3 years; range 0-18 years) admitted to two hospital centers in Dakar. Peripheral blood lymphocytes from 150 healthy donors were used as a control. Conventional cytogenetics, telomere, and centromere staining followed by multiplex FISH, as well as FISH with

resultsCytogenetic analysis identified 19 male and 13 female patients with apparently normal karyotypes, two patients with Turner syndrome, and one patient with Klinefelter syndrome. Additional structural chromosome aberrations were detected in 22% of the patients (8/35). Telomere analysis revealed a reduction in mean telomere lengths of DSD patients compared to those of healthy donors of similar age. This reduction in telomere length was associated with an increased rate of telomere aberrations (telomere loss and the formation of telomere doublets) and the presence of additional chromosomal aberrations.

conclusionsTo the best of our knowledge, this study is the first to demonstrate a correlation between telomere dysfunction and DSDs. Further studies may reveal the link between telomere dysfunction and possible mechanisms involved in the disease itself, such as DNA repair deficiency or specific gene mutations. The present study demonstrates the relevance of implementing telomere analysis in prenatal tests as well as in diagnosed genetic DSD disorders.

Indexed as

chromosomal aberrationsDSDstelomere dysfunctionstelomere shortening

Identifiers

PMID38540177
PMCPMC10968223
OpenAlexW4392379060

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.