Evidence map›Paper›PMID 41342320›Full record

ArticleEndocrine connections2025

Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants.

Khadidja Fouatih, Camille Roussel, Maryse Cartigny, Muriel Houang, Lise Duranteau, Zeina Chakhtoura, Anne-Sophie Lambert, Marie-Agathe Trouvin, Barbara Girerd, Ekaterina Belozertseva and 9 more

Abstract read
In one paragraph

Article in Endocrine connections, 2025. 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
–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

0 citing papers in PubMed.

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

19 authors.

Khadidja FouatihService d'endocrinologie et du diabète de l'enfant, Hôpital Bicêtre, Paris, France.ORCID https://orcid.org/0009-0009-8794-4138
Camille RousselLaboratoire d'Hématologie Générale, Hôpital Necker, APHP & UMR_S1134 - Inserm - Université Paris Cité, Paris, France.
Maryse CartignyService d'Endocrinologie Pédiatrique, CHU Lille, Lille, France.
Muriel HouangExplorations Fonctionnelles Endocriniennes, Centre de Référence Maladies Endocriniennes Rares de la Croissance et du Développement - CRESCENDO, Hôpital Armand Trousseau, APHP, Paris, France.
Lise DuranteauService de Gynécologie médicale, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre, APHP, Le Kremlin-Bicetre, France.
Zeina ChakhtouraService d'Endocrinologie et Médecine de la Reproduction, Hôpital La Pitié-Salpêtrière, Paris, France.ORCID https://orcid.org/0009-0009-9109-560X
Anne-Sophie LambertService d'endocrinologie et du diabète de l'enfant, Hôpital Bicêtre, Paris, France.ORCID https://orcid.org/0000-0002-4232-3882
Marie-Agathe TrouvinService d'endocrinologie et du diabète de l'enfant, Hôpital Bicêtre, Paris, France.
Barbara GirerdService d'endocrinologie et du diabète de l'enfant, Hôpital Bicêtre, Paris, France.
Ekaterina BelozertsevaService d'endocrinologie et du diabète de l'enfant, Hôpital Bicêtre, Paris, France.
Delphine BorgelLaboratoire d'Hématologie Générale, Hôpital Necker, APHP & UMR_S1134 - Inserm - Université Paris Cité, Paris, France.
Stephanie Franchi-AbellaService d'imagerie médicale pédiatrique, Hôpital Bicêtre, Le Kremlin-Bicetre, France.
Jérôme BouligandINSERM UMR-S U1185, Faculté de Médecine, University Paris-Saclay, Le Kremlin Bicêtre, France.
Maureen LopezService de Génétique Moléculaire, Pharmacogénétique et Hormonologie de Bicêtre, Hôpitaux Universitaires Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Hôpital de Bicêtre, Le Kremlin Bicêtre, France.
Kenneth ChappellService de Génétique Moléculaire, Pharmacogénétique et Hormonologie de Bicêtre, Hôpitaux Universitaires Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Hôpital de Bicêtre, Le Kremlin Bicêtre, France.
Pierre BuffetService des Maladies Infectieuses et Tropicales, Hôpital Necker, APHP & UMR_S1134 - Inserm - Université Paris Cité, Paris, France.
Ines BelguithLaboratoire d'Hématologie Générale, Hôpital Necker, APHP & UMR_S1134 - Inserm - Université Paris Cité, Paris, France.
Claire BouvattierService d'endocrinologie et du diabète de l'enfant, Hôpital Bicêtre, Paris, France.
Abd El Kader Ait TayebINSERM UMR-S U1185, Faculté de Médecine, University Paris-Saclay, Le Kremlin Bicêtre, France.ORCID https://orcid.org/0000-0001-6432-1098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Steroidogenic factor 1 (SF-1), encoded by NR5A1, is essential for spleen development and function. NR5A1 variants have been linked to abnormal spleen development. Hyposplenism exposes individuals to severe complications with potentially serious sequelae. This study aimed to determine the prevalence and principal features of hyposplenism in a cohort of French patients with NR5A1 variants. Methods: We conducted a cross-sectional multicentre ancillary study among 34 patients carrying heterozygous NR5A1 variants within the GR-EX cohort, which includes individuals from families affected by red blood cell diseases. All participants underwent splenic imaging (ultrasound, CT, or MRI) and pocked red blood cell (pRBC) quantification. pRBC thresholds of <7%, 7-20%, and >20% corresponded to normal splenic function, moderate hyposplenism, and severe hyposplenism, respectively. The primary endpoints were the prevalence of hyposplenism and its severity. Results: Functional hyposplenism was observed in 21/34 patients (61.7%), including 16/34 (47%) with severe forms. Morphological spleen abnormalities were identified in 15/34 patients (44.1%), with asplenia in 4/34 (11.7%). All patients with morphological spleen abnormalities on imaging also presented functional hyposplenism. Conversely, 6/21 patients (28%) with functional hyposplenism showed no morphological abnormalities on imaging. No association was found between NR5A1 genotypes, gonadal phenotypes, and splenic anomalies. Conclusions: Functional hyposplenism was frequent in this cohort of patients carrying NR5A1 variants, regardless of genotype and gonadal phenotype. Assessing splenic function is mandatory to help manage these patients. Preventive measures are also critical when hyposplenism is present.

Indexed as

asplenismdisorders of sex development (DSD)hyposplenismSF-1/NR5A1spleen development

Identifiers

PMID41342320
PMCPMC12712559

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.