Evidence map›Paper›PMID 41540017›Full record

ArticleNPJ genomic medicine2026

Distinguishing benign from pathogenic duplications involving GPR101 and VGLL1-adjacent enhancers in the clinical setting with the bioinformatic tool POSTRE.

Giampaolo Trivellin, Víctor Sánchez-Gaya, Alexia Grasso, Magdalena Pasińska, Constantine A Stratakis, Di Milnes, Edwin P Kirk, Albert Beckers, Andrea G Lania, Patrick Pétrossians and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in NPJ genomic medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00001595 (A Clinical and Genetic Investigation of Pituitary and Hypothalamic Tumors and Related Disorders), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

NCT00001595 recruitingnot on this map

A Clinical and Genetic Investigation of Pituitary and Hypothalamic Tumors and Related Disorders

TypeobservationalSponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Ran1997Enrolled2,000ConditionsPanhypopituitarism, Gigantism/Acromegaly, Prolactinoma, Cushing DiseaseArmsTissue specimen collection, MRI
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Genetics of familial acromegaly and pituitary gigantism.The Journal of clinical endocrinology and metabolism · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Giampaolo TrivellinDepartment of Biomedical Sciences, Humanitas University, via Rita Levi Montalcini 4, Pieve Emanuele, Milan, Italy. giampaolo.trivellin@hunimed.eu.
Víctor Sánchez-GayaInstitute of Biomedicine and Biotechnology of Cantabria (IBBTEC), CSIC/Universidad de Cantabria, Albert Einstein 22, Santander, Spain.
Alexia GrassoIRCCS Humanitas Research Hospital, Translational Endocrinology and Metabolism Lab, via Manzoni 56, Rozzano, Milan, Italy.
Magdalena PasińskaDepartment of Clinical Genetics, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Bydgoszcz, Poland.
Constantine A StratakisHuman Genetics & Precision Medicine, Institute of Molecular Biology and Biotechnology (IMBB), Foundation for Research and Technology Hellas (FORTH), Heraklion, Greece.
Di MilnesGenetic Health Queensland, Royal Brisbane Women's Hospital, Brisbane, QLD, Australia.
Edwin P KirkNSW Health Pathology East Genomics, Randwick, NSW, Australia.
Albert BeckersDepartment of Endocrinology, Centre Hospitalier Universitaire de Liège, University of Liège, Liège, Belgium.
Andrea G LaniaDepartment of Biomedical Sciences, Humanitas University, via Rita Levi Montalcini 4, Pieve Emanuele, Milan, Italy.
Patrick PétrossiansDepartment of Endocrinology, Centre Hospitalier Universitaire de Liège, University of Liège, Liège, Belgium.
Alvaro Rada-IglesiasInstitute of Biomedicine and Biotechnology of Cantabria (IBBTEC), CSIC/Universidad de Cantabria, Albert Einstein 22, Santander, Spain.
Martin FrankeAndalusian Center for Developmental Biology (CABD), Junta de Andaluciıa- Universidad Pablo de Olavide (UPO) - Consejo Superior de Investigaciones Científicas (CSIC), Seville, Spain.
Adrian F DalyDepartment of Endocrinology, Centre Hospitalier Universitaire de Liège, University of Liège, Liège, Belgium.

Funding

Molecular Genetics of Endocrine Tumors and Related DisordersZIAHD008920 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI STRATAKIS, CONSTANTINE A. · 2012 to 2021
$25.8M
Centre Hospitalier Universitaire de Liège Fonds d'Investissment pour la Recherche Scientifique 2018-2023Eunice Kennedy Shriver National Institute of Child Health and Human Development Z1A HD008920Fondazione Telethon GGP20130Intramural NIH HHS ZIA HD008920'la Caixa' Foundation 100010434Ministero dell'Istruzione, dell'Università e della Ricerca MSCA_0000055NextGenerationEU Generation D initiativeUniversité de Liège FSR-F-2023-FM
6 · The paper itself

Abstract

Structural variants (SVs) that disrupt topologically associating domains can cause disease by rewiring enhancer-promoter interactions. Duplications involving GPR101 are known to cause X-linked acrogigantism (X-LAG) through ectopic GPR101 expression, but not all of these duplications are pathogenic. This presents a diagnostic challenge, especially in the prenatal setting. We evaluated POSTRE, a tool that predicts the regulatory impact of SVs, to distinguish pathogenic from benign GPR101 duplications. We analyzed seven non-pathogenic duplications and 27 known X-LAG-associated duplications. To enable predictions in an X-LAG-relevant tissue, enhancer maps built using H3K27ac ChIP-seq, ATAC-seq, and RNA-seq data derived from human anterior pituitary samples (NIH research protocol 97-CH-0076, Clinicaltrials.gov Identifier NCT00001595, submitted on 11 March 1999) were integrated into POSTRE. POSTRE correctly classified all 34 duplications as benign or pathogenic. In addition, one X-LAG case with mild clinical features (i.e. severe growth hormone hypersecretion without pituitary tumorigenesis) was found to include only 2/5 VGLL1 enhancers, whereas all typical X-LAG cases had ≥4 enhancers duplicated. This suggests that partial enhancer hijacking at VGLL1 could explain the different clinical features in this individual. These findings support the utility of POSTRE to support diagnostic pipelines when interpreting SVs affecting chromatin architecture in pituitary disease and highlight its potential to reduce uncertainty in genetic counseling without requiring chromatin conformation capture assays.

Identifiers

PMID41540017
PMCPMC12890961

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Registered trials

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.