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Record W2898906372 · doi:10.1210/js.2018-00130

Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing

2018· article· en· W2898906372 on OpenAlex
Avinaash Maharaj, Federica Buonocore, Eirini Meimaridou, Gerard Ruiz‐Babot, Leonardo Guasti, Hwei‐Ming Peng, Cameron P. Capper, Neikelyn Burgos-Tirado, Rathi Prasad, Claire Hughes, Ashwini Maudhoo, Elizabeth Crowne, Timothy Cheetham, Caroline Brain, Jenifer P. Suntharalingham, Niccolò Striglioni, Bilgin Yüksel, Fatih Gürbüz, S Gupta, Robert S. Lindsay, Robert Couch, Helen Spoudeas, Tülay Güran, Stephanie Johnson, Dallas Fowler, Louise S. Conwell, Aideen McInerney‐Leo, D. Drui, Bertrand Cariou, Juan Pedro López‐Siguero, Mark Harris, Emma L. Duncan, Peter C. Hindmarsh, Richard J. Auchus, Malcolm Donaldson, John C. Achermann, Louise Metherell

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueJournal of the Endocrine Society · 2018
Typearticle
Languageen
FieldMedicine
TopicAdrenal Hormones and Disorders
Canadian institutionsUniversity of Alberta
FundersNational Institutes of HealthQueensland University of TechnologyGreat Ormond Street Hospital CharityNational Institute for Health and Care ResearchNational Institute of General Medical SciencesMedical Research CouncilWellcomeBarts CharityQueen Mary University of LondonWellcome Trust
KeywordsMissense mutationBiologyEtiologyCohortGeneticsAdrenal insufficiencyAlleleLoss of heterozygosityCholesterol side-chain cleavage enzymeCompound heterozygosityMedicineInternal medicineMutationGene

Abstract

fetched live from OpenAlex

Primary adrenal insufficiency (PAI) is a potentially life-threatening condition that can present with nonspecific features and can be difficult to diagnose. We undertook next generation sequencing in a cohort of children and young adults with PAI of unknown etiology from around the world and identified a heterozygous missense variant (rs6161, c.940G>A, p.Glu314Lys) in CYP11A1 in 19 individuals from 13 different families (allele frequency within undiagnosed PAI in our cohort, 0.102 vs 0.0026 in the Genome Aggregation Database; P < 0.0001). Seventeen individuals harbored a second heterozygous rare disruptive variant in CYP11A1 and two had very rare synonymous changes in trans (c.990G>A, Thr330 = ; c.1173C>T, Ser391 =). Although p.Glu314Lys is predicted to be benign and showed no loss-of-function in an Escherichia coli assay system, in silico and in vitro studies revealed that the rs6161/c.940G>A variant, plus the c.990G>A and c.1173C>T changes, affected splicing and that p.Glu314Lys produces a nonfunctional protein in mammalian cells. Taken together, these findings show that compound heterozygosity involving a relatively common and predicted “benign” variant in CYP11A1 is a major contributor to PAI of unknown etiology, especially in European populations. These observations have implications for personalized management and demonstrate how variants that might be overlooked in standard analyses can be pathogenic when combined with other very rare disruptive changes.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.428
Threshold uncertainty score0.407

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.014
GPT teacher head0.271
Teacher spread0.258 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it