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Record W2898840518 · doi:10.1016/j.ajhg.2018.10.004

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability

2018· article· en· W2898840518 on OpenAlexafffund
Karl P. Schlingmann, Sascha Bandulik, Cherry Mammen, Maja Tarailo‐Graovac, Rikke Holm, Matthias Baumann, Jens König, Jessica J. Y. Lee, Britt I. Drögemöller, Katrin Imminger, Bodo B. Beck, Janine Altmüller, Hölger Thiele, Siegfried Waldegger, William van’t Hoff, Robert Kleta, Richard Warth, Clara van Karnebeek, Bente Vilsen, Detlef Böckenhauer, Martin Konrad

Bibliographic record

VenueThe American Journal of Human Genetics · 2018
Typearticle
Languageen
FieldNursing
TopicMagnesium in Health and Disease
Canadian institutionsAlberta Children's HospitalUniversity of CalgaryUniversity of British Columbia
FundersCanadian Institutes of Health ResearchDeutsche ForschungsgemeinschaftEuropean CommissionKidney Research UKEuropean Geosciences UnionGenome British ColumbiaBC Children’s Hospital FoundationMichael Smith Health Research BCSt Peter’s Trust for Kidney Bladder and Prostate ResearchLundbeckfondenDavid and Elaine Potter FoundationNovo Nordisk FondenKids Kidney ResearchWyethInnovationsfondenSeventh Framework ProgrammeSundhed og Sygdom, Det Frie Forskningsråd
KeywordsHypomagnesemiaGermlineIntellectual disabilityMedicineRefractory (planetary science)GeneticsPediatricsPsychiatryBiologyGeneChemistryMagnesium

Abstract

fetched live from OpenAlex

Over the last decades, a growing spectrum of monogenic disorders of human magnesium homeostasis has been clinically characterized, and genetic studies in affected individuals have identified important molecular components of cellular and epithelial magnesium transport. Here, we describe three infants who are from non-consanguineous families and who presented with a disease phenotype consisting of generalized seizures in infancy, severe hypomagnesemia, and renal magnesium wasting. Seizures persisted despite magnesium supplementation and were associated with significant intellectual disability. Whole-exome sequencing and conventional Sanger sequencing identified heterozygous de novo mutations in the catalytic Na + , K + -ATPase α1 subunit ( ATP1A1 ). Functional characterization of mutant Na + , K + -ATPase α1 subunits in heterologous expression systems revealed not only a loss of Na + , K + -ATPase function but also abnormal cation permeabilities, which led to membrane depolarization and possibly aggravated the effect of the loss of physiological pump activity. These findings underline the indispensable role of the α1 isoform of the Na + , K + -ATPase for renal-tubular magnesium handling and cellular ion homeostasis, as well as maintenance of physiologic neuronal activity.

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.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.026
GPT teacher head0.337
Teacher spread0.311 · 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

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations93
Published2018
Admission routes2
Has abstractyes

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