MétaCan
Menu
← Back to cohort
Record W2763628863 · doi:10.1093/pch/19.6.e35-130

133: The Search for CYP24A1 Mutations in Canadian Children: An Unexpected Presentation with Nephrocalcinosis Despite Normal 1,25(OH)2d and Serum Calcium

2014· article· en· W2763628863 on OpenAlexaffabout
Isabelle Rousseau-Nepton, Glenville Jones, Atul Sharma, Celia Rodd

Bibliographic record

VenuePaediatrics & Child Health · 2014
Typearticle
Languageen
FieldMedicine
TopicVitamin D Research Studies
Canadian institutionsMcGill University
Fundersnot available
KeywordsCYP24A1NephrocalcinosisHypercalciuriaVitamin D and neurologyMedicineInternal medicineMetaboliteEndocrinologyCreatinineUrinary systemGastroenterologyKidneyCalcitriol receptor

Abstract

fetched live from OpenAlex

Idiopathic Hypercalcemia of Infancy (IIH) has been associated with mutations in the vitamin D degrading enzyme CYP24A1. The classic phenotype involves infants who present with hypercalcemia although individuals without an apparent infantile hypercalcemic phase have presented later in life. Typically, at least one vitamin D metabolite is elevated at the time of presentation, and usually CYP24A1 mutations described to date have completely abrogated enzyme activity. The frequency of CYP24A1 mutations and their phenotype is still poorly documented. To recruit children from across Canada with presumed IIH to examine their vitamin D metabolite profile using sensitive LC-MS/MS profiling and mutational analyses. Endocrinologists and nephrologists across Canada were contacted to identify potential cases of hypercalcemia or hypercalciuria without another identifiable etiology. LC-MS/MS was used to determine the ratio of 25(OH)D: 24,25(OH)2D, a marker of CYP24A1 activity. A ratio greater than 80 (ng/mL/ng/mL) is suggestive of CYP24A1 mutations. Mutational analyses were then carried out in all children. To date, five children have been recruited and 25 other cases are pending analyses. Three were infants with serum total calcium >2.90 mM and urine calcium: creatinine ratio >95th CI for age, and two were adolescents presenting with nephrocalcinosis or nephrolithiasis. Almost all had elevated 1,25(OH)2D concentrations and suppressed PTH. All vitamin D metabolite ratios were normal except in one girl who presented at nine years of age with an incidental finding of nephrocalcinosis on ultrasound performed for urinary tract infection. Her labs demonstrated intermittent hypercalciuria (peak 6.2 mmol/d), sporadically suppressed PTH, normal serum calcium, and normal vitamin D metabolites in the clinical laboratory. Family history was positive on both sides for nephrolithiasis. Her vitamin D metabolite ratio was 121; the mutational analysis demonstrated a known homozygous mutation E143del. The full phenotype of CYP24A1 mutations is not yet fully described. Likely other gene mutations are associated with IIH. Clinicians need to consider CYP24A1 mutations in the presence of suppressed PTH concentrations and incidental hypercalciuria or nephrocalcionosis.

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: Case report · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.176
Threshold uncertainty score0.354

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0020.002
Science and technology studies0.0030.001
Scholarly communication0.0010.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0040.000

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 head0.021
GPT teacher head0.327
Teacher spread0.306 · 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 designCase report
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

Citations0
Published2014
Admission routes2
Has abstractyes

Explore more

Same venuePaediatrics & Child Health→Same topicVitamin D Research Studies→French-language works237,207→