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Record W2789290343 · doi:10.21037/aes.2018.ab090

AB090. MOG1, the genetic modifier at 20q13, delays the age-at-onset of glaucoma by 8 to 10 years

2018· article· en· W2789290343 on OpenAlex

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.
aboutThe title or abstract carries a Canadian signal from the geographic lexicon.

Bibliographic record

VenueAnnals of Eye Science · 2018
Typearticle
Languageen
FieldMedicine
TopicGlaucoma and retinal disorders
Canadian institutionsCentre hospitalier universitaire de Québec
Fundersnot available
KeywordsMyocilinGlaucomaEndophenotypeGeneticsMutationAge of onsetGeneDiseaseOpen angle glaucomaBiologyMedicineOphthalmologyInternal medicineNeuroscience

Abstract

fetched live from OpenAlex

Background: Primary open-angle glaucoma (POAG) is a genetically complex disorder caused primarily by gene-gene interactions. To identify these interactions, we studied the CA family, a large French-Canadian pedigree in which the myocilin K423E mutation (MYOCK423E) causes autosomal dominant glaucoma with diagnoses ranging from juvenile-onset OAG (JOAG) to late adult-onset POAG in the heterozygotes (HTZ). To explain this extreme variability, we hypothesized that a second gene, called a modifier, was interacting with MYOC, the primary disease gene. Our goals were (I) to map the modifier on the human genome and; (II) to characterize the symptoms affected genetically by the modifier. These symptoms are called endophenotypes. Methods: Three hundred seventy-five CA members were studied using four quantitative endophenotypes: age of maximal intra-ocular pressures (IOPmax), IOPs progression, progression of cup to disk ratios and age-at-onset (AAO) defined as age at which ocular hypertension (OHT) was first detected with IOP ≥22 mmHg. Genome-wide linkage analysis was performed by genotyping 408 genetic markers in 184 CA members. An unbiased pedigree-based algorithm was designed to identify the individuals who were double-mutants, i.e., these individuals carried one MYOCK423E mutation (i.e., they were HTZ, affected or not) and they also carry simultaneously a DNA mutation within the modifier. Results: Out of the 375 CA family members investigated, 156 were HTZ for the MYOCK423E mutation. 120 HTZ were affected with OAG or OHT with treatment while the remaining 36 HTZ were asymptomatic. AAO ranged from 7 to 63 years old; 4 individuals over 50 years old were still asymptomatic. OHT preceded optic nerve damage in >98% of the HTZ carriers, confirming that AAO reflected the true severity of the disorder. The modifier showed strong inherited effects on 2 of the 4 endophenotypes: AAO and IOPmax. We next mapped with very high confidence the modifier locus for AAO at chromosome 20q13. Saturation genotyping with additional markers refined the locus to a 9 to 10 centimorgan interval, or about 10 million DNA nucleotides, between D20S857 and D20S832. The locus was named modifier of glaucoma 1 (MOG1). When comparing the AAOs of the double mutants versus the median of the AAOs of the MYOCK423E HTZ who carried a wild-type (normal) MOG1 gene and were 1st cousins or closer with the double mutant under investigation, we observed that MOG1 delayed the ages at onset by an average of 8 to 10 years in the double mutants. Conclusions: The MOG1 locus encodes a DNA element that delays the onset of glaucoma by an average of 8–10 years by hampering the first manifestations of OHT. This research will lead to the development of new therapeutic targets for glaucoma. These treatments should prevent optic nerve damage by maintaining IOPs within the normal range.

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)0.001
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: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.741
Threshold uncertainty score0.862

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.002
Scholarly communication0.0000.000
Open science0.0010.000
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 head0.031
GPT teacher head0.325
Teacher spread0.294 · 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