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Record W2921445007 · doi:10.1093/jcag/gwz006.012

A13 PROTEINS AND FIBROSTENOTIC CROHN’S DISEASE; WHO SHOWED UP TO THE PARTY?

2019· article· en· W2921445007 on OpenAlexaff
Cathy Lu, Antoine Dufour, Aito Ueno, Humberto Jijon, K Prowse, Kerri L. Novak, Remo Panaccione, Simon A. Hirota

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2019
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicDermatological and Skeletal Disorders
Canadian institutionsMcMaster UniversityUniversity of Calgary
Fundersnot available
KeywordsCrohn's diseaseMedicineInflammatory bowel diseaseGastroenterologyProteomeInternal medicineUlcerative colitisDiseaseDemographicsPathologyBioinformaticsBiology

Abstract

fetched live from OpenAlex

Crohn’s Disease (CD) is an inflammatory bowel disease mainly affecting the terminal ileum (TI) with three distinct phenotypes including strictures. Despite advances in medical therapy, fibrostenosis remains a therapeutic challenge as there are no available anti-fibrotic treatments. To date, there are no biomarkers to discriminate stricturing CD from other phenotypes. Early studies suggest that protein biomarkers identified from serum profiling may differentiate CD subtypes, and predict biologic therapy response. However, no studies have assessed which cell surface proteins are found in patients with strictures. Utilizing intestinal ultrasound (US), which readily detects fibrostenotic CD strictures, the serum of patients with and without strictures was collected for proteomic characterization. To investigate differences in the serum proteome among CD patients with fibrostenosis, as identified on bowel US, to those without strictures. All consecutive CD patients attending outpatient US appointments received greyscale US. Strictures were defined as a fixed bowel segment with a point of luminal apposition with or without prestenotic dilation. Five patients with ileal strictures were matched with similar ileal CD patients with only inflammatory behaviour, as confirmed on US. Patient sera was collected for quantitative shotgun proteomics using liquid chromatography/mass spectrometry. Statistical analysis was conducted at 1% false discovery rate to identify cell surface proteins to differentiate CD with and without strictures. 10 CD patient samples were collected; five patients allocated to the stricture and five to the non-stricture group. Demographics and age at diagnosis were similar between groups. Mean ileal bowel wall thickness was greater in the strictured (7.5 mm) group than without (4.5mm, p = 0.02). Prestenotic dilation (2 to 5 cm) was present in all with ileal stricture. All patients with a stricture had inflammation (mild/moderate inflammatory fat, hyperemia), while all but one in the non-strictured group had quiescent CD. More than 1,600 proteins were identified. In the strictured group, 4/5 patients had elevated Plexin-A2 and CD5 antigen-like protein, and 3/5 had elevated neogenin and dystonin. Of the non-strictured patients, 3/5 had elevated MMP-16/MT3-MMP (matrix metalloproteinase 16/membrane-type 3 MMP), and 4/5 had elevated vinculin. The sera of patients with and without structuring CD have a unique protein signature. These results provide an initial foundation driving further evaluation to confirm or refine candidate proteins, comparison to patients with resected strictures, and for mechanistic studies. Protein biomarkers may facilitate early stricture detection, monitor CD progression and ultimately identify patients in need of therapies with the greatest stricture risk. None

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 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 score0.052
Threshold uncertainty score0.965

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 head0.004
GPT teacher head0.192
Teacher spread0.188 · 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 teacher head, 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

Citations0
Published2019
Admission routes1
Has abstractyes

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