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Record W2319060123 · doi:10.1158/1538-7445.am2011-3742

Abstract 3742: Gene-environment Interactions in esophageal adenocarcinoma risk: A case-only analysis

2011· article· en· W2319060123 on OpenAlexaff
Rihong Zhai, Yang Zhao, Geoffrey Liu, Monica Ter‐Minassian, Zhao‐Xi Wang, I‐Chen Wu, Li Su, Kofi Asomaning, Feng Chen, Matthew H. Kulke, Xihong Lin, Rebecca S. Heist, John C. Wain, David C. Christiani

Bibliographic record

VenueCancer Research · 2011
Typearticle
Languageen
FieldMedicine
TopicEsophageal Cancer Research and Treatment
Canadian institutionsPrincess Margaret Cancer CentreOntario Institute for Cancer Research
Fundersnot available
KeywordsGERDSingle-nucleotide polymorphismInternal medicineMedicineEsophageal cancerGastroenterologyLogistic regressionIncidence (geometry)EtiologyCancerOncologyDiseaseRefluxBiologyGeneGeneticsGenotype

Abstract

fetched live from OpenAlex

Abstract The incidence of esophageal adenocarcinoma (EA) has increased approximately 500% in Western countries over the last four decades. The rapidly increasing incidence and sporadically development feature of EA suggest that gene-environment (G-E) interactions dominate the etiology. However, how G-E contributes to EA carcinogenesis is still poorly understood. We used a case-only approach to test the effect of G-E interactions in the occurrence of EA. 1330 functional and/or tagging SNPs selected from 354 cancer-associated genes were genotyped in 335 Caucasian EA cases. G-E (gastroesophageal reflux symptoms, GERD; BMI; and smoking) interactions were assessed by a two-step approach. First, we applied random forest (RF) to screen for important SNPs that had main effects as well as interaction effects. Second, we used case-only logistic regression (LR) models to estimate the G-E interaction effect, adjusting for covariates and false-discovery rate (FDR). RF analyses identified three sets of SNPs (94 SNPs-GERD, 38 SNPs-smoking, and 44 SNPs-BMI, respectively) that had the highest importance scores and lowest classification error rates. Further case-only LR analysis revealed that multiple interaction markers were significantly associated with EA risk: GERD*rs2237051 of EGF(OR = 1.39, P = 3.50E-07), GERD*rs2440 of XRCC5 (OR = 1,80, P = 0.0008), GERD*rs2237051*rs2440 (OR = 1.85, P = 0.004), smoking*rs10842514 of KRAS (OR = 0.85, P = 0.012), BMI*rs2305742 of IL12RB1 (OR = 0.84, P = 0.003), BMI*rs11568820 of VDR (OR = 0.97, P = 0.0005), BMI*rs11244142 of ABL1 (OR = 1.47, P = 2.09E-05), BMI*rs2800975 of XPA*rs743572 of CYP17A (OR = 3.62, P = 0.0009), and BMI*rs11244142*rs20547 of IL13 (OR = 1.89, P = 0.023). These results indicate that genetic variability may contribute to EA development through interactions with environmental factors. Our data also suggest that G-E interactions may be G- and E-specific in modulating the risk of EA. Supported by grants: NIH grants CA92824, CA74386, CA90578, and CA119650); Flight Attendant Medical Research Institute (FAMRI) grant 062459_YCSA; the Kevin Jackson Memorial Fund and Alan Brown Chair of Molecular Genomics. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2-6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2011;71(8 Suppl):Abstract nr 3742. doi:10.1158/1538-7445.AM2011-3742

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)0.003
metaresearch head score (Gemma)0.006
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: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.018

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0030.006
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.002
Bibliometrics0.0020.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0060.001

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 head0.130
GPT teacher head0.416
Teacher spread0.286 · 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

Citations0
Published2011
Admission routes1
Has abstractyes

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