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Record W2946343948 · doi:10.1161/circgen.118.002376

Rare Protein-Truncating Variants in <i>APOB</i> , Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease

2019· article· en· W2946343948 on OpenAlex
Gina M. Peloso, Akihiro Nomura, Amit Khera, Mark Chaffin, Hong‐Hee Won, Diego Ardissino, John Danesh, Heribert Schunkert, James G. Wilson, Nilesh J. Samani, Jeanette Erdmann, Ruth McPherson, Hugh Watkins, Danish Saleheen, Shane McCarthy, Tanya M. Teslovich, Joseph B. Leader, H. Lester Kirchner, Jaume Marrugat, Atsushi Nohara, Masa‐aki Kawashiri, Hayato Tada, Frederick E. Dewey, David J. Carey, Aris Baras, Sekar Kathiresan

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.
fundA Canadian funder is recorded on the work.

Bibliographic record

VenueCirculation Genomic and Precision Medicine · 2019
Typearticle
Languageen
FieldMedicine
TopicLipoproteins and Cardiovascular Health
Canadian institutionsUniversity of Ottawa
FundersNational Heart, Lung, and Blood InstituteMedical Research CouncilPerelman School of Medicine, University of PennsylvaniaSamsungTechnische Universität MünchenUniversità degli Studi di ParmaRegeneron PharmaceuticalsUniversität zu LübeckBritish Heart FoundationSungkyunkwan UniversityUniversity of OxfordUniversity of LeicesterUniversity of PennsylvaniaNational Human Genome Research InstituteWellcome TrustUniversity of OttawaCentro de Investigación Biomédica en Red Enfermedades CardiovascularesNational Institute for Health and Care ResearchMassachusetts General Hospital
KeywordsApolipoprotein BInternal medicineMedicineTriglycerideEndocrinologyCholesterolOdds ratioLipoproteinGeneticsBiology

Abstract

fetched live from OpenAlex

Background Familial hypobetalipoproteinemia is a genetic disorder caused by rare protein-truncating variants (PTV) in the gene encoding APOB (apolipoprotein B), the major protein component of LDL (low-density lipoprotein) and triglyceride-rich lipoprotein particles. Whether heterozygous APOB deficiency is associated with decreased risk for coronary heart disease (CHD) is uncertain. We combined family-based and large scale gene-sequencing to characterize the association of rare PTVs in APOB with circulating LDL-C (LDL cholesterol), triglycerides, and risk for CHD. Methods We sequenced the APOB gene in 29 Japanese hypobetalipoproteinemia families, as well as 57 973 individuals derived from 12 CHD case-control studies—18 442 with early-onset CHD and 39 531 controls. We defined PTVs as variants that lead to a premature stop, disrupt canonical splice-sites, or lead to insertions/deletions that shift reading frame. We tested the association of rare APOB PTV carrier status with blood lipid levels and CHD. Results Among 29 familial hypobetalipoproteinemia families, 8 families harbored APOB PTVs. Carrying 1 APOB PTV was associated with 55 mg/dL lower LDL-C ( P =3×10 -5 ) and 53% lower triglyceride level ( P =2×10 -4 ). Among 12 case-control studies, an APOB PTV was present in 0.038% of CHD cases as compared to 0.092% of controls. APOB PTV carrier status was associated with a 43 mg/dL lower LDL-C ( P =2×10 -7 ), a 30% decrease in triglycerides ( P =5×10 -4 ), and a 72% lower risk for CHD (odds ratio, 0.28; 95% CI, 0.12–0.64; P =0.002). Conclusions Rare PTV mutations in APOB which are associated with lower LDL-C and reduced triglycerides also confer protection against CHD.

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 score0.790
Threshold uncertainty score0.882

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
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 head0.014
GPT teacher head0.238
Teacher spread0.224 · 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