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Record W2280176326 · doi:10.1161/atvb.34.suppl_1.43

Abstract 43: The Hypofunctional GPER P16L Variant is Associated With a Gene Dosage-Related Increase in Plasma LDL Cholesterol

2014· article· en· W2280176326 on OpenAlexaffabout
Yasin Hussain, Ross D. Feldman, Qingming Ding, Jozef Chorazyczewski, Matthew R. Ban, Adam D. McIntyre, Rob Gros, Robert A. Hegele

Bibliographic record

VenueArteriosclerosis Thrombosis and Vascular Biology · 2014
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicEstrogen and related hormone effects
Canadian institutionsRobarts Clinical Trials
Fundersnot available
KeywordsGPEREndocrinologyInternal medicineCohortCholesterolBiologyEstrogen receptorPopulationMedicineBreast cancerCancer

Abstract

fetched live from OpenAlex

Introduction: Estrogen deficiency is linked with dyslipidemia, especially in postmenopausal women, through a poorly understood mechanism. GPER is a recently recognized GPCR which is activated by estrogens. However, the role of GPER in mediating estrogen’s effects on lipid metabolism is unknown. We recently identified a common hypofunctional missense variant of GPER, namely P16L (allele frequency ~ 20%). We studied association of this with plasma LDL cholesterol levels. Further, we studied the role of GPER in regulating expression of the LDL receptor. Methods: Our discovery cohort was a genetically isolated population of Northern European descent (n=415), and our validation cohort consisted of 505 normal, healthy subjects 18-56 years of age from London, Ontario. Genomic DNA was extracted from whole blood and genotyped for GPER using a dedicated TaqMan assay. Additionally we examined the role of GPER on the regulation of LDL receptor expression by treatment with the GPER agonist, G1. Results: In the discovery cohort, the GPER P16L genetic variant was associated with a significant gene-dosage related increase in LDL cholesterol (CC [homozygous wild type] =3.18±0.84 (mean+SD); CT [heterozygote] =3.25±0.80; and TT [homozygous variant] =4.25±0.87 mmol/L, p<0.05). Total cholesterol concentrations followed a similar gradient across genotypes. In the validation cohort, the GPER P16L genetic variant was associated with a similar significant gene-dosage related increase in LDL cholesterol (CC =2.16±0.67; CT [heterozygote] =2.29±0.67; TT =2.40±0.84 mmol/L, p<0.05). In HepG2 cells expressing GPER, G1 mediated a concentration-dependent increase in LDL receptor expression. Pre-treating the cells with the GPER antagonist G15 attenuated the effect of G1 on LDL receptor upregulation. Further, downregulation of GPER expression via infection with a shGPER construct also attenuated G1's effect on LDL receptor upregulation. Conclusion: GPER activation upregulates LDL receptor expression. Further, carrying the hypofunctional P16L genetic variant of GPER, increases plasma LDL cholesterol in humans. In aggregate these data suggest an important role of GPER in regulation of LDL receptor expression and consequently LDL metabolism.

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: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.009
Threshold uncertainty score0.024

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.001
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0070.001

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 head0.010
GPT teacher head0.219
Teacher spread0.209 · 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
Published2014
Admission routes2
Has abstractyes

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