Publication Information (EuropePMC) | |
Title | Polygenic Score for β-Blocker Survival Benefit in European Ancestry Patients With Reduced Ejection Fraction Heart Failure. |
PubMed ID | 33012170(Europe PMC) |
doi | 10.1161/circheartfailure.119.007012 |
Publication Date | Oct. 4, 2020 |
Journal | Circ Heart Fail |
Author(s) | Lanfear DE, Luzum JA, She R, Gui H, Donahue MP, O'Connor CM, Adams KF, Sanders-van Wijk S, Zeld N, Maeder MT, Sabbah HN, Kraus WE, Brunner-LaRocca HP, Li J, Williams LK. |
Polygenic Score ID & Name | PGS Publication ID (PGP) | Reported Trait | Mapped Trait(s) (Ontology) | Number of Variants |
Ancestry distribution GWAS Dev Eval |
Scoring File (FTP Link) |
---|---|---|---|---|---|---|
PGS000718 (PRPBB_44) |
PGP000134 | Lanfear DE et al. Circ Heart Fail (2020) |
Beta-blocker survival benefit | response to beta blocker | 44 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS000718/ScoringFiles/PGS000718.txt.gz |
PGS Performance Metric ID (PPM) |
Evaluated Score |
PGS Sample Set ID (PSS) |
Performance Source | Trait |
PGS Effect Sizes (per SD change) |
Classification Metrics | Other Metrics | Covariates Included in the Model |
PGS Performance: Other Relevant Information |
---|---|---|---|---|---|---|---|---|---|
PPM001643 | PGS000718 (PRPBB_44) |
PSS000852| European Ancestry| 1,188 individuals |
PGP000134 | Lanfear DE et al. Circ Heart Fail (2020) |
Reported Trait: Response to beta blocker (reduction in cardiovascular death) in heart failure patients | — | — | P-value (treatment benefit in low vs. high PRP patients): 0.046 | Meta-Analysis Global Group in Chronic Heart Failure Score, beta-blocker propensity score | Low polygenic response predictor score < 30th percentile of derviation group |
PPM001642 | PGS000718 (PRPBB_44) |
PSS000851| European Ancestry| 1,188 individuals |
PGP000134 | Lanfear DE et al. Circ Heart Fail (2020) |
Reported Trait: Response to beta blocker (reduction in all-cause mortality) in heart failure patients | — | — | P-value (treatment benefit in low vs. high PRP patients): 0.024 | Meta-Analysis Global Group in Chronic Heart Failure Score, beta-blocker propensity score | Low polygenic response predictor score < 30th percentile of derviation group |
PGS Sample Set ID (PSS) |
Phenotype Definitions and Methods | Participant Follow-up Time | Sample Numbers | Age of Study Participants | Sample Ancestry | Additional Ancestry Description | Cohort(s) | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
PSS000851 | Cases = number of cardiovascular deathsHFPGR: Patients with left ventricular ejection fraction (LVEF) <50% were included. Beta-blocker (BB) exposure was calculated from pharmacy claims (ie, drug actually dispensed to patient) and was updated over time. Beta-blocker (BB) exposure was calculated from pharmacy claims (ie, drug actually dispensed to patient) and was updated over time. TIME-CHF: Patients with analysable data and a baseline LVEF <50% were included. BB exposure was calculated from the specific drug and dose at baseline, using the same dose-equivalence scheme as HFPGR but implemented without any updates over time and without information on medication dispensing (ie, assumes patients were receiving the dose prescribed). HF-ACTION: BB exposure was calculated from the specific drug and dose at baseline, using the same dose-equivalence scheme as HFPGR but implemented without any updates over time and without information on medication dispensing (ie, assumes patients were receiving the dose prescribed). | — | [
|
— | European | — | HF-ACTION, HFPGR, TIME-CHF | — |
PSS000852 | Cases = number of all cause deaths. HFPGR: Patients with left ventricular ejection fraction (LVEF) <50% were included. Beta-blocker (BB) exposure was calculated from pharmacy claims (ie, drug actually dispensed to patient) and was updated over time. Beta-blocker (BB) exposure was calculated from pharmacy claims (ie, drug actually dispensed to patient) and was updated over time. TIME-CHF: Patients with analysable data and a baseline LVEF <50% were included. BB exposure was calculated from the specific drug and dose at baseline, using the same dose-equivalence scheme as HFPGR but implemented without any updates over time and without information on medication dispensing (ie, assumes patients were receiving the dose prescribed). HF-ACTION: BB exposure was calculated from the specific drug and dose at baseline, using the same dose-equivalence scheme as HFPGR but implemented without any updates over time and without information on medication dispensing (ie, assumes patients were receiving the dose prescribed). | — | [
|
— | European | — | HF-ACTION, HFPGR, TIME-CHF | — |