Abstract 4370493: Hypercholesterolemia polygenic score modulates response to statin therapy

E Elizabeth Cirulli (Helix, Lakeside, California, United States) M Matthew Levy (Helix, San Mateo, California, United States) N Natalie Telis (Helix, Lakeside, California, United States) A Amy Sturm (OSUMC, Columbus, Ohio, United States) C Chad Haldeman-Englert (Cone Health, Greensboro, North Carolina, United States) S STEVEN POWELL (Sanford Health, Sioux Falls, South Dakota, United States) C Christopher Chapman (St. Luke’s University Health Network, Bethlehem, Pennsylvania, United States) C C. Anwar Chahal (WellSpan, York, Pennsylvania, United States) D Douglas Stoller (UNMC, Omaha, Nebraska, United States) D Daniel Judge (Medical University of South Carolina, Charleston, South Carolina, United States) D Douglas Olson (HealthPartners, Minneapolis, Minnesota, United States) J Joseph Grzymski (Desert Research Institute, Reno, Nevada, United States) W William Lee K Kelly Schiabor Barrett (Helix, San Diego, California, United States) A Alexandre Bolze

Abstract

Background: Studies have shown that individuals with high CAD PGS have greater reduction in cardio outcomes from statin use than do those with low PGS. Here, we quantify the effect of a hypercholesterolemia PGS on response to statin therapy. Methods: A retrospective study of real world EMR data from ~200k Helix Research Network participants, enrolled from the general population during routine medical care from >15 health systems across the country. This study utilizes Exome+(R) sequencing; hypercholesterolemia PGS000889; longitudinal LDL levels; and statin start date. We analyzed a median of 9 LDL measurements spanning 8 years and studied percent change in LDL after beginning statins. Results: We analyzed 12,444 individuals who had baseline LDL above 100 mg/dL and then began statins, dropping their LDL by a median of 31%. We found that highPGS individuals (>90%) had less reduction in their LDL compared to lowPGS (<10%). This effect was most pronounced in those with lower baseline LDL: for those with LDL between 100-130, lowPGS individuals saw a 35% reduction, compared to 20% reduction for highPGS, while for those with LDL >160, both high and low PGS experienced a 34% reduction. In contrast, the effect of statins on reducing subsequent CAD was higher for highPGS: a 1.6x reduction in risk for lowPGS vs. a 4.2x reduction for highPGS with baseline LDL 100-300, and a 4.1x reduction for lowPGS vs. 7.1x for highPGS with baseline LDL >160. This observed difference was mostly due to untreated highPGS individuals having high risk even without clinically elevated LDL. Conclusion: Our data shows an association between hypercholesterolemia PGS and CAD risk reduction following statin use. The observed percent LDL reduction appeared lower in highPGS individuals, with the greatest difference in association observed in individuals with relatively low LDL.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (15)

E

Elizabeth Cirulli

Helix, Lakeside, California, United States

M

Matthew Levy

Helix, San Mateo, California, United States

N

Natalie Telis

Helix, Lakeside, California, United States

A

Amy Sturm

OSUMC, Columbus, Ohio, United States

C

Chad Haldeman-Englert

Cone Health, Greensboro, North Carolina, United States

S

STEVEN POWELL

Sanford Health, Sioux Falls, South Dakota, United States

C

Christopher Chapman

St. Luke’s University Health Network, Bethlehem, Pennsylvania, United States

C

C. Anwar Chahal

WellSpan, York, Pennsylvania, United States

D

Douglas Stoller

UNMC, Omaha, Nebraska, United States

D

Daniel Judge

Medical University of South Carolina, Charleston, South Carolina, United States

D

Douglas Olson

HealthPartners, Minneapolis, Minnesota, United States

J

Joseph Grzymski

Desert Research Institute, Reno, Nevada, United States

W

William Lee

K

Kelly Schiabor Barrett

Helix, San Diego, California, United States

A

Alexandre Bolze