Personalizing cholesterol treatment recommendations for primary cardiovascular disease prevention.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
07 01 2022
Historique:
received: 13 07 2021
accepted: 02 12 2021
entrez: 8 1 2022
pubmed: 9 1 2022
medline: 24 2 2022
Statut: epublish

Résumé

Statin therapy is the cornerstone of preventing atherosclerotic cardiovascular disease (ASCVD), primarily by reducing low density lipoprotein cholesterol (LDL-C) levels. Optimal statin therapy decisions rely on shared decision making and may be uncertain for a given patient. In areas of clinical uncertainty, personalized approaches based on real-world data may help inform treatment decisions. We sought to develop a personalized statin recommendation approach for primary ASCVD prevention based on historical real-world outcomes in similar patients. Our retrospective cohort included adults from a large Northern California electronic health record (EHR) aged 40-79 years with no prior cardiovascular disease or statin use. The cohort was split into training and test sets. Weighted-K-nearest-neighbor (wKNN) regression models were used to identify historical EHR patients similar to a candidate patient. We modeled four statin decisions for each patient: none, low-intensity, moderate-intensity, and high-intensity. For each candidate patient, the algorithm recommended the statin decision that was associated with the greatest percentage reduction in LDL-C after 1 year in similar patients. The overall cohort consisted of 50,576 patients (age 54.6 ± 9.8 years) with 55% female, 48% non-Hispanic White, 32% Asian, and 7.4% Hispanic patients. Among 8383 test-set patients, 52%, 44%, and 4% were recommended high-, moderate-, and low-intensity statins, respectively, for a maximum predicted average 1-yr LDL-C reduction of 16.9%, 20.4%, and 14.9%, in each group, respectively. Overall, using aggregate EHR data, a personalized statin recommendation approach identified the statin intensity associated with the greatest LDL-C reduction in historical patients similar to a candidate patient. Recommendations included low- or moderate-intensity statins for maximum LDL-C lowering in nearly half the test set, which is discordant with their expected guideline-based efficacy. A data-driven personalized statin recommendation approach may inform shared decision making in areas of uncertainty, and highlight unexpected efficacy-effectiveness gaps.

Identifiants

pubmed: 34996943
doi: 10.1038/s41598-021-03796-6
pii: 10.1038/s41598-021-03796-6
pmc: PMC8742083
doi:

Substances chimiques

Cholesterol, LDL 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

Subventions

Organisme : NHLBI NIH HHS
ID : K01 HL144607
Pays : United States
Organisme : NHLBI NIH HHS
ID : 1K01HL144607
Pays : United States
Organisme : NHLBI NIH HHS
ID : 1R01HL126172-01A1
Pays : United States

Informations de copyright

© 2022. The Author(s).

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Auteurs

Ashish Sarraju (A)

Division of Cardiovascular Medicine and the Cardiovascular Institute, Center for Academic Medicine, Stanford University School of Medicine, 453 Quarry Road, Stanford, CA, USA.

Andrew Ward (A)

Department of Electrical Engineering, Stanford University, Stanford, CA, USA.

Jiang Li (J)

Palo Alto Foundation Research Institute, Palo Alto, CA, USA.

Areli Valencia (A)

Division of Cardiovascular Medicine and the Cardiovascular Institute, Center for Academic Medicine, Stanford University School of Medicine, 453 Quarry Road, Stanford, CA, USA.

Latha Palaniappan (L)

Palo Alto Foundation Research Institute, Palo Alto, CA, USA.
Division of Primary Care and Population Health, Stanford University School of Medicine, Stanford, CA, USA.

David Scheinker (D)

Department of Management Science and Engineering, Stanford University School of Engineering, Stanford, CA, USA.
Division of Pediatric Endocrinology, Stanford University School of Medicine, Stanford, CA, USA.

Fatima Rodriguez (F)

Division of Cardiovascular Medicine and the Cardiovascular Institute, Center for Academic Medicine, Stanford University School of Medicine, 453 Quarry Road, Stanford, CA, USA. frodrigu@stanford.edu.

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Classifications MeSH