Abstract

The All of Us Research Program was designed to enable broad-based precision medicine research in a cohort of unprecedented scale and diversity. Hypertension (HTN) is a major public health concern. The validity of HTN data and definition of hypertension cases in the All of Us (AoU) Research Program for use in rule-based algorithms is unknown. In this cross-sectional, population-based study, we compare HTN prevalence in the AoU Research Program to HTN prevalence in the 2015–2016 National Health and Nutrition Examination Survey (NHANES). We used AoU baseline data from patient (age ≥ 18) measurements (PM), surveys, and electronic health record (EHR) blood pressure measurements. We retrospectively examined the prevalence of HTN in the EHR cohort using Systemized Nomenclature of Medicine (SNOMED) codes and blood pressure medications recorded in the EHR. We defined HTN as the participant having at least 2 HTN diagnosis/billing codes on separate dates in the EHR data AND at least one HTN medication. We calculated an age-standardized HTN prevalence according to the age distribution of the U.S. Census, using 3 groups (18–39, 40–59, and ≥ 60). Among the 185,770 participants enrolled in the AoU Cohort (mean age at enrollment = 51.2 years) available in a Researcher Workbench as of October 2019, EHR data was available for at least one SNOMED code from 112,805 participants, medications for 104,230 participants, and 103,490 participants had both medication and SNOMED data. The total number of persons with SNOMED codes on at least two distinct dates and at least one antihypertensive medication was 33,310 for a crude prevalence of HTN of 32.2%. AoU age-adjusted HTN prevalence was 27.9% using 3 groups compared to 29.6% in NHANES. The AoU cohort is a growing source of diverse longitudinal data to study hypertension nationwide and develop precision rule-based algorithms for use in hypertension treatment and prevention research. The prevalence of hypertension in this cohort is similar to that in prior population-based surveys.

Highlights

  • The All of Us Research Program was designed to enable broad-based precision medicine research in a cohort of unprecedented scale and diversity

  • Researcher Workbench electronic health record (EHR) and medication data were available on 104,047 participants, Systemized Nomenclature of Medicine (SNOMED) codes were available on 112,468 participants, and 103,270 participants had both medication and SNOMED data

  • We completed the first analysis of HTN using data from the All of Us (AoU) Research Program Researcher Workbench

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Summary

Introduction

The All of Us Research Program was designed to enable broad-based precision medicine research in a cohort of unprecedented scale and diversity. The validity of HTN data and definition of hypertension cases in the All of Us (AoU) Research Program for use in rule-based algorithms is unknown. In this cross-sectional, population-based study, we compare HTN prevalence in the AoU Research Program to HTN prevalence in the 2015–2016 National Health and Nutrition Examination Survey (NHANES). Our rationale for this study was to validate the definition of ­HTN7 in the new resource, the All of Us (AoU) Research Program using rule-based algorithms The validity of this definition based on electronic health record (EHR) data in underrepresented populations is unknown. Our findings may inform the use of AoU data to develop rule-based algorithms based on EHR data for prevention and treatment of hypertension in clinical practice

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