The "All of Us" Research Program

被引:1195
作者
Denny J.C. [1 ]
Rutter J.L. [2 ]
Goldstein D.B. [3 ,4 ]
Philippakis A. [5 ]
Smoller J.W. [5 ,6 ]
Jenkins G. [1 ]
Dishman E. [3 ]
机构
[1] Departments of Biomedical Informatics and Medicine, Vanderbilt University Medical Center, 2525 West End Ave., Nashville, 37203, TN
[2] National Center for Advancing Translational Sciences, Bethesda, MD
[3] Research Program, National Institutes of Health, Bethesda, MD
[4] Institute for Genomic Medicine, Department of Neurology, Columbia University Irving Medical Center, New York
[5] Broad Institute, Cambridge
[6] Center for Genomic Medicine, Department of Psychiatry, Massachusetts General Hospital, Boston, MA
关键词
CORONARY-HEART-DISEASE; HEALTH; ASSOCIATION; GENOMICS; BIOBANK; COHORT; RISK;
D O I
10.1056/NEJMsr1809937
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The U.S. research cohort All of Us was announced in 2015 and launched last year. With more than one fifth of the target enrollment now completed, the investigators report on progress and challenges. Knowledge gained from observational cohort studies has dramatically advanced the prevention and treatment of diseases. Many of these cohorts, however, are small, lack diversity, or do not provide comprehensive phenotype data. The All of Us Research Program plans to enroll a diverse group of at least 1 million persons in the United States in order to accelerate biomedical research and improve health. The program aims to make the research results accessible to participants, and it is developing new approaches to generate, access, and make data broadly available to approved researchers. All of Us opened for enrollment in May 2018 and currently enrolls participants 18 years of age or older from a network of more than 340 recruitment sites. Elements of the program protocol include health questionnaires, electronic health records (EHRs), physical measurements, the use of digital health technology, and the collection and analysis of biospecimens. As of July 2019, more than 175,000 participants had contributed biospecimens. More than 80% of these participants are from groups that have been historically underrepresented in biomedical research. EHR data on more than 112,000 participants from 34 sites have been collected. The All of Us data repository should permit researchers to take into account individual differences in lifestyle, socioeconomic factors, environment, and biologic characteristics in order to advance precision diagnosis, prevention, and treatment.
引用
收藏
页码:668 / 676
页数:9
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