Research Topics
The Laboratory of Heart Disease Phenomics, established in 2021, is dedicated to understanding the evolving burden of cardiovascular diseases (CVD) across diverse populations and its impact on health. Our research spans the entire CVD continuum—from etiology to outcomes (morbidity and mortality)—with a focus on health equity.
We rely on multi-omics approaches, and advanced analytical methods such as machine learning. Using descriptive epidemiology in large-scale, nationally representative datasets, we have documented the prevalence of CVD across different populations and highlighted significant disparities by race and sex. In disease-specific cohorts, we have demonstrated that novel molecular methods, such as proteomics and targeted metabolomics, can significantly enhance the assessment of heart failure (HF) risk, paving the way for precision interventions.
Our initial research focus has been on investigating heart failure (HF) phenotypes, prevention strategies, and outcomes. Despite a more than 40% decline in heart disease mortality in the United States between 1980 and 2000, this positive trend has stalled and even reversed since 2015 due to a significant increase in HF-related deaths. This alarming trend indicates that the HF epidemic, which began gaining attention in 1997, remains unresolved and undermines progress against heart disease mortality. These critical observations underscore the urgent need to address the HF epidemic, recognizing its complex, syndromic nature and its disproportionate impact on diverse populations.
HF is not a single disease and is traditionally classified based on ejection fraction (EF). However, this approach fails to capture the full complexity and heterogeneity of HF and its underlying mechanisms. These gaps in knowledge impede therapeutic progress, and treatment trials for HF with preserved EF have often been disappointing or lack mechanistic explanations when they are promising.
One of our key research areas is the study of novel molecular phenotypes and the application of contemporary analytical methods. Our goal is to identify molecular phenotypes that contribute to understand the mechanisms of HF, while considering its intersection with aging and multimorbidity in diverse populations. Our central objective is to develop a novel approach to HF phenotyping, which will support health equity and lead to the development of new therapeutics.
Our approach integrates molecular assays, robust epidemiological methods, and rigorous analytical techniques. We utilize comprehensive, multidisciplinary longitudinal datasets, including electronic medical records from thousands of community patients with HF, and have access to valuable biospecimens. This approach is grounded in our unwavering commitment to studying and engaging diverse populations.
Our team is committed to mentoring and training the next generation of diverse scientists. We collaborate actively with laboratories within the NHLBI Division of Intramural Research, other NIH institutes (NCI and NIA), and the broader scientific community, both nationally and internationally.
Biography
Dr. Roger received her medical degree in 1986 from Sorbonne University in Paris, France and her Master in Public Health (Epidemiology) at the University of Minnesota in 1996. After training in cardiology at Mayo Clinic, in Rochester Minnesota, she joined the faculty in 1992 and became Professor in Medicine (2002) and Epidemiology (2006). At Mayo Clinic, Dr. Roger served in various leadership positions including Chair of the Department of Health Sciences Research and member of the Mayo Clinic Board of Governors and Board of Trustees.
Dr. Roger served on the NHLBI Advisory Council and the NHLBI Board of Scientific Counselors. She chaired the Epidemiology Council of the American Heart Association 2018-2020 and was recognized as the American Heart Association Distinguished Investigator in 2019.
The unifying theme of Dr. Roger’s work is the epidemiology of heart diseases, and their occurrence and outcomes in diverse communities. As a physician scientist, Dr. Roger has deployed, directly and through collaborations, multidisciplinary methods including epidemiology, outcomes and health care delivery analyses, behavioral sciences and the use of electronic health records in population research applied to case ascertainment, risk prediction and pragmatic trials.
Selected Publications
- Turecamo SE, Xu M, Dixon D, Powell-Wiley TM, Mumma MT, Joo J, Gupta DK, Lipworth L, Roger VL. Association of Rurality With Risk of Heart Failure. JAMA Cardiol. 2023;8(3):231-239.
- Conners KM, Shearer JJ, Joo J, Park H, Manemann SM, Remaley AT, Otvos JD, Connelly MA, Sampson M, Bielinski SJ, Wolska A, Turecamo S, Roger VL. The Metabolic Vulnerability Index: A Novel Marker for Mortality Prediction in Heart Failure. JACC Heart Fail. 2024;12(2):290-300.
- Roger VL, Banaag A, Korona-Bailey J, Wiley TMP, Turner CE, Haigney MC, Koehlmoos TP. Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience. Am J Med. 2023;136(11):1079-1086.e1.
- Kuku KO, Shearer JJ, Hashemian M, Oyetoro R, Park H, Dulek B, Bielinski SJ, Larson NB, Ganz P, Levy D, Psaty BM, Joo J, Roger VL. Development and Validation of a Protein Risk Score for Mortality in Heart Failure : A Community Cohort Study. Ann Intern Med. 2024;177(1):39-49.
- Joo J, Shearer JJ, Wolska A, Remaley AT, Otvos JD, Connelly MA, Sampson M, Bielinski SJ, Larson NB, Park H, Conners KM, Turecamo S, Roger VL. Incremental Value of a Metabolic Risk Score for Heart Failure Mortality: A Population-Based Study. Circ Genom Precis Med. 2024;17(2):e004312.
Related Scientific Focus Areas
This page was last updated on Sunday, December 1, 2024