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American journal of human genetics · 2026

The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessments.

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Limdi Nita, Beasley T Mark, Cortopassi Josh, Davis Brittney, Bangash Hana, Chen Jingheng, Chisholm Rex L, Chung Wendy K, Cimino James J, Connolly John, Crosslin David R, Davis Kyle W, DiVietro Alanna, Esplin Edward D, Freimuth Bob, Gordon Adam, Hakonarson Hakon, Hamed Marwan, He Megan, Hoell Christin, Holm Ingrid, Hripscak George, Irvin Margurite R, Jarvik Gail P, Karavite Dean, Karlson Elizabeth W, Kenny Eimear E, Khan Atlas, Kiryluk Krzysztof, Knerr Sarah, Korf Bruce, Kottyan Leah, Kullo Iftikhar, Larkin Katie, Lennon Niall, Linder Jodell E, Manolio Teri, Martin Lisa J, McNally Elizabeth M, Morse Jennifer, Murphy Shawn, Namjou Bahram, Odgis Jacqueline A, Orlando Lori, Pacheco Jennifer, Peterson Josh F, Pineda-Alvarez Daniel E, Prows Cindy, Puckelwartz Megan, Purcell Jasmine, Rasmussen-Torvik Laura, Rehm Heidi, Roden Dan M, Rosenthal Elisabeth A, Rowley Robb, Sabatello Maya, Schaid Daniel, Sharp Richard, Smith Johanna L, Smoller Jordan W, Soper Emily R, Sterling Rene, Suckiel Sabrina A, Terek Shannon, Thayer Jeritt, Ting Yi-Lee, Tiwari Hemant, Velez-Edwards Digna, Wagholikar Kavishwar B, Walunas Theresa, Wei Wei-Qi, Weng Chunua, Wiesner Georgia, Abul-Husn Noura S, Veenstra David L

Аннотация

The Electronic Medical Records and Genomics (eMERGE) Network developed and implemented a genome-informed risk assessment (GIRA) to communicate genomic (polygenic risk scores [PRSs], integrated risk scores [IRSs], and monogenic results), clinical, and family history-based risk for 11 chronic diseases and provide recommended healthcare recommendations. GIRA reports have now been returned to 23,840 participants and their providers in a large prospective cohort study. We present here the study design and analysis framework for assessing the attributable impact of GIRA return. Pre-specified outcomes include (1) provider/participant adoption of recommended healthcare actions, (2) new diagnosis of disease, (3) treatment initiation/intensification, and (4) clinical outcomes (surrogate markers or clinical events). We assess outcomes in high risk vs. not-high-risk participants, adjusting for covariates. We evaluate the effect of PRS/IRS at pre-established high-risk thresholds using regression discontinuity (RD), a quasi-experimental method that mimics randomization near a cutoff, enabling estimation of causal effects and controlling for unobserved confounders. Monogenic and family history-based risk stratification are analyzed using logistic regression. With 23,840 participants and 12 months of follow-up, the study is powered to detect differences of 2%-11% with 80% power (α = 0.05 in the adoption outcome). Longer follow-up will be required to enable assessment of new disease diagnosis, treatment changes, and clinical outcomes. Through innovative RD analyses and defined outcomes and comparison groups, this study will provide new insights into the real-world clinical impact of genomic risk assessment, address critical evidence gaps, advance understanding of genomic medicine outcomes, and inform future research.

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