Managing Patient Health in the Genomic Era: Family Health History and Adult Disease Risk presents strategies on the practical integration of genomic technologies in conducting accurate family health histories to improve patient management, enhance adult disease risk assessment, provide more precise diagnosis, and support effective interventions and treatment. In more than fourteen evidence-based chapters, the book examines family health history's place in genomic medicine, FHH tools and strategies, how to identify existing and novel genetic markers, how to identify lineage specific variants within families, how to find effective interventions based on genetic testing, gene-environment interactions, FHH social networking, data sharing, and more.
Readers will discover succinct commentary and key examples to assist with their local needs. Relevant principles of genetic biology and inheritance are both explored in-depth, with guidance on available support networks and online resources also provided.
- Presents a practical, accessible resource for primary care providers, allied health professionals, pharmacologists, public health professionals, students and clinical researchers
- Addresses genetic and genomic approaches in managing patient health, conducting and analyzing family health histories, and assessing adult disease risk
- Features an expert author team with direct experience integrating genetics and genomics in primary care and family medicine settings
- Examines the attributes and limitations of family health history, genetic testing, and genomic testing in clinical practice
- Includes detailed explanations following practice-based examples
1. Genomic Medicine Overview
Part I. FHH, Genomics, and Disease Risk 2. Family Health History's Place in Genomic Medicine 3. FHH as a driver of genetic testing 4. FHH contextualizes genetic test results 5. FHH help to identify existing and new genetic markers 6. Lineage specific variants: principles and detection (Brian Shirts) 7. FHH, gene-environment interactions 8. Finding Effective Interventions in the Genomic era 9. Tools for FHH collection and Analysis 10. Applying algorithms, Epidemiology, Evidence-based intervention (Beth Hauser) 11. Genetic counseling: description and purpose (Adam Buchanan) 12. Closing the loop: patient followup
Part III. Primary Care in the Genomic Era 13. Prognosis for FHH-social networking for extended families, consent issues 14. Conclusion: The future: whole genome sequencing, familial variant database, gene editing
Dr. Vincent Henrich is Professor Emeritus of Biology and former Director of the Center for Biotechnology, Genomics, and Health Research at University of North Carolina at Greensboro. His research interests include gene-environment interactions affecting conditions and nuclear receptor biology. Additionally, he has conducted extensive research related to the connection between family health history and genomic and genetic diagnostics, as a basis for assessing an individual's vulnerability to serious medical conditions and diseases. Dr. Henrich and Dr. Lori Orlando collaborate on the Guilford Genomic Medicine Initiative, a project funded by the Department of Defense to implement family health history usage and appropriate genetic testing into primary care settings. His main responsibility for this project is overseeing genetic counseling and education programs for physicians and patients.
Orlando, Lori A.
Dr. Lori Orlando is Associate Professor of Medicine and Director of the Precision Medicine Program in the Center for Applied Genomics and Precision Medicine at Duke University. Her major research interests are decision making and patient preferences, implementation research, risk stratification for preventive health services, and decision modeling. In her work at the Center for Applied Genomics and Precision Medicine, Dr. Orlando leads the development and implementation of MeTree, a patient-facing family health history based risk assessment and clinical decision support initiative. Dr. Orlando collaborates and has published papers with Dr. Henrich related to the Guilford Genomic Medicine Initiative, where she leads the development of clinical protocols to obtain and assess family health history, implement evidence-based medical recommendations to reduce disease risk, and develop follow-up procedures that maintain patient flow.
Shirts, Brian H.
Brian Shirts, M.D., is an Associate Professor and Associate Director of the University of Washington, Department of Laboratory Medicine's Genetics and Solid Tumor Laboratory. Dr. Shirts' specialty is genetic testing for hereditary cancer risk and other complex hereditary traits. His goal is to create systems that allow the highest quality genetic testing possible for all patients. Dr. Shirts earned his M.D. and Ph.D. at the University of Pittsburgh. He is board certified in both Clinical Pathology and Molecular Genetic Pathology. His clinical interests include improving strategies for detection and classification of rare mutations, as well as the clinical classification of rare genetic variants of uncertain significance. Dr. Shirts' research interests include developing communication strategies to help physicians and families learn about complex genetic information. A special interest is in family-centric personalized healthcare using genetic information.