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Energy in Action Podcast Episode 113: Dr. Vockley’s Journey in Mitochondrial Disease Care

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Dr. Jerry Vockley works everyday in the development and advancement of mitochondrialRelated to the mitochondria. disease patient care. He is a Cleveland Family Endowed Chair in Pediatric Research, Professor of Pediatrics and Human Genetics, and Director of the Center for Rare Disease Therapy. 

EPISODE HIGHLIGHTS

What inspired your career in genetics and mitochondrial care?

I stumbled into genetics as an undergraduate and did undergrad research in genetics. My first job was also in genetics. I can’t tell you precisely what triggered my interest in genetics, but it layered on and I can’t imagine a different career. 

What is your research focus and goals for that research?

In clinical and medical genetics when I started in the field, there weren’t the diagnostic advances we have now. The biggest advances came with the development of diagnostic technology. My focus is now on additional improvement and changes in technologies that have allowed us to move forward in therapy. Almost everything I do is therapy-based. The area I’m excited about is that we’re in the process of developing our first gene therapy for a fatty acid oxidation defect and we expect it’ll be in clinical trials in a couple years. Fatty oxidation disorders didn’t exist when I started my career because we didn’t know about them. To go from not knowing about them to being able to cure them is powerful.

When you go into the lab and create experiments and conduct research, is it inspired by the patients you see?

As an example of why we would do something like that, I once saw a 12-year-old girl who had whole-body psoriasis and physicians had only ever treated the psoriasis. I recognized that in addition to the rash, she was small for her age, had a small head size and she hadn’t started showing any signs of sexual maturity. I suspected her case was more than just a rash and sent samples off to look for defects in steroid metabolism. Testing came back normal and so we went into the lab to look more broadly and identified a chemical that should have been there. We were able to confirm a gene that wasn’t working and that led to us determining what the girl had and we were able to establish an effective treatment. 

LINKS & RESOURCES MENTIONED

International Network for Fatty Acid Oxidation Research and Management (INFORM) 

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energy in action, mitochondrial disease care, podcast, research

About the Speaker

Jerry Vockley, MD, PhD, FACMG

Jerry Vockley, MD, PhD, FACMG

Dr. Vockley received his undergraduate degree at Carnegie-Mellon University in Pittsburgh, Pennsylvania, and received his MD and PhD degrees in Medicine and Genetics from the University of Pennsylvania School of Medicine in Philadelphia, Pennsylvania. He completed his pediatric residency at the Denver Children’s Hospital, Denver, Colorado, and his postdoctoral fellowship in Human Genetic and Pediatrics at Yale University School of Medicine in New Haven, Connecticut. Before assuming his current position in Pittsburgh, Dr. Vockley was Chair of Medical Genetics in the Mayo Clinic School of Medicine. 

Dr. Vockley is internationally recognized as a leader in the field of inborn errors of metabolism. His current research focuses on mitochondrial energy metabolism, novel therapies for disorders of fatty acid oxidation and amino acid metabolism, and population genetics of the Plain communities in the United States. He has published over 320 peer reviewed scholarly articles and is the principal or Co-investigator on multiple NIH grants. Dr.Vockley has an active clinical research program and participates in and consults on multiple gene therapy trials. Dr. Vockley has served on numerous national and international scientific boards including the Advisory Committee (to the Secretary of Health and Human Services) on Heritable Disorders in Newborns and Children, where he was chair of the technology committee. He is a Fellow in the American Association for the Advancement of Science. He is a Founding Fellow of the American College of Medical Genetics and Genomics, and currently serves on its board of directors. He is founder and chair of the International Network on Fatty Acid Oxidation Research and Management (INFORM). He has served as chair of the Pennsylvania State Newborn Screening Advisory Committee and is a past president of the International Organizing Committee for the International Congress on Inborn Errors of Metabolism and the Society for the Inherited Metabolic Disorders (SIMD). He is co-founder and editor of the SIMD North American Metabolic Academy. He provides support for numerous family advocacy groups including MitoAction, the United Mitochondrial Disease Foundation, the National PKU Association, and the Organic Acidemia Association. 

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