Melanie B. Gillingham, Ph.D., R.D., L.D.
- Professor of Molecular and Medical Genetics, School of Medicine
- Director, Master's Program, Graduate Programs in Human Nutrition, School of Medicine
- Molecular and Medical Genetics Graduate Program, School of Medicine
- Graduate Programs in Human Nutrition, School of Medicine
- Pediatrics, School of Medicine
- Medicine, Division of Endocrinology, Diabetes and Clinical Nutrition, School of Medicine
- Program in Molecular and Cellular Biosciences, School of Medicine
Education and training
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Degrees
- B.F.A., 1990, Texas Christian University
- B.S., 1990, Texas Christian University
- M.S., 1992, University of Oklahoma Health Science Center
- Ph.D., 2000, University of Wisconsin-Madison
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Fellowship
- Post-doctoral Fellowship, OHSU Department of Molecular and Medical Genetics, 2001-2006
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Certifications
- Certificate in Human Investigations, OHSU 2005
Memberships and associations:
- Genetic Metabolic Dietitians International (GMDI), President 2017-2019
- Society of Inherited Metabolic Diseases (SIMD), Member, Board of Directors 2013-2016
- American Society of Nutrition, member
- Academy of Nutrition and Dietetics, member
- AND Pediatrics Nutrition Practice Group, Research Awards and Chair 2015
- AND SCAN, member
- AND Research DPG, member
Areas of interest
- Fatty acid oxidation, disorders, and essential fatty acids
- Sports nutrition
- Insulin resistance
- Nutritional laboratory assessment
- Retinopathy of LCHAD deficiency
Publications
Publications
D-BHB supplementation before moderate-intensity exercise suppresses lipolysis and selectively blunts exercise-induced long-chain acylcarnitine increase in pilot study of patients with long-chain fatty acid oxidation disorders
Molecular Genetics and MetabolismA proposal for an updated staging system for LCHADD retinopathy
Ophthalmic GeneticsAssociations between daily step count classifications and continuous glucose monitoring metrics in adults with type 1 diabetes
DiabetologiaCardiac phenotype in adolescents and young adults with long-chain 3-hydroxyacyl CoA dehydrogenase (LCHAD) deficiency
Genetics in MedicineCombining uncertainty-aware predictive modeling and a bedtime Smart Snack intervention to prevent nocturnal hypoglycemia in people with type 1 diabetes on multiple daily injections
Journal of the American Medical Informatics AssociationDecline in Isotope Dilution Space Ratio Above Age 60 Could Affect Energy Estimates Using the Doubly Labeled Water Method
Journal of NutritionEarly diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy
Journal of inherited metabolic diseaseFactors Affecting Reproducibility of Change in Glucose During Exercise
Journal of Diabetes Science and TechnologyiPSC-Derived LCHADD Retinal Pigment Epithelial Cells Are Susceptible to Lipid Peroxidation and Rescued by Transfection of a Wildtype AAV-HADHA Vector
Investigative ophthalmology & visual scienceObesity alters the circadian profiles of energy metabolism and glucose regulation in humans
ObesityPatient-reported visual function outcomes agree with visual acuity and ophthalmologist-graded scoring of visual function among patients with long-chain 3-hydroxyacylcoA dehydrogenase deficiency (LCHADD)
Molecular Genetics and Metabolism ReportsThe Association Between Diet Quality and Glycemic Outcomes Among People with Type 1 Diabetes
Current Developments in NutritionThe LCHADD Mouse Model Recapitulates Early-Stage Chorioretinopathy in LCHADD Patients
Investigative Ophthalmology and Visual ScienceA G1528C Hadha knock-in mouse model recapitulates aspects of human clinical phenotypes for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Communications BiologyExamining the Acute Glycemic Effects of Different Types of Structured Exercise Sessions in Type 1 Diabetes in a Real-World Setting
Diabetes careGreater male variability in daily energy expenditure develops through puberty
Biology LettersOptical coherence tomography angiography of choroidal neovascularization in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)
American Journal of Ophthalmology Case ReportsResting and total energy expenditure of patients with long-chain fatty acid oxidation disorders (LC-FAODs)
Molecular Genetics and MetabolismThe Effect of Preoperative Carbohydrate Intake on Length of Stay and Postoperative Recovery Following Laparoscopic Living Donor Nephrectomy
Journal of Renal NutritionThe Type 1 Diabetes and EXercise Initiative
Diabetes Technology and TherapeuticsTotal daily energy expenditure has declined over the past three decades due to declining basal expenditure, not reduced activity expenditure
Nature MetabolismAssessing Mealtime Macronutrient Content
Diabetes Technology and TherapeuticsMaternal dietary fat intake during pregnancy and newborn body composition
Journal of PerinatologyMore Time in Glucose Range during Exercise Days than Sedentary Days in Adults Living with Type 1 Diabetes
Diabetes Technology and TherapeuticsA ketogenic & low-protein diet slows retinal degeneration in rd10 mice
Translational Vision Science and TechnologyCardiac tissue citric acid cycle intermediates in exercised very long-chain acyl-CoA dehydrogenase-deficient mice fed triheptanoin or medium-chain triglyceride
Journal of inherited metabolic diseaseEffects of fasting, feeding and exercise on plasma acylcarnitines among subjects with CPT2D, VLCADD and LCHADD/TFPD
Molecular Genetics and MetabolismNutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controls
Molecular Genetics and Metabolism ReportsBlood cytokine patterns suggest a modest inflammation phenotype in subjects with long-chain fatty acid oxidation disorders
Physiological reports