Supplements and Co-factors in the Treatment of Metabolic Disorders Lynne A. Wolfe, MS, CRNP, BC Metabolic Nurse Practitioner Children’s Hospital of Pittsburgh.

Slides:



Advertisements
Similar presentations
Protein-, Mineral- & Fluid-Modified Diets for Kidney Diseases
Advertisements

NUTRITION A proper diet requires a balance of carbohydrates, fats, and proteins. In addition the body requires many phytochemicals, vitamins, minerals,
1 LECTURES CATABOLISM OF PROTEINS AND AMINO ACID NITROGEN DR SAMEER FATANI BIOCHEMISTRY (METABOLISM)
Approach to Inborn Error of Metabolism in a Neonate Filomena Hazel R. Villa, MD PL2.
Metabolic uses of amino acids ● building blocks for protein synthesis ● precursors of nucleotides and heme ● source of energy ● neurotransmitters ● precursors.
By Nora, Leah, Justin & Taylor. INTRODUCTION  Many athletes use dietary supplements as part of their regular training or competition routine, including.
Inborn Errors of Metabolism Robert D. Steiner, MD Associate Professor, Pediatrics and Molecular and Medical Genetics Head: Division of Metabolism OHSU.
Genetic testing Biochemical genetic testing Cytogenetic testing Direct genetic testing Diagnostic testing Predictive testing Carrier testing Prenatal testing.
Sunlight energy to chemical energy Sunlight is the major energy source for most life. This energy drives the conversion of atmospheric carbon dioxide.
Mosby items and derived items © 2006 by Mosby, Inc. Slide 1 Chapter 7 Vitamins.
Amino Acid Oxidation and the Production of Urea
Inborn Errors Of Metabolism (IEM).
Metabolic Disorders KNH 413.
MAPLE SYRUP URINE DISEASE (MSUD) IS A METABOLISM DISORDER PASSED DOWN THROUGH FAMILIES IN WHICH THE BODY CANNOT BREAK DOWN CERTAIN PARTS OF PROTEINS. URINE.
UNIT 6: PHYSIOLOGY Chapter 32: Digestive and Excretory Systems.
Inborn Errors of Metabolism Monica Egan. Video Links Part 1: – xWwY&feature=plcphttp://
Nutrition, Metabolism, and Temperature Regulation $100 $200 $300 $400 $500 $100$100$100 $200 $300 $400 $500 Nutrition FINAL ROUND Carbohydrate Metabolism.
Amino acid metabolism V. Enzymopathies related to amino acid metabolism Figures: Lehninger-4ed; chapter: 18 (Stryer-5ed; chapter: 23)
Metabolism: FON 241; L. Zienkewicz Metabolism Chapter 7.
Nutrient Role in Bioenergetics Chapter 4 Part 2. Bioenergetics-Glycolysis  Carbohydrates primary function  Energy for cellular work.  Breakdown of.
Metabolism—How do we obtain energy from foods? Susan Algert, Ph.D., R.D.
1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 4: Understanding Inborn Errors of Metabolism Define inborn errors.
Dr Shahida Mushtaq.  provides advanced understanding and applied knowledge in the theory and practice of Clinical Biochemistry  a critical understanding.
Metabolism Transformations and Interactions Copyright 2005 Wadsworth Group, a division of Thomson Learning.
Amino Acid Metabolism. Intestinalsynthesize apoproteins (for lipoproteins) Epithelia:synthesize digestive enzymes glutamine degradation is a primary source.
Chemical level of organization
Anatomy and Physiology
Why is food important?.
18.2 Nitrogen Excretion and the Urea Cycle Produced in liver Blood Kidney  urine.
Nutrition. Nutrients Substances in foods that provide energy and materials for cell development, growth and repair Energy: –Every body activity needs.
Cell Metabolism Chapter 6. Metabolic Pathways  Metabolic Pathways  Break down and manufacture molecules in a sequential set of reactions  Enzyme reaction:
1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 4: Understanding Inborn Errors of Metabolism Define inborn errors.
Lecture 11b-19 November 2014 This lecture is based largely on CHAPTER 23 IN KRAUSE'S FOOD NUTRITION AND DIET THERAPY (ON RESERVE IN LIBRARY) AND CHAPTERS.
Chapter 6 Nutrition and Weight Management. 2 Six Classes of Nutrients Carbohydrates Fats Proteins Vitamins Minerals Water.
Chapter 4 Cellular Metabolism & Digestion Metabolism involves 2 processes: Anabolism- is the buildup of larger molecules from smaller ones and requires.
Nutritional therapy in children with in-born errors of metabolism.
D: HUMAN PHYSIOLOGY D.1: Human nutrition. Essential nutrients Essential nutrients cannot be synthesized by the body. E.g. calcium, vitamins, water, some.
Related Pathways Anaerobic Pathways (4.4) & Alternatives To Glucose (4.3)
KIN 211 Metabolism. The sum total of all chemical reactions that go on in the living cells. Energy Metabolism-the reactions by which the body obtains.
Dr. M Shakiba Subspecialist of pediatric Endocrinology and metabolism.
Nutrition and Nutrient Nutrition Unit Lecture 4. What is Nutrition? Nutrition is the science or study of food and the ways the body uses food. Nutrients.
Copyright © 2011, Pearson Education, Inc., publishing as Pearson Benjamin Cummings. Chapter 7 - Metabolism $100 $200 $300 $400 $500 $100$100$100 $200 $300.
INBORN ERRORS OF METABOLISM (IEM)
Inborn Errors of Metabolism
Chapter 7: Metabolism: From Food to Life
Oxidation of Fatty Acid
Nutrition in glutaric acidemia
Catabolism of amino acid nitrogen
What food do they need more or less of?
Amino acid metabolism.
Chapter 7: Metabolism The Basics Glycolysis TCA Fat Metabolism
Nutrition.
Vet 104 – Cell Metabolism Metabolism – the sum of all the biochemical reactions that occur within an organism, including the synthetic (anabolic) & decomposition.
Muscle Metabolism Dr. Nabil Bashir.
An Approach to Inborn Errors of Metabolism
UNIT 12 CS BASIC CONCEPTS OF METABOLISM
Cardiovascular System
Cardiovascular System
آشنایی با انواع شیرخشک. آشنایی با انواع شیرخشک.
Cardiovascular System
Nutrition, Metabolism, and Temperature Regulation
Pyruvate Dehydrogenase
Chapter 32: Digestive and Excretory Systems
Lecture 11b-26 March 2018 This lecture is based largely on CHAPTER 23 IN KRAUSE'S FOOD NUTRITION AND DIET THERAPY (ON RESERVE IN LIBRARY) AND CHAPTERS.
Alternatives to Glucose
Nutrition Facts Calories 250 Calories from Fat 120 Total Fat 13g 10%
Chapter 32: Digestive and Excretory Systems
NUTRITION FUNCTION OF NUTRIENTS.
Chapter 7 Key Ideas Name the six classes of nutrients.
Presentation transcript:

Supplements and Co-factors in the Treatment of Metabolic Disorders Lynne A. Wolfe, MS, CRNP, BC Metabolic Nurse Practitioner Children’s Hospital of Pittsburgh

UREA CYCLE SUGAR FAT PROTEIN Mitochondria TCA ETC ATP C C Food Groups of Metabolic Disease

Current Therapy for Metabolic Disease Avoid Catabolism Newborn Weight Loss Febrile Illnesses, trauma, surgery Provide Calories from “non-offending” foods groups

Current Therapy of Metabolic Disease Replace “created” deficiencies Calcium and other macro/micronutrients Carnitine Essential Fatty acids

Current Therapy of Metabolic Disease Provide elements not released or able to be used from apoenzyme Biotin - Biotinidase def Cobalamin

Current Therapy of Metabolic Disease Remove Toxic build up Carnitine in OA’s & FOD’s Glycine - Isovaleric acidemia Sodium Benzoate and Dextromethorphan - Nonketotic Hyperglycinemia Sodium Phenylbutyrate - Urea Cycle disorders

Current Therapy of Metabolic Disease Go around metabolic block or create a block we can manage MCT Oil - Long chain FOD’s Orfadine (NTBC) - Tyrosinemia

Current Therapy of Metabolic Disease Augment Enzyme function Riboflavin - FOD’s, GAII Biotin - Propionic acidemia

UREA CYCLE SUGAR FAT PROTEIN Mitochondria TCA ETC ATP C C Food Groups of Metabolic Disease Serum Amino acids Ammonia Abnormal Urine Organic acids Low Carnitine Alanine Lactate / Pyruvate BCAA

Current Treatment Restrict Offending Amino acids Supplement single Amino acids as needed Carnitine supplementation Add calories with carbohydrates and fats Biotin, Glycine in specific disorders +/- Antibiotics (Flagyl)

? Potential New Treatments BH4 supplementation - PKU Enzyme Replacement - PKU CoQ Antioxidant Vitamins LNAA supplementation More aggressive Organ Transplantation

UREA CYCLE SUGAR FAT PROTEIN Mitochondria TCA ETC ATP C C Food Groups of Metabolic Disease Serum Amino acids Ammonia Abnormal Urine Organic acids Nl/Low Carnitine Alanine Lactate / Pyruvate

Current Treatment Strict, very low protein diet Single Amino acid supplements Sodium Phenylbutyrate/Acetate/Benzoate +/- B Vitamins +/- Carnitine

? Potential New Treatments IV Phenylbutyrate/acetate Gene therapy

UREA CYCLE SUGAR FAT PROTEIN Mitochondria TCA ETC ATP C C Food Groups of Metabolic Disease Abnormal Urine Organic acids Nl/Low Carnitine Alanine Lactate/ Pyruvate Abnormal Acylcarnitines

Current Treatment Avoid Fasting Low Fat diet, provide extra calories with Protein and Carbohydrates MCT Oil in long chain defects +/-Essential Fatty acid supplements +/- DHA +/- Riboflavin +/- Carnitine Avoid Toxins (Depakote etc…)

? Potential New Treatments Creatine CoQ Antioxidant Vitamins

Other supplements ? Cornstarch Glutamine Inulin (FOS fiber) Antibiotics Senna Periactin (Cyproheptadine) Zofran (Ondansetron)

QUESTIONS ????? THANK YOU