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Maple Syrup Urine Disease MSUD Information for families after a positive newborn screening ADAPTED Adapted by BY the THE Dietitians DIETITIANS Group GROUP BIMDG British Inherited Metabolic Diseases Group BASED ON THE ORIGINAL TEMPLE WRITTEN BY BASED BURGARD ON AND THE ORIGINAL WENDEL TEMPLE WRITTEN BY WENDEL Reviewed & revised AND BURGARD for North America by: A. Huber This Reviewed version & of revised the TEMPLE for North tool, originally America adapted by: A. by Huber the Dietitians group of the BIMDG for use within the UK and Ireland, has been further adapted by Nutricia North America for use within United States and Canada. This version no longer represents clinical or dietetic practice in the UK or Ireland. TEMPLE Tools Enabling Metabolic Parents LEarning Supported by For more educational tools, visit MedicalFood.com

What is MSUD? MSUD stands for Maple Syrup Urine Disease. It is an inherited metabolic condition. Maple Syrup Urine Disease MSUD 1

What is MSUD? Too much ketoacids in the urine Too much leucine in the blood 2

How does MSUD affect the body? MSUD affects the way the body breaks down protein. Protein is found in our bodies and in many foods. The body needs protein for growth and repair. 3

What is protein? Protein consists of chains of many smaller units called amino acids. A M I A C I N D O S 4

Protein metabolism Metabolism refers to the processes that occur inside the cells of the body. Anabolism Catabolism 5

What do enzymes do? Enzymes help with metabolism by functioning like scissors. They break down proteins into smaller parts, including amino acids. 6

What happens in MSUD? MSUD is due to deficiency of an enzyme complex called branched-chain ketoacid dehydrogenase (BCKAD). Three amino acids called leucine (LEU), isoleucine (ILE) and valine (VAL) also known as branched-chain amino acids (BCAA), cannot be broken down. This means that levels of these amino acids, leucine in particular, build up in the blood and brain. ISO VAL LEU 7 LEU ISO

What can go wrong in MSUD? Leucine and other substances build up to high toxic levels in the blood and brain. It may affect babies and children in different ways. Left unmanaged, some babies develop symptoms such as sleepiness and irritability in the first few days. Babies may deteriorate and even go into a coma which can lead to brain damage. Other children may develop symptoms at a later stage, and this may be caused by an infection such as the flu or vomiting illness. Early management can prevent brain damage and learning difficulties. 8

What about other symptoms? The urine and sweat may smell sweet (like maple syrup) before diagnosis or when unwell. 9

How is MSUD diagnosed? As part of newborn screening, a few drops of blood are collected. The blood sample is then analyzed and LEU, ILE and VAL levels are measured. A high level of these amino acids could mean your child has MSUD, which will prompt your clinician to do further testing to confirm the diagnosis. 10

How is MSUD managed day-to-day? 1. A whole protein restricted diet Avoid high protein foods Include foods low in protein 2. A metabolic formula, prescribed by your clinic 3. When recommended, isoleucine and valine supplements L-ISOLEUCINE METABOLIC FORMULA L-VALINE 11

Avoid high protein foods Foods rich in protein, and therefore BCAA*, should be avoided. This includes meat, fish, eggs, cheese, milk, bread, pasta, nuts, soy and tofu. 12 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

Include foods low in protein These are foods that contain small amounts of BCAA* which can be used in typical quantities. They include many fruits and vegetables, and special medical low protein foods. They provide: an important source of energy variety in the diet 13 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

Low protein cooking Cooking low-protein meals for your child can still be appealing to the eye and taste good. There are many low-protein cookbooks to choose from. Your dietitian may be able to recommend a few favorites. 14

Feeding your baby with metabolic formula BCAA* are essential for normal development and therefore a limited and controlled amount must be taken daily. Breast milk or standard infant formula will provide the BCAA required by your baby prior to the introduction of solids, generally around 4-6 months of age. Your baby will also need a special metabolic formula to provide protein without BCAA. Your dietitian will determine how much breast milk or standard infant formula and metabolic formula to offer. 15 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

BCAA*-free metabolic formula Leucine-, Isoleucine-, and Valine-free metabolic formula is an essential part of meeting your baby s nutritional requirements. Like breast milk or standard infant formula, metabolic formula has carbohydrate, fat, vitamins, minerals and protein in the form of amino acids without BCAA. Metabolic formula, plus the prescribed amount of BCAA, allows your baby to get all the nutrients he or she needs to grow. METABOLIC FORMULA 16 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

Tracking BCAA* As your baby starts to eat solids your clinic will work with you to track BCAA. Foods must be weighed or measured using household measures (1 cup, 1 Tablespoon, etc) to determine BCAA content. Your clinic can help you find the best tools to help determine the BCAA content of foods. 17 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

How is MSUD monitored? By regular blood tests taken at home or in the clinic and reviewed by a dietitian. The sample is tested for the amount of BCAA it contains. The metabolic dietitian will contact you with the result and discuss any changes in management. 18

Metabolic crisis A metabolic crisis causes a build up of leucine and other toxic substances. It is usually triggered by childhood infections or viruses causing high temperatures, vomiting, and diarrhea. It is important to manage a metabolic crisis quickly and properly. 19

How is MSUD managed during illness? During any illness, our bodies need extra energy. The body will start breaking down cell protein, causing blood leucine (LEU) levels to increase. This process is also referred to as catabolism. It is extremely important to start the emergency protocol your metabolic team has developed for you and contact them right away. EMERGENCY PROTOCOL 20

How is MSUD managed during illness? Always follow your medical team s guidance. Contact your medical team at first signs of illness. They may have you: Stop all protein in food & drinks Start the emergency protocol. This is made up of metabolic formula and glucose METABOLIC FORMULA Continue isoleucine and valine supplements, if prescribed L-ISOLEUCINE L-VALINE 21

How is MSUD managed during illness? Always follow your medical team s guidance. Always take full amounts of emergency feeds as prescribed METABOLIC FORMULA If symptoms continue and/or you are worried, go immediately to the hospital Regularly update your metabolic team 22

Most importantly It is essential that you contact your metabolic team immediately if your child is getting sick. Follow their instructions promptly without delay. 23

What else is monitored in MSUD? Blood tests for amino acid and nutrient levels Height and weight Diet is adjusted according to growth and blood tests METABOLIC FORMULA Developmental check 24

What happens in human genetics? Humans have chromosomes composed of DNA. Genes are pieces of DNA that carry the genetic instruction. Each chromosome may have several thousand genes. The word mutation means a change or error in the genetic instruction. We inherit particular chromosomes from the egg of the mother and sperm of the father. The genes on those chromosomes carry the instruction that determines characteristics, which are a combination of the parents. 25

How does one inherit MSUD? MSUD is an inherited condition. There is nothing that could have been done to prevent your child from having MSUD. Everyone has a pair of genes that make the branched chain ketoacid dehydrogenase enzyme. In children with MSUD, neither of these genes works correctly. These children inherit one non-working MSUD gene from each parent. Parents of children with MSUD are carriers of the condition. Carriers do not have MSUD because the other gene of this pair is working correctly. 26

Inheritance Autosomal recessive possible combinations Chances for each child when both parents are carriers Carrier Father Carrier Mother Working gene Non-working gene Non-affected Carrier Carrier Affected 27

Future pregnancies For each pregnancy, when both parents are carriers, the risk to the baby is as follows: 25% chance (1 in 4) baby will not have MSUD nor be a carrier 25% chance (1 in 4) baby will have MSUD 50% chance (2 in 4) baby will be a carrier of MSUD 28

Take home messages MSUD is a serious inherited metabolic disorder that can lead to severe brain damage. Damage can be prevented with a whole protein restricted diet, metabolic formula and appropriate illness management. During illness, it is imperative that emergency feeds are started promptly, followed strictly and there are no delays in management. Regular blood spot tests are essential to monitor blood BCAA* levels. When your child is ill, or not behaving as usual, it is important to communicate with your metabolic team regularly to prevent metabolic crisis. 29 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

Helpful hints Always ensure you have a good supply of your low protein foods, BCAAfree metabolic formula and that they are not expired. Your special dietary products and BCAA-free metabolic formula are prescribed by your metabolic clinic. Always ensure you give the correct amount of BCAA-free formula as prescribed by your metabolic clinic and have your emergency protocol And remember, when correctly managed, your child can enjoy normal growth and development. 30 *Remember BCAA are the amino acids leucine (LEU), isoleucine (ILE) and valine (VAL)

Who s who (contact details) My dietitian Name:... Phone #:... Email:... My nurse Name:... Phone #:... Email:... My doctor Name:... Phone #:... Email:... 31

Notes 32

Notes 33

Notes 34

TEMPLE Tools Enabling Metabolic Parents LEarning ADAPTED BY THE DIETITIANS GROUP British Inherited Metabolic Diseases Group To learn more, visit MedicalFood.com BASED ON THE ORIGINAL TEMPLE WRITTEN BY BASED BURGARD ON AND THE ORIGINAL WENDEL TEMPLE WRITTEN BY WENDEL Reviewed & revised AND BURGARD for North America by: A. Huber This Reviewed version & of revised the TEMPLE for North tool, originally America adapted by: A. by Huber the Dietitians group of the BIMDG for use within the UK and Ireland, has been further adapted by Nutricia North America for use within United States and Canada. This version no longer represents clinical or dietetic practice in the UK or Ireland. 9497350-51096 ZMSUDTB 09/17 Supported by