care for children with rare metabolic disorders07d0901f-86b6-4cd0...errors of metabolism •describe...
TRANSCRIPT
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Care for Children with Rare Metabolic Disorders
Lindsay C. Burrage, M.D., Ph.D.
Department of Molecular and Human Genetics
Baylor College of Medicine
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Objectives
• Understand basic principles of management of inborn errors of metabolism
• Describe 2 metabolic genetic disorders detected by newborn screening
• Discuss the multidisciplinary approach to managing care for affected children
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What is an Inborn Error of Metabolism?
• 1902: Archibald Garrod described Alkaptonuria
• Now, > 300 disorders with new disorders still being discovered!
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General Principles
A B C DEnzyme 1 Enzyme 2 Enzyme 3
• Deficient enzyme activity or deficient transport of a
substrate
• Toxic products accumulate (B, maybe A)
• Important products become deficient
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General Principles of Management
• Limit substrates that produce toxic products (A,B)
- E.g. dietary manipulations
A B C DEnzyme 1 Enzyme 2 Enzyme 3
TOXIC
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General Principles of Management
• Limit substrates that produce toxic products (A,B)
• Enhance excretion of toxic products (B)
- e.g., Medications that bind toxic products and lead to
excretion in the urine
A B C DEnzyme 1 Enzyme 2 Enzyme 3
TOXIC
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General Principles of Management
• Limit substrates that produce toxic products (A,B)
• Enhance excretion of toxic products (B)
• Prevent production of toxic products (B)
- e.g., Medication that blocks upstream enzyme 1
A B C DEnzyme 1 Enzyme 2 Enzyme 3
TOXIC
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General Principles of Management
• Limit substrates that produce toxic products (A,B)
• Enhance excretion of toxic products (B)
• Prevent production of toxic products (B)
• Provide deficient products (C or D)
- E.g. amino acid supplementation
A B C DEnzyme 1 Enzyme 2 Enzyme 3
TOXIC
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General Principles of Management
• Limit substrates that produce toxic products (A,B)
• Enhance excretion of toxic products (B)
• Prevent production of toxic products (B)
• Provide deficient products (C or D)
• Provide vitamins/cofactors for enzymes
- e.g., vitamin or cofactor supplementation
A B C DEnzyme 1 Enzyme 2 Enzyme 3
TOXIC
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General Principles of Management
• Limit substrates that produce toxic products (A,B)
• Enhance excretion of toxic products (B)
• Prevent production of toxic products (B)
• Provide deficient products (C or D)
• Provide vitamins/cofactors for enzymes
• Give enzyme back (e.g. enzyme replacement therapy)
A B C DEnzyme 1 Enzyme 2 Enzyme 3
TOXIC
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Broad Categories of IEM
• Amino Acid Disorders
• Urea Cycle Disorders
• Organic Acid Disorders
• Transport Disorders
• Vitamin Disorders
• Disorders of glucose metabolism
• Fatty acid oxidation disorders
• Mitochondrial Disorders
• Lysosomal Storage Disorders
• Peroxisomal Disorders
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Broad Categories of IEM
• Amino Acid Disorders
• Urea Cycle Disorders
• Organic Acid Disorders
• Transport Disorders
• Vitamin Disorders
• Disorders of glucose metabolism
• Fatty acid oxidation disorders
• Mitochondrial Disorders
• Lysosomal Storage Disorders
• Peroxisomal Disorders
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Newborn Screening
Newborns are screened for a list of genetic disorders in the first days of life so that management can be initiated in treatable
disorders prior to the onset of signs or symptoms of the disorder
Important to note that not all metabolic disorders are
included on newborn screening
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• Phenylketonuria (PKU)
• Citrullinemia (Urea cycle disorder)
Newborn Screening:Two examples
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A Case Example
A 7 year old girl has
difficulties gaining weight.
The PCP notices lack of
weight gain on growth chart.
Thorough work-up reveals
unknown cause for the poor
weight gain. The pediatrician
decides to add a calorie-rich
supplemental formula to
encourage weight gain.
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A Case Example
A 7 year old girl with PKU
has difficulties gaining
weight. The PCP notices
lack of weight gain on growth
chart. Thorough work-up
reveals unknown cause for
the poor weight gain. The
pediatrician decides to add a
calorie-rich supplemental
formula to encourage weight
gain.
Is this the right approach?
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PKU: The First Newborn Screening
CH2
CH
NH3+ COO-
OH
Phenylalanine
Hydroxylase
Tetrahydro-
biopterin
Dihydro-
biopterin
Phenylalanine
(PHE)
Tyrosine
(TYR)
CH2
CH
NH3+ COO-
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Phenylketonuria (PKU)
CH2
CH
NH3+ COO-
OH
Phenylalanine
Hydroxylase
Tetrahydro-
biopterin
Dihydro-
biopterin
Phenylalanine
(PHE)
Tyrosine
(TYR)
• Microcephaly
• Intellectual disability
• Eczema
• Musty or “mousy” odor
CH2
CH
NH3+ COO-
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Phenylketonuria (PKU)
CH2
CH
NH3+ COO-
OH
Phenylalanine
Hydroxylase
Tetrahydro-
biopterin
Dihydro-
biopterin
Phenylalanine
(PHE)
Tyrosine
(TYR)
What treatment will
you provide?
CH2
CH
NH3+ COO-
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Phenylketonuria (PKU): Dietary Therapy
CDC
• Low protein diet
• PHE-free formula with Tyrosine supplementation
• Close coordination with metabolic dietitian
NIH
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Phenylketonuria (PKU): Sapropterin
CH2
CH
NH3+ COO-
OH
Phenylalanine
Hydroxylase
Tetrahydro-
biopterin
Dihydro-
biopterin
Phenylalanine
(PHE)
Tyrosine
(TYR)
CH2
CH
NH3+ COO-
Synthetic form of tetrahydrobiopterin
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Phenylketonuria (PKU): Sapropterin
CH2
CH
NH3+ COO-
OH
Phenylalanine
Hydroxylase
Tetrahydro-
biopterin
Dihydro-
biopterin
Phenylalanine
(PHE)
Tyrosine
(TYR)
CH2
CH
NH3+ COO-
Only a subset of patients respond to this medication
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Phenylketonuria (PKU): Other Treatments in Children
• Dietary therapy
• Sapropterin
• Avoidance of aspartame (a sweetener that contains PHE)
• Specialized dietary therapy (Glycomacropeptide)
• Investigational treatments
Goal : PHE levels of 2-6 mg/dL to
minimize risk for complications
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PKU: Care Requires A Team Approach
• Physicians
• Newborn screening laboratory nurses
• Clinic nurses
• Dietitians
• Social workers
• Parents and families
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PKU in Primary Care
• Avoid medications with aspartame!
• Consult with geneticist and metabolic dietitian before
changing the diet plan
• Encourage adherence to diet plan
• Consult with geneticist and metabolic dietitian IMMEDIATELY
if a patient is considering pregnancy or becomes pregnant
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Maternal PKU:Infants Born to Mothers With Elevated PHE
• Developmental delay
• Small size (IUGR)
• Microcephaly
• Congenital heart defects
Risk is minimized with PHE level in target range at time of conception!
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A Case Example
A 7 year old girl with PKU
has difficulties gaining
weight. The PCP notices
lack of weight gain on growth
chart. Thorough work-up
reveals unknown cause for
the poor weight gain. The
pediatrician contacts the
geneticist and metabolic
dietitian to discuss a plan.
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• Phenylketonuria (PKU)
• Citrullinemia (Urea cycle disorder)
Newborn Screening:Two examples
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• Non-bloody, non-bilious emesis x 2
• No fever, abdominal pain, cough, dysuria
• Review of systems otherwise negative
• Several classmates had a “stomach bug”
• Exam shows no signs of dehydration
• PCP discharges from clinic with an anti-emetic and warning signs for return to clinic
3 year old girl with vomiting
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• Non-bloody, non-bilious emesis x 2
• No fever, abdominal pain, cough, dysuria
• Review of systems otherwise negative
• Several classmates had a “stomach bug”
• Exam shows no signs of dehydration
• PCP discharges from clinic with Zofran and warning signs for return to clinic
3 year old girl with Citrullinemiaand vomiting
Is this the best approach?
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Citrullinemia
Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Protein in dietProtein
Breakdown
Or
Urea
Cycle
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Citrullinemia is Incuded in State Newborn Screening Panel
Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Urea
Cycle
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Citrullinemia
Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Urea
Cycle
Elevated ammonia levels
damage the brain!
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Citrullinemia
Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Urea
Cycle
Elevated ammonia levels cause
confusion, lethargy, headache,
vomiting, coma and death, if
untreated!
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Citrullinemia and Dietary Treatment
Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Urea
Cycle
Reduce protein intake, essential amino
acid formula
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Citrullinemia:Dietary Therapy
CDC
• Low protein diet
• Essential amino acid formula/amino acid supplements
• Close coordination with metabolic dietitian
• Strategies to promote adherence (can be costly!)
NIH
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Citrullinemia and Medications
Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Urea
Cycle
Medications that divert ammonia away
from the cycle to produce safe waste
products
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• Vomiting
• Illness
• Skipped meals
• Surgery
• Skipped medication doses
Potential Triggers of High Ammonia in Citrullinemia
• Delivery/post-partum period
• Certain medications
• Menses
• High protein diet/meals
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• Non-bloody, non-bilious emesis x 2
• No fever, abdominal pain, cough, dysuria
• Review of systems otherwise negative
• Several classmates had a “stomach bug”
• Exam shows no signs of dehydration
• PCP discharges from clinic with Zofran and warning signs for return to clinic
3 year old girl with Citrullinemiaand vomiting
What is a better approach?
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Emergency Planning
• Emergency letters:
Diagnosis
Concerning signs/symptoms
Initial steps in evaluation/management
Contact information for genetics team
• Emergency letters should be carried at all times and copy placed in PCP chart
• Don’t ignore the emergency letter!
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• Non-bloody, non-bilious emesis x 2
• No fever, abdominal pain, cough, dysuria
• Review of systems otherwise negative
• Several classmates had a “stomach bug”
• Exam shows no signs of dehydration
3 year old girl with Citrullinemiaand vomiting
PCP notes risk for high ammonia and
contacts genetics team
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• Non-bloody, non-bilious emesis x 2
• No fever, abdominal pain, cough,dysuria
• Review of systems otherwise negative
• Several classmates had a “stomach bug”
• Exam shows no signs of dehydration
3 year old girl with Citrullinemiaand vomiting
Patient admitted to hospital
for high ammonia level
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• Avoid prolonged fasting (NPO) and work with genetics/anesthesia for safe anesthesia plans
• Consult geneticist/dietitian before making a diet change or suggesting skipped medication doses
• Avoid steroids and valproic acid medications
Other important considerations in Urea Cycle Disorders
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Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGS
Protein in diet Protein
Breakdown
Or
Urea
Cycle
Other important considerations in Urea Cycle Disorders
Some urea cycle disorders ARE
NOT covered on newborn
screen!
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Urea
Citrulline
ASA
Arginine
Ornithine
ASS1
ASL
Carbamoyl phosphate
ARG
OTC
NH3CPS
NAGSProtein in diet
Protein
Breakdown
Or
Urea
Cycle
Other important considerations in Urea Cycle Disorders
Check an ammonia in any patient
with altered mental status of
unclear cause!
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Summary and Conclusions
• Newborn screening facilitates the early diagnosis and
treatment of children with a subset of metabolic disorders
• All metabolic disorders ARE NOT included on the newborn
screen panel
• Emergency planning is important for some metabolic
disorders
• The care for individuals with metabolic disorders requires a
team approach
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