When to think about metabolic disorders in adulthood? Wouter Meersseman · 1) Energy metabolism...
Transcript of When to think about metabolic disorders in adulthood? Wouter Meersseman · 1) Energy metabolism...
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When to think about metabolic disorders in adulthood?
Wouter MeerssemanGeneral Internal Medicine
Adult Metabolic ClinicWouter Meersseman, Leuven, Belgium
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Man, 25 year-old
Normal developmentFrom 15 months to adulthoodRecurrent episodes of hypotonia/weakness/Ataxia/lethargy during fever episodes (about once a year).
In between episodes: polyneuropathy, scoliosisDiagnosis: Charcot Marie Tooth type II (axonal polyneuropathy)
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What features suggest an inborn error of metabolism?
1. Acute relapsing episodes triggered by fever
2. Chronic polyneuropathy
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19 yo: left acute visual loss (left optic neuropathy)
24 yo: right acute visual loss ( right optic neuropathy)
What kind of inborn error of metabolism do you suspect and why?
Energy metabolism disorder because:1) Episodes triggered by fever2) Acute optic neuropathy3) Axonal polyneuropathy
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Mitochondria: the tiniest rotatory motor
DiMauro. Mitochondrial respiratory-chain diseases. N Engl J Med 2003;348:2656-68
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alanine
PDH
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What investigations will you ask for?
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fast Post prandial
Lactates(N<1.8mM)
1.6 mM 2.8 mM
Pyruvate(N<67µM)
173 µM 250 µM
L/P (N<20) 9 11
Amino acids chromatographyHyperalaninemia (789 mM)
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Treatment with thiamine (500 mg/d)
Visual acuity before treatment Right =4/10,Left =1/10
Visual acuity one year later: Right eye=8/10, Left eye=6/10.
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Primary mitochondrial disease: frequently overlooked !!!!Important for internists and neurologistsE.g.- Diabetes-deafness syndrome- Classic MELAS phenotype- Hypertrophic cardiomyopathy, renal failure
and diabetes- Kearns-Sayre syndrome (3th degree AV
block, deafness, retinitis and diabetes)- Myopathy (PEO)- Alpers syndrome: liver–brain–valproic acid
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Leigh Syndrome
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Leigh syndrome
Biotin responsive basal ganglia disease
Pyruvate dehydrogenase deficiency
Complex 3 deficiency
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Acquired causes of « Leigh Syndrome »
Acquired metabolic disorders-Gayet Wernicke’s encephalopathy-Hypoglycemia
Toxic causes-Carbon monoxide poisoning-Cyanide poisoning-Intoxication with Methylbromide-Intoxication with Methanol..
Anoxia-Drowning, hanging, etc…
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Acute encephalopathies/comas
Intoxications
1. Urea cycle defects2. Homocysteine remethylation defects3. Acute porphyrias4. Non ketotic hyperglycinemia5. MSUD
Energy metabolism defects (Leigh syndrome or pseudo-strokes)
Normal MRI Abnormal MRI
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Central nervous system Myopathy 36%Encephalopathy 20%CVA 18%Spasticity 12%Cerebellar syndrome 8%
Growth retardation Neonatal distress 31%Failure to thrive 20%
Cardiac system Cardiomyopathy 24%Hepatic system Acute liver failure 20%Eye system Retinitis pigmentosa 8%Renal system Tubulopathy 8%Ear system Deafness 8%Endocrine system Diabetes 7%
Mitochondrial diseases: diversity of clinical expressions (organs relying on OXPHOS !!!)
Any symptom in any combinations at any ageThink “mitochondrial” when lactic acidosis is present with any of the above
features
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Think mitochondrial if new “strange” symptoms arise following metabolic
stressWhat is in the diagnostic armamentarium?
-Organic acid analysis in the urine (krebs cycle intermediates: lactate, fumarate, methylglutaconic acid)-Mutation analysis-Muscle biopsy
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Mitochondrial mode of inheritanceMaternally transmitted, girls and boys can be affected, only girls
pass it through on to their childrenClinical variability within one family: heteroplasmyVariability in time
Mitotic segregation
HOMOPLASMY
HOMOPLASMY
HETEROPLASMY
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Importance of muscle biopsy
ragged red fibers, Showed by a Gomori stain
Accumulation of abnormal mitochondria at the periphery of the muscle fibreElectron-transport chain assays: defect in complex I
DNA sequencing: G13513A missense mutation, MELAS syndrome
Gomori stain COX mosacism
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Primary mitochondrial diseases
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Mendelian mode of inheritance
4q34-35 →ANT1adenine nucleotide translocator
Autosomal dominant external ophthalmoplegiaLarge-scale mtDNA deletions
Kaukonen Science 2000
Adult medicine: presenting with ptosis, myopathy and/or encephalopathy
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What is relevant for the internalmedicine doctor?
• In case of a known mitochondrial disease: avoid valproate, biguanides, linezolid and barbiturates
• Speak to the relatives: ethical dilemmas• In case of a rare unexplained diagnostic
conundrum: e.g. unexplained encephalopathy, opthalmoplegia, neuropathy, myopathy, lacticacidosis, liver failure: think “mitochondrial” and talk to a metabolic physician
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Woman, 71 yrs
Past history :– Hysterectomy– Progressive spasticity (legs) since 5 yearsExamination: Spastic paraparesisTetrapyramidal syndrome
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What features suggest an inborn error of metabolism?
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Metabolic leukoencephalopathies
-Symetrical-Fascicular-Weak signal intensity
Symetrical Fascicular Weak signal intensity
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Inflammatory leukoencephalopathies
Leukoencephalopathies in vascular diseases
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Metabolic leukoencephalopathy!
Patient
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Krabbe’s disease (galactocerebrosidase deficiency)
What pattern did you recognize?
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Defects in a single metabolic pathway lead to different lysosomal storage diseases
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When faced with leukodystrophy, think metabolic
• If symmetric lesions are present• If there is a constellation of neurlogical
signs and psychiatric signs (such as psychosis, pyramidal tract signs and polyneuropathy signs)
• If there is positive family history (X-linked ALD, autosomal recessive Krabbe’s disease, metachromatic leukodystrophy)
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Leukoencephalopathies
Lipid storage disorders- Polyneuropathy- Deep white matter
1) Metachromatic leukodystrophy2) Krabbe’s disease3) Adrenoleukodystrophy4) Refum’s disease5) Cerebrotendinous xanthomatosis
Intoxications (amino and organic acids)
- normal EMG- Superficial white matter (U
fibres)
1. Organic acidurias2. Aminoacidopathies
(homocysteine, phenylananine)
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Adrenoleukodystrophy
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What about raised CK levels?Woman, age 40 years
Acute rhabdomyolysis following long distance walk in the mountains, dark urine, pain, oliguria
In childhood, muscular pains frequently when doing sport activitity
3 sibs, with one sister with same complaints
CK-level of 40,000 U/ml
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Energy requirement: long-term
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Exercise-related rhabdomyolysis: think metabolic!!!
Carnitine-palmitoyltransferase II deficiëntie Very long chain fatty acid dehydrogenase
deficiency You need oxydation of fatty acids for long
term physical exercise
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Energy requirement on the short-term
Creatine kinase Glycolysis
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Glycogenoses: with exercise related complaints
GSD V: McArdle disease (myofosforylase, 11q, AR)• Onset: 15-25 years• Symptoms
– At the beginning of exercise– ↓ peak capacity– Pain upon start exercise– Rhabdomyolysis, swelling– ‘Second wind’– in 1/3 >40 jaar paresis
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Glycogenosis with exercise-related complaints
GSD V: McArdle disease• Diagnosis
– Permanent CK rise– EMG: myogenic– Fore armtest– DNA
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Man, 38 yo
At the age of 15: cataract
Normal education until the age of 13
Abnormal behavior from the age of 25, regular falls
Brisk reflexes, ataxic gait, xanthomata
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STATINES
Ac CDCA
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– Dosage of Cholestanol/Cholestérol:1/100 (N <1/1000)
– Accumulation of biliairy sterols in serum and urine
Cerebrotendinous xanthomas
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Tendon xanthomata
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Juvenile bilateral cataract 90%
Tendom xanthomata 70%
Chronic diarrhea 33%
Pyramidal syndrome 67%
Cerebellar ataxia 60
Cognitive decline 57%
Epilepsy 24%
Polyneuropathy 24%
Parkinsonian syndrome <10%
Atherosclerosis 10%
95%
MOGHADASIAN, 2004; VERRIPS et al., 2000. BARKHOF et al.,2000
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20-50 years
•Pyramidal signs (90%)•Cataract (90%)•Cerebellar signs (70%)•Dementia (70%)•Polyneuropathy (70%)•Xanthomata (40%)•Psychiatric signs (30%)•Atheroma (30%?)•Epilepsy (20%)
• Learning difficulties (>70%) • Juvenile cataract (50%)•Chronic Diarrhoea (40%)•Tendon xanthomata (10%)• Neonatal Cholestasis (?)
Childhood
Adulthood
Clinical spectrum of cerebrotendinous xanthomatosisEstimated from 124 published cases
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Cerebellar ataxia
Energy metabolism disordersPDH deficiencyRespiratory chain disorders
IntoxicationsUrea cycle disordersHartnup’s disease
Lipid metabolism disorders and some lysosomal diseases
- GM2 gangliosidosis- Niemann Pick C- Cerebrotendinous xanthomatosis- Adrenomyeloneuropathy- Refsum’s disease− α mannosidosis- Sialidosis type 1- Vitamin E deficiency,- Abetalipoproteinemia
Energy metabolism disorders- NARP syndrome- Kearns-Sayre syndrome- Others..
Acute Chronic
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1) Symptoms unexplained by « classical causes »
2) « Incongruous » association of symptoms
3) Acute episodes triggered by fever, exercise,
surgery, drugs etc..
4) Young age at onset
5) Exercise-related rhabdomyolysis
6) Familial history…
Question 1: Could it be an inborn error of metabolism?
In general, think to an IEM when..
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1) Energy metabolism disorders (respiratory chain, PDH, ETF,
biotine)
2) Lipid storage disorders (sphingolipidoses, peroxisomal
disorders, cerberotendinous xanthomatosis, Tangier
disease)
3) Intermediary metabolism disorders (intoxications)
4) Neurotransmitter metabolism diseases (dopamine,
serotonine)
5) Metal storage disorders (copper, iron, manganese)
Question 2: What kind of metabolic pathway could be
involved?