This document summarizes an elective on metabolic disorders. It discusses two cases - acute intermittent porphyria and Wilson disease. For porphyria, it describes the biochemical pathway disruption, clinical symptoms of attacks including abdominal pain and neuropathy, and treatment with intravenous carbohydrates. For Wilson disease, it outlines the hepatic and neurological presentations, Kayser-Fleischer rings, low ceruloplasmin and high urine copper diagnostic tests, and therapies including chelation and zinc supplementation. The document ends with two multiple choice review questions.
This classification system was devised by Dr. Jean Marie Saudubray. Metabolic diseases fall into 3 categories - disorders of intoxication, disorders of energy production or metabolism, and defects of complex molecules.
Acutely presenting, or neurovisceral porphyrias. This is in contrast with the cutaneous porphyrias associated with skin manifestations
The mode of inheritance is autosomal dominant with variable penetrance
Acutely presenting, or neurovisceral porphyrias. This is in contrast with the cutaneous porphyrias associated with skin manifestations
The mode of inheritance is autosomal dominant with variable penetrance
The porphyrias are disorders in the synthesis of heme.
Heme is actively produced predominantly in the bone marrow and the liver
Bone marrow – used for hemoglobin synthesis
Liver – used for production and activation of the cytochrome P450 system, among other important biological pathways
If a drug is ingested/used that requires the cytochrome P-450 system for its metabolism, then the system is stimulated which increases flux through the pathway
This can be problematic if there is a defect in the pathway.
Let’s look more closely….
Those factors that activate the cytochrome P450 enzymes, triggers of a crisis, induce the first enzyme in the pathway, 5-ALA synthase, increasing flux through the pathway,
In acute intermittent porphyria, a deficiency of porphobilinogen deaminase becomes the rate-limiting step and causes elevations in the proximal metabolites – porphobilinogen and 5-aminolevulinic acid – which cause intoxication. These are also the lab metabolites to look for when making a diagnosis
There are several triggers for acute porphyria:
Medications
Hormonal variation, especially menstrual periods
Infections
Nutrition, although it is not so much the types of foods but the carbohydrate content, meaning a low intake of carbs
Stress
Alcohol
The most disturbing of the symptoms that occur in porphyria is the pain. Pain can be excruciating, searing or burning, or sometimes crampy. It is most commonly located in the abdomen but the exam is not necessarily indicative of an acute belly. This can lead to multiple exploratory surgeries that result in no clear cause for the pain.
There can be associated nausea or vomiting
Notably though, there is usually no fever or significant elevation in the white blood cell count
But pain can be described elsewhere as well, in the chest, the head, in the limbs
There are also signs of autonomic dysfunction
Examples
Disturbed bowel motility, diarrhea or constipation, and impaired bladder function
Muscle weakness often starts in the upper extremities but can progress to all limbs and even to the chest
Sensory manifestations can present as a painful neuropathy, or as a loss of sensation
Deep tendon reflexes can be diminished in severe crises
The findings do not necessarily follow a specific nerve distribution, confusing a treating physician
The psychological findings include confusion, hallucinations, depression and/or anxiety, and can result from the intoxication itself, or in part as a response to chronic, severe, unremitting symptoms like pain
Given the combination of subjective symptoms like pain, neurologic symptoms that may not follow a defined nerve distribution, and the presence of psychological symptoms, it is easy to understand how clinicians unfamiliar with porphyria might label affected patients incorrectly as having primary psychiatric disease or as patients who are fabricating their symptoms
Urine porphyrin metabolites when exposed to long-wave ultraviolet light become oxidized and emit light with a different wavelength (reddish) light.
Urine porphyrin metabolites when exposed to long-wave ultraviolet light become oxidized and emit light with a different wavelength (reddish) light.
“Porphyric marble” sarcophagus from Egypt, now in the Vatican Museum
The diagnosis is made by documenting elevated levels of 5-ALA and PBG
Spot testing for porphobilinogen is available for rapid testing
5-aminolevulinic acid measurement is done is a specialized testing laboratory
The approach to treating acute porphyria is to reduce flux through the porphyrin pathway.
Hemin can suppress the activity of the first enzyme in the pathway shutting down the synthesis of the intoxicating agents. Carbohydrates as IV dextrose is more readily available and can also do this but it is not as effective as the use of the heme compound. Very large doses of dextrose are generally required. CHO might be particularly helpful alone in very mild attacks, and it is generally used until the heme arginate becomes available
Small interfering RNA agents. Via RNA interference, they lead to degradation of aminolevulinate synthase 1 (ALAS1) mRNA in hepatocytes, which in turn lowers elevated liver ALAS1 mRNA levels. This decreases circulating levels of the neurotoxic intermediates aminolevulinic acid (ALA) and porphobilinogen (PBG), both of which are linked to attacks and other manifestations of the acute hepatic porphyrias (AHP).
The approach to treating acute porphyria is to reduce flux through the porphyrin pathway.
Hemin can suppress the activity of the first enzyme in the pathway shutting down the synthesis of the intoxicating agents. Carbohydrates as IV dextrose is more readily available and can also do this but it is not as effective as the use of the heme compound. Very large doses of dextrose are generally required. CHO might be particularly helpful alone in very mild attacks, and it is generally used until the heme arginate becomes available
The big caution regarding the treatment of porphyria is prevention. Patients and families need to learn how to prevent attacks by reducing their exposure to trigger agents, like avoiding medications that themselves can trigger or exacerbate a crisis. For example, most of the anti-convulsants are porphyrinogenic.
For more information about triggers, and an updated list of drugs that are dangerous for patients with porphyria, seek out a reliable resource like the American Porphyria Foundation website
Schematic depicting effects of phenotypic defects in the Wilson ATPase7B (ATP7B) inside the hepatocyte. Copper (red circle) is taken up from albumin and other carriers in blood by the copper transporter CTR1 (bottom of the screen). In the hepatocyte, copper is stored bound to metallothionein or distributed to specific sites via copper chaperones (only ATOX1 shown here). ATP7B (orange cylinder with arrow) is located in the trans-Golgi network (TGN), where it receives copper from the copper chaperone ATOX1 (green nicked-diamond). At low copper concentrations (when the body needs more copper), the ATP7B participates in the mechanism for incorporating copper into apoceruloplasmin (blue collar) to generate holoceruloplasmin (blue collar plus Cu) also known as just “ceruloplasmin” in blood, but at high copper concentrations (when the body’s supply of copper is high), it expedites the excretion of copper in bile to be excreted into the intestine. Potential phenotypic defects due to lesions in the gene include (1) absence of any intact Wilson ATPase, (2) misfolding of Wilson ATPase leading to its retention in the endoplasmic reticulum, (3) failure to bind to ATOX1 (not shown), and (4) ineffective interaction with other proteins, which directs the intracellular movement of the ATP7B (not shown). Any type of phenotypic defect can result in copper accumulation and toxicity in hepatocytes.
Legend: BC, bile canaliculus; Mt, metallothionein; RER, rough endoplasmic reticulum; SER, smooth endoplasmic reticulum; TGN, trans-Golgi network.
--The accumulating copper in the liver cells can irritate and inflame the liver, and can cause a wide range of types of liver disease, including hepatitis and cirrhosis.
--Patients can present in liver failure; if untreated, this can proceed to renal failure and death (mortality rate=95%).
--6-12% of those referred for emergency liver transplantation have Wilson disease as the underlying diagnosis.
--Copper from accumulations in the damaged liver leaks out into the blood stream and deposits elsewhere, causing damage in other organs.
--Kayser-Fleischer rings are deposits of copper (beige-yellow in color) at the junction of the cornea and iris.
--The accumulating copper in the liver cells can irritate and inflame the liver, and can cause a wide range of types of liver disease, including hepatitis and cirrhosis.
--Patients can present in liver failure; if untreated, this can proceed to renal failure and death (mortality rate=95%).
--6-12% of those referred for emergency liver transplantation have Wilson disease as the underlying diagnosis.
--Copper from accumulations in the damaged liver leaks out into the blood stream and deposits elsewhere, causing damage in other organs.
--Kayser-Fleischer rings are deposits of copper (beige-yellow in color) at the junction of the cornea and iris.
--Copper from accumulations in the damaged liver leaks out into the blood stream and deposits elsewhere, causing damage in other organs.
--In brain, the deposits can occur in the deep nuclei, called the basal ganglia, responsible for regulating body movements. Their involvement can result in symptoms similar to Parkinson disease, including tremors and rigidity, and problems with gross and fine motor, such as issues with hand-writing.
--Abnormal MRI of the brain of a Wilson disease patient with movement problems.
--The abnormally involved “hyperintensity” regions are highlighted in the next slide, where the copper is deposited and causing active injury.
--The abnormally involved “hyperintensity” regions are highlighted here, where the copper is deposited and causing active injury.
--Take notice of the caudate, pallidum and thalamus. These are the “basal ganglia,” deep motor nuclei of the brain.
--In brain, the deposits can also occur in the cerebral cortex, resulting in a loss of cognitive function and/or psychiatric symptoms, such as depression, neurosis, personality changes.
--The copper also damages red blood cells causing them to hemolyze or disintegrate, resulting in anemia.
--There is a broad age range when symptoms appear, but most commonly, onset occurs during the 2nd or 3rd decade of life.
--Liver disease/jaundice is the most common presentation in younger patients.
--Older patients present more often with neurologic/psychiatric symptoms; in these patients, most patients will have active liver disease if you look for it.
--12% of patients present with an anemia picture (hemolytic).
--This patient talks about her dealing with the liver aspects of Wilson disease.
--It seems that she presented in liver failure, and that her course advanced quickly after that. Priority for transplantation depends on:
>> how advanced the liver disease is (higher priority with advanced disease)
>> if the patient is in the hospital (higher priority if admitted)
>> if the patient is in an ICU (meaning that you are even sicker).
--The video is a bit promotional for Barnes-Jewish Hospital in St. Louis, and she clearly loves her doctors/team.
--This patient presented with the neurologic manifestations of Wilson disease. She was also very depressed; it is not clear if that is part of the disease or due to the fact that she has a severely debilitating chronic disease (or both).
--Nothing is mentioned about any liver involvement.
--When watching the video, take note of the following neurologic findings, specifically the rigidity/stiffness of her muscles:
>> neck muscles (note the way she turns her head or holds it… there may be weakness here as well).
>> limb muscles (too straight with extension at the elbows and knees).
>> finger muscles (kept fully extended and straight with difficulty in using her fingers easily, like closing her fingers around something).
>> facial muscles (her smile or expressions can be excessive or unnatural).
--Notice she doesn’t say anything. It could be that her dysarthria is so severe that it as decided that she not talk during the video.
--If suspecting Wilson disease, do the following easy tests:
>> Complete blood count – is there anemia? If so, look for evidence of hemolysis.
>> Liver function tests (AST and ALT, bilirubin, alkaline phosphatase and GGT, PT, INR and PTT, albumin and total protein), looking at the various types of liver function).
--An eye examination.
--Low ceruloplasmin in blood – in Wilson disease (WD), the copper inside liver cells cannot bind with apoceruloplasmin to form holoceruloplasmin (aka ceruloplasmin in hospital tests), so blood ceruloplasmin levels are low.
--Low total copper in blood. Total copper=free copper and copper bound to ceruloplasmin. Since ceruloplasmin cannot be made, blood total copper levels are low.
--High free copper in blood. Copper leaks out of the damaged liver into the blood so levels there are high.
--High urine copper. The elevated free copper in urine leaks out into the urine so levels are high there.
--High liver copper. There is a massive accumulation of copper in liver tissue since it can’t get out.
--Note the scoring system for diagnosing a patient with Wilson disease.
--Biochemical signs do not necessarily correlate with physical signs. If the patient has few clinical signs, looking at the biochemistry or biopsying the liver for copper stores can confirm the diagnosis. And, of course, molecular analysis can easily confirm the diagnosis as well.
--Obvious.
--Patients with active disease need to be ”decoppered” in which chelating agents actively bind copper internally and help to clear the copper excess; this results in higher urine copper levels. After copper stores are cleared, patients continue taking a chelator on a maintenance dose.
--Also, patients should follow a low copper diet, especially around the time they are diagnosed. High copper foods include nuts, shellfish, organ meats (liver, brain), chocolate, mushrooms.
--Metallothionein binds copper in cells. Zinc salts (like zinc sulfate) induces the synthesis of metallothionein in cells, including in the enterocytes that absorb nutrients (including copper) from digested food in the gut. The metallothionein binds the copper there. Enterocytes are continuously shed (into the stools) as new cells take over; the excess bound copper is shed with the old enterocytes.
--With advanced liver failure, replacement of the liver normalizes liver function and provides new (donor) ATP7B molecules.