Tuesday, March 30, 2021

Porphyria (Acute Intermittent Porphyria) Case File

Posted By: Medical Group - 3/30/2021 Post Author : Medical Group Post Date : Tuesday, March 30, 2021 Post Time : 3/30/2021
Porphyria (Acute Intermittent Porphyria) Case File
Eugene C.Toy, MD, William E. Seifert, Jr., PHD, Henry W. Strobel, PHD, Konrad P. Harms, MD

A 21-year-old healthy male college student went to celebrate his birthday with some friends at a bar. His friends convinced him to have his first beer since he just turned 21. After consuming the beer, he began to experience intense, worsening abdominal pain that was nonspecific in location and described as cramping. Nausea and vomiting then ensued and he was taken to the ER. Upon arrival to the ER, he was found to be very anxious with hallucinations. He was noted to be hypertensive, tachycardic, and diaphoretic. Peripheral neuropathy was also noticed on examination. Initial laboratory test revealed a normal CBC, drug screen, and EtOH level. Serum and urine aminolevulinic acid (ALA) and prophobilinogen (PBG) were both found to be elevated.

◆ What is the likely diagnosis?

◆ What is the underlying biochemical problem?


Summary: A 21-year-old healthy male patient with sudden onset abdominal pain, nausea and vomiting, hypertension, tachycardia, and peripheral neuropathy after consumption of first alcoholic beverage. Further testing revealed elevated levels of both serum and urine ALA and PBG.

Diagnosis: Porphyria (likely acute intermittent porphyria, i.e., variegate)

Biochemical problem: Enzymatic deficiency in heme biosynthetic pathway

Porphyrias are inherited disorders in the heme biosynthetic pathway. Porphyrias are classified as either hepatic or erythropoetic depending on primary site of accumulation. Inheritance is usually autosomal dominate. Patients often are asymptomatic unless exposed to factors that increase production of porphyrias (drugs, alcohol, sunlight). Erythropoetic etiologies primarily present with photosensitivity. Hepatic porphyrias present with primarily neurovisceral symptoms such as: abdominal pain, nausea and vomiting, tachycardia and hypertension, peripheral neuropathy, and mental symptoms (hallucinations, anxiety, seizures). Diagnosis is confirmed with elevated levels of ALA and PBG in the urine and serum. Specific tests can be performed to detect which enzyme is deficient (i.e., variegate porphyria is caused by deficiency in the PPO enzyme). Treatment is supportive with avoidance of triggers in the future.


1. Describe the biosynthesis of heme.
2. Explain why certain triggers (such as EtOH) cause an increase in ALA and PBG.
3. Explain why treatment with intravenous heme or hematin is effective.


Aminolevulinic acid synthase (ALAS): Mitochondrial matrix enzyme that catalyzes the rate-limiting synthesis of ALA via condensation of succinyl-CoA and glycine.
ALA dehydratase (ALAD): Cytosolic enzyme that catalyzes the asymmetric condensation of two molecules of ALA to form PBG.
Autonomic neuropathy: Autonomic nervous disruption or deregulation affecting the cardiovascular, urogenital, gastrointestinal systems; symptoms include abdominal pain, nausea and vomiting, tachycardia and hypertension; (aka visceral neuropathy).
Coproporphyrinogen oxidase (CPO): Mitochondrial enzyme that catalyzes specifically the conversion of coproporphyrinogen III to protoporphyrinogen IX.
Ferrochelatase: Assists in the insertion of the ferrous iron into the protoporphyrin IX; the final step in heme synthesis.
Hematin: Compound similar in structure to heme, except that the iron is in the ferric state (tetracoordinated with the pyrrole nitrogens and a hydroxyl group); can restore negative regulation of ALAS.
Heme: An essential metalloorganic cofactor, consisting of one ferrous iron atom coordinated within a tetrapyrrole ring, protoporphyrin IX.
Porphobilinogen deaminase (PBGD): Cytosolic enzyme that processes six PBG molecules through a hexapyrrole adduct to catalyze the formation of a free linear tetrapyrrole, hydroxymethylbilane (aka uroporphyrinogen I synthase).
Porphyria: Any of a number of diseases characterized by derangement in porphyrin metabolism; many are caused by genetic defects in the biosynthetic enzymes.
Protoporphyrinogen oxidase (PPO): Catalyzes the oxidation of protoporphyrinogen IX to produce protoporphyrin IX.
Pyridoxal phosphate: Coenzyme active derivative of vitamin B6.
Uroporphyrinogen (URO) III cosynthase: Cytosolic enzyme that catalyzes formation of the URO III isomer from hydroxymethylbilane.
URO decarboxylase (UROD): Cytosolic enzyme that catalyzes the removal of the carboxyl groups from the side chains of both URO isoforms converting them to their respective coproporphyrinogens (i.e., COPRO I and COPRO III).

The cofactor heme is required for numerous processes throughout the body. Most importantly, the heme iron facilitates systemic oxygen transfer via hemoglobin, participates in mitochondrial electron transport, and mediates oxidative drug metabolism in the liver through various cytochromes P450. All cellular tissues are capable of synthesizing heme, but expression of the pathway enzymes and levels of intermediates are greatest in erythropoietic and hepatic tissues due to high demand for heme incorporation into hemoglobin and cytochromes, respectively. Heme is a metalloorganic compound, consisting of one ferrous iron atom coordinated within a tetrapyrrole ring, protoporphyrin IX. Protoporphyrin IX is derived from eight molecules each of succinyl-CoA and glycine. Heme is a relatively planar molecule and highly stabilized by strong resonance throughout the tetrapyrrole ring system. The structure of heme is shown in Figure 44-1.

Structure of heme

Figure 44-1. Structure of heme.

The biosynthetic pathway includes eight steps, shown in Figure 44-2. The first step is the rate-limiting condensation reaction between succinyl-CoA and glycine to form δ-aminolevulinic acid (ALA). This reaction is catalyzed by a mitochondrial matrix enzyme, ALA synthase (ALAS), and requires the cofactor pyridoxal phosphate. The ALAS protein is produced in the cytosol but remains unfolded or inactive until it is directed to the mitochondrial matrix where its N-terminal signaling sequence is cleaved. Additionally, this enzyme catalyzes the primary regulatory step in heme biosynthesis and is negatively regulated by any accumulation of free heme in the mitochondrial matrix. In the next step of the pathway, ALA dehydratase catalyzes the asymmetric condensation of two molecules of ALA to form porphobilinogen (PBG). Through the addition of water and the removal of four amino groups, PBG deaminase produces the linear tetrapyrrole intermediate, hydroxymethylbilane (HMB) from four molecules of PBG. At this point, HMB can close either in an enzyme-independent manner to form uroporphyrinogen (URO) I, or in an enzyme-dependent manner through uroporphyrinogen III cosynthase to form uroporphyrinogen III, the intermediate that will ultimately lead to heme formation. URO I and URO III differ in the order of the carboxymethyl and carboxyethyl substituents around the tetrapyrrole ring. In the last cytosolic

Heme biosynthetic pathway

Figure 44-2. Heme biosynthetic pathway involving (1) ALAS, (2) ALAD, (3) PBGD, (4) UROS, (5) UROD, (6) CPO, (7) PPO, and (8) Ferrochelatase. HMB = hydroxymethylbilane; CM = carboxymethyl; CE = carboxyethyl; M = methyl; V = vinyl.

steps, uroporphyrinogen decarboxylase (UROD) recognizes either isomer URO I or III and removes specific carboxyl groups leaving coproporphyrinogen I or III, respectively. Coproporphyrinogen oxidase (CPO) acts exclusively on the type III isomer of coproporphyrinogen; after its substrate enters the mitochondrion CPO catalyzes the conversion of COPRO III to protoporphyrinogen III. This intermediate is oxidized by protoporphyrinogen oxidase (PPO) to form protoporphyrin IX. In the final step of heme synthesis, the enzyme ferrochelatase inserts a ferrous iron into water-insoluble protoporphyrin IX. The excess protoporphyrin IX not converted to heme is removed via biliary excretion into the intestine.

The porphyrias are a group of inherited disorders resulting from specific enzymatic defects of the heme biosynthetic pathway. Figure 44-3 shows the heme biosynthetic pathway and characteristics of porphyrias associated with each step. A derangement in any of the involved enzymes can result in an overproduction or backlog of heme precursors prior to the deficient enzymatic step. All of the intermediate compounds in this pathway are potentially toxic. The disorders are divided into two broad groups, erythropoietic and hepatic porphyrias, based on the primary source of precursor accumulation. Furthermore, the porphyrias are also categorized based on the appearance of distinctive acute or chronic symptoms. Pressure to overcome the metabolic “roadblock” contributes to the rapid accumulation of precursors in acute attacks. Early pathway intermediates, that is, ALA and PBG are associated with acute neurovisceral symptoms, whereas later intermediates (which undergo porphyrinogen-porphyrin conversions upon exposure to light) cause skin photosensitivity through free-radial damage. The porphyrins can be detected and identified by spectrofluorometry based on characteristic excitation and emission wavelengths for each porphyrin. For example, serum uroporphyrin levels can be determined by detection at 615 nm after excitation at

Heme biosynthetic

Figure 44-3. Heme biosynthetic pathway and characteristics associated with specific enzyme-deficiency porphyrias. ADP = ALA dehydratase deficiency porphyria; AIP = acute intermittent porphyria; CEP = congenital erythropoietic porphyria; PCT = porphyria cutanea tarda; HEP = hepatoerythropoietic porphyria; HCP = hereditary coproporphyria; VP = variegate porphyria; EPP = erythropoietic protoporphyria.

395 nm to 398 nm, while protoporphyrin is detected at 626 nm. The excretion pathway of the porphyrins is determined by their water solubility. The first possible porphyrin byproduct of the heme biosynthetic pathway, uroporphyrin is by far the most water-soluble, while protoporphyrin the least soluble. Accordingly, uroporphyrin is excreted predominantly in urine, coproporphyrin in urine and in bile, and protoporphyrin exclusively in bile.

In most cases, these disorders are inherited in an autosomal dominant manner where the individual carries one normal allele and one loss-of-function allele. Under normal circumstances, the wild type allele allows for expression of enough functional enzymes to meet the individual’s requirement for heme (symptom-free carriers). However certain environmental triggers for example, drugs, alcohol, steroids, fasting, trauma, and/or high stress can increase this demand beyond a level which can be compensated by the single functional allele. Upon exposure to the trigger(s), patients with acute hepatic porphyrias can shift from a compensated phase to a decompensated latent phase (increased precursor production and excretion without symptoms) or to a clinically manifest stage (marked by abdominal, peripheral neurologic, cardiovascular, and psychiatric symptoms).

Alcohol ingestion induces increased activity of ALAS significantly in the liver and moderately in peripheral tissues. This effect is mediated by alleviating the negative regulation of ALAS by free heme. Mitochondrial concentrations of free heme are diminished by increased heme utilization and/or reduced activity of downstream pathway enzymes. In the liver, the demand for heme is exacerbated by requirement for heme incorporation into alcoholeliminating cytochromes P450. Upon increased activity of ALAS, a genetic defect in either ALAD or PBGD would cause the rapid accumulation of ALA or both ALA and PBG, resulting in ALAD deficiency porphyria (very rare) or acute intermittent porphyria, respectively. During an attack, excess ALA and PBG produced in the liver are secreted into systemic circulation and are later excreted in the urine. In circulation, these neurotoxic compounds have the greatest effect on the autonomic and peripheral nervous systems resulting in the peripheral neuropathy and neurovisceral symptoms, that is, abdominal pain, nausea and vomiting, tachycardia, and hypertension.

Alternatively, patients with cutaneous porphyrias, for example, porphyria cutanea tarda or hereditary coproporphyria, chronic symptoms develop as a result of sun exposure (400 nm radiation). The excess porphyrins accumulated in the skin can absorb light energy and transfer it to damaging chemical reactions, such as peroxidation of membrane lipids. This manifests as thickening of the dermal vessel walls leading to damage of the epidermal basement membrane, excessive fragility, blistering, and scarring. In variegate porphyria, patients can present with neurovisceral symptoms (acute symptoms are identical but often milder than those of AIP) and/or cutaneous symptoms.

Porphyrias are diagnosed after demonstration and biochemical identification of the increased porphyrin precursor(s). Acute porphyrias are often misdiagnosed, and attacks can be fatal. The intravenous administration of heme or hematin can aid in reestablishing the negative regulation of ALAS during acute attacks. With ALAS activity attenuated, the precursor backlog at the enzymatic deficient step can begin to return to manageable levels, and the patient’s condition can shift back to the compensated, symptom-free phase. After diagnosis of acute porphyria is confirmed, strict avoidance of environmental triggers can prevent acute attacks. Most patients with acute porphyrias can lead a normal life; however, complications such as hypertension, chronic renal failure, and hepatoma can become problematic.


For Questions 44-1 and 44-2 refer to the following case:
A 30-year-old white woman enters the emergency room complaining of nausea, severe abdominal pain, and prolonged constipation. She appeared distraught and was sweating. She described beginning an extremely low calorie diet within the past 2 months in an attempt to lose weight. Physical examination determined rapid heart rate, moderate hypertension, and weakness in the extremities. Also noted were mild dermatitis/blistering on her hands and scarring on her face.
[44.1] You suspect porphyria. Which biochemical laboratory test(s) would be sufficient to determine the type of porphyria?
A. Urinary ALA and PBG.
B. Urinary and fecal PBG and porphyrins.
C. Porphyrin spectrofluorometry (plasma scan).
D. None of the above is sufficient alone.

[44.2] Laboratory tests revealed elevated urinary PBG and coproporphyrin, and plasma fluorescence emission at 626 nm. Which type of porphyria does the patient have and what is the most likely biochemical explanation?
A. Acute intermittent porphyria; PBGD heterozygous enzyme deficiency causing PBG backlog.
B. Porphyria cutanea tarda; UROD homozygous enzyme deficiency causing uroporphyrin backlog.
C. Variegate porphyria; PPO heterozygous deficiency causing protoporphyrin IX backlog. 
D. Variegate porphyria; PPO homozygous deficiency causing protoporphyrin IX backlog.

[44.3] The second enzyme in the heme pathway, ALAD, is very sensitive to inhibition by heavy metals, for example, lead. Which of the following test results would distinguish lead-based poisoning from acute intermittent porphyria?
A. Decreased serum and urinary ALA and PBG
B. Increased serum and urinary ALA and PBG
C. Increased serum and urinary ALA, decreased serum and urinary PBG
D. Decreased serum and urinary ALA, increased serum and urinary PBG

[44.1] C. Given the patient’s symptoms, neurologic and cutaneous, the main porphyrias to consider are hereditary coproporphyria and variegate porphyria. Both HCP and VP show elevated ALA and PBG during acute attacks, so urine and serum tests for these molecules would not distinguish. Similarly both disorders show coproporphyrin in stool. In this case, only a spectrofluorometric assay to distinguish between coproporphyrin and protoporphyrin in plasma would be sufficient.

[44.2] C. Variegate porphyria patients present with the same, but generally milder, symptoms as AIP. The emission wavelength at 626 nm is characteristic of protoporphyrin IX; the compound is responsible for the skin sensitivity not observed in AIP. PCT can also be ruled out because the characteristic fluorescence emission for uroporphyrin is 615 nm. Homozygous deletion of PPO is unlikely because the patient’s symptoms were triggered by stress in the form of caloric restriction. Patients with homozygous deficiency in the heme synthesis enzymes show early onset and more severe symptoms.

[44.3] C. An increase in urine/serum ALA without concomitant increase in PBG indicates disrupted activity of ALA dehydratase. ALA alone can cause the same neurovisceral symptoms as ALA and PBG together cause in AIP. ALAD-deficiency porphyria is an extremely rare autosomal recessive disorder.

❖ The porphyrias are a group of inherited disorders resulting from specific enzymatic defects of the heme biosynthetic pathway.

❖ The major types of porphyria are each caused by mutations in one of the genes required for heme production.

❖ The first step in heme formation is the rate-limiting condensation reaction between succinyl-CoA and glycine to form δ-aminolevulinic acid (ALA). This reaction is catalyzed by a mitochondrial matrix enzyme, ALA synthase (ALAS).

❖ Forms of porphyria include ALAS deficiency porphyria, acute intermittent porphyria, congenital erythropoietic porphyria, erythropoietic protoporphyria, hepatoerythropoietic porphyria, hereditary coproporphyria, porphyria cutanea tarda, and variegate porphyria.


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Kauppinen R. Porphyrias. Lancet 2005; 365(9455):241–52. 

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