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Year : 2018  |  Volume : 66  |  Issue : 6  |  Page : 1802--1804

Mitochondrial acetoacetyl-CoA thiolase enzyme deficiency in a 9-month old boy: Atypical urinary metabolic profile with a novel homozygous mutation in ACAT1 gene

Soumya Sundaram1, Muralidharan Nair1, Sheela Namboodhiri2, Ramshekhar N Menon1,  
1 Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India
2 Department of Pediatric Genetics, Amrita Institute of Medical Sciences, Kochi, Kerala, India

Correspondence Address:
Dr. Soumya Sundaram
Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala
India




How to cite this article:
Sundaram S, Nair M, Namboodhiri S, Menon RN. Mitochondrial acetoacetyl-CoA thiolase enzyme deficiency in a 9-month old boy: Atypical urinary metabolic profile with a novel homozygous mutation in ACAT1 gene.Neurol India 2018;66:1802-1804


How to cite this URL:
Sundaram S, Nair M, Namboodhiri S, Menon RN. Mitochondrial acetoacetyl-CoA thiolase enzyme deficiency in a 9-month old boy: Atypical urinary metabolic profile with a novel homozygous mutation in ACAT1 gene. Neurol India [serial online] 2018 [cited 2019 May 21 ];66:1802-1804
Available from: http://www.neurologyindia.com/text.asp?2018/66/6/1802/246264


Full Text



Sir,

Mitochondrial acetoacetyl-CoA thiolase enzyme (also known as 2-methyl-acetoacetyl-CoA thiolase and beta-ketothiolase; abbreviated as T2) plays an essential role in isoleucine and ketone body metabolism. T2 deficiency is a rare autosomal recessive inherited metabolic disorder characterized by a normal early development followed by intermittent episodes of metabolic encephalopathy with ketoacidosis between 6 months to 2 years of age.[1] Urinary organic acid analysis by gas chromatography-mass spectrometer (GC-MS) typically shows marked excretion of 2-methylacetoacetate, 2-methyl-3-hydroxybutyric acid and tiglylglycine, which are the intermediate metabolites in the isoleucine pathway.[2]

Here we describe a boy who presented with acute encephalopathy and metabolic ketoacidosis with a confirmed novel homozygous ACAT1 missense mutation with an atypical urinary metabolic profile.

An eleven-month old boy presented with a history of regression of milestones following an episode of metabolic encephalopathy. He was born of third degree consanguinity with normal birth history except for low birth weight (2.2 kg) and had normal development until 9 months of age.

At 5 months of age, he developed one episode of simple febrile seizure and recovered uneventfully. At 9 months of age, he developed fever along with multiple episodes of non-projectile vomiting and diarrhea. The next day, he developed breathlessness and became lethargic. He had an episode of seizure characterized by a brief period of uprolling of eyeballs lasting for 10 seconds. The child was intubated due to his poor respiratory effort and was kept on ventilatory support for 7 days. The parents noted that he was not making any eye contact, had lost head control and was floppy.

He presented to our hospital 2 months after this event. He did not develop any further seizures or metabolic encephalopathy. The child was alert, but was floppy and had failure to thrive. His arterial blood gas analysis (ABG) on initial admission at the local hospital had shown severe metabolic acidosis (pH-7.09, PCO2-24 mm Hg, HCO3-5.5 mmol/L), hyperammonemia (192.6 mmol/L) and mildly elevated serum lactate (4.63 mmol/L). The urine was positive for ketone bodies (ketones ++). His routine hemogram, renal function and liver function tests were normal. Magnetic resonance imaging (MRI) of the brain showed symmetric T2 weighted and FLAIR hyperintensities involving bilateral caudate nuclei, putamina and globus pallidi [Figure 1].{Figure 1}

Our initial impression based on the clinical and blood parameters was in favor of an inherited metabolic disorder related to the intermediate metabolism affecting a branched chain amino acid in the ketolytic pathway, urea cycle, or mitochondrial pathways. He was evaluated in our hospital considering the above differential diagnoses [Figure 2]. His ABG (pH-7.36, PCO2-31 mm Hg, HCO3-11.9 mmol/L) was suggestive of compensated metabolic acidosis with mildly elevated lactate (4.2 mmol/L) with resolution of ketonuria and hyperammonemia. Tandem mass spectrometry analysis of serum showed normal levels of amino acids, carnitine, and fatty acids. The urine analysis showed three times elevation of 3-methylglutaric acid and 3-methyl glutaconic acid whereas 2-methylacetoacetate, 2-methyl-3-hydroxybutyricacid and tiglylglycine were not detected. The genetic testing for 3-methylglutaconic aciduria type 1 (AUH gene), type II (TAZ), type III (OPA 3), type IV (TMEM70) and type V (DNAJC19) were negative. We proceeded with next generation sequencing for genetic defects in other organic acidurias, which revealed a homozygous missense substitution mutation c.764A>C(p. Glu255Ala, chromosome 11.108012365A>C) in exon 8 of ACAT1 gene in our patient. The child was started and maintained on a low protein, high carbohydrate (hepatic) diet and had no further episodes of encephalopathy.{Figure 2}

Mitochondrial acetoacetyl-CoA thiolase (beta-ketothiolase or T2) enzyme is involved in the isoleucine metabolism, ketone body formation in liver, and ketolysis in extrahepatic tissues.[2] This patient had the classic presentation described in the literature with acute metabolic encephalopathy in the presence of hyperammonemia with ketoacidosis at 9 months of age. The mild elevation of 3-methyl glutaconic acid and 3-methylglutaric acid in urine was unusual since these are intermediate metabolites in the leucine pathway.[3] Blood and urine amino acid profile by the gas chromatography–mass spectrometry(GC-MS) analysis in our patient was done 2 months after the encephalopathy episode (due to his late referral to our institute), which might have resulted in lack of detection of the typical metabolic profile in him. Since 2-methylacetoacetate is unstable and volatile, it may not be detected in the urine, whereas 2-methyl-3-hydroxybutyric acid and tiglylglycine may not be increased when the patient has mild mutations and when he/she is unstressed.[1],[4] Hence, the patients with T2 deficiency can be missed if the typical metabolites are analyzed under stable non-episodic conditions, which had happened in our case. Some reports of an abnormal urinary excretion of 3-methyl 3-hydroxyglutaric acid have been described in propionic acidemia and T2 deficiency.[5]

Since the first report of T2 deficiency by Daum et al., around 100 cases have been reported from many countries with only one case report from India which identified a homozygous novel c.578T>G (M193R) mutation.[6],[7] Numerous mutations (more than 50) have been described in the ACAT1 gene with either completely absent or with variable residual enzymatic activity.[1],[4] The gene locus ACAT1 is located at chromosome 11q22.3-q23.1. The mutations in T2 deficiency are heterogeneous and no common mutation has been identified so far.[1],[8],[9] We have identified a novel homozygous missense substitution at c.764A>C (p. Glu255Ala, chromosome 11.108012365A>C) in exon 8 of ACAT1 gene in our patient.

Bilateral symmetric basal ganglia involvement is well described in other organic acidurias such as isovaleric acidemia, propionic acidemia, 3-methyl glutaconic aciduria and methymalonic acidemia.[2] However, the basal ganglia involvement which was seen in our patient, is a rare observation in T2 deficiency.[7],[10]

The limitation in this particular case study was that we did not obtain T2 enzyme assay from the fibroblast culture. The metabolic profile was also determined when the patient was in a stable phase and without any isoleucine challenge test. Moreover, such assays are not widely available in India, and hence, we considered mutational analysis for confirmation of the diagnosis.

This case illustrates the need for the clinician to maintain a broad perspective in evaluating a child with inborn errors of metabolism. An atypical presentation warrants a meticulous genetic evaluation with clinical exome sequencing to arrive at a specific diagnosis.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

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