Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary management
© Grünert et al.; licensee BioMed Central Ltd. 2013
Received: 6 May 2013
Accepted: 2 July 2013
Published: 5 July 2013
Ornithine transcarbamylase (OTC) deficiency is the most common urea cycle defect. The clinical presentation in female manifesting carriers varies both in onset and severity. We report on a female with insulin dependent diabetes mellitus and recurrent episodes of hyperammonemia. Since OTC activity measured in a liver biopsy sample was within normal limits, OTC deficiency was initially excluded from the differential diagnoses of hyperammonemia. Due to moderately elevated homocitrulline excretion, hyperornithinemia-hyperammonemia-homocitrullinuria-syndrome was suggested, but further assays in fibroblasts showed normal ornithine utilization. Later, when mutation analysis of the OTC gene became available, a known pathogenic missense mutation (c.533C>T) in exon 5 leading to an exchange of threonine-178 by methionine (p.Thr178Met) was detected. Skewed X-inactivation was demonstrated in leukocyte DNA. In the further clinical course the girl developed marked obesity. By initiating physical activities twice a week, therapeutic control of both diabetes and OTC deficiency improved, but obesity persisted. In conclusion, our case confirms that normal hepatic OTC enzyme activity measured in a single liver biopsy sample does not exclude a clinical relevant mosaic of OTC deficiency because of skewed X-inactivation. Mutation analysis of the OTC gene in whole blood may be a simple way to establish the diagnosis of OTC deficiency. The joint occurrence of OTC deficiency and diabetes in a patient has not been reported before.
KeywordsOrnithine transcarbamylase deficiency Ornithine carbamoyltransferase deficiency OTC deficiency Urea cycle disorder Insulin-dependent diabetes mellitus Hyperammonemia Insulin
Ammonia which is predominantly formed by degradation of amino acids is bound as urea by action of the urea cycle. Urea cycle defects (UCDs) are a group of inborn errors of metabolism comprising 6 enzymatic defects (five core enzymes and one activating enzyme) as well as a mitochondrial ornithine/citrulline antiporter defect. Among UCDs, ornithine transcarbamylase (ornithin carbamoyltransferase, OTC, E.C. 220.127.116.11) deficiency (OMIM #311250) is the most prevalent with an incidence of 1:14.000 newborns [1–4]. OTC, a mitochondrial matrix enzyme, catalyzes the biosynthesis of citrulline from ornithine and carbamoyl phosphate. The corresponding gene is located on Xp11.4. While hemizygote males usually present with severe neonatal hyperammonemic coma which often proves to be fatal [2, 5], the clinical picture in female carriers of this X-linked disease is extremely variable, depending on the degree of inactivation of the mutated X chromosome.
Survival is better among those who have late onset of symptoms like some female carriers or males with only slightly reduced OTC activity [6–8]. While neonatal onset cases are usually diagnosed reliably using biochemical parameters (like excretion of large amounts of orotic acid and uracil and a typical amino acid pattern with elevated glutamine and very low or not detectable citrulline levels) diagnosis may be more complicated in late onset cases . The mainstay of dietary treatment is protein restriction with supplementation of essential amino acids to minimize nitrogen load . An adequate intake of calories is necessary to prevent protein catabolism . In order to deplete the hepatic nitrogen pool, oral sodium benzoate and/or sodium phenylbutyrate can be applied to eliminate ammonia without stressing the urea cycle. The only curative treatment of OTC deficiency available is liver transplantation [9, 11–15]. In this article we report the joint occurrence of OTC deficiency and type 1 diabetes and describe the diagnostic pitfalls and challenges of dietary therapy.
Decline of ALAT, ASAT and ammonia after starting of a protein-restricted diet at the age of 11 months
normal range 15–55 μmol/l
normal range < 22 U/l
normal range < 15 U/l
start of protein restriction (0.93 g/kg/d)
Diagnostic parameters in plasma and urine before treatment at the age of 11 months
Ornithine in plasma
Glutamine in plasma
Arginine in plasma
Citrulline in plasma
no reference range given
Lysine in plasma
Homocitrulline in urine
17 mmol/mol creatinine
Orotic acid in urine
> 8280 mmol/mol creatinine
1.3-8.5 mmol/mol creatinine
At the age of 4 years, the girl developed insulin-dependent diabetes (islet-cell antibodies positive, but insulin antibodies negative). The treatment had now to include carbohydrate control and insulin injections following a 2 insulin injection regime. The further clinical course was characterized by intermittent periods of both hyperammonemia and ketoacidosis, which were readily controlled by sodium benzoate (up to 350 mg/kg/d), arginine-HCl (2 mmol/kg/d) and glucose-insulin infusions as well as oral phenylbutyrate (100–300 mg/kg/d) during several hospital stays. Later on, diabetes management was switched to intensive insulin therapy (4 insulin injection regime). Nevertheless, diabetes treatment was suboptimal and HbA1c levels were intermittently elevated up to 111 mmol/mol Hb (normal 20–42 mmol/mol Hb).
As a complication of her diet, the girl developed progressive obesity. At the age of 15 years, she reached a BMI of 32.3 kg/m2. At that time she started a sports program with other diabetic adolescents and performed physical activities twice a week. Subsequently, her diabetes control improved, HbA1c-levels decreased from 86 mmol/mol Hb to 60 mmol/mol Hb and serum fructosamine levels from 497 to 290 μmol/l (normal 208–269 μmol/l). Moreover, during that time no hospitalizations because of hyperammonemia or ketoacidosis were necessary. However, during the following years, her compliance to therapy was not always satisfactory and HbA1c values ranged from 62–89 mmol/mol.
The patient finished school and became a nurse. Her psychomotor development is normal. IQ-testing at the age of 26 years revealed an IQ of 94 (Wechsler Intelligenztest für Erwachsene). Now, at the age of 27 years, she lives an independent adult live and works as a nurse in an intensive care unit.
Genomic DNA was isolated from peripheral blood leukocytes using proteinase K/sodium dodecyl sulfate treatment and phenol/dichloromethane extraction .
Mutation analysis of the OTC gene was performed by bidirectional sequencing of all 10 exons including adjacent intronic sequences. Exons 7 and 8 were amplified as a single PCR product including intron 7 (80 bp).
X-inactivation analysis was performed by a PCR methylation assay for the human androgen receptor (HUMARA) gene locus comparing HpaII digested versus undigested samples, as described previously . PCR products of X-chromosomal alleles were analyzed on a ABI3130xl capillary sequencer (Applied Biosystems) and visualized by Peak Scanner Software v1.0 (Applied Biosystems). For each sample, absolute values for the major peak heights of the two alleles were determined (ignoring any stutter peaks) and converted into relative peak heights, based on the sum of both allele peaks as 100%. Peak ratios were calculated by dividing the signal of the allele with the longer fragment size by the signal of the allele with the shorter fragment size.
OTC deficient males are often severely affected  whereas female carriers present with a wide phenotypic variability [19, 20]. Some may be entirely asymptomatic, while others have severe hyperammonemia leading to brain damage or death [9, 21]. This clinical variability is explained by X-inactivation in the liver. In females, X-inactivation is a random process inactivating either the maternal or the paternal allele. If X-inactivation results in predominant expression of the mutated allele, female carriers may be affected due to decreased OTC enzyme activity. In our patient a skewed X-inactivation pattern was found in leukocytes (see Figure 1). It has been shown by Yorifuji et al. that the X-inactivation pattern may differ significantly even within the same hepatic tissue but correlates well with the OTC activity in all liver samples . Thus, it was concluded that a single liver biopsy is not adequate for the assessment of residual enzyme activity in females. This is underlined by our case where normal OTC activity was detected in a single liver biopsy despite symptomatic OTC deficiency. Therefore, according to the recently published guidelines for the diagnosis of urea cycle disorders  mutation analysis of the OTC gene is the diagnostic gold standard and permits to identify carrier females. However, in about 20% of patients the mutation is not identified with standard techniques . The c.533C>T mutation found in our patient was first described in a male suffering from severe neonatal onset OTC deficiency . In the majority of female patients and in some male patients the mutation appears de novo and the mother is not a disease carrier , as was the case in our patient.
To our knowledge, this is the first report on a symptomatic female with OTC deficiency with additional insulin-dependent diabetes.
In view of the two underlying diseases, a vicious cycle aggravating metabolic decompensations in our patient can be hypothesized: In case of insulin deficiency, glucose cannot enter the cells properly, thus leading to energy deficiency and catabolism. Apart from endogeneous protein catabolism resulting in hyperammonemia, increased hepatic glucose production and decreased peripheral glucose utilization may lead to hyperglycemia. The increased blood glucose levels, in turn, might result in glucosuria and loss of calories further enhancing catabolism and thereby aggravating hyperammonemia. Several hospital admissions were necessary for induction of anabolism by intravenous glucose-insulin and fat infusions, but also for intensified detoxification of ammonia by sodium benzoate and phenylbutyrate supplementation.
There is a large body of evidence that, on average, diabetic patients have a higher body weight and body mass index compared to healthy controls  and therefore should control their calorie intake. On the other hand, for patients with urea cycle disorders a sufficient calorie intake is required to prevent catabolism. The diet of our patient was complicated by the restriction of both carbohydrates and protein due to her diabetes and OTC deficiency, respectively. Subsequently, the resulting increased fat intake may have contributed to obesity. Regular physical activity did not only improve the patient’s diabetes control, reflected by a marked decrease in HbA1c levels and stabilization of blood glucose levels, but also her metabolic control. Moderate physical exercise may induce protein anabolism and simultaneously lower glucose levels.
In conclusion, our case report illustrates that liver OTC activity assays are not reliable in the diagnosis of OTC deficiency in females due to the mosaicism caused by X-inactivation. Mutation analysis of the OTC gene is a safer and less invasive approach to confirm the diagnosis. Since OTC deficiency and diabetes have different dietary implications the treatment is challenging.
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Glycosylated hemoglobin A
- HHH syndrome:
We thank Prof. Vivian E. Shih for the 14C-ornithine incorporation measurements in fibroblasts.
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