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January 2007

Ornithine Transcarbamylase Deficiency Presenting as Encephalopathy During Adulthood Following Bariatric Surgery

Author Affiliations

Author Affiliations: Departments of Neurology (Drs Hu, Kantarci, Dyck, Lucchinetti, and Tippmann-Peikert), Medical Genetics (Drs Merritt and McGrann), and Pulmonary and Critical Care Medicine (Dr Tippmann-Peikert), Mayo Clinic College of Medicine, Rochester, Minn.

Arch Neurol. 2007;64(1):126-128. doi:10.1001/archneur.64.1.126

Background  Neurological complications following bariatric surgery are rare. Whereas nutritional deficiencies are the most common cause of neurological symptoms, the unmasking of previously subclinical metabolic disorders can also lead to significant morbidity.

Objective  To characterize the clinical presentation, serum biochemical fluctuations, and functional enzymatic analysis of a case of functional ornithine transcarbamylase deficiency unmasked by a dietary change following bariatric surgery.

Design  Case report.

Setting  Tertiary referral center, hospital (inpatient) setting.

Patient  A 29-year-old woman who presented with intermittent encephalopathy associated with recurrent hyperammonemia.

Interventions  Clinical, biochemical, and mutational studies.

Results  The pattern of intermittent hyperammonemia and encephalopathy following oral and parenteral nutrition suggested a urea cycle abnormality. Functional enzymatic assay results showed markedly reduced ornithine transcarbamylase activity in the absence of known coding mutations.

Conclusion  Previously asymptomatic ornithine transcarbamylase deficiency should be suspected in adult patients who develop recurrent hyperammonemia and encephalopathy following bariatric surgery.

Obesity and overweight affect more than 60% of the adults in the United States and pose a major challenge in health care.1 Bariatric surgery is highly effective in reducing weight and improving the morbidity and mortality associated with obesity.2 Neurological complications following bariatric surgery are infrequent and may include peripheral neuropathy and encephalopathy.3,4 Deficiencies in vitamin B12 and folate represent common causes of neurological complications associated with bariatric surgery, but other neurological disorders, including stroke and central pontine myelinolysis, have been reported.5,6

Herein we describe a patient who developed encephalopathy following bariatric surgery secondary to a previously undiagnosed urea cycle disorder.

Report of a case

A 29-year-old right-handed white woman with morbid obesity underwent elective bariatric surgery. She had no complications in the immediate postoperative period and was placed on a high-protein, high-fat, and low-carbohydrate diet, along with an over-the-counter multivitamin formulation for nutritional supplementation. Four weeks later, she was hospitalized with proximal, painful paresthesias in her legs that spread gradually, significant extremity weakness, and confusion. Magnetic resonance imaging showed symmetrically increased T2 hyperintensities in the anterosuperior cerebellar hemispheres consistent with posterior reversible encephalopathy syndrome. Intravenous thiamine replacement was initiated because her multivitamin formulation contained insufficient thiamine, but she continued to have fluctuating symptoms of mild encephalopathy. Six months after bariatric surgery, she again became intermittently encephalopathic with symptoms of somnolence, perseveration, echolalia, and difficulties with short-term memory. Her serum ammonia level was found to be elevated at 72 μg of nitrogen per deciliter (42.3 μmol/L), with markedly abnormal liver function test results showing an aspartate aminotransferase level of 467 U/L and an alanine aminotransferase level of 251 U/L. She was treated with oral lactulose, and the ammonia level gradually normalized. Repeat magnetic resonance imaging showed resolution of the cerebellar abnormalities. No clear etiology for the encephalopathy was identified, and she continued to have recurrent symptomatic hyperammonemia, which was effectively treated with lactulose and intravenous hydration. However, aggressive hydration and prolonged malnutrition also led to significant hypoalbuminemia and peripheral edema. Given her recurrent episodes of somnolence and cognitive changes, she was transferred to our institution for further evaluation. The patient's family history was unknown because she had been adopted. She had no children or history of miscarriage.

Physical examination revealed an obese, ill-appearing young woman with marked generalized edema, skin hyperpigmentation, and hyperkeratotic changes over her joints. Neurological examination showed her to be anxious but alert with no cranial nerve dysfunction. She had diffuse weakness in all extremities with marked allodynia. Limb movement was further impeded by severe peripheral edema. Deep tendon reflexes were absent throughout and plantar responses were flexor bilaterally. She was unable to stand owing to pain and weakness. Liver function test results showed mildly elevated levels of aspartate aminotransferase (58 U/L), alanine aminotransferase (44 U/L), and serum ammonia (51 μg of nitrogen per deciliter [29.9 μmol/L] [reference range, <50 μg/dL (<29.4 μmol/L)]). Other laboratory abnormalities included hypoalbuminemia of 2.1 g/dL (reference range, 3.4-4.7 g/dL), an elevated manganese level of 1.2 ng/mL (21.84 nmol/L) (reference range, 0.4-0.85 ng/mL [7.3-15.5 nmol/L]), a low serum copper level of 57 μg/dL (8.9 μmol/L) (reference range, 75-145 μg/dL [11.78-22.77 μmol/L]), and a low serum zinc level of 30 μg/dL (4.6 μmol/L) (reference range, 66-110 μg/dL [10.1-16.83 μmol/L]). Serum levels of vitamins B12 and E, thiamine, and folate were all within normal limits. Intravenous thiamine hydrochloride supplementation was continued. Because the ammonia level had normalized, lactulose therapy was discontinued and a regular diet was initiated on hospital day 1.

On hospital day 5, she became acutely obtunded without any new focal neurological deficits. The serum ammonia level was elevated at 156 μg of nitrogen per deciliter (91.6 μmol/L), with an elevated γ-glutamyltransferase level of 351 U/L. Lactulose therapy was reinitiated and her serum ammonia level started to decrease (Figure, open arrow). On hospital day 7, total parenteral nutrition was begun to improve her caloric intake. This led to another elevation of her serum ammonia level despite continued lactulose treatment (Figure, black arrow). Because of recurrent hyperammonemia after protein loading, an inborn error of metabolism was suspected. The urine level of orotic acid was found to be mildly elevated at 3.2 mmol per mole of creatinine (reference range, 0.4-1.2 mmol per mole of creatinine). Quantitative plasma amino acid analysis showed an elevated glutamine level at 29.5 mg/dL (2018 μmol/L) (reference range, 3.0-11.0 mg/dL [205-753 μmol/L]), a low normal citrulline level of 0.25 mg/dL (17 μmol/L) (reference range, 0.21-0.96 mg/dL [12-55 μmol/L]), and a normal arginine level of 1.78 mg/dL (102 μmol/L) (reference range, 0.26-2.18 mg/dL [15-128 μmol/L]). The elevated glutamine level was thought to reflect the persistent increase in her serum ammonia level. Other biochemical studies, including urine organic acid, plasma acylcarnitine, lactate, creatine kinase, biotinidase, and urine porphyrin profiles, were normal. A liver biopsy specimen showed moderate steatohepatitis. The serum analysis suggested a biochemical diagnosis of ornithine transcarbamylase (OTC) deficiency. Genetic testing for OTC mutations was negative for known coding mutations, but functional testing using fresh frozen liver tissue from the biopsy revealed less than 1% of normal enzymatic activity. Modified low-protein total parenteral nutrition with carnitine supplementation was begun. The patient's serum ammonia level and mental status normalized and remained stable during the remainder of the hospitalization even after discontinuation of lactulose therapy and institution of an oral limited-protein diet. Further inquiry revealed that, since childhood, the patient had routinely felt nauseated after eating meat, leading to avoidance of such products; however, she had increased her intake of protein and fat after the bariatric surgery. In a follow-up visit 1 year later, her cognitive function continued to be stable without any further episodes of encephalopathy.

Levels of serum ammonia in relation to oral and parenteral nutrition during hospitalization. Two peaks of the serum ammonia level corresponded to increased oral intake (open arrow) and full-dose total parenteral nutrition (TPN) (black arrow). No ammonia levels were measured on days 3 and 4 because the patient was asymptomatic. Her serum ammonia level remained normal despite discontinuation of lactulose therapy following institution of an oral low-protein diet. To convert ammonia to micromoles per liter, multiply by 0.587.

Levels of serum ammonia in relation to oral and parenteral nutrition during hospitalization. Two peaks of the serum ammonia level corresponded to increased oral intake (open arrow) and full-dose total parenteral nutrition (TPN) (black arrow). No ammonia levels were measured on days 3 and 4 because the patient was asymptomatic. Her serum ammonia level remained normal despite discontinuation of lactulose therapy following institution of an oral low-protein diet. To convert ammonia to micromoles per liter, multiply by 0.587.


Bariatric surgery remains the most effective therapy for weight reduction in extent and duration,2 and the number of bariatric surgical procedures performed in the United States has more than tripled from 1997 to 2002.7 Neurological complications of bariatric surgery include polyneuropathy, encephalopathy, rhabdomyolysis, stroke, and Guillain-Barré syndrome.3,4 Among patients who develop encephalopathy, thiamine deficiency accounts for nearly 90% of all cases.3,4 Although thiamine deficiency could have initially contributed to this patient's encephalopathy, her recurrent episodic cognitive decline was clearly temporally associated with hyperammonemia following oral or parenteral feedings with a high protein content (Figure). Posterior reversible encephalopathy syndrome was considered an alternate cause of her early encephalopathy because the syndrome is associated with mental status changes in addition to headache, vomiting, and seizures. However, her encephalopathy persisted on resolution of brain magnetic resonance imaging abnormalities, and she had a rapid recovery after the correction of hyperammonemia. Thus, her cyclical encephalopathy was most likely the result of the underlying urea cycle abnormality. Before the diagnosis of functional OTC deficiency, intravenous hydration and lactulose therapy resulted in reduction of the serum ammonia concentration and resolution of the associated encephalopathy. In the absence of severe liver disease, clinical suspicion for a metabolic cause of hyperammonemic encephalopathy led to the correct diagnosis. Allopurinol loading as an alternative diagnostic test was not performed in our patient because the diagnosis was attempted through genetic and enzymatic activity assays.8 Additional DNA and enzymatic studies in family members were not possible because she had been adopted.

Ornithine transcarbamylase deficiency is an X-linked disorder of the urea cycle and has an incidence of 1 in 80 000 live births.9 Female carriers have variable clinical symptoms and age at onset, possibly as a consequence of random X-chromosome inactivation. Approximately 85% of female carriers will remain asymptomatic during their lifetime, but serious neurological complications, including coma, have been reported in previously healthy female carriers.10,11 Healthy carriers may voluntarily restrict their daily protein intake, reflected in a decreased amount of excreted urea nitrogen and total nitrogen.8 Mutational analysis of OTC will detect 70% to 80% of coding mutations,12 and a mutation in the noncoding regions or a larger gene deletion that alters the level of enzyme expression may explain the low level of OTC activity in our patient. It is surprising that this very low enzyme activity was associated with symptomatic onset after childhood. However, there is substantial nitrogen incorporation into urea even in patients with very low in-vitro OTC activity and late-onset OTC deficiency.13 Hence, our patient's lifelong dietary pattern may reflect subclinical disease that manifested fully only after her bariatric surgery. She is at increased risk for postpartum encephalopathy with future pregnancies10,11 and for metabolic decompensation with future stressors such as surgery or catabolic states.

In summary, we present a woman with functional OTC deficiency who developed recurrent encephalopathy after bariatric surgery temporally associated with hyperammonemia. Her lifelong pattern of meat avoidance was a possible clue to her subclinical disease, and the postsurgical diet pattern change and total parenteral nutrition for malnutrition likely served as provocative protein loads. In adult patients who develop ammonia-related encephalopathy after bariatric surgery, OTC deficiency and other urea cycle abnormalities should be strongly considered.

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Article Information

Correspondence: Maja Tippmann-Peikert, MD, Department of Neurology, Mayo Clinic College of Medicine, Mayo Building, East 8, 200 First St SW, Rochester MN 55905 (tippmannpeikert.maja@mayo.edu).

Accepted for Publication: July 7, 2006.

Author Contributions: Drs Hu and Kantarci contributed equally to this manuscript. Study concept and design: Hu, Dyck, and Tippmann-Peikert. Acquisition of data: Hu, Kantarci, Merritt, McGrann, Lucchinetti, and Tippmann-Peikert. Analysis and interpretation of data: Hu, Kantarci, Merritt, McGrann, Dyck, and Tippmann-Peikert. Drafting of the manuscript: Hu, Kantarci, and Tippmann-Peikert. Critical revision of the manuscript for important intellectual content: Hu, Kantarci, Merritt, McGrann, Dyck, Lucchinetti, and Tippmann-Peikert. Study supervision: Kantarci, Merritt, McGrann, Dyck, Lucchinetti, and Tippmann-Peikert.

Financial Disclosure: None reported.

National Center for Health Statistics Health United States 2003 With Chartbook on Trends in the Health of Americans.  Hyattsville, Md: National Center for Health Statistics; 2003
Christou  NVSampalis  JSLiberman  M  et al.  Surgery decreases long-term mortality, morbidity, and health care use in morbidly obese patients.  Ann Surg 2004;240416- 423PubMedGoogle ScholarCrossref
Koffman  BMGreenfield  LJAli  IIPirzada  NA Neurologic complications after surgery for obesity.  Muscle Nerve 2006;33166- 176PubMedGoogle ScholarCrossref
Thaisetthawatkul  PCollazo-Clavell  MLSarr  MGNorell  JEDyck  PJ A controlled study of peripheral neuropathy after bariatric surgery.  Neurology 2004;631462- 1470PubMedGoogle ScholarCrossref
Alvarez-Leite  JI Nutrient deficiencies secondary to bariatric surgery.  Curr Opin Clin Nutr Metab Care 2004;7569- 575PubMedGoogle ScholarCrossref
Bloomberg  RDFleishman  ANalle  JEHerron  DMKini  S Nutritional deficiencies following bariatric surgery: what have we learned?  Obes Surg 2005;15145- 154PubMedGoogle ScholarCrossref
Flum  DRSalem  LElrod  JADellinger  EPCheadle  AChan  L Early mortality among Medicare beneficiaries undergoing bariatric surgical procedures.  JAMA 2005;2941903- 1908PubMedGoogle ScholarCrossref
Maestri  NELord  CGlynn  MBale  ABrusilow  SW The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.  Medicine (Baltimore) 1998;77389- 397PubMedGoogle ScholarCrossref
Brusilow  SWHorwich  AL Urea Cycle Enzymes.  New York, NY: McGraw-Hill Co; 1995
Arn  PHHauser  ERThomas  GHHerman  GHess  DBrusilow  SW Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus: a cause of postpartum coma.  N Engl J Med 1990;3221652- 1655PubMedGoogle ScholarCrossref
Cordero  DRBaker  JDorinzi  DToffle  R Ornithine transcarbamylase deficiency in pregnancy.  J Inherit Metab Dis200528237240 [published correction appears in J Inherit Metab Dis. 2005;28:811]. PubMedGoogle Scholar
Tuchman  MMorizono  HRajagopal  BSPlante  RJAllewell  NM The biochemical and molecular spectrum of ornithine transcarbamylase deficiency.  J Inherit Metab Dis 1998;21(suppl 1)40- 58PubMedGoogle ScholarCrossref
McCullough  BAYudkoff  MBatshaw  MLWilson  JMRaper  SETuchman  M Genotype spectrum of ornithine transcarbamylase deficiency: correlation with the clinical and biochemical phenotype.  Am J Med Genet 2000;93313- 319PubMedGoogle ScholarCrossref