Neuroimaging and Neuropsychological Outcomes in Urea Cycle Disorders (UCD)

  • STATUS
    Recruiting
  • End date
    Dec 26, 2024
  • participants needed
    56
  • sponsor
    Children's National Research Institute
Updated on 16 February 2022
cognitive impairment
deficiency
encephalopathy
brain damage
coma
neurological injury
ornithine
citrulline
brain pathology
hyperammonemia
argininosuccinic aciduria
citrullinemia
arginosuccinate
myo-inositol
Accepts healthy volunteers

Summary

In proximal urea cycle disorders (UCD), particularly ornithine transcarbamylase deficiency (OTCD), hyperammonemia (HA) causes increased brain glutamine (Gln) which perturbation is thought to be at the core of the neurological injury. In contrast, in distal UCD such as citrullinemia (argininosuccinate synthetase deficiency; (ASSD) and argininosuccinic aciduria (argininosuccinate lyase deficiency); (ASLD) cognitive impairment and neuropsychiatric disease are common even in the absence of acute HA. As a consequence, both citrulline and argininosuccinate (ASA) or their metabolic products have been implicated as neurotoxic. In this project the investigators will use state-of- the-art neuroimaging and neuropsychological methods to investigate whether patients with OTCD have chronically elevated brain Gln and reduced myo-inositol (mI) levels that correlate with regional brain structural abnormalities and neurocognitive dysfunction. The researchers will further investigate whether during an acute episode of HA elevated brain Gln and decreased mI levels correlate with the magnitude of cytotoxic edema and whether a Gln/mI ratio threshold can be identified at which the cytotoxic edema is followed by cell loss. Finally, the researchers will investigate whether regions of brain damage in ASSD and/or ASLD are distinct from those in OTCD and compare brain Gln levels in ASSD and ASLD in the absence of HA to those in OTCD. The investigators will also seek to determine if brain citrulline and ASA can be identified in the brains of patients with distal UCD and whether they correlate with brain abnormalities seen in MRI and neuropsychological testing. This project will elucidate the chronology of brain pathology both in acute hyperammonemia and chronic UCD and whether, proximal and distal UCD differ in their pathophysiology of brain damage.

Description

UCDs are a group of rare genetic diseases that affect how protein is broken down in the body. The cause of UCDs is a deficiency in one of eight enzymes responsible for removing ammonia, a waste product of protein metabolism, from the bloodstream. Normally, ammonia is converted into urea and then removed from the body in the form of urine. However, in people with UCDs, ammonia accumulates unchecked and is not removed from the body. Toxic levels of ammonia can build up and cause irreversible neurologic damage that can affect metabolism, cognition, sensation, and movement. This study will focus on the most common enzyme disorder among UCDs, ornithine transcarbamylase deficiency (OTCD), a disorder inherited from mothers. Using different types of magnetic resonance imaging (MRI), this study will evaluate how UCD-related neurologic injuries affect metabolism, cognition, sensation, and movement in adults with OTCD.

This study will be separated into three sections. The first study will study longitudinal changes in OTCD. The second section will study the recovery of OTCD participants from a hyperammonemic episode over time. The third section will be a longitudinal study of the distal urea cycle disorders. In all cases, participants in this study will attend an initial study visit that will include a review of medical history, current symptoms, impairments, and diet history; a physical exam; a full neurological exam; and cognitive and motor testing. During this visit, participants will undergo imaging studies and additional cognitive and motor testing over a 1-2-day period. This will include standard MRI studies and four sessions consisting of functional MRI (fMRI) (CNMC only), diffusion tensor imaging, and 1H magnetic resonance spectroscopy. For the fMRI study, participants perform various motor and behavioral tasks while in the imaging scanner. Magnetic resonance spectroscopy (MRS) is used to study and evaluate the chemical makeup of specific brain areas. Diffusion tensor imaging is used to assess myelination of major brain pathways and their alteration in disease states. This study will involve multiple time point participation. The study will be conducted at Children's National Medical Center and Boston Children's Hospital.

Details
Condition Urea Cycle Disorders
Treatment MRI, Behavioral, Behavioral
Clinical Study IdentifierNCT02935283
SponsorChildren's National Research Institute
Last Modified on16 February 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Inclusion criteria for group 1
Confirmed diagnosis of ornithine transcarbamylase deficiency (OTCD) by genetic analysis (genotype) and/or enzyme analysis with at least a single episode of HA hyperammonemic (HA) encephalopathy
Ability to undergo MRI without sedation
Ages 7 - 50 years
Ability to provide informed consent or assent to the procedures
Healthy controls (age and gender matched)
Inclusion criteria for group 2
Males and females with a UCD who are having an acute metabolic crisis, with ammonia levels between 100-300 M
Subjects must be awake, and not comatose and able to maintain patent airway on their own and in the opinion of the examining physician, medically stable without risk for acute decompensation and must continue to be stable based on visual contact, vital sign measurement and voice contact with subjects while in the scanner
Age range 7-30 years
Able to undergo neuroimaging safely (i.e. without ferromagnetic devices)
Sexually active female of childbearing potential must agree to urine pregnancy test
Admitted to the hospital for treatment of HA at one of the 4 sites for this study
Can be subjects who were originally enrolled in aim 1 who then have HA (they will cross over to aim 2)
Inclusion criteria for group 3
Confirmed diagnosis of arginosuccinate ASSD, and ASLD by genotype and/or enzyme analysis or healthy age and gender matched control
Ability to undergo MRI without sedation
Age 7 - 30 years
Able to provide informed consent or assent to the procedures

Exclusion Criteria

Exclusion Criteria for group 1
Inability to undergo MRI without sedation
Metal implants, including orthodontic braces
Other health conditions contra-indicated in MRI
Medically unstable at time of scheduled research visit
Unable to provide informed consent or assent to the procedures
Exclusion criteria for group 2
Ammonia level > 300 M, or <100 M
Presence of coma and/or inability to maintain a patent airway
Age <7 or >30 years
Subject with ferromagnetic device that precludes safe MRI imaging
Pregnant female
Unstable medically, at risk for decompensations
Combative, or severely neurologically compromised irrespective of ammonia level and showing declining medical status in the scanner based on visual, voice contact and electronic HR monitoring
Subjects must be awake, and not comatose and able to maintain patent airway on
their own
Exclusion criteria for group 3
Inability to undergo MRI without sedation
Metal implants, including orthodontic braces
Other health conditions contra-indicated for MRI
Medically unstable at time of scheduled research visit
Unable to provide informed consent or assent
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