PhenylketonuriaNCT02297347
The Brain and Neuropsychological Functioning in Adults With Sapropterin Dihydrochloride Treated Phenylketonuria
An observational study of Phenylketonuria, run by Boston Children's Hospital at 1 site in United States.
Trial summary
Newborn screening and early treatment prevent the most severe manifestations of phenylketonuria (PKU). However, executive functioning deficits, attention deficit disorder, slow processing speed, and visual-motor problems commonly occur. Many adults with this disorder also suffer depression and anxiety. Read more about this study
- Who is it for?
- Ages 18 to 55 yearsHealthy volunteers can take part
- Conditions the study is for
- Phenylketonuria
- How many people
- 10 participants
- Where
- 1 siteUnited States
- Study dates
- Apr 2015to Apr 2017
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 55 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Adults with PKU on Kuvan treatment for at least one month prior to enrolling in the study.
Who may be able to join
- Adult with classic PKU currently on Kuvan treatment for at least one month.
- Age 18-55 years
- Medical Records available that include blood phenylalanine levels during the first 6 years of life.
- Capable of providing informed consent
- Able to undergo MRI procedures without sedating medication
- Does not have metal implants, braces, or permanent retainers.
Who cannot join
- Mild PKU or mild hyperphenylalaninemia
- Less than 18 years old or greater than 55 years old
- No medical records available for the first 6 years of life
- Not capable of providing informed consent
- Not able to undergo MRI without sedating medication
- Has metal implants, braces or permanent retainers
- Currently involved in any clinical trial
Trial locations and contacts
1 site in 1 country.
United States1 site
Boston Children's Hospital
Boston, Massachusetts, 02115
About this study
Official title: The Brain, Neurological Features and Neuropsychological Functioning in Adults With Sapropterin Dihydrochloride Treated Phenylketonuria
Newborn screening and early treatment prevent the most severe manifestations of phenylketonuria (PKU). However, executive functioning deficits, attention deficit disorder, slow processing speed, and visual-motor problems commonly occur. Many adults with this disorder also suffer depression and anxiety. In this study the investigators will examine adults with PKU on sapropterin dihydrochloride (Kuvan) treatment for PKU and compare their results to those of subjects with PKU not on Kuvan. Using magnetic resonance imaging (MRI) techniques, including novel MR spectroscopy (MRS) the investigators hope to discover why this distinct constellation of deficits occurs in PKU. Adult subjects with PKU will undergo a comprehensive MRI evaluations, including a novel method of MR spectroscopy to determine brain phenylalanine levels. In addition, participants will receive neurological and neuropsychological examinations and dietary evaluation.
Read the detailed description
Phenylketonuria (PKU, OMIM 261600), an autosomal recessive disorder, affects approximately 1:11,000 individuals in the United States. In PKU, mutations in the gene responsible for the liver enzyme phenylalanine hydroxylase (PAH) result in reduced or absent conversion of phenylalanine (Phe) to tyrosine (Tyr) and subsequently to elevated plasma concentrations of Phe and reduced concentrations of Tyr (Scriver and Kaufman, 2001). Untreated PKU results in progressive, neurological decline by 6-12 months of age (Koch et al, 1971). Even with early detection and treatment with a Phe-restricted diet, patients experience neurocognitive deficits (Waisbren et al, 1994) and psychiatric disturbances as they get older (Brumm et al, 2010; Bilder et al, 2013; Weglage et al, 2013) as well as white matter abnormalities detected through magnetic resonance imaging (MRI) (Mastrangelo et al, 2015).
In treated PKU, neuropsychological functioning is associated with exposure to elevated blood phenylalanine levels (Jahja et a;. 2017; and decreased blood tyrosine (Luciana, Sullivan, Nelson, 2001). However, the extent to which these biomarkers confer risks to cognitive and emotional well-being varies dramatically, with some individuals experiencing serious deficits and others functioning normally despite equally high phenylalanine or depleted tyrosine levels in blood (Rajabi, Waisbren and Levy, 2016; Manti et al, 2017 ). One explanation is that blood Phe and Tyr do not represent exposure in the brain (Diamond et al, 1997; Surtees and Blau, 2000).
Previously, we reported on an improved method for measuring brain Phe and brain Tyr in PKU (Waisbren et al, 2016) using two dimensional shift correlated magnetic resonance spectroscopy (COSY) (Thomas et al, 2001). This allows for the unambiguous identification of cerebral metabolites that could not be detected using conventional MRS methods due to spectral overlap. By obtaining multiple acquisitions at different echo times, a second chemical shift domain allows for metabolites to be identified by two chemical shifts instead of just one based on scalar coupling of different proton groups. The concentration of the metabolite is therefore shown in the third dimension. By visualizing the COSY data in three dimensions, smaller resonances that would have been obscured by larger resonances can be measured (Figure 1). Different brain regions, separating white and gray matter tissue, can be assessed with this method as a smaller voxel can be used.
In our previous study, we demonstrated that COSY could be used to quantify brain Phe and brain Tyr in two brain regions in adults with treated PKU without the need for a phenylalanine load. We also examined the relationship between these biomarkers and neuropsychological functioning and found that associations were in the expected direction, with higher brain Phe and lower brain Tyr related to poorer functioning (Waisbren et al, 2016).
The aims of the study reported here were to examine the relationships between blood and brain concentrations of Phe and Tyr in patients on sapropterin dihydrochloride (BH4 or Kuvan) and to assess the relationships between these biomarkers and neuropsychological functioning.
- Conditions
- Phenylketonuria
- Medical subject headings
- Phenylketonurias
What is being measured
The primary outcome is the main question the study is designed to answer.
Phenylalanine (phe) level in the brain as determined by MR Spectroscopy
Brain phe described as umol/L through MR Spectroscopy in both the , posterior cingulate gyrus (PCG) and parietal white matter (PWM)
Measured: one day
Secondary outcomes (2)
Full Scale IQ
Full Scale IQ is obtained from the Wechsler Abbreviated Scale of Intelligence
Measured: one day
Brain tyrosine (tyr) level as determined by MR Spectroscopy
Brain tyr described as umol/L through MR Spectroscopy in both the , posterior cingulate gyrus (PCG) and parietal white matter (PWM)
Measured: one day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Nov 2014 (estimated)
- Study startApr 2015
- Primary completionApr 2017
- Study completionApr 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for PhenylketonuriaStudies of the same condition, open and under way.
- More trials run by Boston Children's HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boston Children's Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Susan Waisbren, Boston Children's Hospital
- Investigators
- Susan E. Waisbren, PhD, Principal investigator, Boston Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02297347
- Sponsor's protocol ID
- IRB-P00015326
- Status last verified
- Feb 2018
- First submitted
- 19 Nov 2014
- Last updated
- 5 Feb 2018
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Feb 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Brain, Neurological Features and Neuropsychological Functioning in Adults With Sapropterin Dihydrochloride Treated Phenylketonuria
- ClinicalTrials.gov ID
- NCT02297347
- Acronym / sponsor ID
- IRB-P00015326
- Conditions
- Phenylketonuria
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- Boston Children's HospitalUniversity, hospital or other
- Collaborators
- Beth Israel Deaconess Medical Center, Brigham and Women's Hospital
- Study start
- Apr 2015
- Primary completion
- Apr 2017 (actual)
- Study completion
- Apr 2017 (actual)
- First posted
- 21 Nov 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Newborn screening and early treatment prevent the most severe manifestations of phenylketonuria (PKU). However, executive functioning deficits, attention deficit disorder, slow processing speed, and visual-motor problems commonly occur. Many adults with this disorder also suffer depression and anxiety. In this study the investigators will examine adults with PKU on sapropterin dihydrochloride (Kuvan) treatment for PKU and compare their results to those of subjects with PKU not on Kuvan. Using magnetic resonance imaging (MRI) techniques, including novel MR spectroscopy (MRS) the investigators hope to discover why this distinct constellation of deficits occurs in PKU. Adult subjects with PKU will undergo a comprehensive MRI evaluations, including a novel method of MR spectroscopy to determine brain phenylalanine levels. In addition, participants will receive neurological and neuropsychological examinations and dietary evaluation.
Detailed description
Phenylketonuria (PKU, OMIM 261600), an autosomal recessive disorder, affects approximately 1:11,000 individuals in the United States. In PKU, mutations in the gene responsible for the liver enzyme phenylalanine hydroxylase (PAH) result in reduced or absent conversion of phenylalanine (Phe) to tyrosine (Tyr) and subsequently to elevated plasma concentrations of Phe and reduced concentrations of Tyr (Scriver and Kaufman, 2001). Untreated PKU results in progressive, neurological decline by 6-12 months of age (Koch et al, 1971). Even with early detection and treatment with a Phe-restricted diet, patients experience neurocognitive deficits (Waisbren et al, 1994) and psychiatric disturbances as they get older (Brumm et al, 2010; Bilder et al, 2013; Weglage et al, 2013) as well as white matter abnormalities detected through magnetic resonance imaging (MRI) (Mastrangelo et al, 2015).
In treated PKU, neuropsychological functioning is associated with exposure to elevated blood phenylalanine levels (Jahja et a;. 2017; and decreased blood tyrosine (Luciana, Sullivan, Nelson, 2001). However, the extent to which these biomarkers confer risks to cognitive and emotional well-being varies dramatically, with some individuals experiencing serious deficits and others functioning normally despite equally high phenylalanine or depleted tyrosine levels in blood (Rajabi, Waisbren and Levy, 2016; Manti et al, 2017 ). One explanation is that blood Phe and Tyr do not represent exposure in the brain (Diamond et al, 1997; Surtees and Blau, 2000).
Previously, we reported on an improved method for measuring brain Phe and brain Tyr in PKU (Waisbren et al, 2016) using two dimensional shift correlated magnetic resonance spectroscopy (COSY) (Thomas et al, 2001). This allows for the unambiguous identification of cerebral metabolites that could not be detected using conventional MRS methods due to spectral overlap. By obtaining multiple acquisitions at different echo times, a second chemical shift domain allows for metabolites to be identified by two chemical shifts instead of just one based on scalar coupling of different proton groups. The concentration of the metabolite is therefore shown in the third dimension. By visualizing the COSY data in three dimensions, smaller resonances that would have been obscured by larger resonances can be measured (Figure 1). Different brain regions, separating white and gray matter tissue, can be assessed with this method as a smaller voxel can be used.
In our previous study, we demonstrated that COSY could be used to quantify brain Phe and brain Tyr in two brain regions in adults with treated PKU without the need for a phenylalanine load. We also examined the relationship between these biomarkers and neuropsychological functioning and found that associations were in the expected direction, with higher brain Phe and lower brain Tyr related to poorer functioning (Waisbren et al, 2016).
The aims of the study reported here were to examine the relationships between blood and brain concentrations of Phe and Tyr in patients on sapropterin dihydrochloride (BH4 or Kuvan) and to assess the relationships between these biomarkers and neuropsychological functioning.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 55 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Adults with PKU on Kuvan treatment for at least one month prior to enrolling in the study.
Key inclusion criteria (6 listed)
- Adult with classic PKU currently on Kuvan treatment for at least one month.
- Age 18-55 years
- Medical Records available that include blood phenylalanine levels during the first 6 years of life.
- Capable of providing informed consent
- Able to undergo MRI procedures without sedating medication
Key exclusion criteria (7 listed)
- Mild PKU or mild hyperphenylalaninemia
- Less than 18 years old or greater than 55 years old
- No medical records available for the first 6 years of life
- Not capable of providing informed consent
- Not able to undergo MRI without sedating medication
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Phenylalanine (phe) level in the brain as determined by MR Spectroscopy
Time frame: one day
Brain phe described as umol/L through MR Spectroscopy in both the , posterior cingulate gyrus (PCG) and parietal white matter (PWM)
2 secondary outcomes
Full Scale IQ
Time frame: one day
Brain tyrosine (tyr) level as determined by MR Spectroscopy
Time frame: one day
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Feb 2018.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Susan E. Waisbren, PhD principal investigator
Boston Children's Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Phenylketonuria, run by Boston Children's Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 5 Feb 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Phenylalanine (phe) level in the brain as determined by MR Spectroscopy (time frame: one day). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Feb 2018.