Impact of Phenylalanine Elevations on Brain and Cognition in Adult PKU Carriers

Официальное название

The Impact of Phenylalanine Elevations on Metabolic, Cognitive, and Neural Functioning in Adults Heterozygous for Phenylketonuria (PKU)

Обзор

The goal of this clinical trial is to advance our understanding of the cognitive and neurophysiologic sequelae associated with suboptimal phenylalanine (Phe) metabolism in heterozygous carriers of phenylketonuria (PKU). The main questions it aims to answer are: * Do PKU carriers experience prolonged elevations in brain Phe levels following oral ingestion of dietary Phe? * Do PKU carriers experience disruptions in cognitive functioning following oral ingestion of dietary Phe? * Do PKU carriers experience atypical brain activity following oral ingestion of dietary Phe? Researchers will compare PKU carriers and non-carriers following oral ingestion of dietary Phe and a placebo. Participants will: * Consume Phe or a placebo at two separate visits to our facility * At each visit, they will complete a series of MRIs and cognitive tests throughout the day

Подробное описание

Limitations inherent in past studies of phenylketonuria (PKU) carriers (e.g., poor genetic characterization of sample resulting in inclusion of homozygous non-PKU relatives, reliance on rudimentary or overly broad behavioral assessment tools) make it difficult to conclude the extent to which neurophysiologic and cognitive processes are affected in these individuals. To address this gap in the literature, we propose to conduct a double-blind crossover study in a sample of genetically-confirmed sample of 18 heterozygous PKU carriers and 18 non-carriers. A principled investigation of the effects of elevated phenylalanine (Phe) on neurocognition will involve participants performing an fMRI n-back WM task, resting state scan, and a battery of select cognitive tests at 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo. Blood and brain levels of Phe and Tyr will also be assessed at each timepoint.

Вмешательства

• Пищевая добавка Phenylalanine (Phe)
  Oral ingestion of phenylalanine (Phe)
• Пищевая добавка Placebo
  Oral ingestion of Placebo (Vitamin C)

Первичные конечные точки

• Blood Phenylalanine Levels [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Brain Phenylalanine Levels [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Brain Phenylalanine-to-Tyrosine Ratio [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Neural Activity during Go/No-Go Task [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Operational Span Task [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Multi-Source Interference Task [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Grooved Pegboard Test [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• Resting-State Functional Connectivity [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]

Вторичные конечные точки (9)

• Brain concentrations of glutamate, glutathione, creatine, and other metabolites [Срок оценки: 3 timepoints: baseline (pre-load), 2 hours and 4 hours after starting oral administration of Phe or placebo]
• PROMIS Anxiety - Short Form 8a [Срок оценки: Baseline only]
• PROMIS Depression - Short Form 8a [Срок оценки: Baseline only]
• PROMIS Sleep - Short Form 8a [Срок оценки: Baseline only]
• PROMIS Fatigue - Short Form 8a [Срок оценки: Baseline only]
• PROMIS Cognitive Function - Short Form 8a [Срок оценки: Baseline only]
• • Executive Function, Attention, and Speed Symptom Inventory (EASSI) [Срок оценки: Baseline only]
• Adult ADHD Self-Report Scale (ASRS) [Срок оценки: Baseline only]
• Matrix Reasoning subtest from the WASI-2 [Срок оценки: Baseline only]

Критерии участия

Критерии включения

• Age 18-60 years
• For the PKU carrier group: Individuals who are the parent of an individual with PKU or who are otherwise have confirmed PKU carrier status (e.g., a sibling of someone with PKU who has had genetic testing done)
• For the non-carrier group: Individuals who do not have PKU or a family history of PKU

Критерии исключения

• Obesity as defined by a body mass index (BMI) over 30\*
• Taking oral contraceptives on the day of testing session\*
• Positive cotinine urine test showing nicotine use
• History of major neurologic condition (e.g., multiple sclerosis, severe closed head injury, Parkinson's disease)) unrelated to PKU and known to adversely impact brain health and function
• Contraindications for safe MRI participation such as (a) pregnancy or plans to become pregnant during period of study enrollment; or (b) metallic objects inside the body (e.g., surgical staples left in the body following surgery, middle ear prosthesis, metal foreign objects lodged inside the eye, heart pacemakers).

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Перекрёстный дизайн

Маскирование

Двойное слепое

Основная цель

Фундаментальное исследование

Центры проведения

США · 1 центр

• University of Missouri-Columbia — Columbia

Идентификаторы

NCT: NCT07220265 · 2092228 · R21HD115129-01A1

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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