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Brain Aging in Phenylketonuria

Brain Aging in Patients With Phenylketonuria

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Background: Historically, the primary goal in managing phenylketonuria (PKU) has been to prevent severe and irreversible intellectual disability, as well as to address nutritional deficiencies that could lead to growth impairments or intellectual decline. Since the introduction of neonatal PKU screening in the mid-1960s, early treatment during childhood with a low phenylalanine diet or pharmacological interventions have been effective and prevent severe long-term sequelae. However, concerns persist that insufficient treatment during adulthood may cause subtle and, over time, possibly increasing cognitive and brain alterations. Recently, the first generation of early-treated patients has reached mid-adulthood. Hence, there is an urgent need to understand how PKU and metabolic control impact cognitive and brain aging and vice versa. The investigators preliminary cross-sectional findings suggest that brain aging trajectories may diverge significantly between patients with PKU and healthy controls in mid-adulthood. Until now, no comprehensive research has longitudinally tracked brain aging in patients with PKU through MRI markers and their correlation with cognition, metabolic control, and cardiometabolic risk factors. The "brain age" approach enables the identification of individual health characteristics and risk patterns for age-related changes. The evaluation of brain age in addition to the chronological age allows for the development and monitoring of personalized neuroprotective treatments and interventions. Advancing the investigators understanding of disease progression during aging in patients with PKU and identifying strategies for preventing potential harm later in life is of utmost importance for patients' well-being and clinical practice and, through this, follows the WHO's brain health plan. Study aims: This longitudinal study will, for the first time, investigate the trajectory of brain aging relative to chronological aging across early and middle adulthood in individuals with PKU compared to healthy controls. Data collected in the investigators previous SNSF study (Nr 192706; 184453) will serve as baseline data and allow the examination of brain health by means of brain age modeling. The association between brain age trajectories and cognitive performance, metabolic control, and cardiometabolic risk factors will be studied to disentangle risk patterns of accelerated brain aging in patients with a rare disease. Relevance of the study: This study will show whether and how the brain aging trajectory is accelerated in patients with PKU and will determine the functional relevance of brain aging with respect to cognitive performance and metabolic control (i.e., phenylalanine levels). This is one of the first studies to closely examine long-term brain and cognitive changes in PKU during early and mid-adulthood. Its findings could provide valuable insights into the long-term effects of PKU on brain structure and aging processes. Furthermore, the results may support the development of future treatment strategies and improve the quality of life for adults with PKU.

Who May Be Eligible (Plain English)

Patients with PKU Who May Qualify: - Participation in PICO-Study and/or: - PKU diagnosed after a positive newborn screening - Treatment with Phe-restricted diet starting within the first 30 days of life - Age ≥18 years - Written willing to sign a consent form Who Should NOT Join This Trial: - Patients with PKU not following a Phe-restricted diet within 6 months before the study - Phe concentration above 1600 µmol/L within 6 months before the study - Concomitant disease states suspected to significantly affect primary or secondary outcomes - Women who are pregnant or who are breast feeding - Conditions interfering with MRI such as magnetic (metallic) particles in the skull or brain, cardiac pacemaker, deep brain stimulators, cochlear implant, braces or permanent retainers Healthy controls Who May Qualify: - Age ≥18 years - Written willing to sign a consent form Who Should NOT Join This Trial: - Concomitant disease states suspected to significantly affect primary or secondary outcomes - Women who are pregnant or who are breast feeding - Inability to follow the procedures of the study, e. g. due to language problems (lack of fluency in German or French), psychological disorders, dementia, etc. of the participant - Conditions interfering with MRI such as magnetic (metallic) particles in the skull or brain, cardiac pacemaker, deep brain stimulators, cochlear implant, braces or permanent retainers Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Patients with PKU Inclusion Criteria: * Participation in PICO-Study and/or: * PKU diagnosed after a positive newborn screening * Treatment with Phe-restricted diet starting within the first 30 days of life * Age ≥18 years * Written informed consent Exclusion Criteria: * Patients with PKU not following a Phe-restricted diet within 6 months before the study * Phe concentration above 1600 µmol/L within 6 months before the study * Concomitant disease states suspected to significantly affect primary or secondary outcomes * Women who are pregnant or who are breast feeding * Conditions interfering with MRI such as magnetic (metallic) particles in the skull or brain, cardiac pacemaker, deep brain stimulators, cochlear implant, braces or permanent retainers Healthy controls Inclusion Criteria: * Age ≥18 years * Written informed consent Exclusion Criteria: * Concomitant disease states suspected to significantly affect primary or secondary outcomes * Women who are pregnant or who are breast feeding * Inability to follow the procedures of the study, e. g. due to language problems (lack of fluency in German or French), psychological disorders, dementia, etc. of the participant * Conditions interfering with MRI such as magnetic (metallic) particles in the skull or brain, cardiac pacemaker, deep brain stimulators, cochlear implant, braces or permanent retainers

Locations (1)

University Hospital Inselspital, Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism (UDEM)
Bern, Switzerland