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Quantitative Requirements of Docosahexaenoic Acid for Neural Function in Children With Phenylketonuria

Not Applicable
Completed
Conditions
Phenylketonuria
Interventions
Dietary Supplement: microalgal oil
Dietary Supplement: high oleic sunflower oil
Registration Number
NCT00909012
Lead Sponsor
Ludwig-Maximilians - University of Munich
Brief Summary

Patients with phenylketonuria (PKU) have an inborn error in the metabolism of the amino acid phenylalanine (Phe) and thus must follow a strictly controlled protein-restricted diet from early infancy. This protein-restricted diet is devoid of natural dietary sources of n-3 long chain polyunsaturated fatty acids (LC-PUFA), such as eggs, meat, milk or fish. Therefore, blood concentrations of n-3 LC-PUFA, especially of docosahexaenoic acid (DHA) are reduced in PKU children compared to healthy controls. DHA availability is considered important for optimal neurological function. Previous studies have shown that neural function of PKU children is improved by high dose supplementation of fish oil providing DHA, as shown by significant improvements of both visual evoked potential latencies and of fine motor skills and coordination, but no dose response relationship has been established so far.

This multicentric double-blind randomized trial aims at determining quantitative DHA requirements for optimal neural function in PKU children. Patients with classical PKU from several major treatment centers in Europe will be randomized to receive between 0 and 8 mg of DHA per kg body weight daily for a duration of 6 months. Biochemical (fatty acid composition of plasma phospholipids, lipoprotein metabolism and metabolic profiles), and functional testing (visual evoked potentials, fine motor skills, cognitive function and markers of immune function) will be performed at baseline and after 6 months. Intake per kg body weight will be related to outcome parameters and thus a possible dose response relationship will be defined. The results from this study are expected to contribute to the improvement of the diet of PKU patients, but they also have the potential to help defining quantitative DHA needs of healthy children.

The primary hypothesis is that supplementation with DHA improves visual function in children with PKU.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
114
Inclusion Criteria
  • Children with classical PKU, who have been diagnosed and treated from the newborn period onwards
  • Classical PKU must have been established by a baseline plasma phenylalanine (PHE) level >1200 µmol/L or detection of underlying mutations
  • Children are clinically healthy besides classical PKU
  • Good metabolic control (a minimum of 2 Phe-values during the last 6 months are needed with average Phe values being below 480 µmol/L in the last 6 months)
  • No n-3 LC-PUFA supplementation for at least 6 months before enrolment
  • Written informed consent of parents exists
Exclusion Criteria
  • Severe neurological symptoms
  • History of neurological disease
  • Children are unable to take DHA-capsules regularly
  • Acute illness, especially infections at the time of clinical examination/testing
  • Children with weight/height over the 97th percentile or below the 3rd percentile
  • Known hypersensitivity to fish oil products

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
2microalgal oil-
3microalgal oil-
1high oleic sunflower oil-
4microalgal oil-
5microalgal oil-
Primary Outcome Measures
NameTimeMethod
latency of visually evoked potentialsassessed basally (before intervention start) and at the end of the 6 month intervention period
Secondary Outcome Measures
NameTimeMethod
fatty acid composition of plasma phospholipidsassessed basally (before intervention start) and at the end of the 6 month intervention period
test of reaction timeassessed basally (before intervention start) and at the end of the 6 month intervention period
fine motor skillsassessed basally (before intervention start) and at the end of the 6 month intervention period

Trial Locations

Locations (6)

Zentrum für Kinder- und Jugendmedizin

🇩🇪

Heidelberg, Germany

LMU

🇩🇪

Muenchen, Germany

Department of Pediatrics, San Paolo Hospital Milano

🇮🇹

Milano, Italy

The Childrens Hospital Birmingham

🇬🇧

Birmingham, United Kingdom

Department of Pediatrics, IFIMAV-Hospital M. Valdecill

🇪🇸

Santander, Spain

Department of Pediatrics, Great Ormond Street Hospital for Sick Children

🇬🇧

London, United Kingdom

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