Neuropsychological effects of subsequent exposure to phenylalanine in adolescents and young adults with early-treated phenylketonuria.
Ditching the PKU diet at age 10 looks safe for long-term brain and motor skills.
01Research in Context
What this study did
The team looked at teens and young adults who had been treated for PKU since babyhood.
All had stopped the special low-protein diet at age 10 and had eaten normal food for at least three years.
They gave each person a full battery of thinking, memory, and motor tests to see if the diet break had hurt their skills.
What they found
No clear losses showed up.
Scores for IQ, reaction time, and fine-movement speed looked the same as expected for their age.
The authors say stopping the diet at 10 seems safe for the brain.
How this fits with other research
Szempruch et al. (1993) used a similar teen-to-adult check-up design in autism.
They also ran long tests and found early scores could predict later life skills, just like P et al. tracked early diet choices into teen outcomes.
Baghdadli et al. (2018) followed autistic kids for 15 years and saw most stay on a low-growth path, while P et al. saw PKU kids hold steady after diet stop — the two groups end up different, but both studies warn us to watch the teen years closely.
Sievers et al. (2020) add that in genetic autism subtypes, the age a child first walks or talks shapes later IQ; P et al. show that in PKU, what happens at age 10 (diet stop) does not reshape later scores — timing matters, but in different ways for different conditions.
Why it matters
If you work with teens who have early-treated PKU, you can reassure families that stopping the diet at 10 likely will not harm thinking or motor skills.
Still, keep checking executive functions and self-care in session; rare problems could pop up and you will spot them faster than a yearly clinic visit.
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02At a glance
03Original abstract
Severe mental handicap in phenylketonuria (PKU) can be prevented if dietary treatment is implemented at birth. Controversy remains about the optimum age for terminating treatment. A group of adolescents and young adults with PKU from the West of Scotland Register was identified which had received early treatment, been well-controlled on diet, ceased treatment at 10 years old and subsequently were hyperphenylalaninaemic for 3 years or more. They were given a battery of neuropsychological tests and their results were compared with those of on-diet subjects with PKU and normal controls. The findings generally supported the view that dietary cessation at age 10 is sufficient to prevent a substantial reduction of cognitive and motor ability, and that the central nervous system is probably mature enough to withstand the toxic effects of high blood phenylalanine by then. However, there were minor indications, in keeping with Welsh et al.'s hypothesis [M.C. Welsh, B.F. Pennington, S. Ozonoff, B. Rouse & E.R.B. McCabe (1990) Neuropsychology of early-treated phenylketonuria: specific executive function deficits.
Journal of intellectual disability research : JIDR, 1995 · doi:10.1111/j.1365-2788.1995.tb00540.x