Assessment & Research

Neuropsychological effects of subsequent exposure to phenylalanine in adolescents and young adults with early-treated phenylketonuria.

Griffiths et al. (1995) · Journal of intellectual disability research : JIDR 1995
★ The Verdict

Ditching the PKU diet at age 10 looks safe for long-term brain and motor skills.

✓ Read this if BCBAs who treat teens with PKU in clinic or school settings.
✗ Skip if Practitioners who only serve clients without metabolic disorders.

01Research in Context

01

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.

02

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.

03

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.

04

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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→ Action — try this Monday

During your next teen session with PKU, run a quick fine-motor timing task and note any slow or errant responses to flag rare late issues.

02At a glance

Intervention
not applicable
Design
quasi experimental
Population
other
Finding
null
Magnitude
negligible

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