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Improved attention linked to sustained phenylalanine reduction in adults with early‐treated phenylketonuria

Deborah A. Bilder, Georgianne L. Arnold, David Dimmock, Mitzie Grant, Darren Janzen, Nicola Longo, Mina Nguyen‐Driver, Elaina Jurecki, Markus Meriläinen, Gianni Amato, Susan E. Waisbren

2021American Journal of Medical Genetics Part A21 citationsDOIOpen Access PDF

Abstract

Pegvaliase is approved to reduce phenylalanine (Phe) levels for people with phenylketonuria (PKU). PRISM-1 (NCT01819727) and PRISM-2 (NCT01889862) data were analyzed to evaluate the relationship between Phe and inattention in adult participants with PKU. In the modified-intent-to-treat population (N = 156), baseline mean (SE) plasma Phe was 1263 (29) μmol/L and the Attention Deficit Hyperactivity Disorder Rating Scale-IV Inattentive (IA) symptoms score was 9.8 (0.5). Mean (SE) IA scores fell 9.0 (1.1) in Quartile 1 (Phe reduction between 1166 and 2229 μmol/L) versus 4.3 (0.7) in Quartile 4 (Phe reduction of 139 μmol/L to increase of 934 μmol/L), p = 0.004. Least squares mean (SE) change from baseline IA score was -7.9 (0.7) for participants with final Phe ≤ 360 μmol/L and -4.5 (0.7) for final Phe > 360 μmol/L, p < 0.001. In the inattention subgroup, IA scores fell 13.3 (1.5) in Quartile 1 (Phe reduction between 1288 and 2229 μmol/L) versus 6.2 (1.3) in Quartile 4 (Phe reduction of 247 to increase of 934 μmol/L), p = 0.009. Inattention symptoms improved among those whose Phe levels decreased, particularly those with high baseline IA scores. IA improvements were larger among participants with the greatest plasma Phe reductions, supporting this value as a therapeutic goal.

Topics & Concepts

QuartileMedicinePhenylalanineInternal medicinePopulationAttention deficit hyperactivity disorderEndocrinologyChemistryPsychiatryConfidence intervalBiochemistryAmino acidEnvironmental healthMetabolism and Genetic DisordersDiet and metabolism studiesMitochondrial Function and Pathology
Improved attention linked to sustained phenylalanine reduction in adults with early‐treated phenylketonuria | Litcius