Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-22T07:30:49.296Z Has data issue: false hasContentIssue false

Pilot study to evaluate the effects of tetrahydrobiopterin on adult individuals with phenylketonuria with measurable maladaptive behaviors

Published online by Cambridge University Press:  17 October 2014

Kathryn D. Moseley*
Affiliation:
Genetics Division, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles County+University of Southern California Medical Center, Los Angeles, California, USA
Martha J. Ottina
Affiliation:
Genetics Division, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles County+University of Southern California Medical Center, Los Angeles, California, USA
Colleen G. Azen
Affiliation:
Clinical and Translational Science Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA
Shoji Yano
Affiliation:
Genetics Division, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles County+University of Southern California Medical Center, Los Angeles, California, USA
*
*Address for correspondence: Kathryn D. Moseley, M.S., R.D., Genetics Division, Department of Pediatrics, Keck School of Medicine, University of Southern California, LAC+USC Medical Center, 1801 Marengo St., Rm. 1G-24, Los Angeles, CA 90033, USA. (Email: [email protected])

Abstract

Objectives

To evaluate the effects of tetrahydrobiopterin (BH4) on maladaptive behavior in patients with phenylketonuria (PKU).

Methods

In an effort to determine if BH4 has any effects on the central nervous system, we studied 10 individuals with PKU and measurable maladaptive behaviors for 1 year. Behavioral assessments using the Vineland Adaptive Behavior Scales–Second Edition and a PKU Behavior Checklist were obtained at baseline, 6 months, and at the end of the study. Biochemical measures including plasma amino acids were obtained quarterly, and phenylalanine (Phe) and tyrosine (Tyr) were obtained monthly.

Results

Out of the 10 subjects, 2 were responders to BH4, as determined by a blood Phe reduction >30%. While blood Phe in the 8 nonresponders did not change significantly throughout the study, their Tyr levels were significantly higher at 6 months (p=0.012), but not at 12 months (p=0.23). By the end of the study, 8 subjects exhibited fewer maladaptive behaviors on the components of the Vineland Maladaptive Behavior Index, and all 10 had lower total scores on the PKU Behavior Checklist.

Conclusion

These findings suggest that there may be direct effects of BH4 on the central nervous system, independent of lowering blood Phe.

Type
Original Research
Copyright
© Cambridge University Press 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

The authors wish to thank Dr. Richard Koch, who was a key contributor to this study.

References

1. Niu, DM. Disorders of BH4 metabolism and the treatment of patients with 6-pyruvoyl tetrahydropterin synthase deficiency in Taiwan. Brain Dev. 2011; 33(10): 847855.Google Scholar
2. Kaufman, S, Kapatos, G, McInnes, RR, Schulman, JD, Rizzo, WB. Use of tetrahydropterins in the treatment of hyperphenylalaninemia due to defective synthesis of tetrahydrobiopterin: evidence that peripherally administered tetrahydropterins enter the brain. Pediatrics. 1982; 70(3): 376380.Google Scholar
3. Scriver, CR, Kaufman, S. Hyperphenylalaninemias: phenylalanine hydroxylase deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vopgelstein B, eds. The Metabolic and Molecular Bases of Inherited Disease, 8th ed. New York: McGraw-Hill; 2001.Google Scholar
4. Pietz, J, Landwehr, R, Kutscha, A, Schmidt, H, de Sonneville, L, Trefz, FK. Effect of high-dose tyrosine supplementation on brain function in adults with phenylketonuria. J Pediatr. 1995; 127(6): 936943.Google Scholar
5. Bickel, H, Gerard, J, Hickmans, EM. Influence of phenylalanine intake on the phenylketonurics. Lancet. 1953; 2(6790): 812813.Google Scholar
6. Levy, HL, Milanowski, A, Chakrapani, A, et al. Efficacy of sapropterindihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomized placebo-controlled study. Lancet. 2007; 370(9586): 504510.Google Scholar
7. Kure, S, Hou, D-CH, Ohura, T, et al. Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. J Pediatr. 1999; 135(3): 375378.Google Scholar
8. Burnett, JR. Sapropterin dihydrochloride (Kuvan/Phenoptin), an orally active synthetic form of BH4 for the treatment of phenylketonuria. IDrugs. 2007; 10(11): 805813.Google Scholar
9. Yannicelli, S, Ryan, A. Improvements in behaviour and physical manifestations in previously untreated adults with phenylketonuria using a phenylalanine-restricted diet: a national survey. J Inherit Metab Dis. 1995; 18(2): 131134.Google Scholar
10. Williams, K. Benefits of normalizing plasma phenylalanine: impact on behavior and health. A case report. J Inherit Metab Dis. 1998; 21(8): 785790.Google Scholar
11. Lee, PJ, Amos, A, Robertson, L, et al. Adults with late diagnosed PKU and severe challenging behavior: a randomized placebo-controlled trial of a phenylalanine-restricted diet. J Neurol Neurosurg Psychiatry. 2009; 80(6): 631635.Google Scholar
12. Fitzgerald, B, Morgan, J, Keene, N, Rollinson, R, Hodgson, A, Dalrymple-Smith, J. An investigation into diet treatment for adults with previously untreated phenylketonuria and severe intellectual disability. J Intellect Disabil Res. 2000; 44(Pt 1): 5359.Google Scholar
13. Sparrow, SS, Ciccetti, DV, Balla, DA. Vineland Adaptive Behavior Scales. 2–– ed. Circle Pines, MN: American Guidance Service; 2005.Google Scholar
14. Baumeister, AA, Baumeister, AA. Dietary treatment of destructive behavior associated with hyperphenylalaninemia. Clin Neuropharmacol. 1998; 21(1): 1827.Google Scholar
15. Kappock, TJ, Caradonna, JP. Pterin-dependent amino acid hydroxylases. Chem Rev. 1996; 96(7): 26592756.Google Scholar
16. Lykkelund, D, Nielsen, JB, Lou, HC, et al. Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of tyrosine. Eur J Pediatr. 1998; 148(3): 238245.Google Scholar
17. Lou, HC, Lykkelund, C, Gerdes, AM, Udesen, H, Bruhn, P. Increased vigilance and dopamine synthesis by large doses of tyrosine or phenylalanine restriction in phenylketonuria. Acta Paediatr Scand. 1987; 76(4): 560565.Google Scholar
18. Nielsen, JB, Lou, HC, Guttler, F. Effects of diet discontinuation and dietary tryptophan supplementation on neurotransmitter metabolism in phenylketonuria. Brain Dysfunction. 1988; 1: 5156.Google Scholar
19. Fernstrom, JD, Fernstrom, MH. Tyrosine, phenylalanine, and catecholamine synthesis and function in the brain. J Nutr. 2007; 137(6 Suppl 1): 1539S1547S.Google Scholar
20. Thöny, B, Calva, AC, Scherer, T, et al. Tetrahydrobiopterin shows chaperone activity for tyrosine hydroxylase. J Neurochem. 2008; 106(2): 672681.Google Scholar