Literature DB >> 29030855

Extended Experience of Lower Dose Sapropterin in Irish Adults with Mild Phenylketonuria.

S Doyle1,2, M O'Regan3, C Stenson3, J Bracken1, U Hendroff1, A Agasarova1, D Deverell4, E P Treacy5,6,7.   

Abstract

Adherence to dietary and treatment recommendations is a long-standing concern for adults and adolescents with PKU and treating clinicians. In about 20-30% of PKU patients, Phe levels may be controlled by tetrahydrobiopterin (BH4) therapy. The European PKU 2017 Guidelines recommends treatment with BH4 for cases of proven long-term BH4 responsiveness, with a recommended dosage of Sapropterin 10-20 mg/kg/day.We report four young Irish patients with mild PKU, known to be BH4 responsive, who were treated with lower doses of Sapropterin for over 7 years.Case 1: Female, currently age 20. Genotype p. 165T/p/F39L, c.[194T>C]; [117C>G]. Newborn Phe: 851 μmol/L. Pre-Sapropterin Phe tolerance: 600 mg Phe/day to maintain Phe levels <400 μmol/L. Commenced on Sapropterin 400 mg (6.5 mg/kg/day) with increase in Phe tolerance to 800 mg/day.Case 2: Female, currently age 23. Genotype p. 165T/pF39L; c.[194T>C]; [117C>G]. Newborn Phe: 714 μmol/L. Pre-Sapropterin Phe tolerance: 700 mg Phe/day. Commenced on Sapropterin 400 mg (8 mg/kg/day) with increase in Phe tolerance to 800 mg/day.Case 3: Male, currently age 22. Genotype p. 165T/p.S349P; c.[194T>C][1045T>C]. Newborn Phe: 1,036 μmol/L. Pre-Sapropterin Phe tolerance: 600 mg Phe/day. Commenced on Sapropterin 400 mg (5.4 mg/kg/day). Increased to 1,600 mg Phe/day.Case 4: Female, currently age 29. Genotype p.R408W/p/p.Y414C; c.[1222C>T], [1241A>G]. Newborn Phe: 1,600 μmol/L. Pre-Sapropterin tolerance: 450 mg/day. Commenced on Sapropterin 400 mg (5.0 mg/kg/day). Increased to 900 mg Phe/day.Almost 7 years of surveillance for these four patients has shown that this dose of Sapropterin (range 5-8 mg/kg day) was well tolerated and effective with a significant response to treatment and a marked improvement in quality of life at these lower Sapropterin doses.

Entities:  

Year:  2017        PMID: 29030855      PMCID: PMC6121967          DOI: 10.1007/8904_2017_63

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  18 in total

Review 1.  Key European guidelines for the diagnosis and management of patients with phenylketonuria.

Authors:  Francjan J van Spronsen; Annemiek Mj van Wegberg; Kirsten Ahring; Amaya Bélanger-Quintana; Nenad Blau; Annet M Bosch; Alberto Burlina; Jaime Campistol; Francois Feillet; Maria Giżewska; Stephan C Huijbregts; Shauna Kearney; Vincenzo Leuzzi; Francois Maillot; Ania C Muntau; Fritz K Trefz; Margreet van Rijn; John H Walter; Anita MacDonald
Journal:  Lancet Diabetes Endocrinol       Date:  2017-01-10       Impact factor: 32.069

2.  A Systematic Review of BH4 (Sapropterin) for the Adjuvant Treatment of Phenylketonuria.

Authors:  Mary Lou Lindegren; Shanthi Krishnaswami; Tyler Reimschisel; Christopher Fonnesbeck; Nila A Sathe; Melissa L McPheeters
Journal:  JIMD Rep       Date:  2012-07-29

3.  Adherence to clinic recommendations among patients with phenylketonuria in the United States.

Authors:  E R Jurecki; S Cederbaum; J Kopesky; K Perry; F Rohr; A Sanchez-Valle; K S Viau; M Y Sheinin; J L Cohen-Pfeffer
Journal:  Mol Genet Metab       Date:  2017-01-06       Impact factor: 4.797

4.  Sapropterin treatment does not enhance the health-related quality of life of patients with phenylketonuria and their parents.

Authors:  Reinhold Feldmann; Eva Wolfgart; Josef Weglage; Frank Rutsch
Journal:  Acta Paediatr       Date:  2017-03-19       Impact factor: 2.299

Review 5.  Tetrahydrobiopterin, its mode of action on phenylalanine hydroxylase, and importance of genotypes for pharmacological therapy of phenylketonuria.

Authors:  Caroline Heintz; Richard G H Cotton; Nenad Blau
Journal:  Hum Mutat       Date:  2013-05-01       Impact factor: 4.878

6.  How practical are recommendations for dietary control in phenylketonuria?

Authors:  J H Walter; F J White; S K Hall; A MacDonald; G Rylance; A Boneh; D E Francis; G J Shortland; M Schmidt; A Vail
Journal:  Lancet       Date:  2002-07-06       Impact factor: 79.321

7.  Prevalence of stimulant use for attentional dysfunction in children with phenylketonuria.

Authors:  G L Arnold; C J Vladutiu; C C Orlowski; E M Blakely; J DeLuca
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

8.  A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics.

Authors:  Barbara K Burton; Lauren Leviton; Hazel Vespa; Hilary Coon; Nicola Longo; Bridget D Lundy; Maria Johnson; Andrew Angelino; Ada Hamosh; Deborah Bilder
Journal:  Mol Genet Metab       Date:  2012-11-15       Impact factor: 4.797

9.  Assessment of the impact of phenylketonuria and its treatment on quality of life of patients and parents from seven European countries.

Authors:  Annet M Bosch; Alberto Burlina; Amy Cunningham; Esther Bettiol; Flavie Moreau-Stucker; Ekaterina Koledova; Khadra Benmedjahed; Antoine Regnault
Journal:  Orphanet J Rare Dis       Date:  2015-06-18       Impact factor: 4.123

10.  Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride.

Authors:  Teresa D Douglas; Usha Ramakrishnan; Julie A Kable; Rani H Singh
Journal:  Health Qual Life Outcomes       Date:  2013-12-30       Impact factor: 3.186

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