Evidence map›Paper›PMID 29030855›Full record

ArticleJIMD reports2018

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

S Doyle, M O'Regan, C Stenson, J Bracken, U Hendroff, A Agasarova, D Deverell, E P Treacy

Abstract read
In one paragraph

Article in JIMD reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

S DoyleNational Centre for Inherited Metabolic Disorders, The Mater Misericordiae University Hospital, Dublin, Ireland.
M O'ReganNational Centre for Inherited Metabolic Disorders, The Children's University Hospital, Dublin, Ireland.
C StensonNational Centre for Inherited Metabolic Disorders, The Children's University Hospital, Dublin, Ireland.
J BrackenNational Centre for Inherited Metabolic Disorders, The Mater Misericordiae University Hospital, Dublin, Ireland.
U HendroffNational Centre for Inherited Metabolic Disorders, The Mater Misericordiae University Hospital, Dublin, Ireland.
A AgasarovaNational Centre for Inherited Metabolic Disorders, The Mater Misericordiae University Hospital, Dublin, Ireland.
D DeverellDepartment of Pathology, The Children's University Hospital, Dublin, Ireland.
E P TreacyNational Centre for Inherited Metabolic Disorders, The Mater Misericordiae University Hospital, Dublin, Ireland. etreacy@mater.ie.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Identifiers

PMID29030855
PMCPMC6121967

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