Suppr超能文献

Improving sapropterin administration efficacy in PKU: Clinical practice case studies.

作者信息

Tosi Martina, Daly Anne, Ashmore Catherine, Pinto Alex, Vijay Suresh, Verduci Elvira, Evans Sharon, MacDonald Anita

机构信息

Department of Health Sciences, University of Milan, Milan, Italy.

Department of Pediatrics, Vittore Buzzi Children's Hospital, Milan, Italy.

出版信息

Mol Genet Metab Rep. 2025 Sep 16;45:101252. doi: 10.1016/j.ymgmr.2025.101252. eCollection 2025 Dec.

Abstract

In patients with phenylketonuria (PKU), sapropterin dihydrochloride (sapropterin) lowers blood phenylalanine (Phe) and may enhance Phe tolerance in sapropterin responsive patients. Attention to its administration, particularly the timing, and giving it with food with appropriate macronutrient composition, is important. We describe two boys with PKU who improved their Phe tolerance and metabolic control when they adjusted their method of sapropterin administration. Case 1: aged 7.25 years with mild PKU experienced a 40 % reduction in blood Phe after a 30-day sapropterin trial (20 mg/kg). Initially, he took sapropterin once daily dissolved in water. This increased his protein tolerance from 26 g to 50 g/day and reduced his protein equivalent from protein substitute to 20 g/day. His blood Phe was a median of 230 μmol/L (range: 130-300). After six months, twice-daily dosing further improved his protein tolerance to 60 g/day, with a lower median blood Phe (130 μmol/L, range: 80-220). By age 8 years, he swallowed tablets intact with meals, ate an unrestricted protein intake (∼80 g/day), stopped protein substitute, maintained excellent metabolic control with perceived cognitive improvement. Case 2: a boy who aged 4.992 years with mild PKU had a 33 % reduction in blood Phe after a 30-day sapropterin (20 mg/kg) trial. Initially, he took sapropterin once daily dissolved in water, increasing his protein tolerance from 14 g to 55 g/day, and reducing protein equivalent from protein substitute to 20 g/day. Median blood Phe was 240 μmol/L (range: 120-320). At age 6.92 years, twice-daily dosing and swallowing intact tablets further lowered his blood Phe, to a mean of 130 μmol/L (range: 100-130). He stopped dietary protein restriction and protein substitute intake. These case studies showed clinical and dietary benefits with adjustment of sapropterin administration. It was unclear if the improvements observed were associated with twice daily sapropterin administration, attention to taking it with fat containing meals, swallowing the tablets intact, or a combination of these. Further research to monitor the efficacy and safety of administration change is necessary.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c74/12465036/c7b6509245b2/gr1.jpg

相似文献

1
Improving sapropterin administration efficacy in PKU: Clinical practice case studies.
Mol Genet Metab Rep. 2025 Sep 16;45:101252. doi: 10.1016/j.ymgmr.2025.101252. eCollection 2025 Dec.
5
Sapropterin dihydrochloride for phenylketonuria.
Cochrane Database Syst Rev. 2010 Jun 16(6):CD008005. doi: 10.1002/14651858.CD008005.pub2.
6
Sapropterin dihydrochloride for phenylketonuria.
Cochrane Database Syst Rev. 2015 Mar 27;2015(3):CD008005. doi: 10.1002/14651858.CD008005.pub4.
7
Sapropterin dihydrochloride for phenylketonuria.
Cochrane Database Syst Rev. 2012 Dec 12;12:CD008005. doi: 10.1002/14651858.CD008005.pub3.

本文引用的文献

2
Current Advances and Material Innovations in the Search for Novel Treatments of Phenylketonuria.
Adv Healthc Mater. 2024 Oct;13(26):e2401353. doi: 10.1002/adhm.202401353. Epub 2024 May 31.
3
Metabolic control and clinical outcome in adolescents with phenylketonuria.
Mol Genet Metab. 2023 Nov;140(3):107684. doi: 10.1016/j.ymgme.2023.107684. Epub 2023 Aug 12.
7
PKU dietary handbook to accompany PKU guidelines.
Orphanet J Rare Dis. 2020 Jun 30;15(1):171. doi: 10.1186/s13023-020-01391-y.
8
Long-term comparative effectiveness of pegvaliase versus standard of care comparators in adults with phenylketonuria.
Mol Genet Metab. 2019 Sep-Oct;128(1-2):92-101. doi: 10.1016/j.ymgme.2019.07.018. Epub 2019 Aug 7.
9
International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria.
Mol Genet Metab. 2019 May;127(1):1-11. doi: 10.1016/j.ymgme.2019.04.004. Epub 2019 Apr 26.
10
The complete European guidelines on phenylketonuria: diagnosis and treatment.
Orphanet J Rare Dis. 2017 Oct 12;12(1):162. doi: 10.1186/s13023-017-0685-2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验