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苯丙酮尿症中盐酸沙丙蝶呤的反应性:探索综合患者监测差距的病例系列

Sapropterin Dihydrochloride Responsiveness in Phenylketonuria: A Case Series Exploring Gaps in Comprehensive Patient Monitoring.

作者信息

Lo Bianco Manuela, Leonardi Roberta, Migliore Alessia, Moliteo Evelina, Sciacca Monica, Rinella Sergio, Pappalardo Maria Grazia, La Spina Luisa, Messina Marianna, Iacobacci Riccardo, Ruggieri Martino, Meli Concetta, Polizzi Agata

机构信息

Unit of Pediatric Clinic, A.O.U. Policlinico "G. Rodolico-San Marco", P.O. "G. Rodolico"-University of Catania, 95123 Catania, Italy.

Postgraduate Residency Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, 95123 Catania, Italy.

出版信息

Nutrients. 2025 Sep 7;17(17):2892. doi: 10.3390/nu17172892.

Abstract

: Phenylketonuria (PKU) is a rare autosomal recessive metabolic disorder caused by mutations in the phenylalanine hydroxylase () gene, leading to hyperphenylalaninemia (HPA). Untreated, elevated phenylalanine (Phe) levels cause severe neurocognitive, developmental, and psychiatric complications. Management relies on a Phe-restricted diet, which is challenging to maintain, particularly in adolescents and adults. Sapropterin dihydrochloride, a synthetic form of tetrahydrobiopterin (BH4), can enhance residual PAH activity, lowering blood Phe levels and increasing dietary tolerance in responsive patients. However, real-world alignment with best practices remains underexplored. This study aims to report a tertiary referral center's experience with sapropterin treatment in PKU and assess adherence to international guidelines. : We retrospectively analyzed 23 PKU patients treated with sapropterin from 2007 to 2025. Patients with baseline Phe levels of 360-2000 µmol/L underwent a 10 mg/kg/day loading test over two weeks. Responsiveness was defined as a ≥30% reduction in blood Phe levels. Phe levels were measured pre- and post-test, and dietary tolerance was evaluated. Adherence to best practices was critically reviewed. : All patients showed significant Phe reductions (mean 71.43%, < 0.0001), exceeding responsiveness thresholds. Most achieved substantial increases in dietary Phe tolerance, with three patients partially responsive (800-1200 mg/day). Responsiveness was unrespectful of the patient's genotype, for those individuals for whom this was known (8/23 patients). Although effective, the test dose and duration differed from guideline recommendations (20 mg/kg/day). Neuropsychological and QoL assessments were not systematically performed, representing a key limitation. : Sapropterin dihydrochloride effectively identified responders and improved dietary flexibility even with lower dosing protocols. Greater adherence to international standards, particularly regarding long-term neuropsychological monitoring, is needed to optimize patient care.

摘要

苯丙酮尿症(PKU)是一种罕见的常染色体隐性代谢紊乱疾病,由苯丙氨酸羟化酶(PAH)基因突变引起,导致高苯丙氨酸血症(HPA)。未经治疗,苯丙氨酸(Phe)水平升高会导致严重的神经认知、发育和精神并发症。治疗依赖于低苯丙氨酸饮食,而维持这种饮食具有挑战性,尤其是在青少年和成年人中。盐酸沙丙蝶呤是四氢生物蝶呤(BH4)的合成形式,可增强残余PAH活性,降低血液Phe水平并提高有反应患者的饮食耐受性。然而,现实世界中与最佳实践的一致性仍未得到充分探索。本研究旨在报告一家三级转诊中心在PKU患者中使用沙丙蝶呤治疗的经验,并评估对国际指南的依从性。:我们回顾性分析了2007年至2025年期间接受沙丙蝶呤治疗的23例PKU患者。基线Phe水平为360 - 2000 µmol/L的患者在两周内进行了10 mg/kg/天的负荷试验。反应性定义为血液Phe水平降低≥30%。在试验前后测量Phe水平,并评估饮食耐受性。严格审查对最佳实践的依从性。:所有患者的Phe水平均显著降低(平均降低71.43%,P < 0.0001),超过反应性阈值。大多数患者的饮食Phe耐受性大幅提高,3例患者部分有反应(800 - 1200 mg/天)。对于已知基因型的患者(23例患者中的8例),反应性与患者基因型无关。虽然有效,但试验剂量和持续时间与指南建议(20 mg/kg/天)不同。神经心理学和生活质量评估未系统进行,这是一个关键限制。:即使采用较低的给药方案,盐酸沙丙蝶呤也能有效识别有反应者并提高饮食灵活性。需要更好地遵守国际标准,特别是在长期神经心理学监测方面,以优化患者护理。

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The Genetic Landscape and Epidemiology of Phenylketonuria.苯丙酮尿症的遗传景观和流行病学。
Am J Hum Genet. 2020 Aug 6;107(2):234-250. doi: 10.1016/j.ajhg.2020.06.006. Epub 2020 Jul 14.
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