Systematic literature review of the somatic comorbidities experienced by adults with phenylketonuria

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-08-12 DOI:10.1186/s13023-024-03203-z
Kaleigh B. Whitehall, Sarah Rose, Gillian E. Clague, Kirsten K. Ahring, Deborah A. Bilder, Cary O. Harding, Álvaro Hermida, Anita Inwood, Nicola Longo, François Maillot, Ania C. Muntau, André L. S. Pessoa, Júlio C. Rocha, Fran Rohr, Serap Sivri, Jack Said, Sheun Oshinbolu, Gillian C. Sibbring
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Abstract

Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism that, if untreated, causes Phe accumulation in the brain leading to neurophysiologic alterations and poor outcomes. Lifelong management centers on dietary Phe restriction, yet long-term complete metabolic control is unachievable for many adults. High blood Phe levels or chronic Phe and intact protein restriction in the diet may lead to somatic comorbidities. A systematic literature review was conducted to evaluate somatic comorbidities experienced by adults with PKU. Clinical and observational studies reporting somatic comorbidities experienced by individuals with PKU aged ≥ 16 years (or classified as adults) evaluating a Phe-restricted diet with or without pharmacologic therapy versus no therapeutic intervention (including healthy controls), or pharmacologic therapy versus a Phe-restricted diet alone, were identified. PubMed® was searched (February 1, 2022 and updated November 1, 2023), using a pre-defined search strategy, followed by two-stage screening and data extraction. Included studies were grouped by PKU population comparison. 1185 records were screened; 51 studies across 12,602 individuals were extracted. Bone-related abnormalities were the most reported outcome (n = 21); several outcome measures were used. Original study groupings included: Phe-restricted diet versus healthy controls or reference values (n = 40); treatment-adherent versus those non-adherent (n = 12). Additional groups added as part of a protocol amendment included: different Phe-restricted diets (n = 4); severe versus less severe disease (n = 5). Vote counting indicated a higher burden of ≥ 1 comorbidity (or outcome measure) for the Phe-restricted diet group by 37 of 38 studies included in the analysis of Phe-restricted diet versus healthy controls; higher burden in healthy controls was reported in 12 studies. Vote counting was similar between those treatment adherent (n = 7) versus non-adherent (n = 10). Adults with PKU have a higher comorbidity burden than a non-PKU population. More robust studies are needed to better understand the relationship between effective metabolic control and comorbidity burden, using consistent outcome measures. This SLR was supported by BioMarin Pharmaceutical Inc., Novato, CA, and is registered with the Research Registry (reviewregistry1476).
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苯丙酮尿症成人躯体合并症的系统文献综述
苯丙酮尿症(PKU)是一种先天性苯丙氨酸(Phe)代谢异常,如不及时治疗,会导致 Phe 在大脑中蓄积,从而引起神经生理改变和不良后果。终生治疗的核心是限制饮食中的 Phe,但对于许多成年人来说,长期完全的代谢控制是无法实现的。血液中 Phe 含量过高或饮食中长期限制 Phe 和完整蛋白质可能会导致躯体并发症。为了评估患有 PKU 的成年人的躯体并发症,我们进行了一项系统性文献综述。对年龄≥ 16 岁(或被归类为成人)的 PKU 患者进行了临床和观察性研究,报告了他们的躯体并发症,这些研究评估了有或无药物治疗的 Phe 限制饮食与无治疗干预(包括健康对照组)的比较,或药物治疗与单纯 Phe 限制饮食的比较。采用预先确定的检索策略对 PubMed® 进行了检索(2022 年 2 月 1 日,2023 年 11 月 1 日更新),随后进行了两阶段筛选和数据提取。纳入的研究按 PKU 群体比较进行分组。共筛选出 1185 条记录;提取了 51 项研究,涉及 12602 人。与骨骼相关的异常是报告最多的结果(n = 21);使用了多种结果测量方法。最初的研究分组包括限制 Phe 饮食与健康对照组或参考值组(n = 40);坚持治疗与非坚持治疗组(n = 12)。作为方案修订的一部分,新增的分组包括:不同的 Phe 限制饮食(n = 4);重症与轻症(n = 5)。在 38 项关于 Phe 限制饮食与健康对照分析的研究中,有 37 项研究的计票结果表明,Phe 限制饮食组的合并症(或结果指标)负担≥ 1 种;有 12 项研究报告健康对照组的负担较重。坚持治疗组(7 例)与非坚持治疗组(10 例)的投票计数相似。与非北京大学人群相比,患有北京大学的成年人的合并症负担更高。为了更好地了解有效的代谢控制与并发症负担之间的关系,需要使用一致的结果测量方法进行更深入的研究。本 SLR 得到了加利福尼亚州诺瓦托市 BioMarin 制药公司的支持,并已在研究注册中心注册 (reviewregistry1476)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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