成人苯丙酮尿与心血管系统的关系-机制和风险的见解。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Yann Dos Santos, Friedrich Trefz, Maria Giżewska, Annemiek M J van Wegberg, Bruno Lefort, François Labarthe, Francjan van Spronsen, François Maillot
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引用次数: 0

摘要

对PKU成人患者的研究主要集中在无法维持推荐的终生饮食的个体可能出现的神经精神并发症。最近的一些流行病学研究建议考虑其他并发症。因此,迄今为止,心血管(CV)问题一直是很少研究的主题。本综述的目的是收集和讨论PKU患者CV并发症的传统风险、该人群的潜在CV表型以及各种非传统风险和潜在相关机制的文献数据。报道的合并症患病率表明PKU成人CV并发症的风险增加,主要发生在晚期诊断的患者中。关于与PKU相关的特定CV表型的研究具有启发性,尽管需要进一步的研究。该人群的氧化应激数据是一致的,并证实心血管风险增加。至于其他可能的机制,尚不能断定成年PKU患者是否有低度炎症、血脂异常、肾脏损害或是否有高同型半胱氨酸血症。测量与心血管并发症相关的潜在生物标志物,如同型半胱氨酸、不对称二甲基精氨酸和犬尿氨酸(喹啉酸),将是一项有趣的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relationship between adult phenylketonuria and the cardiovascular system - insights into mechanisms and risks.

Studies in adults with PKU have mainly focused on the neuropsychiatric complications that may arise in individuals who are unable to maintain the recommended lifetime diet. Some recent epidemiological studies suggest to consider other complications. As such, cardiovascular (CV) issues have been the subject of few studies to date. The aim of this review is to gather and discuss data from the literature on the traditional risks of CV complications in PKU, a potential CV phenotype in this population and the various non-traditional risks and potential associated mechanisms. The reported prevalence of comorbidities suggests an increased risk of CV complications in adults with PKU, mostly in late-diagnosed patients. Studies about a specific CV phenotype associated with PKU are suggestive, although further studies are needed. The data on oxidative stress in this population are consistent and confirm an increased CV risk. Regarding other potential mechanisms, it is not possible to conclude whether adult PKU patients have low grade inflammation, dyslipidemia, kidney impairment or if they have hyperhomocysteinemia. It would be of interest to measure potential biomarker associated with CV complications, such as homocysteine, asymmetric dimethylarginine and kynurenines (quinolic acid).

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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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