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角膜轮纹状和肢端感觉异常可有效区分法布里病的严重程度簇。

Cornea verticillata and acroparesthesia efficiently discriminate clusters of severity in Fabry disease.

机构信息

Internal Medicine Department, Reference Center for Lysosomal Storage Disorders, Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France.

UMRS 974, INSERM, Sorbonne Université, Paris, France.

出版信息

PLoS One. 2020 May 22;15(5):e0233460. doi: 10.1371/journal.pone.0233460. eCollection 2020.

Abstract

BACKGROUD

Fabry disease (OMIM #301 500), the most prevalent lysosomal storage disease, is caused by enzymatic defects in alpha-galactosidase A (GLA gene; Xq22.1). Fabry disease has historically been characterized by progressive renal failure, early stroke and hypertrophic cardiomyopathy, with a diminished life expectancy. A nonclassical phenotype has been described with an almost exclusive cardiac involvement. Specific therapies with enzyme substitution or chaperone molecules are now available depending on the mutation carried. Numerous clinical and fundamental studies have been conducted without stratifying patients by phenotype or severity, despite different prognoses and possible different pathophysiologies. We aimed to identify a simple and clinically relevant way to classify and stratify patients according to their disease severity.

METHODS

Based on data from the French Fabry Biobank and Registry (FFABRY; n = 104; 54 males), we applied unsupervised multivariate statistics to determine clusters of patients and identify clinical criteria that would allow an effective classification of adult patients. Thanks to these criteria and empirical clinical considerations we secondly elaborate a new score that allow the severity stratification of patients.

RESULTS

We observed that the absence of acroparesthesia or cornea verticillata is sufficient to classify males as having the nonclassical phenotype. We did not identify criteria that significantly cluster female patients. The classical phenotype was associated with a higher risk of severe renal (HR = 35.1; p <10-3) and cardiac events (HR = 4.8; p = 0.008) and a trend toward a higher risk of severe neurological events (HR = 7.7; p = 0.08) compared to nonclassical males. Our simple, rapid and clinically-relevant FFABRY score gave concordant results with the validated MSSI.

CONCLUSION

Acroparesthesia and cornea verticillata are simple clinical criteria that efficiently stratify Fabry patients, defining 3 different groups: females and males with nonclassical and classical phenotypes of significantly different severity. The FFABRY score allows severity stratification of Fabry patients.

摘要

背景

法布里病(OMIM#301500)是最常见的溶酶体贮积病,由α-半乳糖苷酶 A(GLA 基因;Xq22.1)酶缺陷引起。法布里病的历史特征是进行性肾功能衰竭、早发性中风和肥厚型心肌病,预期寿命缩短。现已描述一种无经典表型,几乎仅心脏受累。根据携带的突变,现在有特定的酶替代或伴侣分子治疗。尽管预后不同,可能存在不同的病理生理学,但许多临床和基础研究都是在未按表型或严重程度对患者进行分层的情况下进行的。我们旨在确定一种简单且临床相关的方法,根据疾病严重程度对患者进行分类和分层。

方法

基于法国法布里生物库和登记处(FFABRY;n=104;54 名男性)的数据,我们应用无监督多元统计确定患者聚类并确定临床标准,以有效分类成年患者。根据这些标准和经验临床考虑,我们其次制定了一个新的评分,允许对患者进行严重程度分层。

结果

我们观察到无肢端感觉异常或角膜涡纹足以将男性分类为无经典表型。我们没有发现能显著聚类女性患者的标准。经典表型与严重肾脏事件(HR=35.1;p<10-3)和心脏事件(HR=4.8;p=0.008)的风险增加相关,与非经典男性相比,严重神经系统事件的风险也有增加趋势(HR=7.7;p=0.08)。我们简单、快速且具有临床相关性的 FFABRY 评分与经过验证的 MSSI 结果一致。

结论

肢端感觉异常和角膜涡纹是简单的临床标准,可有效地分层法布里病患者,定义 3 个不同的组:女性和具有明显不同严重程度的非经典和经典表型的男性。FFABRY 评分可对法布里病患者进行严重程度分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca6f/7244174/8f549d19b368/pone.0233460.g001.jpg

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