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以法布里病为例改进基于数据挖掘的罕见病诊断支持工具:需要考虑性别差异。

Improving a data mining based diagnostic support tool for rare diseases on the example of M. Fabry: Gender differences need to be taken into account.

作者信息

Hahn Philipp, Lechner Werner, Siefen Rainer-Georg, Lampe Christina, Nordbeck Peter, Grigull Lorenz, Lücke Thomas

机构信息

University Children's Hospital, Ruhr-University Bochum, Bochum, Germany.

KIMedi GmbH, Ulm, Germany.

出版信息

PLoS One. 2025 Jun 30;20(6):e0326372. doi: 10.1371/journal.pone.0326372. eCollection 2025.

Abstract

BACKGROUND

Rare diseases often present with a variety of clinical symptoms and therefore are challenging to diagnose. Fabry disease is an x-linked rare metabolic disorder. The severity of symptoms is usually different in men and women. Since therapeutic options for Fabry disease exist, early diagnosis is important. An artificial intelligence (AI)-based diagnosis support algorithm for rare diseases has been developed in preliminary studies.

OBJECTIVE

Our aim was to extend and train the questionnaire-based AI, capable of distinguishing patients with from those without rare diseases, to achieve satisfactory sensitivity for the detection of a single rare disease, Fabry disease, taking into account gender differences in disease perception.

METHODS

We collected 33 complete datasets from patients with confirmed Fabry disease. These records contained answered AI questionnaires, general information on disease progression, demographic information and quality of life (QoL) measures. The AI was trained to distinguish patients with Fabry disease from patients with relevant differential diagnoses. Its performance was assayed using stratified eleven-fold cross-validation and ROC curve calculation. Variables influencing the performance of the AI were examined with linear regression and calculation of the coefficient of determination.

RESULT

We were able to show that a relatively small sample is sufficient to achieve a sensitivity of 88.12% for the presence of Fabry disease, taking into account gender-specific differences in the disease perception during the pre-diagnostic phase. No confounders of the tool's performance could be found in the data collected concerning the patients' quality of life and diagnostic history.

CONCLUSION

This study illustrates on the example of Fabry disease that differences between female and male Fabry patients, not only in the expression of symptoms, but also with regard to disease perception, might be relevant influencing variables for improving the performance of AI-based diagnostic support tools for rare diseases.

摘要

背景

罕见病通常表现出多种临床症状,因此诊断具有挑战性。法布里病是一种X连锁的罕见代谢紊乱疾病。症状的严重程度在男性和女性中通常有所不同。由于存在法布里病的治疗选择,早期诊断很重要。在初步研究中已开发出一种基于人工智能(AI)的罕见病诊断支持算法。

目的

我们的目标是扩展并训练基于问卷的人工智能,该人工智能能够区分患有罕见病和未患罕见病的患者,考虑到疾病认知中的性别差异,对单一罕见病法布里病的检测实现令人满意的灵敏度。

方法

我们收集了33份来自确诊法布里病患者的完整数据集。这些记录包含已回答的人工智能问卷、疾病进展的一般信息、人口统计学信息和生活质量(QoL)测量。训练人工智能以区分法布里病患者和具有相关鉴别诊断的患者。使用分层十一折交叉验证和ROC曲线计算来测定其性能。通过线性回归和决定系数计算来检查影响人工智能性能的变量。

结果

我们能够表明,考虑到诊断前阶段疾病认知中的性别特异性差异,相对较小的样本足以实现法布里病存在时88.12%的灵敏度。在所收集的关于患者生活质量和诊断史的数据中未发现该工具性能的混杂因素。

结论

本研究以法布里病为例说明,法布里病男女患者之间的差异,不仅在症状表达方面,而且在疾病认知方面,可能是提高基于人工智能的罕见病诊断支持工具性能的相关影响变量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/12208464/ce9e16f4d1c9/pone.0326372.g001.jpg

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