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一种从新生儿到青少年患者的克里斯波尼/冷诱导出汗综合征1(CISS1/CISS)颅面再现的人工智能方法。

An Artificial Intelligence Approach to the Craniofacial Recapitulation of Crisponi/Cold-Induced Sweating Syndrome 1 (CISS1/CISS) from Newborns to Adolescent Patients.

作者信息

Pascolini Giulia, Didona Dario, Tarani Luigi

机构信息

Genetic Counselling Unit, Istituto Dermopatico Dell'immacolata, IDI-IRCCS, Via dei Monti di Creta 104, 00167 Rome, Italy.

Rare Diseases Center, Istituto Dermopatico Dell'immacolata, IDI-IRCCS, 00167 Rome, Italy.

出版信息

Diagnostics (Basel). 2025 Feb 21;15(5):521. doi: 10.3390/diagnostics15050521.

Abstract

: Crisponi/cold-induced sweating syndrome 1 (CISS1/CISS, MIM#272430) is a genetic disorder due to biallelic variants in (MIM*604237). The related phenotype is mainly characterized by abnormal thermoregulation and sweating, facial muscle contractions in response to tactile and crying-inducing stimuli at an early age, skeletal anomalies (camptodactyly of the hands, scoliosis), and craniofacial dysmorphisms, comprising full cheeks, micrognathia, high and narrow palate, low-set ears, and a depressed nasal bridge. The condition is associated with high lethality during the neonatal period and can benefit from timely symptomatic therapy. : We collected frontal images of all patients with CISS1/CISS published to date, which were analyzed with Face2Gene (F2G), a machine-learning technology for the facial diagnosis of syndromic phenotypes. In total, 75 portraits were subdivided into three cohorts, based on age (Cohort 1 and 2) and the presence of the typical facial trismus (Cohort 3). These portraits were uploaded to F2G to test their suitability for facial analysis and to verify the capacity of the AI tool to correctly recognize the syndrome based on the facial features only. The photos which passed this phase (62 images) were fed to three different AI algorithms-DeepGestalt, Facial D-Score, and GestaltMatcher. : The DeepGestalt algorithm results, including the correct diagnosis using a frontal portrait, suggested a similar facial phenotype in the first two cohorts. Cohort 3 seemed to be highly differentiable. The results were expressed in terms of the area under the curve (AUC) of the receiver operating characteristic (ROC) curve and Value. The Facial D-Score values indicated the presence of a consistent degree of dysmorphic signs in the three cohorts, which was also confirmed by the GestaltMatcher algorithm. Interestingly, the latter allowed us to identify overlapping genetic disorders. : This is the first AI-powered image analysis in defining the craniofacial contour of CISS1/CISS and in determining the feasibility of training the tool used in its clinical recognition. The obtained results showed that the use of F2G can reveal valid support in the diagnostic process of CISS1/CISS, especially in more severe phenotypes, manifesting with facial contractions and potentially lethal consequences.

摘要

克里斯波尼/冷诱导出汗综合征1(CISS1/CISS,MIM#272430)是一种由(MIM*604237)双等位基因变异引起的遗传性疾病。相关表型的主要特征是体温调节和出汗异常,早年对触觉和诱发哭泣的刺激出现面部肌肉收缩,骨骼异常(手部屈曲挛缩、脊柱侧弯),以及颅面畸形,包括脸颊丰满、小颌畸形、高而窄的腭、低位耳和鼻梁凹陷。该病症在新生儿期具有较高的致死率,及时的对症治疗可能有益。

我们收集了迄今为止已发表的所有CISS1/CISS患者的正面图像,并用Face2Gene(F2G)进行分析,这是一种用于面部诊断综合征表型的机器学习技术。总共75张肖像根据年龄(队列1和2)以及典型面部牙关紧闭的存在情况(队列3)分为三个队列。这些肖像被上传到F2G,以测试它们是否适合面部分析,并验证人工智能工具仅基于面部特征正确识别该综合征的能力。通过此阶段的照片(62张图像)被输入到三种不同的人工智能算法——DeepGestalt、面部D评分和格式塔匹配器。

DeepGestalt算法的结果,包括使用正面肖像进行的正确诊断,表明前两个队列具有相似的面部表型。队列3似乎具有高度可区分性。结果以受试者操作特征(ROC)曲线的曲线下面积(AUC)和 值表示。面部D评分值表明三个队列中存在一致程度的畸形体征,格式塔匹配器算法也证实了这一点。有趣的是,后者使我们能够识别重叠的遗传性疾病。

这是首次利用人工智能进行图像分析来定义CISS1/CISS的颅面轮廓,并确定训练用于其临床识别的工具的可行性。获得的结果表明,使用F2G在CISS1/CISS的诊断过程中可以提供有效的支持,特别是在更严重的表型中,表现为面部收缩并可能产生致命后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee1f/11898923/1ced32a5f033/diagnostics-15-00521-g001.jpg

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