Neumann Michael, Kothare Hardik, Ramanarayanan Vikram
Modality.AI, Inc., San Francisco, CA, USA.
University of California, San Francisco, CA, USA.
medRxiv. 2024 Jun 27:2024.06.26.24308811. doi: 10.1101/2024.06.26.24308811.
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that severely impacts affected persons' speech and motor functions, yet early detection and tracking of disease progression remain challenging. The current gold standard for monitoring ALS progression, the ALS functional rating scale - revised (ALSFRS-R), is based on subjective ratings of symptom severity, and may not capture subtle but clinically meaningful changes due to a lack of granularity. Multimodal speech measures which can be automatically collected from patients in a remote fashion allow us to bridge this gap because they are continuous-valued and therefore, potentially more granular at capturing disease progression. Here we investigate the responsiveness and sensitivity of multimodal speech measures in persons with ALS (pALS) collected via a remote patient monitoring platform in an effort to quantify how long it takes to detect a clinically-meaningful change associated with disease progression. We recorded audio and video from 278 participants and automatically extracted multimodal speech biomarkers (acoustic, orofacial, linguistic) from the data. We find that the timing alignment of pALS speech relative to a canonical elicitation of the same prompt and the number of words used to describe a picture are the most responsive measures at detecting such change in both pALS with bulbar ( = 36) and non-bulbar onset ( = 107). Interestingly, the responsiveness of these measures is stable even at small sample sizes. We further found that certain speech measures are sensitive enough to track bulbar decline even when there is no patient-reported clinical change, i.e. the ALSFRS-R speech score remains unchanged at 3 out of a total possible score of 4. The findings of this study have the potential to facilitate improved, accelerated and cost-effective clinical trials and care.
肌萎缩侧索硬化症(ALS)是一种进行性神经退行性疾病,严重影响患者的言语和运动功能,但疾病进展的早期检测和跟踪仍然具有挑战性。目前监测ALS进展的金标准,即修订后的ALS功能评定量表(ALSFRS-R),是基于对症状严重程度的主观评分,由于缺乏粒度,可能无法捕捉到细微但具有临床意义的变化。多模态言语测量可以以远程方式自动从患者那里收集,这使我们能够弥合这一差距,因为它们是连续值的,因此在捕捉疾病进展方面可能更具粒度。在这里,我们研究了通过远程患者监测平台收集的ALS患者(pALS)多模态言语测量的反应性和敏感性,以努力量化检测与疾病进展相关的具有临床意义的变化需要多长时间。我们记录了278名参与者的音频和视频,并从数据中自动提取了多模态言语生物标志物(声学、口面部、语言)。我们发现,pALS言语相对于相同提示的标准诱发的时间对齐以及用于描述图片的单词数量是检测延髓性(=36)和非延髓性起病(=107)的pALS中这种变化最具反应性的测量方法。有趣的是,即使在小样本量下,这些测量方法的反应性也是稳定的。我们进一步发现,某些言语测量足够敏感,能够跟踪延髓功能衰退,即使没有患者报告的临床变化,即ALSFRS-R言语评分在总分4分中的3分保持不变。这项研究的结果有可能促进改进、加速和具有成本效益的临床试验及护理。