尿尿性脊柱疾病的深度学习研究评估全球和区域严重程度并检测隐匿治疗状态

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Kendall A. Flaharty, Vibha Chandrasekar, Irene J. Castillo, Dat Duong, Carlos R. Ferreira, Suzanna Ledgister Hanchard, Ping Hu, Rebekah L. Waikel, Francis Rossignol, Wendy J. Introne, Benjamin D. Solomon
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引用次数: 0

摘要

深度学习(DL)越来越多地用于分析医学成像,但在罕见的情况下却不太完善,这需要新的预处理和分析方法。为了在罕见疾病的背景下评估DL,本研究重点研究了尿酸尿症(AKU),这是一种影响脊柱并伴有其他后遗症的罕见疾病;治疗方法包括使用尼替西酮。由于评估x射线来确定疾病严重程度可能是一个缓慢的人工过程,需要相当多的专业知识,因此本研究旨在确定这些DL方法是否能够准确识别脊柱特定区域的整体脊柱严重程度,以及患者是否接受了尼替西酮。通过颈椎和腰椎x线片评估DL表现。DL模型预测的整体严重程度评分(30分制)与专家临床医生的颈椎评分(1.72±1.96分)和腰椎x线片评分(2.51±1.96分)之间的差异。对于特定区域的指标,评估每个椎间隙(IVS)的狭窄程度、钙和真空盘现象。该模型的缩小评分与临床评分(6分制)相差0.191-0.557分,预测钙的准确率为78%-90%(存在、缺失或椎间盘融合),而真空椎间盘现象的预测不太一致(41%-90%)。有趣的是,DL模型预测尼替西酮治疗状态的准确率为68%-77%,而专家临床医生似乎无法识别尼替西酮的状态(准确率为51%)(p = 2.0 × 10−9)。这突出了DL在增加罕见疾病的某些类型的临床评估方面的潜力,以及识别诸如治疗状态之类的隐匿特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Learning Study of Alkaptonuria Spinal Disease Assesses Global and Regional Severity and Detects Occult Treatment Status

Deep learning (DL) is increasingly used to analyze medical imaging, but is less refined for rare conditions, which require novel pre-processing and analytical approaches. To assess DL in the context of rare diseases, this study focused on alkaptonuria (AKU), a rare disorder that affects the spine and involves other sequelae; treatments include the medication nitisinone. Since assessing x-rays to determine disease severity can be a slow, manual process requiring considerable expertise, this study aimed to determine whether these DL methods could accurately identify overall spine severity at specific regions of the spine and whether patients were receiving nitisinone. DL performance was evaluated versus clinical experts using cervical and lumbar spine radiographs. DL models predicted global severity scores (30-point scale) within 1.72 ± 1.96 points of expert clinician scores for cervical and 2.51 ± 1.96 points for lumbar radiographs. For region-specific metrics, the degrees of narrowing, calcium, and vacuum disc phenomena at each intervertebral space (IVS) were assessed. The model's narrowing scores were within 0.191–0.557 points from clinician scores (6-point scale), calcium was predicted with 78%–90% accuracy (present, absent, or disc fusion), and vacuum disc phenomenon predictions were less consistent (41%–90%). Intriguingly, DL models predicted nitisinone treatment status with 68%–77% accuracy, while expert clinicians appeared unable to discern nitisinone status (51% accuracy) (p = 2.0 × 10−9). This highlights the potential for DL to augment certain types of clinical assessments in rare disease, as well as identifying occult features like treatment status.

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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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