Identifying brain networks to predict treatment resistance and post-surgical outcome: An ENIGMA-Epilepsy initiative

识别大脑网络以预测治疗抵抗和术后结果：ENIGMA-癫痫计划

• 批准号: 10443866
• 负责人: CARRIE R MCDONALD
• 金额: $ 61.84万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-15 至 2026-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10443866
• 关键词: Address; Affect; Age; Benchmarking; Bilateral; Brain; Characteristics; Clinical; Clinical Data; Communities; Complement; Country; Coupled; Data; Data Set; Databases; Development; Diagnosis; Diagnostic; Diffusion Magnetic Resonance Imaging; Disease; Drug resistance; Ensure; Epilepsy; Evaluation; Failure; Fibrinogen; Freedom; Frontal Lobe Epilepsy; Generalized Epilepsy; Genetic; Genetic Markers; Genetic Risk; Genetic Variation; Geography; Grant; Health; Heterogeneity; Human; Image; Individual; Infrastructure; Intractable Epilepsy; Lesion; Lifting; Lobe; Longitudinal Studies; Machine Learning; Magnetic Resonance Imaging; Medical Genetics; Methods; Modeling; National Institute of Neurological Disorders and Stroke; Neurologic; Newly Diagnosed; Operative Surgical Procedures; Outcome; Partial Epilepsies; Patient-Focused Outcomes; Patients; Pattern; Persons; Pharmaceutical Preparations; Play; Postoperative Period; Prediction of Response to Therapy; Property; Reproducibility; Reproducibility of Results; Research; Resources; Risk Factors; Role; Sample Size; Sampling; Seizures; Series; Site; Syndrome; Temporal Lobe Epilepsy; Testing; Treatment outcome; United States National Institutes of Health; Visual; base; brain abnormalities; clinical biomarkers; clinical risk; cohort; comorbidity; connectome; data harmonization; design; determinants of treatment resistance; frontal lobe; genetic risk factor; imaging biomarker; imaging genetics; improved; individual patient; insight; interest; large datasets; large scale data; nervous system disorder; network models; neuroimaging; patient response; polygenic risk score; predicting response; quantitative imaging; response; surgery outcome; treatment planning

ABSTRACT Epilepsy is a devastating neurological illness that affects over 50 million people worldwide. Approximately one-third of patients do not respond to anti-seizure medication (ASM) and require additional diagnostic work-up, including consideration for surgery. Structural neuroimaging plays a pivotal role in the diagnostic evaluation of epilepsy, identifying visible lesions in many patients that co-localize with the seizure focus. However, up to 40% of patients have normal-appearing MRIs and this number is growing. As a result, there is increased interest in identifying subtle brain network abnormalities that could help to delineate the epileptogenic network and aid in the prediction of treatment response (i.e., response to ASMs and surgical outcomes). Unfortunately, methods for reliably identifying which patients will be drug-responsive versus drug- resistant, and which patients will achieve successful versus unsuccessful surgical outcomes are lacking. A major barrier to progress in this field has been obtaining quantitative imaging, including structural MRI (sMRI) and diffusion-weighted imaging (dMRI), clinical, and genetic data on large, geographically diverse samples of patients in whom different treatment outcomes can be evaluated. In the past, sample sizes have been insufficient to detect subtle, but reliable, brain abnormalities in patients with focal or generalized epilepsies that are genuinely associated with epilepsy and not with vicissitudes related to small or geographically restricted samples. A new, large-scale data initiative, ENIGMA4-Epilepsy, coupled with technological advancements that enable improved data harmonization are now lifting these barriers and allowing us to combine multi-site sMRI/dMRI, clinical, genetic data to predict important clinical outcomes, and making the results generalizable to a global epilepsy community. In this grant, we will leverage data collected through ENIGMA-Epilepsy—a consortium of 24 epilepsy centers from 14 countries (more than 2,250 patient and 1,727 healthy control sMRI/dMRI datasets) and the Human Epilepsy Project (HEP). We will include new network models (i.e., individualized connectomes) and polygenic risk scores (PRS) to test whether a combination of imaging, clinical, and genetic risk can accurately predict two clinical outcomes: drug-resistance and post-operative seizure outcome. Our scientific premise is that MRI-based assessment of whole-brain network properties, in combination with clinical data and PRS derived from genetic data, are able to predict (i) drug response in recently diagnosed epilepsy cases and (ii) postsurgical outcomes in individuals with drug-resistant epilepsy. This R01 addresses NIH's call for more reproducible studies by introducing a highly-powered design capable of capturing variability across patients with diverse clinical characteristics and treatment outcomes. This grant is also directly aligned with NINDS's 2020 Epilepsy Benchmarks (IIIB), which encourage the identification of genetic, clinical, and imaging biomarkers capable of predicting treatment response in epilepsy.

摘要 癫痫是一种毁灭性的神经系统疾病，影响着全世界超过5000万人。 大约三分之一的患者对抗癫痫药物（ASM）没有反应，需要额外的治疗。 诊断检查，包括考虑手术。结构神经影像学在神经功能缺损的诊断中起着关键作用。 癫痫的诊断评估，在许多患者中识别与癫痫发作共定位的可见病变 专心点然而，高达40%的患者的MRI表现正常，而且这个数字还在增长。因此，在本发明中， 人们对识别细微的脑网络异常越来越感兴趣，这些异常有助于描绘出 癫痫网络并有助于预测治疗反应（即，对ASM和手术的反应 成果）。不幸的是，用于可靠地鉴定哪些患者将对药物敏感， 耐药，以及哪些患者将获得成功与不成功的手术结果是缺乏的。 在这一领域取得进展的一个主要障碍是获得定量成像，包括结构MRI （sMRI）和弥散加权成像（dMRI），临床和遗传数据的大型，地理上不同的 可以评估不同治疗结果的患者样本。在过去，样本量 在局灶性或全身性脑梗死患者中， 真正与癫痫相关的癫痫，而不是与小的或 地理限制的样本。 一项新的大规模数据计划，ENIGMA 4-癫痫，加上技术进步， 现在，我们正在消除这些障碍，使我们能够将联合收割机多站点 sMRI/dMRI、临床、遗传学数据预测重要的临床结局，并使结果具有普遍性 to a global全球epilepsy癫痫community社区.在这项资助中，我们将利用通过ENIGMA-Epilepsy-a 来自14个国家24个癫痫中心的联盟（超过2,250名患者和1,727名健康对照 sMRI/dMRI数据集）和人类癫痫项目（HEP）。我们将包括新的网络模型（即， 个体化的连接体）和多基因风险评分（PRS）来测试成像， 临床和遗传风险可以准确预测两种临床结局：耐药性和术后 癫痫发作结果。我们的科学前提是，基于MRI的全脑网络特性评估， 与临床数据和源自遗传数据的PRS组合，能够预测（i）药物应答， 最近诊断的癫痫病例和（ii）耐药性癫痫患者的术后结局。 该R 01通过引入高性能设计解决了NIH对更多可重复研究的要求 能够捕获具有不同临床特征和治疗结果的患者之间的变异性。 这笔赠款也直接与NINDS的2020年癫痫基准（IIIB）保持一致，该基准鼓励 鉴定能够预测癫痫治疗反应的遗传、临床和成像生物标志物。