Improving Prediction of Medical Responsiveness and Clinical Outcomes in Crohn's Disease

改善克罗恩病医疗反应和临床结果的预测

• 批准号: 9306838
• 负责人: Ryan William Stidham
• 金额: $ 19.44万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-08-03 至 2020-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9306838
• 关键词: Acute; Affect; Agreement; Anti-Inflammatory Agents; Anti-inflammatory; Award; Bioinformatics; Biological Markers; Blood; Caliber; Characteristics; Childhood; Chronic; Cicatrix; Clinical; Clinical Research; Collaborations; Colonoscopy; Crohn' s disease; Data; Data Set; Decision Support Systems; Development; Development Plans; Diagnosis; Disease; Disease Management; Disease Progression; Excision; Failure; Fatty acid glycerol esters; Feces; Fibrosis; Focus Groups; Foundations; Future; Gastroenterologist; Gastroenterology; Goals; Grant; Hospitalization; Image; Image Analysis; Immunosuppression; Immunosuppressive Agents; Individual; Inflammation; Inflammatory; Inflammatory Bowel Diseases; Inflammatory disease of the intestine; Influentials; Injury; Internal Medicine; International; Intestinal Fibrosis; Intestines; Journals; K-Series Research Career Programs; Laboratories; Lead; Machine Learning; Measurement; Measures; Medical; Medical Imaging; Medicine; Mentors; Mentorship; Methodology; Methods; Michigan; Modernization; Morphology; Mucositis; Newly Diagnosed; Operative Surgical Procedures; Organ; Outcome; Patients; Pennsylvania; Phenotype; Physicians; Population; Probability; Process; Prospective Studies; Proteomics; Public Health Schools; Publishing; Recording of previous events; Research; Research Design; Research Proposals; Research Training; Residencies; Resources; Risk; Serum; Standardization; Statistical Data Interpretation; Steroids; Surgical Management; Therapeutic; Thick; Time; Training; Treatment Failure; Ultrasonography; United States; Universities; Variant; Virginia; Work; X-Ray Computed Tomography; base; biomarker development; biomarker discovery; blood-based biomarker; career; career development; clinical practice; clinical predictors; cohort; cost; digital imaging; disease phenotype; experience; glycoproteomics; improved; large bowel Crohn' s disease; learning strategy; lecturer; matriculation; novel; novel marker; personalized medicine; predict clinical outcome; predictive modeling; prevent; prognostic; prognostic tool; programs; prospective; public health relevance; quantitative imaging; research and development; response; skills; statistics; success; support tools; tool development; translational impact; translational scientist; treatment response

 DESCRIPTION (provided by applicant): This is a K23 career development award resubmission for Dr. Ryan Stidham, a gastroenterologist at the University of Michigan. Dr. Stidham's long-term career goal is to develop objective prognostics to personalize treatment decisions for patients with inflammatory bowel disease. The immediate goals of the proposal are to evaluate both analytic morphomics, an image analysis platform to quantify CT scan findings, and serum glycoproteomic profiles to predict therapeutic response in patients with Crohn's disease. Dr. Stidham's integrated research and career development plan align with goals of developing himself as a collaborative translational investigator, skilled in statistical analysis o large datasets, applying novel prognostics to improve clinical outcomes in Crohn's disease. Crohn's disease (CD) affects over 700,000 patients in the United States. Nearly 60% of CD patients require surgical resection for medically-unresponsive disease within 10 years of diagnosis. Frequently, patients present with deep bowel injury composed of both medically-responsive inflammatory and non- responsive fibrotic injury. Despite the presence of an inflammatory target, medical therapy may be futile and timely surgical management should be pursued. Further, strategies using early high-intensity immunosuppression to prevent future fibrostenotic disease are likely to over treat portions of the CD population. Therefore, therapeutic decisions are predicated on (1) the probability that existing disease activity will respond to medical therapy and (2) the probability of developing future fibrostenotic complications. Assessment using colonoscopy and surrogates of inflammation including imaging, blood, and stool-based biomarkers fail to provide comprehensive and quantitative assessments of bowel injury, including fibrosis. Despite its importance, there are no measures to account for deep bowel wall injury and intestinal fibrosis. This research proposal will utilize quantitative imaging findings of deep bowel injury in conjunction with blood-based biomarkers reflecting disease phenotypes to predict medical failure, defined as requiring future bowel resection, hospitalization, and prolonged steroid use. To achieve our imaging aims (Aim 1) we will use analytic morphomics, a computer image analysis method, to quantify body and bowel composition from over 4,000 CT-enterographies in a longitudinal 1200 patient CD cohort. In Aim 2, serum glycoproteome variance will be characterized in carefully phenotyped inflammatory and stricturing subjects to refine our preexisting biomarkers of fibrosis. We have demonstrated that variations of the serum glycoproteome reflect the degree of intestinal fibrosis present and expect that serum glycoproteomics can differentiate inflammatory from fibrotic phenotypes in CD. Optimized serum glycoproteome profiles will be used to predict future conversion from B1- inflammatory disease to B2/3 fibrostenotic disease in a pediatric prospective-inception cohort (RISK study). Aim 3 entails a prospective study combining analytic morphomics and serum glycoproteome profiles to predict therapeutic response and clinical outcomes; providing preliminary data for future R03/R01 studies. Dr. Stidham is a Lecturer of Medicine at the University of Michigan Division of Gastroenterology. He earned his medical degree from the University of Virginia (AOA), completed an internal medicine residency at the University of Pennsylvania, and was a T-32 research fellow at the University of Michigan (2011). His research background combines laboratory and clinical experience with Dr. Peter Higgins (primary mentor), focusing on novel biomarker development. Dr. Stidham has been awarded several prior grants for pilot work, including a MICHR-CTSA T32 Pilot Grant for Proteomics and a Crohn's and Colitis Foundation Career Development Award for ultrasound imaging research. He is in the process of completing a Masters program in Clinical Research Design and Statistical Analysis at the University of Michigan School of Public Health (matriculation in April 2015). He has published in several gastroenterology journals, presented research internationally, and has built the independent collaborations featured in this proposal. Central to this career development award, the candidate will leverage the expertise of several mentors and collaborators to develop deep foundational skillsets in analytic imaging, translational proteomics, bioinformatics, and machine learning methods. The University of Michigan houses a nationally recognized Inflammatory Bowel Disease Program, internationally recognized proteomics expertise, and a dedicated Analytic Morphomics Group focused on computational image analysis of organs. The mentored research training will be supplemented with focused graduate-level coursework in bioinformatics, medical image analysis, machine learning methodologies, and decision support systems provided through the University of Michigan Center for Computational Medicine and Bioinformatics and the School of Public Health. The Division of Gastroenterology and Department of Medicine have a history of strong support for Dr. Stidham and will provide the time, resources, and mentorship necessary to achieve his professional and research goals. The training provided through this career development award will be pivotal for the candidate's development as an independent translational investigator focused on individualizing therapeutic management. This research will provide the foundation for future collaborative studies to further develop these and other prognostic tools for the inflammatory bowel diseases.

 描述（由申请人提供）：这是密歇根大学胃肠病学家Ryan Stidham博士重新提交的K23职业发展奖。Stidham博士的长期职业目标是开发客观的诊断学，为炎症性肠病患者提供个性化的治疗决策。该提案的直接目标是评估分析形态学，量化CT扫描结果的图像分析平台，以及预测克罗恩病患者治疗反应的血清糖蛋白质组学。Stidham博士的综合研究和职业发展计划与发展自己作为协作翻译研究者的目标相一致，擅长大型数据集的统计分析，应用新的统计学来改善克罗恩病的临床结果。克罗恩病（CD）在美国影响超过70万患者。近60%的CD患者在诊断后10年内需要手术切除医学无反应的疾病。通常，患者存在由医学反应性炎性和非反应性纤维化损伤组成的深部肠损伤。尽管存在炎症靶点，但药物治疗可能无效，应及时进行手术治疗。此外，使用早期高强度免疫抑制来预防未来纤维狭窄疾病的策略可能过度治疗部分CD人群。因此，治疗决策取决于（1）现有疾病活动对药物治疗有反应的概率和（2）未来发生纤维狭窄并发症的概率。使用结肠镜检查和炎症替代物（包括成像、血液和基于粪便的生物标志物）的评估无法提供对肠损伤（包括纤维化）的全面和定量评估。尽管它的重要性，有没有措施来解释深肠壁损伤和肠纤维化。这项研究提案将利用定量成像结果的深部肠损伤结合血液为基础的生物标志物反映疾病表型预测医疗失败，定义为需要未来肠切除术，住院治疗，并延长类固醇的使用。为了实现我们的成像目标（目标1），我们将使用分析形态学，一种计算机图像分析方法，从纵向1200例CD患者队列的4,000多例CT肠道造影中量化身体和肠道成分。在目标2中，将在仔细分型的炎性和狭窄受试者中表征血清糖蛋白组变异，以改进我们先前存在的纤维化生物标志物。我们已经证明血清糖蛋白组的变化反映了肠纤维化的程度，并期望血清糖蛋白组学可以区分CD的炎症和纤维化表型。优化的血清糖蛋白谱将用于预测未来从B1炎症性疾病向B2/3纤维狭窄性疾病的转化，这是一项儿科前瞻性初始队列研究（RISK研究）。目的3需要一项前瞻性研究，结合分析形态学和血清糖蛋白质组谱来预测治疗反应和临床结局;为未来的R 03/R 01研究提供初步数据。Stidham博士是密歇根大学胃肠病学分部的医学讲师。他获得了弗吉尼亚大学（AOA）的医学学位，在宾夕法尼亚大学完成了内科住院医师，并在密歇根大学（2011年）担任T-32研究员。他的研究背景结合了Peter Higgins博士（主要导师）的实验室和临床经验，专注于新型生物标志物的开发。Stidham博士曾获得多项试点工作的赠款，包括MICHR-CTSA T32蛋白质组学试点资助和克罗恩病和结肠炎基金会超声成像研究职业发展奖。他正在密歇根大学公共卫生学院完成临床研究设计和统计分析硕士课程（2015年4月入学）。他曾在多个胃肠病学期刊上发表文章，在国际上发表研究成果，并建立了本提案中的独立合作。的核心 这个职业发展奖，候选人将利用几个导师和合作者的专业知识，在分析成像，翻译蛋白质组学， 生物信息学和机器学习方法。密歇根大学拥有全国公认的炎症性肠病计划，国际公认的蛋白质组学专业知识，以及专注于器官计算图像分析的专门分析形态学小组。指导的研究培训将辅以生物信息学，医学图像分析，机器学习方法和决策支持系统的重点研究生课程，通过密歇根大学计算医学和生物信息学中心和公共卫生学院提供。胃肠病学和医学系的部门有一个强有力的支持博士的历史. Stidham并将提供必要的时间，资源和指导，以实现他的专业和研究目标。通过这个职业发展奖提供的培训将是候选人的发展作为一个独立的翻译研究者专注于个性化治疗管理的关键。这项研究将为未来的合作研究提供基础，以进一步开发这些和其他炎症性肠病的预后工具。