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Emerging Prognostic Markers to Determine Crohns Disease Natural History and Improve Management Strategies

机译:新兴的预后指标以确定克罗恩病的自然历史并改善管理策略

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摘要

Because Crohn's disease (CD) is a chronic, incurable condition, patients require life-long therapeutic approaches to initiate and maintain symptom control, improve quality of life, avoid hospitalizations and surgery, and minimize short- and long-term toxicity and complications such as stricturing, fistulae, osteoporosis and associated bony fractures, and linear growth failure in pediatric patients. Many physicians use symptom-based classifications, such as those published in the American College of Gastroenterology Practice Guidelines, to classify disease severity. However, all current classifications for CD focus predominantly on treating the present symptoms and not on the long-term treatment goal of altering the natural history of the disease. If physicians were able to identify disease phenotypes; at diagnosis, they could advise a course of robust intervention or more. conservative therapeutic modalities with a lower risk of toxicity, as appropriate. Over the past several years, much interest has developed in the role of genetic and serologic markers as prognostic tools in CD. With these genetic and serologic data in mind, clinicians have a growing ability to harness laboratory and genetic testing information in order to stratify patients relative to their risk of disease progression from the time of diagnosis, allowing for a more individualized treatment plan for each patient.
机译:由于克罗恩病(CD)是一种慢性无法治愈的疾病,因此患者需要终生治疗方法来启动和维持症状控制,改善生活质量,避免住院和手术,并最大程度地减少短期和长期毒性及并发症,例如小儿患者的狭窄,瘘管,骨质疏松症和相关的骨性骨折以及线性生长衰竭。许多医师使用基于症状的分类(例如在美国胃肠病学实践指南中发布的分类)对疾病的严重程度进行分类。但是,当前所有的CD分类主要集中于治疗当前症状,而不是改变疾病自然史的长期治疗目标。如果医师能够识别疾病表型;在诊断时,他们可以建议采取强有力的干预措施或更多措施。适当的保守治疗方法,具有较低的毒性风险。在过去的几年中,人们对遗传和血清标志物作为CD预后工具的作用产生了浓厚的兴趣。考虑到这些遗传和血清学数据,临床医生具有越来越多的能力利用实验室和遗传检测信息,以便从诊断之日起将患者相对于其疾病进展风险进行分层,从而为每个患者制定更个性化的治疗计划。

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