Cardiovascular Complications Are Increased in Inflammatory Bowel Disease: A Path Toward Achievement of a Personalized Risk Estimation.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Vito Annese, Maria Laura Annunziata, Guglielmo Albertini Petroni, Emanuele Orlando, Sofia Cinque, Marzio Parisi, Paolo Biamonte, Giuseppe Dell'Anna, Anna Latiano, Serenella Castelvecchio
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引用次数: 0

Abstract

Background/Objectives: The global burden of inflammatory bowel diseases (IBDs) continues to rise, with up to 50% of patients experiencing extraintestinal manifestations. Cardiovascular diseases (CVDs) are of particular concern, ranking as the second leading cause of mortality in this population. Despite a comparatively lower prevalence of traditional cardiovascular (CV) risk factors, the persistent inflammatory milieu and immune dysregulation inherent to IBD may contribute to heightened CVD risk. In this study, following a review of the current literature, an ongoing prospective trial designed to clarify CV risk profiles in IBD patients is detailed. Methods: A cohort of patients with IBD is being enrolled for comprehensive baseline evaluation of CV risk factors, lifestyle metrics, and disease characteristics. The incidence of major adverse cardiovascular events (MACEs) will be tracked and contrasted with a gender- and age-matched non-IBD cohort over a 2-year follow-up period. In cases of MACE occurrence, a multi-omics analysis-including genomic, proteomic, transcriptomic, and microbiome profiling-will be performed, along with a parallel evaluation in matched IBD controls without MACE. An artificial intelligence (AI) framework will support the analysis of this complex dataset. Results: To date, over 150 patients with IBD have been enrolled, and detailed phenotypic data and biological samples have been collected. Conclusions: We aim to introduce an IBD-specific correction factor for existing CV risk scores upon study completion. This is particularly relevant for individuals under 40 years of age, who are often inadequately assessed by current risk stratification models.

炎症性肠病的心血管并发症增加:实现个性化风险评估的途径
背景/目的:全球炎症性肠病(IBDs)负担持续上升,高达50%的患者出现肠外症状。心血管疾病(cvd)尤其令人关注,它是这一人群的第二大死亡原因。尽管传统心血管(CV)危险因素的患病率相对较低,但IBD固有的持续炎症环境和免疫失调可能导致CVD风险增加。在本研究中,在回顾了当前文献后,详细介绍了一项正在进行的前瞻性试验,旨在阐明IBD患者的心血管风险概况。方法:纳入一组IBD患者,对心血管危险因素、生活方式指标和疾病特征进行综合基线评估。主要不良心血管事件(mace)的发生率将被跟踪,并在2年的随访期间与性别和年龄匹配的非ibd队列进行对比。在发生MACE的病例中,将进行多组学分析,包括基因组学、蛋白质组学、转录组学和微生物组分析,同时对没有MACE的匹配IBD对照进行平行评估。人工智能(AI)框架将支持对这一复杂数据集的分析。结果:迄今为止,已有150多名IBD患者入组,并收集了详细的表型数据和生物学样本。结论:我们的目标是在研究完成后为现有的CV风险评分引入ibd特异性校正因子。这对40岁以下的人尤其重要,目前的风险分层模型对他们的评估往往不充分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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