溃疡性结肠炎:发病机制、生物标志物和治疗策略的进展。

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Pharmacogenomics & Personalized Medicine Pub Date : 2025-09-05 eCollection Date: 2025-01-01 DOI:10.2147/PGPM.S536459
Siyuan Bu, Xiaozhen Cheng, Meng Chen, Yongduo Yu
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引用次数: 0

摘要

溃疡性结肠炎是一种由多种因素引起的炎症性肠病,以结肠黏膜持续炎症为特征,可导致预期寿命缩短,需要结肠切除术以及发展为结直肠癌的可能性增加。尽管全世界大约有500万人受到溃疡性结肠炎的影响,但其复杂的机制仍然没有得到充分的定义,这阻碍了有效治疗方法的发展。肠外并发症,包括肠病性关节炎,也在疾病负担和管理的背景下得到解决。这篇综述探讨了溃疡性结肠炎的多方面发病机制,强调了上皮屏障异常、不规则免疫反应、炎症介质的释放和肠道微生物群组成的改变等关键因素。我们还强调了最近在提高疾病检测和监测准确性的诊断性生物标志物方面取得的进展。传统的药物策略与生物疗法的出现一起进行了回顾,特别是那些针对肿瘤坏死因子(TNF)、白细胞介素和整合素的疗法,它们显著地改变了治疗方法。已建立的治疗方法(如5-氨基水杨酸,皮质类固醇)和新兴药物(如JAK抑制剂,S1P调节剂)被清楚地描述。联合策略-如双重生物方案或JAK抑制剂联合抗整合素药物-也在专门的小节中讨论。我们讨论了利用小分子靶向的新疗法,特别是那些抑制Janus激酶(JAK)和调节鞘氨醇-1-磷酸(S1P)受体的疗法,为治疗提供了有希望的途径。此外,粪便微生物群移植(FMT)被评估为一种治疗选择,因为它显示出恢复微生物平衡的希望。总的来说,这些进展强调了免疫失调、生物治疗和微生物群调节在重塑溃疡性结肠炎精确治疗中的关键作用。当前知识的综合强调了继续研究以完善治疗策略和改善溃疡性结肠炎患者预后的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ulcerative Colitis: Advances in Pathogenesis, Biomarkers, and Therapeutic Strategies.

Ulcerative Colitis: Advances in Pathogenesis, Biomarkers, and Therapeutic Strategies.

Ulcerative Colitis: Advances in Pathogenesis, Biomarkers, and Therapeutic Strategies.

Ulcerative colitis represents an inflammatory bowel disease with multiple contributing factors, marked by persistent inflammation of the colonic mucosa, which can lead to a reduced life expectancy and an elevated likelihood of requiring colectomy as well as developing colorectal cancer. Despite impacting roughly 5 million individuals worldwide, the intricate mechanisms underlying ulcerative colitis are still inadequately defined, hindering the development of effective treatments. Extra-intestinal complications, including enteropathic arthritis, are also addressed in the context of disease burden and management. This review explores the multifaceted pathogenesis of ulcerative colitis, emphasizing critical factors such as abnormalities in the epithelial barrier, irregular immune responses, the release of inflammatory mediators, and alterations in gut microbiota composition. We also underscore recent advancements in diagnostic biomarkers that improve the accuracy of disease detection and monitoring. Conventional medicinal strategies are reviewed alongside the emergence of biological therapies, notably those that target tumor necrosis factor (TNF), interleukins, and integrins, which have significantly altered management approaches. Established therapies (eg, 5-aminosalicylic acid, corticosteroids) and emerging agents (eg, JAK inhibitors, S1P modulators) are clearly delineated. Combination strategies-such as dual biologic regimens or JAK inhibitors combined with anti-integrin agents-are also discussed in dedicated subsections. We discuss novel therapies that utilize small molecule targeting, particularly those that inhibit Janus kinase (JAK) and modulate sphingosine-1-phosphate (S1P) receptors, presenting promising avenues for treatment. Additionally, fecal microbiota transplantation (FMT) is evaluated as a therapeutic option, as it shows promise in restoring microbial balance. Collectively, these advances underscore the pivotal roles of immune dysregulation, biologic therapies, and microbiota modulation in reshaping precision management of ulcerative colitis. This synthesis of current knowledge underscores the necessity for continued research to refine therapeutic strategies and improve patient outcomes in ulcerative colitis.

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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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