Advanced Therapies in Elderly Patients With Inflammatory Bowel Disease: A Comparative Retrospective Cohort Study in Taiwan.

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics
Therapeutics and Clinical Risk Management Pub Date : 2025-04-25 eCollection Date: 2025-01-01 DOI:10.2147/TCRM.S518405
Shih-Hua Lin, Horng-Yih Chiu, Chia-Jung Kuo, Chien-Ming Chen, Ming-Yao Su, Ren-Chin Wu, Cheng-Tang Chiu, Chen-Wang Chang, Chen-Shuan Chung, Yu-Bin Pan, Puo-Hsien Le
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引用次数: 0

Abstract

Purpose: Inflammatory Bowel Disease (IBD) predominantly affects younger individuals, but emerging data indicates a shift toward older populations. Elderly-onset IBD (diagnosed at 60 years or older) differs from younger-onset IBD, presenting with atypical symptoms and higher risks of infections and malignancies. However, drug persistence is underexplored in the elderly IBD group, warranting further investigation to optimize treatment strategies for this demographic.

Patients and methods: This retrospective cohort study included IBD patients receiving advanced therapies at the Chang Gung IBD Center from October 2017 to September 2023. Patients were stratified into two groups: elderly-onset (≥60 years) and control (<60 years). We compared one-year persistence of advanced therapies, opportunistic infections, IBD-related admissions, complications, surgeries, and acute flare-ups between the groups. Specifically, we analyzed the one-year persistence of various advanced therapies within the elderly-onset cohort.

Results: The study included 511 IBD patients, 107 of whom were elderly-onset. Elderly-onset patients had a higher body mass index, a higher proportion of ulcerative colitis, fewer smokers, and lower levels of white blood cells, hemoglobin, and albumin. Differences were noted in Montreal classifications and a higher use of Vedolizumab. Clinical outcomes, including steroid-free remission rates, one-year therapy persistence, infections, complications, surgeries, and flare-ups, were comparable between groups. In Crohn's disease (CD), Infliximab and Ustekinumab exhibited higher one-year persistence. Predictors of one-year therapy persistence included Montreal L1 (OR: 6.722; 95% CI: 1.296-34.852; P=0.023), Ustekinumab use (OR: 5.672; 95% CI: 1.138-28.267; P=0.034), and hemoglobin level (OR: 1.612; 95% CI: 1.210-2.147; P=0.001) with an optimal cutoff of 11.65 g/dL.

Conclusion: Elderly-onset IBD patients display unique clinical characteristics and therapy persistence, particularly in CD, highlighting the necessity for customized therapeutic strategies.

台湾老年炎症性肠病患者的先进治疗:一项比较回顾性队列研究。
目的:炎症性肠病(IBD)主要影响年轻人,但新数据表明其向老年人转移。老年发病的IBD(诊断年龄在60岁或以上)不同于年轻发病的IBD,表现为非典型症状,感染和恶性肿瘤的风险更高。然而,老年IBD组的药物持久性尚未得到充分研究,需要进一步研究以优化这一人群的治疗策略。患者和方法:本回顾性队列研究纳入了2017年10月至2023年9月在长庚IBD中心接受先进治疗的IBD患者。将患者分为老年发病组(≥60岁)和对照组(结果:纳入511例IBD患者,其中107例为老年发病组)。老年发病患者体重指数较高,溃疡性结肠炎比例较高,吸烟者较少,白细胞、血红蛋白和白蛋白水平较低。在蒙特利尔分类和Vedolizumab的较高使用中注意到差异。临床结果,包括无类固醇缓解率、一年治疗持续性、感染、并发症、手术和突发事件,在两组之间具有可比性。在克罗恩病(CD)中,英夫利昔单抗和乌斯特金单抗表现出更高的一年持久性。一年治疗持续的预测因子包括蒙特利尔L1 (OR: 6.722;95% ci: 1.296-34.852;P=0.023), Ustekinumab的使用(OR: 5.672;95% ci: 1.138-28.267;P=0.034),血红蛋白水平(OR: 1.612;95% ci: 1.210-2.147;P=0.001),最佳临界值为11.65 g/dL。结论:老年IBD患者表现出独特的临床特征和治疗持久性,特别是在CD中,突出了定制治疗策略的必要性。
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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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