The Impact of Concomitant Hypothyroid Disease on the Course of Inflammatory Bowel Disease.

IF 2.5 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Digestive Diseases and Sciences Pub Date : 2025-05-01 Epub Date: 2025-03-01 DOI:10.1007/s10620-025-08956-6
Maaz Ahsan, Jahnavi Udaikumar, Simon Hong, Adam S Faye, Seymour Katz, Olivia Delau, Jordan Axelrad
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引用次数: 0

Abstract

Background: Inflammatory bowel disease (IBD) is a chronic, immune-mediated inflammatory disorder of the gastrointestinal tract. In IBD, systemic inflammation and immune dysregulation may also impact extraintestinal organs, such as the thyroid gland. Despite this, little is known about the influence of concomitant hypothyroidism on the clinical course of IBD.

Methods: A retrospective analysis was conducted among adult patients with IBD and at least one thyroid stimulating hormone (TSH) measurement within a large healthcare network. Patient charts were reviewed, and baseline demographics, disease characteristics, biomarkers, healthcare utilization, medication use, and other comorbidities were extracted. Patients were stratified by those with IBD only and those with concomitant IBD and hypothyroidism. Multivariable logistic regression was used to identify factors associated with concomitant hypothyroidism. Concomitant disease as an independent predictor for lab abnormalities and increased healthcare utilization was also assessed using multivariable logistic and negative binomial regression.

Results: We identified 287 adult patients with IBD, including 146 (50.9%) with Crohn's disease (CD) and 141 (49.1%) with ulcerative colitis (UC). Among this sample, 178 (62.0%) patients had concomitant hypothyroidism. Concomitant disease was associated with older age (adjOR 1.04, 95% CI 1.02, 1.06), female sex (adjOR 1.78, 95% CI 1.01, 3.16), and the presence of other extraintestinal manifestations (adjOR 2.30, 95% CI 1.06, 5.00). Concomitant disease was also found to be a significant predictor for increased healthcare utilization, specifically, higher number of radiation-based abdominal imaging (RBAI) studies (adjIRR: 1.89, 95% CI 1.08, 3.32).

Conclusion: Patients with both IBD and hypothyroidism have an increased likelihood of other extraintestinal manifestations compared to individuals who have IBD without hypothyroidism. Furthermore, patients with concomitant disease exhibited greater healthcare utilization, specifically, increased rates of RBAI studies. The presence of concomitant hypothyroidism may be associated with a more severe course of IBD.

伴发性甲状腺功能减退对炎症性肠病病程的影响。
背景:炎症性肠病(IBD)是一种慢性、免疫介导的胃肠道炎症性疾病。在IBD中,全身炎症和免疫失调也可能影响肠外器官,如甲状腺。尽管如此,关于合并甲状腺功能减退对IBD临床病程的影响知之甚少。方法:回顾性分析在大型医疗保健网络中对IBD和至少一种促甲状腺激素(TSH)测量的成年患者进行了分析。回顾了患者图表,提取了基线人口统计学、疾病特征、生物标志物、医疗保健利用、药物使用和其他合并症。患者分为单纯IBD患者和合并IBD和甲状腺功能减退患者。采用多变量logistic回归来确定与甲状腺功能减退相关的因素。使用多变量逻辑回归和负二项回归评估了伴随疾病作为实验室异常和医疗保健利用率增加的独立预测因子。结果:我们确定了287例IBD成年患者,其中146例(50.9%)患有克罗恩病(CD), 141例(49.1%)患有溃疡性结肠炎(UC)。其中178例(62.0%)患者伴有甲状腺功能减退。伴发疾病与年龄较大(adjOR 1.04, 95% CI 1.02, 1.06)、女性(adjOR 1.78, 95% CI 1.01, 3.16)和其他肠外表现相关(adjOR 2.30, 95% CI 1.06, 5.00)。研究还发现,伴随疾病是医疗保健利用率增加的重要预测因素,特别是基于放射的腹部成像(RBAI)研究的数量增加(adjIRR: 1.89, 95% CI 1.08, 3.32)。结论:与没有甲状腺功能减退的IBD患者相比,同时患有IBD和甲状腺功能减退的患者出现其他肠外症状的可能性增加。此外,伴有疾病的患者表现出更高的医疗保健利用率,特别是RBAI研究的发生率增加。伴有甲状腺功能减退可能与IBD更严重的病程有关。
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
Digestive Diseases and Sciences
Digestive Diseases and Sciences 医学-胃肠肝病学
CiteScore
6.40
自引率
3.20%
发文量
420
审稿时长
1 months
期刊介绍: Digestive Diseases and Sciences publishes high-quality, peer-reviewed, original papers addressing aspects of basic/translational and clinical research in gastroenterology, hepatology, and related fields. This well-illustrated journal features comprehensive coverage of basic pathophysiology, new technological advances, and clinical breakthroughs; insights from prominent academicians and practitioners concerning new scientific developments and practical medical issues; and discussions focusing on the latest changes in local and worldwide social, economic, and governmental policies that affect the delivery of care within the disciplines of gastroenterology and hepatology.
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