内脏脂肪组织对克罗恩病抗肿瘤坏死因子-α的影响。

IF 4.2 3区 医学
Kangrong Li, Pan Gong, Yongbin Zhang, Minji Liu, Zinan Zhang, Xiaoyu Yu, Mingmei Ye, Li Tian
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引用次数: 0

摘要

背景:目前尚不清楚内脏脂肪组织(VAT)是否可以预测克罗恩病(CD)患者对抗肿瘤坏死因子-α (anti-TNF-α)治疗的反应。目的:本研究旨在探讨VAT是否能预测英夫利昔单抗(IFX)对不同部位CD的疗效及其与血清TNF-α水平和IFX血清谷浓度的关系。设计:这是一项多中心回顾性研究。方法:纳入2014年1月至2021年1月期间接受IFX治疗的CD患者。通过计算机断层扫描(CT)获得内脏脂肪区域的周长。根据病变部位(L1、L2和L3)和内脏脂肪面积对参与者进行分类。参与者被分为结肠不受累的非内脏肥胖(L1-VATL)、结肠不受累的内脏肥胖(L1-VATH)、结肠受累的非内脏肥胖(L2 + L3-VATL)和结肠受累的内脏肥胖(L2 + L3-VATH)组。本研究的终点设定为6个月和12个月的疾病缓解状态。结果:最终队列包括140例患者。在6个月和12个月的疗效方面,L1-VATL组(73.8%比36.8%,p = 0.006)和L1-VATH组(81.0%比47.4%,p = 0.008)的疗效差异有统计学意义。在血清TNF-α水平和IFX血清谷浓度分析中,L1-VATL与L1-VATH (59.5 pg/mL vs 236.0 pg/mL, pTNF-α = 0.006)、(10.0 μg/mL vs 0.4 μg/mL, pIFX = 0.000)以及L1-VATH与L2 + L3-VATH (78.7 pg/mL vs 118.6 pg/mL, pTNF-α = 0.031)、(0.4 μg/mL vs 6.40 μg/mL, pIFX = 0.017)之间存在显著差异。结论:在L1患者中,VAT值预测IFX的疗效,VAT值高表明疗效差。VAT水平可能是预测IFX对不同类型CD患者疗效的有用放射学指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of visceral adipose tissue on anti-tumour necrosis factor-α in Crohn's disease.

Effects of visceral adipose tissue on anti-tumour necrosis factor-α in Crohn's disease.

Effects of visceral adipose tissue on anti-tumour necrosis factor-α in Crohn's disease.

Effects of visceral adipose tissue on anti-tumour necrosis factor-α in Crohn's disease.

Background: It remains unclear whether visceral adipose tissue (VAT) can predict the response of patients with Crohn's disease (CD) to anti-tumour necrosis factor-α (anti-TNF-α) therapy.

Objectives: This study aimed to investigate whether VAT predicts the efficacy of infliximab (IFX) for different sites of CD and its relationship with serum TNF-α levels and IFX serum trough concentration.

Design: This is a multicentre retrospective study.

Methods: Patients with CD treated with IFX from January 2014 to January 2021 were included. The perimeter of the visceral adipose area was obtained by a Computed Tomography (CT) scan. Participants were classified according to the lesion site (L1, L2, and L3) and visceral fat area. The participants were divided into colon-uninvolved non-visceral obesity (L1-VATL), colon-uninvolved visceral obesity (L1-VATH), colon-involved non-visceral obesity (L2 + L3-VATL), and colon involved visceral obesity (L2 + L3-VATH) groups. The end points of this study were set as disease remission status at 6 and 12 months.

Results: The final cohort included 140 patients. Regarding efficacy at 6 and 12 months, there was a significant difference between L1-VATL (73.8% versus 36.8%, p = 0.006) and L1-VATH (81.0% versus 47.4%, p = 0.008) groups. In the analysis of serum TNF-α levels and IFX serum trough concentrations, there was a significant difference between L1-VATL and L1-VATH (59.5 pg/mL versus 236.0 pg/mL, pTNF-α = 0.006), (10.0 μg/mL versus 0.4 μg/mL, pIFX = 0.000), and L1-VATH and L2 + L3-VATH (78.7 pg/mL versus 118.6 pg/mL, pTNF-α = 0.031), (0.4 μg/mL versus 6.40 μg/mL, pIFX = 0.017).

Conclusion: In L1 patients, the VAT level predicted the efficacy of IFX, with high VAT values indicating poor efficacy. The VAT level may be a useful radiological marker to predict the efficacy of IFX in patients with various types of CD.

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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology Medicine-Gastroenterology
自引率
2.40%
发文量
103
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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