• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

自身免疫性协议饮食治疗炎症性肠病的疗效。

Efficacy of the Autoimmune Protocol Diet for Inflammatory Bowel Disease.

机构信息

*Division of Gastroenterology, Scripps Clinic, La Jolla, California; †Scripps Translational Science Institute, La Jolla, California; ‡Division of Cardiology, Scripps Clinic, La Jolla, California; §Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; ‖School of Exercise and Nutritional Sciences, San Diego State University, San Diego, California; and ¶Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California.

出版信息

Inflamm Bowel Dis. 2017 Nov;23(11):2054-2060. doi: 10.1097/MIB.0000000000001221.

DOI:10.1097/MIB.0000000000001221
PMID:28858071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5647120/
Abstract

INTRODUCTION

Data suggest dietary modification can improve clinical responses in inflammatory bowel disease (IBD). The goal of this study was to determine the efficacy of an autoimmune protocol diet in patients with Crohn's disease and ulcerative colitis.

METHODS

We enrolled adults with active IBD (Harvey-Bradshaw index ≥ 5 or partial Mayo score ≥3 and erosions on endoscopy and/or elevated fecal calprotectin). For the autoimmune protocol, patients underwent 6-week elimination followed by 5-week maintenance phase. Clinical indices, laboratories, and biomarkers were assessed at baseline and weeks 6 and 11. Endoscopy was performed at study completion.

RESULTS

The final cohort included 15 patients with IBD, with mean disease duration 19 years (SD 14.6) and active biological use in 7 (47%) patients. Nutrient repletion was initiated for deficiencies in vitamin D (n = 3) and iron (n = 6). From week 0 to weeks 6 and 11, mean partial Mayo score significantly improved from 5.8 (SD 1.2) to 1.2 (SD 2.0) and 1.0 (SD 2.0) for ulcerative colitis, and mean Harvey-Bradshaw index significantly improved from 7 (SD 1.5) to 3.6 (SD 2.1) and 3.4 (SD 2.6) for Crohn's disease. C-reactive protein did not significantly change during study. Mean fecal calprotectin improved from 471 (SD 562) to 112 (SD 104) at week 11 (P = 0.12). Among those with follow-up endoscopy at week 11 (n = 7), improvements were noted in simple endoscopic score for Crohn's disease (n = 1), Rutgeerts score (n = 1), and Mayo endoscopy subscore (n = 4).

DISCUSSION

Dietary elimination can improve symptoms and endoscopic inflammation in patients with IBD. Randomized controlled trials are warranted.

摘要

介绍

有数据表明,饮食调整可以改善炎症性肠病(IBD)患者的临床反应。本研究的目的是确定克罗恩病和溃疡性结肠炎患者采用自身免疫协议饮食的疗效。

方法

我们招募了患有活动期 IBD(Harvey-Bradshaw 指数≥5 或部分 Mayo 评分≥3 且内镜下有糜烂和/或粪便钙卫蛋白升高)的成年人。对于自身免疫协议,患者进行 6 周的排除期,然后进入 5 周的维持期。在基线、第 6 周和第 11 周评估临床指标、实验室和生物标志物。在研究完成时进行内镜检查。

结果

最终队列包括 15 名 IBD 患者,平均疾病持续时间为 19 年(SD 14.6),7 名(47%)患者正在使用生物制剂。因维生素 D(n=3)和铁(n=6)缺乏而开始补充营养。从第 0 周到第 6 周和第 11 周,溃疡性结肠炎的部分 Mayo 评分从 5.8(SD 1.2)显著改善至 1.2(SD 2.0)和 1.0(SD 2.0),克罗恩病的 Harvey-Bradshaw 指数从 7(SD 1.5)显著改善至 3.6(SD 2.1)和 3.4(SD 2.6)。研究期间 C 反应蛋白没有明显变化。粪便钙卫蛋白在第 11 周时从 471(SD 562)降至 112(SD 104)(P=0.12)。在第 11 周进行了内镜随访的 7 名患者中,克罗恩病的简单内镜评分(n=1)、Rutgeerts 评分(n=1)和 Mayo 内镜亚评分(n=4)均有改善。

讨论

饮食排除可改善 IBD 患者的症状和内镜下炎症。需要进行随机对照试验。

相似文献

1
Efficacy of the Autoimmune Protocol Diet for Inflammatory Bowel Disease.自身免疫性协议饮食治疗炎症性肠病的疗效。
Inflamm Bowel Dis. 2017 Nov;23(11):2054-2060. doi: 10.1097/MIB.0000000000001221.
2
Low Fecal Calprotectin Correlates with Histological Remission and Mucosal Healing in Ulcerative Colitis and Colonic Crohn's Disease.低粪便钙卫蛋白与溃疡性结肠炎和结肠克罗恩病的组织学缓解及黏膜愈合相关。
Inflamm Bowel Dis. 2016 Mar;22(3):623-30. doi: 10.1097/MIB.0000000000000652.
3
High Percentage of IBD Patients with Indefinite Fecal Calprotectin Levels: Additional Value of a Combination Score.炎症性肠病患者粪便钙卫蛋白水平不确定的比例较高:联合评分的附加价值。
Dig Dis Sci. 2017 Feb;62(2):465-472. doi: 10.1007/s10620-016-4397-6. Epub 2016 Dec 8.
4
A longitudinal study of fecal calprotectin and the development of inflammatory bowel disease in ankylosing spondylitis.一项关于粪便钙卫蛋白与强直性脊柱炎患者炎症性肠病发生发展的纵向研究。
Arthritis Res Ther. 2017 Feb 2;19(1):21. doi: 10.1186/s13075-017-1223-2.
5
Disease activity assessment in IBD: clinical indices and biomarkers fail to predict endoscopic remission.炎症性肠病的疾病活动度评估:临床指标和生物标志物无法预测内镜缓解。
Inflamm Bowel Dis. 2015 Apr;21(4):824-31. doi: 10.1097/MIB.0000000000000341.
6
Evaluation of disease activity in IBD at the time of diagnosis by the use of clinical, biochemical, and fecal markers.在诊断时通过临床、生化和粪便标志物评估炎症性肠病的疾病活动度。
Scand J Gastroenterol. 2011 Sep;46(9):1081-91. doi: 10.3109/00365521.2011.584897. Epub 2011 May 30.
7
Fecal calprotectin is a surrogate marker for endoscopic lesions in inflammatory bowel disease.粪便钙卫蛋白是炎症性肠病内镜下病变的替代标志物。
Inflamm Bowel Dis. 2012 Dec;18(12):2218-24. doi: 10.1002/ibd.22917. Epub 2012 Feb 16.
8
Capsule endoscopic findings correlate with fecal calprotectin and C-reactive protein in patients with suspected small-bowel Crohn's disease.在疑似小肠克罗恩病患者中,胶囊内镜检查结果与粪便钙卫蛋白及C反应蛋白相关。
Scand J Gastroenterol. 2014 Sep;49(9):1084-90. doi: 10.3109/00365521.2014.920915. Epub 2014 May 22.
9
Neopterin is a novel reliable fecal marker as accurate as calprotectin for predicting endoscopic disease activity in patients with inflammatory bowel diseases.新型蝶呤可作为一种可靠的粪便标志物,其预测炎症性肠病患者内镜下疾病活动的准确性与钙卫蛋白相当。
Inflamm Bowel Dis. 2013 Apr;19(5):1043-52. doi: 10.1097/MIB.0b013e3182807577.
10
Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease.儿童炎症性肠病临床症状与炎症生物标志物的关系。
Eur J Pediatr. 2016 Oct;175(10):1335-42. doi: 10.1007/s00431-016-2762-2. Epub 2016 Aug 29.

引用本文的文献

1
Early life factors, diet and microbiome, and risk of inflammatory bowel disease.早期生活因素、饮食与微生物群以及炎症性肠病风险
J Can Assoc Gastroenterol. 2025 Feb 21;8(Suppl 2):S44-S50. doi: 10.1093/jcag/gwae039. eCollection 2025 Mar.
2
Autoimmune protocol diet: A personalized elimination diet for patients with autoimmune diseases.自身免疫性疾病饮食方案:一种针对自身免疫性疾病患者的个性化排除饮食法。
Metabol Open. 2024 Dec 30;25:100342. doi: 10.1016/j.metop.2024.100342. eCollection 2025 Mar.
3
Assessing the Nutrient Composition of a Carnivore Diet: A Case Study Model.评估肉食动物饮食的营养成分:一个案例研究模型。
Nutrients. 2024 Dec 31;17(1):140. doi: 10.3390/nu17010140.
4
Lithium Coupled with C6-Carboxyl Improves the Efficacy of Oligoguluronate in DSS-Induced Ulcerative Colitis in C57BL/6J Mice.锂与C6-羧基结合可提高低聚古罗糖醛酸对C57BL/6J小鼠DSS诱导的溃疡性结肠炎的疗效。
Mar Drugs. 2024 Dec 21;22(12):573. doi: 10.3390/md22120573.
5
The Gut Microbiome Advances Precision Medicine and Diagnostics for Inflammatory Bowel Diseases.肠道微生物组推动炎症性肠病的精准医学和诊断进展。
Int J Mol Sci. 2024 Oct 19;25(20):11259. doi: 10.3390/ijms252011259.
6
Restore Intestinal Barrier Integrity: An Approach for Inflammatory Bowel Disease Therapy.恢复肠道屏障完整性:一种炎症性肠病的治疗方法。
J Inflamm Res. 2024 Aug 14;17:5389-5413. doi: 10.2147/JIR.S470520. eCollection 2024.
7
Inflammatory Bowel Disease: A Comprehensive Analysis of Molecular Bases, Predictive Biomarkers, Diagnostic Methods, and Therapeutic Options.炎症性肠病:分子基础、预测生物标志物、诊断方法和治疗选择的综合分析。
Int J Mol Sci. 2024 Jun 27;25(13):7062. doi: 10.3390/ijms25137062.
8
Sterile Diet Causes Gut Microbiome Collapse of Cancer Patients Post Hematopoietic Cell Transplantation, But Normal Diet Recovers Them.无菌饮食导致造血细胞移植后癌症患者的肠道微生物组崩溃,但正常饮食可使其恢复。
Adv Sci (Weinh). 2024 Sep;11(34):e2403991. doi: 10.1002/advs.202403991. Epub 2024 Jul 8.
9
Ultra-processed foods and food additives in gut health and disease.超加工食品和食品添加剂与肠道健康和疾病。
Nat Rev Gastroenterol Hepatol. 2024 Jun;21(6):406-427. doi: 10.1038/s41575-024-00893-5. Epub 2024 Feb 22.
10
Intestinal microbiota regulates the gut-thyroid axis: the new dawn of improving Hashimoto thyroiditis.肠道微生物群调节肠道-甲状腺轴:改善桥本甲状腺炎的新曙光。
Clin Exp Med. 2024 Feb 22;24(1):39. doi: 10.1007/s10238-024-01304-4.

本文引用的文献

1
Dietary emulsifiers directly alter human microbiota composition and gene expression ex vivo potentiating intestinal inflammation.膳食乳化剂可直接改变人体微生物群组成并在体外增强肠道炎症,从而影响基因表达。
Gut. 2017 Aug;66(8):1414-1427. doi: 10.1136/gutjnl-2016-313099. Epub 2017 Mar 21.
2
Development of the IBD Disk: A Visual Self-administered Tool for Assessing Disability in Inflammatory Bowel Diseases.炎症性肠病圆盘的开发:一种用于评估炎症性肠病残疾情况的视觉自我管理工具。
Inflamm Bowel Dis. 2017 Mar;23(3):333-340. doi: 10.1097/MIB.0000000000001033.
3
Clinical and Fecal Microbial Changes With Diet Therapy in Active Inflammatory Bowel Disease.活动性炎症性肠病饮食疗法的临床及粪便微生物变化
J Clin Gastroenterol. 2018 Feb;52(2):155-163. doi: 10.1097/MCG.0000000000000772.
4
Diet as a Trigger or Therapy for Inflammatory Bowel Diseases.饮食作为炎症性肠病的诱因或疗法。
Gastroenterology. 2017 Feb;152(2):398-414.e6. doi: 10.1053/j.gastro.2016.10.019. Epub 2016 Oct 25.
5
Patients Perceive Clinical Benefit with the Specific Carbohydrate Diet for Inflammatory Bowel Disease.炎症性肠病患者认为特定碳水化合物饮食具有临床益处。
Dig Dis Sci. 2016 Nov;61(11):3255-3260. doi: 10.1007/s10620-016-4307-y. Epub 2016 Sep 16.
6
The intestinal microbiome, barrier function, and immune system in inflammatory bowel disease: a tripartite pathophysiological circuit with implications for new therapeutic directions.炎症性肠病中的肠道微生物群、屏障功能和免疫系统:一个三方病理生理回路及其对新治疗方向的启示
Therap Adv Gastroenterol. 2016 Jul;9(4):606-25. doi: 10.1177/1756283X16644242. Epub 2016 Apr 19.
7
Low Fecal Calprotectin Correlates with Histological Remission and Mucosal Healing in Ulcerative Colitis and Colonic Crohn's Disease.低粪便钙卫蛋白与溃疡性结肠炎和结肠克罗恩病的组织学缓解及黏膜愈合相关。
Inflamm Bowel Dis. 2016 Mar;22(3):623-30. doi: 10.1097/MIB.0000000000000652.
8
Specific carbohydrate diet for pediatric inflammatory bowel disease in clinical practice within an academic IBD center.学术性炎症性肠病中心临床实践中针对儿童炎症性肠病的特殊碳水化合物饮食
Nutrition. 2016 Apr;32(4):418-25. doi: 10.1016/j.nut.2015.08.025. Epub 2015 Nov 30.
9
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.关联分析确定了38个炎症性肠病的易感基因座,并突出了不同人群间共有的遗传风险。
Nat Genet. 2015 Sep;47(9):979-986. doi: 10.1038/ng.3359. Epub 2015 Jul 20.
10
Deregulation of intestinal anti-microbial defense by the dietary additive, maltodextrin.膳食添加剂麦芽糊精对肠道抗菌防御的失调作用。
Gut Microbes. 2015;6(1):78-83. doi: 10.1080/19490976.2015.1005477.