Zachos M, Tondeur M, Griffiths A M
Hospital for Sick Children, Division of Gastroenterology, Hepatology and Nutrition, 555 University Avenue, Toronto, Ontario, Canada, M5G 1X8.
Cochrane Database Syst Rev. 2007 Jan 24(1):CD000542. doi: 10.1002/14651858.CD000542.pub2.
The role of enteral nutrition in Crohn's disease is controversial. Increasing research on the mechanisms by which nutritional therapy improves the clinical well being of patients with Crohn's disease has led to novel formula design and trials comparing two different forms of enteral nutrition. This meta-analysis aims to provide an update on the existing effectiveness data for both corticosteroids versus enteral nutrition and for one form of enteral nutrition versus another for inducing remission of active Crohn's disease.
To evaluate the effectiveness of exclusive enteral nutrition (EN) as primary therapy to induce remission in Crohn's disease and to examine the importance of formula composition on effectiveness.
Studies were selected using a computer-assisted search of the on-line bibliographic databases MEDLINE (1966-2006) and EMBASE (1984-2006), as well as the Science Citation Index on Web of Science. Additional citations were sought by manual search of references of articles retrieved from the computerized search, abstracts submitted to major gastroenterologic meetings and published in the journals: American Journal of Gastroenterology, Gut, Gastroenterology, Journal of Pediatric Gastroenterology and Nutrition, and Journal of Parenteral and Enteral Nutrition, and from the reviewers' personal files or contact with leaders in the field.
All randomized and quasi-randomized controlled trials involving patients with active Crohn's disease defined by a clinical disease activity index were considered for review. Studies evaluating the administration of one type of enteral nutrition to one group of patients and another type of enteral nutrition or conventional corticosteroids to the other group were selected for review.
Data were extracted independently by two authors and any discrepancies were resolved by rereading and discussion. For the dichotomous variable, achievement of remission, individual and pooled trial statistics were calculated as odds ratios (OR) with 95% confidence intervals (CI); both fixed and random effect models were used. The results for each analysis were tested for heterogeneity using the chi square statistic. The studies were separated into two groups: A. one form of enteral nutrition compared with another form of enteral nutrition and B. one form of enteral nutrition compared with corticosteroids. Subgroup analyses were conducted on the basis of clinical or disease criteria and formula composition. Sensitivity analyses were conducted on the basis of the inclusion of abstract publications, methodologic quality and by random or fixed effects models.
In part A, of the 15 included eligible trials (one abstract) comparing different formulations of EN for the treatment of active CD, 11 compared one (or more) elemental formula to a non-elemental one, three compared enteral diets of similar protein composition but different fat composition, and one compared non-elemental diets differing only in glutamine enrichment. Meta-analysis of ten trials comprising 334 patients demonstrated no difference in the efficacy of elemental versus non-elemental formulas (OR 1.10; 95% CI 0.69 to 1.75). Subgroup analyses performed to evaluate the different types of elemental and non-elemental diets (elemental, semi-elemental and polymeric) showed no statistically significant differences. Further analysis of seven trials including 209 patients treated with EN formulas of differing fat content (low fat: < 20 g/1000 kCal versus high fat: > 20 g/1000 kCal) demonstrated no statistically significant difference in efficacy (OR 1.13; 95% CI 0.63 to 2.01). Similarly, the effect of very low fat content (< 3 g/1000 kCal) or type of fat (long chain triglycerides) were investigated, but did not demonstrate a difference in efficacy in the treatment of active CD, although a non significant trend was demonstrated favoring very low fat and very low long chain triglyceride content. This result should be interpreted with caution due to statistically significant heterogeneity and small sample size. Sensitivity analyses had no significant effects on the results. The role of specific fatty acids or disease characteristics on response to therapy could not be evaluated. In part B, eight trials (including two abstracts) comparing enteral nutrition to steroid therapy met the inclusion criteria for review. Meta-analysis of six trials that included 192 patients treated with enteral nutrition and 160 treated with steroids yielded a pooled OR of 0.33 favouring steroid therapy (95% CI 0.21 to 0.53). A sensitivity analysis including the abstracts resulted in an increase in the number of participants to 212 in the enteral nutrition group and 179 in the steroid group but the meta-analysis yielded a similar result (OR 0.36; 95% CI 0.23 to 0.56). There were inadequate data from full publications to perform further subgroup analyses by age, disease duration and disease location.
AUTHORS' CONCLUSIONS: Corticosteroid therapy is more effective than enteral nutrition for inducing remission of active Crohn's disease as was found in previous systematic reviews. Protein composition does not influence the effectiveness of EN in the treatment of active CD. A non significant trend favouring very low fat and/or very low long chain triglyceride content exists but larger trials are required to explore the significance of this finding.
肠内营养在克罗恩病中的作用存在争议。对营养治疗改善克罗恩病患者临床状况机制的研究不断增加,这促使了新型配方的设计以及比较两种不同形式肠内营养的试验。本荟萃分析旨在更新关于皮质类固醇与肠内营养以及一种肠内营养形式与另一种肠内营养形式在诱导活动性克罗恩病缓解方面的现有有效性数据。
评估全肠内营养(EN)作为诱导克罗恩病缓解的主要治疗方法的有效性,并研究配方组成对有效性的重要性。
通过计算机辅助检索在线书目数据库MEDLINE(1966 - 2006年)、EMBASE(1984 - 2006年)以及科学网的科学引文索引来选择研究。通过人工检索从计算机检索中获取的文章参考文献、提交给主要胃肠病学会议并发表在以下期刊上的摘要来寻找其他引文:《美国胃肠病学杂志》《肠道》《胃肠病学》《儿科胃肠病学与营养杂志》以及《肠外与肠内营养杂志》,还从审稿人的个人档案或与该领域的领军人物联系中获取。
所有涉及通过临床疾病活动指数定义的活动性克罗恩病患者的随机和半随机对照试验均纳入综述。选择评估向一组患者给予一种类型的肠内营养而向另一组给予另一种类型的肠内营养或传统皮质类固醇的研究进行综述。
由两位作者独立提取数据,任何差异通过重新阅读和讨论解决。对于二分变量,即缓解的达成情况,计算个体和汇总试验统计量为比值比(OR)及95%置信区间(CI);使用固定效应模型和随机效应模型。使用卡方统计量对每项分析的结果进行异质性检验。研究分为两组:A. 一种肠内营养形式与另一种肠内营养形式比较;B. 一种肠内营养形式与皮质类固醇比较。根据临床或疾病标准以及配方组成进行亚组分析。基于摘要出版物的纳入、方法学质量以及随机或固定效应模型进行敏感性分析。
在A部分,纳入的15项符合条件的试验(1篇摘要)比较了不同配方的EN用于治疗活动性CD,其中11项将一种(或多种)要素配方与非要素配方进行比较,3项比较了蛋白质组成相似但脂肪组成不同的肠内饮食,1项比较了仅在谷氨酰胺富集方面不同的非要素饮食。对包含334例患者的10项试验进行的荟萃分析表明,要素配方与非要素配方的疗效无差异(OR 1.10;95% CI 0.69至1.75)。为评估不同类型的要素和非要素饮食(要素、半要素和聚合型)进行的亚组分析未显示出统计学显著差异。对7项试验(包括209例接受不同脂肪含量EN配方治疗的患者,低脂:<20 g/1000 kCal与高脂:>20 g/1000 kCal)的进一步分析表明,疗效无统计学显著差异(OR 1.13;95% CI 0.63至2.01)。同样,研究了极低脂肪含量(<3 g/1000 kCal)或脂肪类型(长链甘油三酯)的影响,但在治疗活动性CD方面未显示出疗效差异,尽管显示出有利于极低脂肪和极低长链甘油三酯含量的非显著趋势。由于统计学显著的异质性和小样本量,该结果应谨慎解释。敏感性分析对结果无显著影响。无法评估特定脂肪酸或疾病特征对治疗反应的作用。在B部分,8项比较肠内营养与类固醇治疗且符合纳入标准的试验(包括2篇摘要)纳入综述。对6项试验(包括192例接受肠内营养治疗的患者和160例接受类固醇治疗的患者)进行的荟萃分析得出汇总OR为0.33,支持类固醇治疗(95% CI 0.21至0.53)。纳入摘要的敏感性分析使肠内营养组的参与者人数增加到212例,类固醇组增加到179例,但荟萃分析得出类似结果(OR 0.36;95% CI 0.23至0.56)。来自完整出版物的数据不足,无法按年龄分组、疾病持续时间和疾病部位进行进一步的亚组分析。
如先前系统评价所发现的,皮质类固醇治疗在诱导活动性克罗恩病缓解方面比肠内营养更有效。蛋白质组成不影响EN治疗活动性CD的有效性。存在有利于极低脂肪和/或极低长链甘油三酯含量的非显著趋势,但需要更大规模的试验来探究这一发现的意义。