Letter: Inflammatory Potential of the Diet and Risk of Crohn's Disease and Ulcerative Colitis. Authors' Reply

IF 6.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Antoine Meyer, Aurélien Amiot
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引用次数: 0

Abstract

We thank Drs. Zhou, Sun Liu for their interest in our study [1, 2]. We suggest that a high inflammatory score of the diet (ISD) is associated with a higher risk of developing Crohn's disease (CD) but not ulcerative colitis (UC).

First, Zhou et al. suggested that results might be biased as the number of food items included In the Food Frequency Questionnaires ranged from 98 to 2059 across centres. However, this potential bias was taken into account by stratifying the analyses by centre as stated in the statistical analysis section of the manuscript.

Second, Zhou et al. stated that no false discovery rate was performed for multiple comparisons. However, in our study, there was only one exposure (inflammatory score of the diet) for two outcomes (CD and UC). Correcting for false discovery rate does not modify our results (Ptrend = 0.009 for CD and 0.208 for UC) [3]. Additional analyses according to sex or to items of the inflammatory score of the diet are only exploratory and do not require adjustment for multiple testing [4].

Third, Zhou et al. suggested that our analyses were underpowered to study an interaction between the ISD and sex for this risk of CD/UC, and that we should include a larger sample size, particularly men. However, the EPIC cohort is one of the largest cohorts worldwide as 394,255 participants from eight European countries, including 268,599 women and 125,656 men were included in the analyses. Even if a population as large as possible is desirable, this objective seems difficult to achieve. As the interaction tests for ISD between women and men and the risk of developing CD were not significant (p = 0.44 for quartile 2, 0.99 for quartile 3, and 0.66 for quartile 4), a differential effect of ISD between women and men is unlikely.

Finally, Zhou et al. mentioned that the analyses were not adjusted for some confounders such as antibiotic use, breastfeeding history, and prior gut infections. Indeed, these potential confounding factors were not available in our database. Therefore, as in all non-randomised epidemiology studies, residual confounding cannot be excluded.

In conclusion, our results suggest that a high inflammatory score of the diet is associated with a higher risk of developing CD but not UC. These results are in agreement with those reported in another study that used similar methodology with another inflammatory score (empirical dietary inflammatory pattern) [5].

Antoine Meyer: conceptualization, validation, writing – original draft. Aurélien Amiot: validation, conceptualization, writing – review and editing.

This article is linked to Meyer and Zhou et al. papers. To view these articles, visit https://doi.org/10.1111/apt.18497 and https://doi.org/10.1111/apt.70124.

信:饮食的炎症潜力和克罗恩病和溃疡性结肠炎的风险。作者的回复
我们感谢 Zhou、Sun Liu 博士对我们研究的关注[1, 2]。我们认为,膳食炎症评分(ISD)高与患克罗恩病(CD)的风险较高有关,但与患溃疡性结肠炎(UC)的风险无关。首先,Zhou 等人认为结果可能存在偏差,因为各中心的食物频率调查表中包含的食物数量从 98 种到 2059 种不等。然而,正如手稿中统计分析部分所述,通过按中心进行分层分析,这种潜在的偏倚已被考虑在内。其次,Zhou 等人指出没有对多重比较进行假发现率分析。然而,在我们的研究中,两个结果(CD 和 UC)只有一个暴露(饮食的炎症评分)。对虚假发现率进行校正并不会改变我们的结果(Ptrend = 0.009 用于 CD,0.208 用于 UC)[3]。根据性别或膳食炎症评分项目进行的其他分析只是探索性的,不需要进行多重检验调整[4]。第三,Zhou 等人认为,我们的分析不足以研究 ISD 与性别在 CD/UC 风险中的交互作用,我们应该纳入更大的样本量,尤其是男性样本。然而,EPIC队列是全球最大的队列之一,因为来自8个欧洲国家的394255名参与者(包括268599名女性和125656名男性)被纳入了分析。即使希望研究对象的规模越大越好,这一目标似乎也很难实现。最后,Zhou 等人提到,分析未对一些混杂因素进行调整,如抗生素使用、母乳喂养史和既往肠道感染。事实上,我们的数据库中没有这些潜在的混杂因素。因此,与所有非随机流行病学研究一样,不能排除残余混杂因素。总之,我们的研究结果表明,饮食中的高炎症评分与较高的 CD 发病风险有关,但与 UC 无关。这些结果与另一项研究的结果一致,该研究采用了类似的方法,并使用了另一种炎症评分(经验性饮食炎症模式)[5]。
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
CiteScore
15.60
自引率
7.90%
发文量
527
审稿时长
3-6 weeks
期刊介绍: Alimentary Pharmacology & Therapeutics is a global pharmacology journal focused on the impact of drugs on the human gastrointestinal and hepato-biliary systems. It covers a diverse range of topics, often with immediate clinical relevance to its readership.
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