饮食和生活方式的胰岛素电位、血浆代谢组和憩室炎风险:一项前瞻性队列研究。

IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS American Journal of Clinical Nutrition Pub Date : 2024-09-20 DOI:10.1016/j.ajcnut.2024.09.017
Jane Ha, Yilun Wu, Dong Hoon Lee, Fred K Tabung, Edward L Giovannucci, Lisa L Strate, Wenjie Ma, Andrew T Chan
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引用次数: 0

摘要

背景:饮食和生活方式因素与憩室炎的发病有关。然而,这些关联是否由新陈代谢紊乱(如高胰岛素血症和相应的代谢组学干扰)介导仍是一个未知数:我们研究了饮食、生活方式(饮食、体力活动、体重)和代谢组学模式的胰岛素血症潜能与憩室炎发病风险的关系:我们进行了一项前瞻性队列研究,研究对象包括美国三个全国性健康专业人员队列中的参与者。根据高胰岛素血症经验饮食指数(EDIH)和高胰岛素血症经验生活方式指数(ELIH)的五分位数估算了憩室炎的发病风险。在一部分进行了代谢组学测量的参与者中,我们制定了高胰岛素血症代谢组学饮食指数(MDIH)和高胰岛素血症代谢组学生活方式指数(MLIH),这两个代谢组学指数分别与 EDIH 和 ELIH 相关,并测试了它们与憩室炎后续风险的关联。我们还研究了 EDIH 和 ELIH 与憩室炎的关联是否由代谢物特征评分介导:在 184,508 名参与者(中位年龄 51 [IQR,46-56]岁)中,我们记录了 3,419,945 人年中的 9,123 例憩室炎病例。与最低五分位数的参与者相比,高胰岛素饮食和生活方式(EDIH 和 ELIH 的最高五分位数)最严重的参与者罹患憩室炎的风险比分别为 1.22(95% CI,1.13-1.31)和 1.69(95% CI,1.57-1.81)。同样,代谢物特征评分与憩室炎风险也有显著相关性,在比较极端五分位数时,MDIH 的几率比为 1.96(95% CI,1.47-2.60),MLIH 的几率比为 1.93(95% CI,1.48-2.51)。MDIH和MLIH可解释的EDIH和ELIH相关憩室炎风险比例分别为70%(95% CI,6%-99%)和57%(95% CI,23%-86%)(P 结论:MDIH和MLIH可解释的EDIH和ELIH相关憩室炎风险比例分别为70%(95% CI,6%-99%)和57%(95% CI,23%-86%):胰岛素潜能值较高的饮食和生活方式的参与者患憩室炎的风险增加,这可能是由代谢组学特征介导的。
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Dietary and lifestyle insulinemic potentials, plasma metabolome, and risk of diverticulitis: a prospective cohort study.

Background: Diet and lifestyle factors have been linked to developing diverticulitis. However, it remains largely unknown whether the associations are mediated by metabolic disturbance, such as hyperinsulinemia and corresponding metabolomic perturbations.

Objective: We investigated associations of the insulinemic potential of diet, lifestyle (diet, physical activity, body weight), and metabolomic patterns with the risk of incident diverticulitis.

Design: We conducted a prospective cohort study including participants in three nationwide cohorts of US health professionals. The risk of incident diverticulitis was estimated according to quintiles of the empirical dietary index for hyperinsulinemia (EDIH) and empirical lifestyle index for hyperinsulinemia (ELIH). In a subset of participants with metabolomic measurements, we developed metabolomic dietary index for hyperinsulinemia (MDIH) and metabolomic lifestyle index for hyperinsulinemia (MLIH), metabolite profile scores correlating with EDIH and ELIH, respectively, and tested their associations with subsequent risk of diverticulitis. We also examined whether the associations of EDIH and ELIH with diverticulitis were mediated by the metabolite profile scores.

Results: Among 184,508 participants (median age, 51 [IQR, 46-56] years), we documented 9,123 incident diverticulitis cases over 3,419,945 person-years. Compared with those in the lowest quintile, participants with the most hyperinsulinemic diets and lifestyles (highest quintiles of EDIH and ELIH) had a hazard ratio for the risk of diverticulitis of 1.22 (95% CI, 1.13-1.31) and 1.69 (95% CI, 1.57-1.81), respectively. Similarly, the metabolite profile scores were significantly associated with the diverticulitis risk with odds ratio of 1.96 for MDIH (95% CI, 1.47-2.60) and 1.93 for MLIH (95% CI, 1.48-2.51) when comparing extreme quintiles. The explainable proportions of EDIH- and ELIH-related diverticulitis risk by MDIH and MLIH were 70% (95% CI, 6%-99%) and 57% (95% CI, 23%-86%), respectively (P <.0001 for both).

Conclusions: Participants with dietary and lifestyle patterns corresponding to higher insulinemic potential had an increased risk of diverticulitis, which might be mediated by metabolomic profiles.

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来源期刊
CiteScore
12.40
自引率
4.20%
发文量
332
审稿时长
38 days
期刊介绍: American Journal of Clinical Nutrition is recognized as the most highly rated peer-reviewed, primary research journal in nutrition and dietetics.It focuses on publishing the latest research on various topics in nutrition, including but not limited to obesity, vitamins and minerals, nutrition and disease, and energy metabolism. Purpose: The purpose of AJCN is to: Publish original research studies relevant to human and clinical nutrition. Consider well-controlled clinical studies describing scientific mechanisms, efficacy, and safety of dietary interventions in the context of disease prevention or health benefits. Encourage public health and epidemiologic studies relevant to human nutrition. Promote innovative investigations of nutritional questions employing epigenetic, genomic, proteomic, and metabolomic approaches. Include solicited editorials, book reviews, solicited or unsolicited review articles, invited controversy position papers, and letters to the Editor related to prior AJCN articles. Peer Review Process: All submitted material with scientific content undergoes peer review by the Editors or their designees before acceptance for publication.
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