Clinical and Translational Epidemiology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States; Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Department of Biostatistics, Yale School of Public Health, New Haven, CT, United States.
Am J Clin Nutr. 2024 Nov;120(5):1053-1062. doi: 10.1016/j.ajcnut.2024.09.017. Epub 2024 Sep 20.
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.
We investigated associations of the insulinemic potential of diet, lifestyle (diet, physical activity, body weight), and metabolomic patterns with the risk of incident diverticulitis.
We conducted a prospective cohort study including participants in 3 nationwide cohorts of United States 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.
Among 184,508 participants [median age, 51 (interquartile range, 46-56) y], we documented 9123 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% confidence interval (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 < 0.0001 for both).
Participants with dietary and lifestyle patterns corresponding to higher insulinemic potential had an increased risk of diverticulitis, which might be mediated by metabolomic profiles.
饮食和生活方式因素与憩室炎的发生有关。然而,代谢紊乱(如高胰岛素血症)及其相应的代谢组学改变是否在其中起中介作用,目前仍知之甚少。
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生成潜力与新发憩室炎风险之间的关联。
我们进行了一项前瞻性队列研究,纳入了美国三个全国性健康专业人员队列中的参与者。根据经验性高胰岛素血症饮食指数(EDIH)和经验性高胰岛素血症生活方式指数(ELIH)的五分位数,估计新发憩室炎的风险。在具有代谢组学测量值的参与者亚组中,我们分别开发了代谢组学高胰岛素血症饮食指数(MDIH)和代谢组学高胰岛素血症生活方式指数(MLIH),以及与 EDIH 和 ELIH 相关的代谢物谱评分,并检测它们与随后憩室炎风险的相关性。我们还研究了 EDIH 和 ELIH 与憩室炎的关联是否由代谢物谱评分介导。
在 184508 名参与者中(中位年龄 51 岁[四分位距 46-56 岁]),我们在 3419945 人年中记录了 9123 例新发憩室炎病例。与最低五分位数的参与者相比,饮食和生活方式胰岛素生成潜力最高(EDIH 和 ELIH 最高五分位数)的参与者发生憩室炎的风险比为 1.22(95%置信区间[CI]:1.13,1.31)和 1.69(95% CI:1.57,1.81)。同样,代谢物谱评分与憩室炎风险显著相关,MDIH 的比值比为 1.96(95% CI:1.47,2.60),MLIH 的比值比为 1.93(95% CI:1.48,2.51),当比较极端五分位数时。MDIH 和 MLIH 可解释 EDIH 和 ELIH 相关憩室炎风险的比例分别为 70%(95% CI:6%,99%)和 57%(95% CI:23%,86%)(均 P < 0.0001)。
饮食和生活方式模式与更高胰岛素生成潜力相关的参与者发生憩室炎的风险增加,这可能是由代谢组学特征介导的。