Rohrmann Sabine, Shvetsov Yurii B, Morimoto Yukiko, Wilkens Lynne R, Monroe Kristine R, Le Marchand Loïc, Franke Adrian A, Kolonel Laurence N, Maskarinec Gertraud
Division of Chronic Disease Epidemiology, Epidemiology, Biostatistics and Prevention Institute (EBPI), University of Zurich, Hirschengraben 84, 8001, Zürich, Switzerland.
Epidemiology Program, University of Hawaii Cancer Center, Honolulu, HI, USA.
Cancer Causes Control. 2018 Jun;29(6):601-607. doi: 10.1007/s10552-018-1034-z. Epub 2018 Apr 18.
To examine if dietary intake of foods rich in flavonoids, which have been shown to be inversely associated with chronic diseases, is associated with inflammatory processes.
This analysis includes controls of case-control studies nested within the Multiethnic Cohort (MEC) who completed a validated food frequency questionnaire at cohort entry. Biomarkers were assessed in blood donated during follow-up (mean = 9.6 years). We used multivariate linear regression adjusted for potential confounders to estimate associations between intake of flavanones, flavonols, and isoflavones and levels of adiponectin, leptin, C-reactive protein, interleukin (IL)-1β, IL-6, IL-10, and tumor necrosis factor-α.
Among the 1,287 participants, the respective median intakes of flavanones, flavonols, and isoflavones were 26.5, 12.4, and 1.3 mg/day at cohort entry. With the exception of flavanone intake, which was statistically significantly inversely associated with adiponectin (p = 0.01) and IL-6 concentrations (p = 0.01), none of the examined flavonoids was related with levels of adipokines or inflammatory markers. Heterogeneity by ethnicity was only observed for flavonol intake and IL-10 (p = 0.04) and may be the result of multiple testing. These null findings were confirmed in a subset of participants who completed a second dietary history within 2.6 years of blood draw.
The current results do not support a consistent association between dietary intake of flavonoids and markers of inflammatory processes.
研究富含类黄酮的食物的饮食摄入量是否与炎症过程相关,此前研究表明类黄酮摄入量与慢性病呈负相关。
本分析纳入了多民族队列(MEC)中病例对照研究的对照组,这些参与者在队列入组时完成了一份经过验证的食物频率问卷。在随访期间(平均9.6年)采集的血液中评估生物标志物。我们使用多元线性回归,并对潜在混杂因素进行调整,以估计黄烷酮、黄酮醇和异黄酮的摄入量与脂联素、瘦素、C反应蛋白、白细胞介素(IL)-1β、IL-6、IL-10和肿瘤坏死因子-α水平之间的关联。
在1287名参与者中,队列入组时黄烷酮、黄酮醇和异黄酮的各自中位数摄入量分别为26.5、12.4和1.3毫克/天。除黄烷酮摄入量与脂联素(p = 0.01)和IL-6浓度(p = 0.01)呈统计学显著负相关外,所检测的类黄酮均与脂肪因子或炎症标志物水平无关。仅在黄酮醇摄入量和IL-10方面观察到种族异质性(p = 0.04),这可能是多次检验的结果。在采血后2.6年内完成第二次饮食史调查的参与者亚组中,这些阴性结果得到了证实。
目前的结果不支持类黄酮的饮食摄入量与炎症过程标志物之间存在一致关联。