Vogiatzoglou Anna, Mulligan Angela A, Bhaniani Amit, Lentjes Marleen A H, McTaggart Alison, Luben Robert N, Heiss Christian, Kelm Malte, Merx Marc W, Spencer Jeremy P E, Schroeter Hagen, Khaw Kay-Tee, Kuhnle Gunter G C
Department of Food & Nutritional Sciences, University of Reading, UK.
Department of Public Health and Primary Care, University of Cambridge, UK.
Free Radic Biol Med. 2015 Jul;84:1-10. doi: 10.1016/j.freeradbiomed.2015.03.005. Epub 2015 Mar 17.
Dietary intervention studies suggest that flavan-3-ol intake can improve vascular function and reduce the risk of cardiovascular diseases (CVD). However, results from prospective studies failed to show a consistent beneficial effect. Associations between flavan-3-ol intake and CVD risk in the Norfolk arm of the European Prospective Investigation into Cancer and Nutrition (EPIC-Norfolk) were investigated. Data were available from 24,885 (11,252 men; 13,633 women) participants, recruited between 1993 and 1997 into the EPIC-Norfolk study. Flavan-3-ol intake was assessed using 7-day food diaries and the FLAVIOLA Flavanol Food Composition database. Missing data for plasma cholesterol and vitamin C were imputed using multiple imputation. Associations between flavan-3-ol intake and blood pressure at baseline were determined using linear regression models. Associations with CVD risk were estimated using Cox regression analyses. Median intake of total flavan-3-ols was 1034mg/d (range: 0-8531mg/d) for men and 970mg/d (0-6695mg/d) for women, median intake of flavan-3-ol monomers was 233mg/d (0-3248mg/d) for men and 217 (0-2712mg/d) for women. There were no consistent associations between flavan-3-ol monomer intake and baseline systolic and diastolic blood pressure (BP). After 286,147 person-years of follow-up, there were 8463 cardiovascular events and 1987 CVD related deaths; no consistent association between flavan-3-ol intake and CVD risk (HR 0.93, 95% CI: 0.87; 1.00; Q1 vs Q5) or mortality was observed (HR 0.93, 95% CI: 0.84; 1.04). Flavan-3-ol intake in EPIC-Norfolk is not sufficient to achieve a statistically significant reduction in CVD risk.
饮食干预研究表明,摄入黄烷-3-醇可改善血管功能并降低心血管疾病(CVD)风险。然而,前瞻性研究结果未能显示出一致的有益效果。本研究调查了欧洲癌症与营养前瞻性调查(EPIC-Norfolk)诺福克分部中黄烷-3-醇摄入量与CVD风险之间的关联。数据来自1993年至1997年招募到EPIC-Norfolk研究中的24,885名参与者(11,252名男性;13,633名女性)。使用7天食物日记和FLAVIOLA黄烷醇食物成分数据库评估黄烷-3-醇摄入量。血浆胆固醇和维生素C的缺失数据采用多重填补法进行填补。使用线性回归模型确定基线时黄烷-3-醇摄入量与血压之间的关联。使用Cox回归分析估计与CVD风险的关联。男性总黄烷-3-醇的中位数摄入量为1034mg/d(范围:0 - 8531mg/d),女性为970mg/d(0 - 6695mg/d),黄烷-3-醇单体的中位数摄入量男性为233mg/d(0 - 3248mg/d),女性为217mg/d(0 - 2712mg/d)。黄烷-3-醇单体摄入量与基线收缩压和舒张压(BP)之间没有一致的关联。经过286,147人年的随访,有8463例心血管事件和1987例CVD相关死亡;未观察到黄烷-3-醇摄入量与CVD风险(HR 0.93,95%CI:0.87;1.00;Q1与Q5)或死亡率之间存在一致的关联(HR 0.93,95%CI:0.84;1.04)。EPIC-Norfolk研究中的黄烷-3-醇摄入量不足以在统计学上显著降低CVD风险。