4.4 Article

Effects of isoflavone-containing soya protein on ex vivo cholesterol efflux, vascular function and blood markers of CVD risk in adults with moderately elevated blood pressure: a dose-response randomised controlled trial

期刊

BRITISH JOURNAL OF NUTRITION
卷 117, 期 10, 页码 1403-1413

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S000711451700143X

关键词

HDL function; Central blood pressure; Arterial stiffness; Augmentation index

资金

  1. DuPont Nutrition and Health
  2. Penn State Clinical & Translational Research Institute, Pennsylvania State University Clinical and Translational Science Award (CTSA), National Institutes of Health/National Center for Advancing Translational Science (NIH/NCATS) [UL1 TR000127]

向作者/读者索取更多资源

Emerging CVD risk factors (e.g. HDL function and central haemodynamics) may account for residual CVD risk experienced by individuals who meet LDL-cholesterol and blood pressure (BP) targets. Recent evidence suggests that these emerging risk factors can be modified by polyphenol-rich interventions such as soya, but additional research is needed. This study was designed to investigate the effects of an isoflavone-containing soya protein isolate (delivering 25 and 50 g/d soya protein) on HDL function (i.e. ex vivo cholesterol efflux), macrovascular function and blood markers of CVD risk. Middle-aged adults (n 20; mean age=516 (sem 66) years) with moderately elevated brachial BP (mean systolic BP=129 (sem 9) mmHg; mean diastolic BP=825 (sem 84) mmHg) consumed 0 (control), 25 and 50 g/d soya protein in a randomised cross-over design. Soya and control powders were consumed for 6 weeks each with a 2-week compliance break between treatment periods. Blood samples and vascular function measures were obtained at baseline and following each supplementation period. Supplementation with 50 g/d soya protein significantly reduced brachial diastolic BP (-23 mmHg) compared with 25 g/d soya protein (Tukey-adjusted P=003) but not the control. Soya supplementation did not improve ex vivo cholesterol efflux, macrovascular function or other blood markers of CVD risk compared with the carbohydrate-matched control. Additional research is needed to clarify whether effects on these CVD risk factors depend on the relative health of participants and/or equol producing capacity.

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