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.
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.
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DOI:
10.1017/s000711451700143x
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发表时间:
2017-05
期刊:
影响因子:
--
通讯作者:
Kris-Etherton PM
中科院分区:
文献类型:
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作者:
Richter CK;Skulas-Ray AC;Fleming JA;Link CJ;Mukherjea R;Krul ES;Kris-Etherton PM
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 50g/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 = 51.6 (SEM 6.6) years) with moderately elevated brachial BP (mean systolic BP = 129 (SEM 9) mmHg; mean diastolic BP = 82.5 (SEM 8.4)mmHg) consumed 0 (control), 25 and 50g/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 (−2.3 mmHg) compared with 25 g/d soya protein (Tukey-adjusted P = 0.03) 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.