University of Surrey, Guildford, United Kingdom.
Ann Intern Med. 2011 May 17;154(10):656-65. doi: 10.7326/0003-4819-154-10-201105170-00005.
High selenium status has been linked to elevated blood cholesterol levels in cross-sectional studies.
To investigate the effect of selenium supplementation on plasma lipids.
Randomized, placebo-controlled, parallel-group study stratified by age and sex. Participants, research nurses, and persons assessing outcomes were blinded to treatment assignment. (International Standard Randomised Controlled Trial Number Register registration number: ISRCTN25193534)
4 general practices in the United Kingdom.
501 volunteers aged 60 to 74 years.
Participants received selenium, 100 mcg/d (n = 127), 200 mcg/d (n = 127), or 300 mcg/d (n = 126), as high-selenium yeast or a yeast-based placebo (n = 121) for 6 months.
Total and high-density lipoprotein (HDL) cholesterol concentrations were measured in nonfasting plasma samples stored from participants in the UK PRECISE (United Kingdom PREvention of Cancer by Intervention with SElenium) Pilot Study at baseline (n = 454) and at 6 months (n = 394). Non-HDL cholesterol levels were calculated.
Mean plasma selenium concentration was 88.8 ng/g (SD, 19.2) at baseline and increased statistically significantly in the treatment groups. The adjusted difference in change in total cholesterol levels for selenium compared with placebo was -0.22 mmol/L (-8.5 mg/dL) (95% CI, -0.42 to -0.03 mmol/L [-16.2 to -1.2 mg/dL]; P = 0.02) for 100 mcg of selenium per day, -0.25 mmol/L (-9.7 mg/dL) (CI, -0.44 to -0.07 mmol/L [-17.0 to -2.7 mg/dL]; P = 0.008) for 200 mcg of selenium per day, and -0.07 mmol/L (-2.7 mg/dL) (CI, -0.26 to 0.12 mmol/L [-10.1 to 4.6 mg/dL]; P = 0.46) for 300 mcg of selenium per day. Similar reductions were observed for non-HDL cholesterol levels. There was no apparent difference in change in HDL cholesterol levels with 100 and 200 mcg of selenium per day, but the difference was an adjusted 0.06 mmol/L (2.3 mg/dL) (CI, 0.00 to 0.11 mmol/L [0.0 to 4.3 mg/dL]; P = 0.045) with 300 mcg of selenium per day. The total-HDL cholesterol ratio decreased progressively with increasing selenium dose (overall P = 0.01).
The duration of supplementation was limited, as was the age range of the participants.
Selenium supplementation seemed to have modestly beneficial effects on plasma lipid levels in this sample of persons with relatively low selenium status. The clinical significance of the findings is unclear and should not be used to justify the use of selenium supplementation as additional or alternative therapy for dyslipidemia. This is particularly true for persons with higher selenium status, given the limitations of the trial and the potential additional risk in other metabolic dimensions.
The Cancer Research Campaign (now Cancer Research UK) and the University of Surrey.
多项横断面研究表明,高硒状态与血液胆固醇水平升高有关。
研究硒补充剂对血浆脂质的影响。
按年龄和性别分层的随机、安慰剂对照、平行组研究。参与者、研究护士和评估结果的人员对治疗分配均不知情。(国际标准随机对照试验注册号:ISRCTN25193534)
英国的 4 家普通诊所。
年龄在 60 岁至 74 岁的 501 名志愿者。
参与者接受硒补充剂,100 μg/d(n=127)、200 μg/d(n=127)或 300 μg/d(n=126),形式为高硒酵母或酵母安慰剂(n=121),持续 6 个月。
在英国 PRECISE(通过干预硒预防癌症)试点研究中,从 UK PRECISE 研究的参与者中采集非禁食状态下的血浆样本并储存,在基线时(n=454)和 6 个月时(n=394)测量总胆固醇和高密度脂蛋白(HDL)胆固醇浓度。计算非高密度脂蛋白胆固醇水平。
基线时血浆硒浓度的平均值为 88.8 ng/g(SD,19.2),且治疗组的浓度呈统计学显著升高。与安慰剂相比,硒的总胆固醇水平变化的调整差异为-0.22 mmol/L(-8.5 mg/dL)(95%CI,-0.42 至-0.03 mmol/L [-16.2 至-1.2 mg/dL];P=0.02),每天补充 100 μg 硒;-0.25 mmol/L(-9.7 mg/dL)(CI,-0.44 至-0.07 mmol/L [-17.0 至-2.7 mg/dL];P=0.008),每天补充 200 μg 硒;-0.07 mmol/L(-2.7 mg/dL)(CI,-0.26 至 0.12 mmol/L [-10.1 至 4.6 mg/dL];P=0.46),每天补充 300 μg 硒。非高密度脂蛋白胆固醇水平也观察到类似的降低。每天补充 100 和 200 μg 硒时,HDL 胆固醇水平的变化没有明显差异,但 300 μg 硒时的差异为调整后 0.06 mmol/L(2.3 mg/dL)(CI,0.00 至 0.11 mmol/L [0.0 至 4.3 mg/dL];P=0.045)。随着硒剂量的增加,总胆固醇/高密度脂蛋白胆固醇比值逐渐降低(总体 P=0.01)。
补充剂的持续时间有限,参与者的年龄范围也有限。
在这个相对低硒状态的人群样本中,硒补充似乎对血浆脂质水平有适度的有益影响。研究结果的临床意义尚不清楚,不应作为治疗血脂异常的额外或替代疗法来使用硒补充剂。对于硒状态较高的人群,尤其如此,因为试验存在局限性,而且在其他代谢方面可能会有额外的风险。
英国癌症研究协会(现为英国癌症研究)和萨里大学。