Macular Pigment Research Group, Department of Chemical and Life Sciences, Waterford Institute of Technology, Waterford, Ireland.
Invest Ophthalmol Vis Sci. 2011 Nov 29;52(12):9207-17. doi: 10.1167/iovs.11-8025.
This study was designed to investigate serum and macular response to, and safety of supplementation with, meso-zeaxanthin (MZ), lutein (L), and zeaxanthin (Z), the carotenoids that constitute macular pigment (MP).
Forty-four healthy subjects were recruited into this randomized, placebo-controlled, clinical trial. Subjects consumed one tablet per day containing 10.6 mg MZ, 5.9 mg L, and 1.2 mg Z (intervention, I group) or placebo (P group). The spatial profile of MP optical density (MPOD) was measured with customized heterochromatic flicker photometry (cHFP), and serum concentrations of L and Z were quantified by using high performance liquid chromatography (HPLC). Subjects were assessed at baseline and at 3 and 6 months. Clinical pathology analysis was performed at baseline and 6 months.
Serum concentrations of L and Z increased significantly in the I group (P = 0.001 and 0.003, respectively) and remained stable in the P group (P > 0.05). There was a significant increase in central MPOD in the I group (0.25°: P = 0.001; 0.5°: P = 0.001), with no significant change in the P group (P > 0.05). Clinical pathology analysis confirmed that all variables remained within the normal reference range, with the exception of total cholesterol and low-density lipoprotein (LDL), which exhibited baseline values outside the accepted normal reference range before supplementation.
Subjects supplemented with MZ, L, and Z exhibited significant increases in serum concentrations of these carotenoids and a subsequent increase in central MPOD. Pathology analysis suggested no adverse clinical implications of consuming these carotenoids. (http://isrctn.org number, ISRCTN60816411).
本研究旨在探讨血清和黄斑对中-玉米黄质(MZ)、叶黄素(L)和玉米黄质(Z)(构成黄斑色素(MP)的类胡萝卜素)补充的反应和安全性。
将 44 名健康受试者纳入这项随机、安慰剂对照、临床试验。受试者每天服用一片含有 10.6 毫克 MZ、5.9 毫克 L 和 1.2 毫克 Z(干预,I 组)或安慰剂(P 组)的片剂。使用定制的双色闪烁光度计(cHFP)测量 MP 光学密度(MPOD)的空间分布,并用高效液相色谱法(HPLC)定量测量血清中 L 和 Z 的浓度。在基线和 3 个月和 6 个月时对受试者进行评估。在基线和 6 个月时进行临床病理分析。
I 组血清 L 和 Z 浓度显著升高(P = 0.001 和 0.003),而 P 组则保持稳定(P > 0.05)。I 组中央 MPOD 显著增加(0.25°:P = 0.001;0.5°:P = 0.001),而 P 组无明显变化(P > 0.05)。临床病理分析证实,除总胆固醇和低密度脂蛋白(LDL)外,所有变量均保持在正常参考范围内,这些变量在补充前的基线值超出了可接受的正常参考范围。
补充 MZ、L 和 Z 的受试者血清中这些类胡萝卜素的浓度显著增加,随后中央 MPOD 也增加。病理学分析表明,食用这些类胡萝卜素没有不良的临床影响。(http://isrctn.org 编号,ISRCTN60816411)。