Kim Keewan, Bloom Michael S, Fujimoto Victor Y, Bell Erin M, Yucel Recai M, Browne Richard W
Department of Environmental Health Sciences, University at Albany, State University of New York, School of Public Health Rm. #157, One University Place, Rensselaer, 12144, NY, USA.
Department of Epidemiology and Biostatistics, University at Albany, State University of New York, Rensselaer, NY, USA.
J Assist Reprod Genet. 2016 Mar;33(3):423-430. doi: 10.1007/s10815-016-0648-x. Epub 2016 Jan 12.
The purpose of this study was to examine the biological variability of follicular fluid (FF) high density lipoprotein (HDL) particle components measured in ipsilateral ovarian follicles.
We collected FF from two ipsilateral follicles among six women undergoing in vitro fertilization (IVF). We measured concentrations of 19 FF HDL particle components, including HDL cholesterol, free cholesterol, four cholesteryl esters, phospholipids, triglycerides, paraoxonase and arylesterase activities, apolipoproteins A-1 and A-2 (ApoA-1 and ApoA-2), and seven lipophilic micronutrients, by automated analysis and with high-performance liquid chromatography. We assessed biological variability using two-stage nested analysis of variance and compared values with those previously published for contralateral follicles.
For most FF HDL analytes, there was little variability between follicles relative to the variability between women (i.e., %σ(2) F:%σ(2) B <0.5). Intraclass correlation coefficients were >0.80 for HDL cholesterol (0.82), phospholipids (0.89), paraoxonase (0.96), and arylesterase (0.91) activities, ApoA-1 (0.89), and ApoA-2 (0.90), and single specimen collections were required to estimate the subject-specific mean, demonstrating sufficient reliability for use as biomarkers of the follicular microenvironment in epidemiologic and clinical studies.
These preliminary results raise the possibility for tighter regulation of HDL in follicles within the same ovary vs. between ovaries. Thus, collection of a single FF specimen may be sufficient to estimate HDL particle components concentrations within a single ovary. However, our results should be interpreted with caution as the analysis was based on a small sample.
本研究旨在检测在同侧卵巢卵泡中测得的卵泡液(FF)高密度脂蛋白(HDL)颗粒成分的生物学变异性。
我们从6名接受体外受精(IVF)的女性的两个同侧卵泡中收集了卵泡液。我们通过自动分析和高效液相色谱法测量了19种卵泡液HDL颗粒成分的浓度,包括HDL胆固醇、游离胆固醇、四种胆固醇酯、磷脂、甘油三酯、对氧磷酶和芳基酯酶活性、载脂蛋白A-1和A-2(ApoA-1和ApoA-2)以及七种亲脂性微量营养素。我们使用两阶段嵌套方差分析评估生物学变异性,并将数值与先前发表的对侧卵泡的数值进行比较。
对于大多数卵泡液HDL分析物,相对于女性之间的变异性,卵泡之间的变异性很小(即,%σ(2)F:%σ(2)B<0.5)。HDL胆固醇(0.82)、磷脂(0.89)、对氧磷酶(0.96)和芳基酯酶(0.91)活性、ApoA-1(0.89)和ApoA-2(0.90)的组内相关系数>0.80,并且需要单次样本采集来估计个体特异性均值,这表明其具有足够的可靠性,可在流行病学和临床研究中用作卵泡微环境的生物标志物。
这些初步结果增加了同一卵巢内卵泡与不同卵巢间HDL调控更严格的可能性。因此,采集单个卵泡液样本可能足以估计单个卵巢内HDL颗粒成分的浓度。然而,由于分析基于小样本,我们的结果应谨慎解释。