Thyagarajan Bharat, Howard Annie Green, Durazo-Arvizu Ramon, Eckfeldt John H, Gellman Marc D, Kim Ryung S, Liu Kiang, Mendez Armando J, Penedo Frank J, Talavera Gregory A, Youngblood Marston E, Zhao Lihui, Sotres-Alvarez Daniela
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, United States.
Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, United States.
Clin Chim Acta. 2016 Dec 1;463:129-137. doi: 10.1016/j.cca.2016.10.019. Epub 2016 Oct 15.
Biomarker variability, which includes within-individual variability (CV), between-individual variability (CV) and methodological variability (CV) is an important determinant of our ability to detect biomarker-disease associations. Estimates of CV and CV may be population specific and little data exists on biomarker variability in diverse Hispanic populations. Hence, we evaluated all 3 components of biomarker variability in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) using repeat blood collections (n=58) and duplicate blood measurements (n=761-929 depending on the biomarker).
We estimated the index of individuality (II) ((CV+CV)/CV) for 41 analytes and evaluated differences in the II across sexes and age groups.
Biomarkers such as fasting glucose, triglycerides and ferritin had substantially higher inter-individual variability and lower II in HCHS/SOL as compared to the published literature. We also found significant sex-specific differences in the II for neutrophil count, platelet count, hemoglobin, % eosinophils and fasting glucose. The II for fasting insulin, post oral glucose tolerance test glucose and cystatin C was significantly higher among the 18-44y age group as compared to the 45+y age group.
The implications of these findings for determining biomarker-disease associations in Hispanic populations need to be evaluated in future studies.
生物标志物变异性,包括个体内变异性(CV)、个体间变异性(CV)和方法学变异性(CV),是我们检测生物标志物与疾病关联能力的重要决定因素。CV和CV的估计可能因人群而异,关于不同西班牙裔人群生物标志物变异性的数据很少。因此,我们在西班牙裔社区健康研究/拉丁裔研究(HCHS/SOL)中,利用重复采血(n = 58)和重复血液测量(根据生物标志物不同,n = 761 - 929)评估了生物标志物变异性的所有三个组成部分。
我们估计了41种分析物的个体性指数(II)((CV + CV)/CV),并评估了不同性别和年龄组之间II的差异。
与已发表的文献相比,HCHS/SOL中的空腹血糖、甘油三酯和铁蛋白等生物标志物个体间变异性显著更高,个体性指数更低。我们还发现中性粒细胞计数、血小板计数、血红蛋白、嗜酸性粒细胞百分比和空腹血糖的个体性指数存在显著的性别差异。与45岁及以上年龄组相比,18 - 44岁年龄组的空腹胰岛素、口服葡萄糖耐量试验后血糖和胱抑素C的个体性指数显著更高。
这些发现对确定西班牙裔人群中生物标志物与疾病关联的意义需要在未来的研究中进行评估。