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Analytical quality goals for 25-vitamin D based on biological variation

机译:基于生物学差异的25种维生素D的分析质量目标

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Background: Measurement of 25-hydroxyvitamin D, (25D) is central in the investigation of pathologies of bone and mineral ion metabolism and in determining a patient's vitamin D status. More recently much research interest has lead to investigating the role it can play in decreasing the risk of many chronic illnesses, including common cancers, autoimmune diseases, infectious diseases, and cardiovascular disease. Knowledge of the biological variation of an analyte forms an essential part of evaluating a new analyte enabling the objective assessment of the changes in serial results, the utility of reference intervals as well as establishing laboratory quality specifications. Methods: This study determined the biological variation of 25D in 20 healthy individuals that was calculated according to the familiar methods outlined by Fraser and Harris. Results: The within-subject variation was 12.1% and the between subject variation was 40.3%. The critical difference for sequential values significant at P0.05 was calculated as 38.4%. The within-subject variation forms a relatively small part of the reference interval shown by the low index of individuality of 0.3. Objective analytical quality goals have also been established which have shown achievable minimum performance for imprecision of ~6%. The desirable analytical bias goal was ~10%. Conclusion: This study has objectively shown that the analytical precision of current instruments is being achieved contrary to the known problems surrounding the analytical bias for 25D assays. The limitations of using reference intervals for 25D, both in diagnoses and monitoring are shown. J. Clin. Lab. Anal. 25:130–133, 2011. ? 2011 Wiley-Liss, Inc.
机译:背景:25-羟基维生素D(25D)的测量在骨骼和矿物质离子代谢的病理研究以及确定患者的维生素D状态中至关重要。最近,许多研究兴趣促使人们研究它在降低许多慢性疾病(包括常见癌症,自身免疫性疾病,传染性疾病和心血管疾病)风险中的作用。了解分析物的生物学变化是评估新分析物的重要部分,从而能够客观评估连续结果的变化,参考区间的实用性以及建立实验室质量规格。方法:本研究确定了20位健康个体中25D的生物学变异,该变异是根据Fraser和Harris概述的熟悉方法计算得出的。结果:受试者内部变异为12.1%,受试者之间变异为40.3%。计算出P <0.05时显着的连续值的临界差计算为38.4%。受试者内的变异形成参考区间的相对较小的部分,该指数由0.3的低个性指数表示。还建立了客观的分析质量目标,这些目标显示出〜6%的不精确度可以达到的最低性能。理想的分析偏差目标为〜10%。结论:这项研究客观地表明,与围绕25D分析的分析偏差相关的已知问题相反,当前仪器的分析精度正在实现。显示了在诊断和监视中使用25D参考间隔的局限性。 J.临床。实验室肛门25:130–133,2011.? 2011年Wiley-Liss,Inc.

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