首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Evaluation of vitamin D standardization program protocols for standardizing serum 25-hydroxyvitamin D data: A case study of the program's potential for national nutrition and health surveys
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Evaluation of vitamin D standardization program protocols for standardizing serum 25-hydroxyvitamin D data: A case study of the program's potential for national nutrition and health surveys

机译:评估标准化血清25-羟基维生素D数据的维生素D标准化计划协议:该计划在全国营养和健康调查中的潜力的案例研究

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Background: The Vitamin D Standardization Program (VDSP) has developed protocols for standardizing procedures of 25-hydroxyvitamin D [25(OH)D] measurement in National Health/Nutrition Surveys to promote 25(OH)D measurements that are accurate and comparable over time, location, and laboratory procedure to improve public health practice. Objective: We applied VDSP protocols to existing ELISA-derived serum 25(OH)D data from the Irish National Adult Nutrition Survey (NANS) as a case-study survey and evaluated their effectiveness by comparison of the protocol-projected estimates with those from a reanalysis of survey serums by using liquid chromatography-tandem mass spectrometry (LC-tandem MS). Design: The VDSP reference system and protocols were applied to ELISA-based serum 25(OH)D data from the representative NANS sample (n = 1118). A reanalysis of 99 stored serums by using standardized LC-tandem MS and resulting regression equations yielded predicted standardized serum 25(OH)D values, which were then compared with LC-tandem MS reanalyzed values for all serums. Results: Year-round prevalence rates for serum 25(OH)D concentrations <30, <40, and <50 nmol/L were 6.5%, 21.9%, and 40.0%, respectively, via original ELISA measurements and 11.4%, 25.3%, and 43.7%, respectively, when VDSP protocols were applied. Differences in estimates at <30- and <40-nmol/L thresholds, but not at the <50-nmol/L threshold, were significant (P < 0.05). A reanalysis of all serums by using LC-tandem MS confirmed prevalence estimates as 11.2%, 27.2%, and 45.0%, respectively. Prevalences of serum 25(OH)D concentrations >125 nmol/L were 1.2%, 0.3%, and 0.6% by means of ELISA, VDSP protocols, and LC-tandem MS, respectively. Conclusion: VDSP protocols hold a major potential for national nutrition and health surveys in terms of the standardization of serum 25(OH)D data.
机译:背景:维生素D标准化计划(VDSP)开发了用于在国家健康/营养调查中标准化25-羟基维生素D [25(OH)D]测量程序的规程,以促进25(OH)D测量的准确性和长期可比性,位置和实验室程序,以改善公共卫生实践。目的:我们将VDSP方案应用于来自爱尔兰国家成人营养调查(NANS)的现有ELISA衍生的血清25(OH)D数据作为案例研究,并通过将方案预测的估计值与来自国家的成人估计值的估计值进行比较来评估其有效性液相色谱-串联质谱法(LC-串联质谱)对被调查血清进行重新分析。设计:将VDSP参考系统和方案应用于来自代表性NANS样品(n = 1118)的基于ELISA的血清25(OH)D数据。使用标准的LC串联质谱对99种储存的血清进行重新分析,并使用回归方程得出预测的标准血清25(OH)D值,然后将其与所有血清的LC串联MS再分析值进行比较。结果:通过最初的ELISA测量,血清25(OH)D浓度<30,<40和<50 nmol / L的全年患病率分别为6.5%,21.9%和40.0%,分别为11.4%,25.3% ,当应用VDSP协议时分别为43.7%。在<30-nmol / L阈值和<40-nmol / L阈值下,估计值差异显着(P <0.05)。使用LC串联质谱对所有血清进行的重新分析证实患病率分别为11.2%,27.2%和45.0%。通过ELISA,VDSP方案和LC串联质谱分析,血清25(OH)D浓度> 125 nmol / L的患病率分别为1.2%,0.3%和0.6%。结论:就血清25(OH)D数据的标准化而言,VDSP方案在全国营养和健康调查中具有重大潜力。

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