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Individualized correction of insulin measurement in hemolyzed serum samples

机译:溶血血清样品中胰岛素测量的个性化校正

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Insulin measurement plays a key role in the investigation of patients with hypoglycemia, subtype classification of diabetes mellitus, insulin resistance, and impaired beta cell function. However, even slight hemolysis can negatively affect insulin measurement due to RBC insulin-degrading enzyme (IDE). Here, we derived and validated an individualized correction equation in an attempt to eliminate the effects of hemolysis on insulin measurement. The effects of hemolysis on insulin measurement were studied by adding lysed self-RBCs to serum. A correction equation was derived, accounting for both percentage and exposure time of hemolysis. The performance of this individualized correction was evaluated in intentionally hemolyzed samples. Insulin concentration decreased with increasing percentage and exposure time of hemolysis. Based on the effects of hemolysis on insulin measurement of 17 donors (baseline insulin concentrations ranged from 156 to 2119 pmol/L), the individualized hemolysis correction equation was derived: INScorr = INSmeas/(0.705lgHb(plasma)/Hb(serum) - 0.001Time - 0.612). This equation can revert insulin concentrations of the intentionally hemolyzed samples to values that were statistically not different from the corresponding insulin baseline concentrations (p = 0.1564). Hemolysis could lead to a negative interference on insulin measurement; by individualized hemolysis correction equation for insulin measurement, we can correct and report reliable serum insulin results for a wide range of degrees of sample hemolysis. This correction would increase diagnostic accuracy, reduce inappropriate therapeutic decisions, and improve patient satisfaction with care.
机译:胰岛素测量在调查中对低血糖患者,糖尿病患者,胰岛素抵抗和β细胞功能受损的关键作用。然而,甚至轻微的溶血也会对由于RBC胰岛素降解酶(IDE)产生负面影响胰岛素测量。这里,我们得出并验证了个性化的校正方程,以消除溶血对胰岛素测量的影响。通过将裂解的自rbcs加入血清来研究溶血对胰岛素测量的影响。衍生校正方程,占溶血的百分比和暴露时间。在有意溶血样品中评估了这种个体化校正的性能。胰岛素浓度随着溶血的百分比和暴露时间而降低。基于溶血对17个供体的胰岛素测量的影响(基线胰岛素浓度为156至2119pmol / L),衍生出个体化溶解校正方程:INSCORR = INSMEA /(0.705LGHB(血浆)/ HB(血清) - 0.001Time - 0.612)。该等式可以将有意溶血样品的胰岛素浓度还原为与相应的胰岛素基线浓度有统计学上的值(P = 0.1564)。溶血可能导致胰岛素测量的负面干扰;通过胰岛素测量的个体化溶血校正方程,我们可以校正并报告可靠的血清胰岛素,从而为各种样品溶血度进行培养。这种矫正将提高诊断准确性,减少不恰当的治疗决策,并通过护理提高患者满意度。

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