Pitfalls in the lab assessment of hypopituitarism

Katharina Schilbach, Martin Bidlingmaier
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Abstract

The diagnostic approach to hypopituitarism involves many disciplines. Clinical symptoms rarely are specific. Imaging techniques are helpful but cannot prove the specific functional defects. Therefore, the definitive diagnosis of pituitary insufficiency is largely based on laboratory tests. However, also laboratory methods come with inherent limitations, and it is essential for the clinician to know and recognize typical pitfalls. Most factors potentially impairing the quality of hormone measurements are introduced in the preanalytical phase, i.e. before the hormones are measured by the laboratory. For example, the timing of blood drawing with respect to circadian rhythm, stress, and medication can have an influence on hormone concentrations. During the actual analysis of the hormones, cross-reactions with molecules present in the sample presenting the same or similar epitopes than the intended analyte may affect immunoassays. Interference can also come from heterophilic or human anti-animal antibodies. Unexpected problems can also be due to popular nutritional supplements which interfere with the measurement procedures. An important example in this respect is the interference from biotin. It became only clinically visible when the use of this vitamin became popular among patients. The extreme serum concentrations reached when patients take it as a supplement can lead to incorrect measurements in immunoassays employing the biotin-streptavidin system. To some extent, hormone analyses using liquid chromatography mass spectrometry (LCMS) can overcome problems, although availability and cost-effectiveness of this method still imposes restrictions. In the post-analytical phase, appropriateness of reference intervals and cut-offs with respect to the specific analytical method used is of outmost importance. Furthermore, for interpretation, additional biological and pharmacological factors like BMI, age and concomitant diseases must be considered to avoid misinterpretation of the measured concentrations. It is important for the clinician and the laboratory to recognize when one or more laboratory values do not match the clinical picture. In an interdisciplinary approach, the search for the underlying cause should be initiated.

实验室评估垂体功能减退症的误区
垂体功能减退症的诊断方法涉及多个学科。临床症状很少具有特异性。影像学技术很有帮助,但无法证明具体的功能缺陷。因此,垂体功能不全的明确诊断主要依靠实验室检查。然而,实验室方法也有其固有的局限性,临床医生必须了解并识别典型的误区。大多数可能影响激素测量质量的因素都出现在分析前阶段,即在实验室测量激素之前。例如,与昼夜节律、压力和药物有关的抽血时间会对激素浓度产生影响。在实际分析激素的过程中,样本中与目标分析物具有相同或相似表位的分子发生的交叉反应可能会影响免疫测定。嗜异性抗体或人类抗动物抗体也会造成干扰。流行的营养补充剂也可能造成意想不到的问题,干扰测量程序。生物素的干扰就是这方面的一个重要例子。在临床上,只有当这种维生素在患者中流行起来时,这种干扰才会显现出来。当患者将生物素作为补充剂服用时,血清中的生物素浓度会达到极高的水平,从而导致采用生物素-链霉亲和素系统的免疫测定中出现错误的测量结果。在某种程度上,使用液相色谱质谱法(LCMS)进行激素分析可以克服这些问题,但这种方法的可用性和成本效益仍然受到限制。在分析后阶段,参照区间和临界值与所使用的特定分析方法是否合适至关重要。此外,在进行解释时,还必须考虑其他生物和药物因素,如体重指数、年龄和伴随疾病,以避免对测量浓度产生误解。当一个或多个实验室数值与临床情况不符时,临床医生和实验室必须识别出来。在跨学科方法中,应开始寻找根本原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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