多发性骨髓瘤的假性高磷血症:干扰副蛋白的去除。

IF 1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY
Michelle De Bruyn, Matthias Cuykx
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引用次数: 0

摘要

背景:多发性骨髓瘤患者可能出现虚假的血清磷酸盐水平升高,这是由于在磷酸钼酸盐紫外测定中干扰副蛋白的存在。如果不认识到这一现象,患者可能会接受不必要的治疗。这篇简短的报告强调了与副蛋白相关的假性高磷血症的存在,并旨在提供消除这种干扰的可行解决方案。材料和方法在已知的IgG多发性骨髓瘤和不明原因的高磷血症患者中,评估血清磷酸盐水平(磷钼酸盐紫外法)和IgG浓度(免疫比浊法)之间的相关性。为了研究副蛋白对磷酸盐水平的影响,通过稀释、用磺基水杨酸或硫酸锌沉淀蛋白质或超滤,测量了一份血清样品在去除蛋白质前后的磷酸盐水平。结果1例多发性骨髓瘤患者出现原因不明的高磷血症,高磷血症与血清IgG浓度呈正相关。当血清稀释使磷酸盐水平正常化时,假设在测定反应中副蛋白的沉淀干扰了测量并导致假高磷血症。用磺基水杨酸或硫酸锌沉淀法去除蛋白质可以有效地将IgG水平降低到检测限以下,但不能得到可靠的磷酸盐测量结果。通过超滤获得了成功的蛋白质去除和更可靠的血清磷酸盐测量。结论副蛋白可干扰磷钼酸盐紫外测定中的反应组分,引起假高磷血症。如果确定存在这种现象,则可以在样品超滤后获得可靠的磷酸盐浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudohyperphosphatemia in multiple myeloma: Removal of interfering paraproteins.

BackgroundMultiple myeloma patients may present with spuriously elevated serum phosphate levels resulting from the presence of paraproteins interfering in the phosphomolybdate UV assay. If this phenomenon is not recognized, patients possibly receive unnecessary treatments. This short report highlights the existence of paraprotein-related pseudohyperphosphatemia, and aims to provide accessible solutions to eliminate this interference.Material and MethodsIn a patient known with IgG multiple myeloma and unexplained hyperphosphatemia, the correlation between serum phosphate levels (phosphomolybdate UV assay) and IgG concentrations (immunoturbidimetry) was evaluated. To investigate the effect of the paraprotein on phosphate levels, phosphate was measured in one serum sample before and after protein removal by either dilution, protein precipitation with sulfosalicylic acid or zinc sulphate, or ultrafiltration.ResultsA patient with multiple myeloma presented with an unexplained hyperphosphatemia which correlated positively with serum IgG concentrations. As serum dilution normalized the phosphate level, it was hypothesized that precipitation of the paraprotein during the assay reaction interfered with the measurement and resulted in pseudohyperphosphatemia. Protein removal by precipitation with sulfosalicylic acid or zinc sulphate efficiently reduced the IgG level below the detection limit but did not result in a reliable phosphate measurement. Successful removal of proteins and a serum phosphate level that matched the patient's other biochemistry parameters and clinical condition were obtained by ultrafiltration.ConclusionParaproteins can interfere with the reaction components in the phosphomolybdate UV assay and result in pseudohyperphosphatemia. If the presence of this phenomenon is established, a reliable phosphate concentration can be obtained after ultrafiltration of the sample.

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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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