Hattori Naoki, Aisaka Kohzo, Shimatsu Akira
Clin Chem Lab Med. 2016 Apr;54(4):603-8. doi: 10.1515/cclm-2015-0484.
Macroprolactinaemia is a major cause of hyperprolactinaemia. The detectability of macroprolactin varies widely among different immunoassay systems, but the causes are not fully known. This study aimed to identify the factors influencing the detectability of macroprolactin by immunoassay systems.
The study included 1544 patients who visited an obstetric and gynaecological hospital. Macroprolactinaemia was screened using the polyethylene glycol (PEG) method and confirmed using gel filtration chromatography and the protein G method. The prolactin (PRL) values determined by enzyme immunoassay (EIA) were compared with those of a chemiluminescence immunoassay system (Centaur) that is known to cross-react the least with macroprolactin.
Macroprolactinaemia was found in 62 of 1544 patients (4.02%) who visited an obstetric and gynaecological hospital. The ratio of EIA-determined total PRL to free PRL in the supernatant after PEG precipitation was significantly elevated in all 62 serum samples with macroprolactin compared to those in 1482 serum samples without macroprolactin. In contrast, the ratio of Centaur-determined total PRL to free PRL was significantly elevated in 32 serum samples (group 1) and was within the normal range in 30 (group 2) of 62 serum samples with macroprolactin. The prevalence of non-IgG-type macroprolactin was significantly higher in group 1 than in group 2. Centaur diagnosed hyperprolactinaemia less frequently than EIA (n=2 vs. 16) in 62 patients with macroprolactinaemia. Those two hyperprolactinaemic patients diagnosed by Centaur had non-IgG-type macroprolactin.
Macroprolactinaemia was present in 4% of patients visiting an obstetric and gynaecological hospital. The nature of macroprolactin (IgG-type or non-IgG-type) may partly explain why macroprolactin detectability varies among different immunoassay systems.
巨泌乳素血症是高泌乳素血症的主要原因。不同免疫分析系统对巨泌乳素的检测能力差异很大,但其原因尚不完全清楚。本研究旨在确定影响免疫分析系统检测巨泌乳素能力的因素。
该研究纳入了1544名到妇产科医院就诊的患者。采用聚乙二醇(PEG)法筛查巨泌乳素血症,并通过凝胶过滤色谱法和蛋白G法进行确认。将酶免疫分析(EIA)测定的催乳素(PRL)值与已知与巨泌乳素交叉反应最少的化学发光免疫分析系统(Centaur)测定的值进行比较。
在1544名到妇产科医院就诊的患者中,有62名(4.02%)被发现患有巨泌乳素血症。与1482名无巨泌乳素血症的血清样本相比,所有62份含有巨泌乳素的血清样本中,PEG沉淀后上清液中EIA测定的总PRL与游离PRL的比值显著升高。相比之下,在62份含有巨泌乳素的血清样本中,32份血清样本(第1组)中Centaur测定的总PRL与游离PRL的比值显著升高,30份(第2组)在正常范围内。第1组中非IgG型巨泌乳素的患病率显著高于第2组。在62名患有巨泌乳素血症的患者中,Centaur诊断高泌乳素血症的频率低于EIA(2例对16例)。Centaur诊断出的这两名高泌乳素血症患者患有非IgG型巨泌乳素。
到妇产科医院就诊的患者中,4%存在巨泌乳素血症。巨泌乳素的性质(IgG型或非IgG型)可能部分解释了为什么不同免疫分析系统对巨泌乳素的检测能力存在差异。