Nerenz Robert D, Butch Anthony W, Woldemariam Getachew A, Yarbrough Melanie L, Grenache David G, Gronowski Ann M
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States; Current institution: Department of Pathology and Laboratory Medicine, University of Kentucky Medical Center, Lexington, KY, United States.
Department of Pathology and Laboratory Medicine, UCLA Geffen School of Medicine, Los Angeles, CA, United States.
Clin Biochem. 2016 Feb;49(3):282-6. doi: 10.1016/j.clinbiochem.2015.10.020. Epub 2015 Nov 2.
Elevated urine concentrations of hCG beta core fragment (hCGβcf) are known to cause false negative qualitative point-of-care hCG test results, but limited information is available regarding urine hCGβcf. In this study, we evaluate the relationship between serum and urine hCG concentrations and the frequency of elevated urine hCGβcf concentrations.
Paired serum and urine specimens were obtained from 60 women at various stages of pregnancy and hCG was measured using the Abbott Architect and Roche Cobas e602 assays. Urine specimens with the greatest difference in urine hCG concentrations between these two instruments were tested using a qualitative point-of-care device and hCGβcf was quantified using LC-MS/MS.
Urine hCG concentrations were lower than serum and the magnitude of the difference depended on whether the hCG assay detected hCGβcf. Elevated hCGβcf concentrations (>280,000pmol/L) were observed in 12% of specimens from an unselected patient population. There was a significant correlation (r=0.97; p<0.0001) between the difference (Roche hCG-Abbott hCG) and the hCGβcf concentration as measured by LC-MS/MS (Roche-Abbott difference IU/L=(hCGβcf (pmol/L)∗0.131+656)).
A correlation exists between serum and urine hCG concentrations but this correlation is variable. hCGβcf concentrations can be estimated using two automated assay reagent platforms that differ in their recognition of hCGβcf.
已知尿液中人绒毛膜促性腺激素β核心片段(hCGβcf)浓度升高会导致即时检验hCG定性检测结果出现假阴性,但关于尿液hCGβcf的信息有限。在本研究中,我们评估血清和尿液hCG浓度之间的关系以及尿液hCGβcf浓度升高的频率。
从60名处于不同孕期阶段的女性中获取配对的血清和尿液标本,并使用雅培Architect和罗氏Cobas e602检测法测量hCG。使用即时检验定性设备对这两种仪器检测的尿液hCG浓度差异最大的尿液标本进行检测,并使用液相色谱-串联质谱法(LC-MS/MS)对hCGβcf进行定量。
尿液hCG浓度低于血清,差异的大小取决于hCG检测法是否能检测到hCGβcf。在未经过筛选的患者群体的12%的标本中观察到hCGβcf浓度升高(>280,000pmol/L)。(罗氏hCG - 雅培hCG)差值与通过LC-MS/MS测量的hCGβcf浓度之间存在显著相关性(r = 0.97;p < 0.0001)(罗氏 - 雅培差值IU/L =(hCGβcf(pmol/L)∗0.131 + 656))。
血清和尿液hCG浓度之间存在相关性,但这种相关性是可变的。可以使用两种对hCGβcf识别不同的自动化检测试剂平台来估计hCGβcf浓度。