Department of Medical Laboratory Diagnostics, 119195 University Hospital "Sveti Duh" , Zagreb, Croatia.
Department of Obstetrics and Gynecology, 119195 University Hospital "Sveti Duh" , Zagreb, Croatia.
Clin Chem Lab Med. 2024 Apr 2;62(10):2048-2061. doi: 10.1515/cclm-2023-1109. Print 2024 Sep 25.
The aims of this study were to verify the bile acids (BA) method and to establish reference intervals (RIs) for bile acids (BA) and biochemical and haematological parameters in Croatian pregnant women.
BA spectrophotometric method verification was performed on Siemens Atellica Solution CH 930 automated analyser using Sentinel reagent. Stability, precision, trueness, linearity, and RIs, as well as lipemia interference were tested according to CLSI guidelines. BA, biochemical, and haematological parameters were measured in serum (BA, biochemical) and whole blood (haematological) samples of fasting healthy third-trimester pregnant women from Croatia (n=121). The establishment of the RIs was done according to the CLSI EP28-A3C:2010 guideline. Selected reference individuals' data were analysed using parametric, non-parametric, and robust methods.
Stability study showed that BA are stable in serum samples for 2 days at 20 °C, 14 days at 4-8 °C, and 22 days at -20 °C. The precision study and adult RIs verification met the criteria. Linearity was verified for the concentration range of 3.5-172.1 μmol/L whereas the lipemia interference test showed a positive bias (%) in BA concentration. The determined reference limits generally exhibited better precision for haematological parameters, being lower than the upper recommended value 0.2, unlike biochemical parameters. Haematological parameters showed notable differences between pregnant and non-pregnant women, while many biochemical parameters' RIs remained similar. Only ALT and GGT showed lower non-comparable RI upper limits in the population pregnant women.
Spectrophotometric BA method showed satisfactory performance and all examined parameters were within the set criteria. Moreover, RIs for key biochemical and haematological parameters, including BAs, have been established for the first time in the population of Croatian pregnant women.
本研究旨在验证胆汁酸(BA)方法,并建立克罗地亚孕妇胆汁酸(BA)和生化及血液参数的参考区间(RI)。
采用西门子 Atellica Solution CH 930 全自动分析仪和 Sentinel 试剂对 BA 分光光度法进行验证。根据 CLSI 指南测试稳定性、精密度、准确度、线性和 RI,以及脂血干扰。在克罗地亚(n=121)空腹健康晚期妊娠的血清(BA、生化)和全血(血液)样本中测量 BA、生化和血液参数。RI 的建立是根据 CLSI EP28-A3C:2010 指南进行的。使用参数、非参数和稳健方法分析选定参考个体的数据。
稳定性研究表明,BA 在 20°C 下血清样本中稳定 2 天,在 4-8°C 下稳定 14 天,在-20°C 下稳定 22 天。精密度研究和成人 RI 验证符合标准。验证了浓度范围为 3.5-172.1 μmol/L 的线性,而脂血干扰测试显示 BA 浓度呈正偏倚(%)。所确定的参考限值通常对血液参数具有更好的精密度,低于推荐的上限 0.2,与生化参数不同。血液参数在孕妇和非孕妇之间存在明显差异,而许多生化参数的 RI 仍然相似。只有 ALT 和 GGT 在孕妇人群中显示出较低的不可比 RI 上限。
分光光度法 BA 方法表现出令人满意的性能,所有检查的参数都在设定的标准范围内。此外,还首次在克罗地亚孕妇人群中建立了关键生化和血液参数(包括 BA)的 RI。