Tislarić-Medenjak Dubravka, Zec Ivana, Simundić Ana-Maria, Sabolović-Rudman Senka, Kos Milan, Megla Zeljka Bukovec
Laboratory of Endocrinology, Clinics of Oncology and Nuclear Medicine, University Hospital "Sestre milosrdnice", Zagreb, Croatia.
BMC Res Notes. 2010 Jul 14;3:194. doi: 10.1186/1756-0500-3-194.
The variability of maternal serum biochemical markers for Down syndrome, free beta-hCG and PAPP-A can have a different impact on false-positive rates between the 10+0 and 13+6 week of gestation. The study population comprised 2883 unaffected, singleton, spontaneously conceived pregnancies in Croatian women, who delivered apparently healthy child at term. Women were separated in 4 groups, dependently on the gestational week when the analyses of biochemical markers were performed. The concentrations of free beta-hCG and PAPP-A in maternal serum were determined by solid-phase, enzyme-labeled chemiluminiscent immunometric assay (Siemens Immulite). Concentrations were converted to MoMs, according to centre-specific weighted regression median curves for both markers in unaffected pregnancies. The individual risks for trisomies 21, 18 and 13 were computed by Prisca 4.0 software.
There were no significant differences between the sub-groups, regarding maternal age, maternal weight and the proportion of smokers. The difference in log10 MoM free beta-hCG values, between the 11th and 12th gestational week, was significant (p = 0.002). The difference in log10 MoM PAPP-A values between the 11th and 12th, and between 12th and 13th week of gestation was significant (p = 0.006 and p = 0.003, respectively). False-positive rates of biochemical risk for trisomies were 16.1% before the 11th week, 12.8% in week 12th, 11.9% in week 13th and 9.9% after week 13th. The differences were not statistically significant.
Biochemical markers (log10 MoMs) showed gestation related variations in the first-trimester unaffected pregnancies, although the variations could not be attributed either to the inaccuracy of analytical procedures or to the inappropriately settled curves of median values for the first-trimester biochemical markers.
唐氏综合征的母体血清生化标志物游离β-人绒毛膜促性腺激素(free beta-hCG)和妊娠相关血浆蛋白A(PAPP-A)的变异性,在妊娠10⁺⁰周和13⁺⁶周之间对假阳性率可能有不同影响。研究人群包括2883例未受影响的克罗地亚单胎自然受孕孕妇,她们足月分娩了明显健康的婴儿。根据进行生化标志物分析时的孕周,将孕妇分为4组。采用固相酶标记化学发光免疫分析法(西门子Immulite)测定母体血清中游离β-hCG和PAPP-A的浓度。根据未受影响妊娠中两种标志物的中心特异性加权回归中位数曲线,将浓度转换为中位数倍数(MoMs)。使用Prisca 4.0软件计算21-三体、18-三体和13-三体的个体风险。
各亚组在产妇年龄、产妇体重和吸烟者比例方面无显著差异。妊娠第11周和第12周之间,log₁₀ MoM游离β-hCG值的差异具有统计学意义(p = 0.002)。妊娠第11周和第12周之间以及第12周和第13周之间,log₁₀ MoM PAPP-A值的差异具有统计学意义(分别为p = 0.006和p = 0.003)。13-三体生化风险的假阳性率在第11周之前为16.1%,第12周为12.8%,第13周为11.9%,第13周之后为9.9%。这些差异无统计学意义。
在孕早期未受影响的妊娠中,生化标志物(log₁₀ MoMs)显示出与孕周相关的变化,尽管这些变化既不能归因于分析程序的不准确,也不能归因于孕早期生化标志物中位数曲线设定不当。