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The impact of temporal variability of biochemical markers PAPP-A and free β-hCG on the specificity of the first-trimester Down syndrome screening: a Croatian retrospective study

机译:生化指标PAPP-A和游离β-hCG随时间变化对孕早期唐氏综合症筛查特异性的影响:一项克罗地亚回顾性研究

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Background The variability of maternal serum biochemical markers for Down syndrome, free β-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 β-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. Findings 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 β-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. Conclusions 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.
机译:背景:唐氏综合症,游离β-hCG和PAPP-A的孕妇血清生化标志物的变异性可能在妊娠的10 + 0和13 + 6周之间对假阳性率产生不同的影响。研究人群包括2883名克罗地亚妇女,这些妇女未受影响,单身,自发怀孕,足月分娩的妇女显然健康。根据孕周进行生化标志物分析时,将妇女分为4组。母体血清中游离β-hCG和PAPP-A的浓度通过固相酶标记化学发光免疫测定法(Siemens Immulite)测定。根据未受影响的妊娠中两个指标的中心特异性加权回归中值曲线,将浓度转换为MoMs。 Trisomies 21、18和13的个体风险通过Prisca 4.0软件计算。结果在孕产妇年龄,孕产妇体重和吸烟者比例方面,亚组之间无显着差异。 11 th 和12 10 MoM无β-hCG值的差异胎龄 显着(p = 0.002)。 log 10 MoM PAPP-A值在第11 th 和12 ,并且介于12 th 和13 妊娠第3周显着(分别为p = 0.006和p = 0.003)。三体组生化风险的假阳性率在第11周之前为16.1%,在第12周为12.8%。 > ,第13周 的11.9%,第13周 之后的9.9% sup>。差异无统计学意义。结论生化标志物(log 10 MoMs)显示了妊娠前三个月未受孕的妊娠相关变异,尽管该变异既不能归因于分析方法的不准确性或孕中期生化指标中位数的不适当沉降曲线。

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