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首页> 外文期刊>Journal of inherited metabolic disease >The influence of sex, gestational age, birth weight, blood transfusion, and timing of the heel prick on the pancreatitis-associated protein concentration in newborn screening for cystic fibrosis
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The influence of sex, gestational age, birth weight, blood transfusion, and timing of the heel prick on the pancreatitis-associated protein concentration in newborn screening for cystic fibrosis

机译:新生儿筛查性囊性纤维化时,性别,胎龄,出生体重,输血和足跟刺的时间对胰腺炎相关蛋白浓度的影响

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Background: Pancreatitis-associated protein (PAP) is currently discussed as a marker in newborn screening (NBS) for cystic fibrosis (CF). However, it is not known if PAP concentrations are influenced by sex, gestational age, birth weight, blood transfusion or time of collection and what this would mean for NBS for CF. Methods: In 2008 all newborns in part of the Netherlands were screened for CF by an IRT/PAP protocol. PAP concentration was determined by the MucoPAP ELISA (DynaBio), which was modified to a Dissociation Enhanced Lanthanide Fluoroimmunoassay (DELFIA) method following a protocol of PerkinElmer. Results: In healthy newborns, the median PAP concentration was 0.5 μg/l (Interquartile range (IQR 0.3-0.8) whereas this was 3.2 μg/l (IQR 2.0-12.5) in CF infants. PAP concentrations were lower in premature infants 0.94 and 0.91 times for 25 to 31 + 6 weeks GA and 32 to 36 + 6 weeks respectively. A higher PAP concentration was observed in low-birth-weight infants (<2500 gram)(p = 0.001), per 100 gram birth weight gained the PAP concentration decreased with 0.1 %. PAP levels were higher after a blood transfusion, the 95th percentile increased from 1.3 to 3.6 μg/l leading to a higher false-positive rate. The PAP concentration increased when newborn screening was performed more than 168 hours (day 7) after birth (β = 1.63), the 95th percentile increased from 1.3-1.6 μg/l to 4.0 μg/l after 168 hours (72,874 newborns were screened). Conclusion: Sex, birth weight, and gestational age lead to small differences in PAP concentrations without consequences for the screening algorithm. However, blood transfusion as well as performance of the heel prick after 168 hours (7 days) lead to clinically significant higher PAP levels and to a higher risk on a false-positive screening test result.
机译:背景:胰腺炎相关蛋白(PAP)目前被认为是囊性纤维化(CF)新生儿筛查(NBS)的标志物。但是,尚不清楚PAP浓度是否受性别,胎龄,出生体重,输血或采集时间的影响,这对于CF的NBS意味着什么。方法:2008年,通过IRT / PAP方案对荷兰部分地区的所有新生儿进行CF筛查。通过MucoPAP ELISA(DynaBio)测定PAP浓度,该酶按照PerkinElmer的规程修改为离解增强镧系元素荧光免疫测定法(DELFIA)。结果:在健康的新生儿中,CF婴儿的PAP浓度中位数为0.5μg/ l(四分位间距(IQR 0.3-0.8),而CF婴儿的PAP浓度中位数为3.2μg/ l(IQR 2.0-12.5),早产儿的PAP浓度较低,为0.94和0.94。 25至31 + 6周的GA和32至36 + 6周的0.91倍,低出生体重婴儿(<2500克)的PAP浓度较高(p = 0.001),每增加100克体重PAP浓度降低0.1%。输血后PAP浓度升高,第95个百分位数从1.3μg/ l增加至假阳性率。当新生儿筛查超过168小时时,PAP浓度升高(出生后第7天(β= 1.63),第168小时(筛查了72,874名新生儿)后,第95个百分位数从1.3-1.6μg/ l增加到4.0μg/ l结论:性别,出生体重和胎龄导致体重下降PAP浓度的差异而不会影响筛选算法。 168小时(7天)后的od输注以及脚后跟刺的表现会导致临床上明显更高的PAP水平,并导致假阳性筛查结果的风险更高。

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