A re-evaluation of the influence of maternal insulin-dependent diabetes on fetal nuchal translucency thickness and first-trimester maternal serum biochemical markers of aneuploidy

被引:30
作者
Spencer, K. [1 ]
Cowans, N. J.
Spencer, C. E.
Achillea, N.
机构
[1] King George Hosp, Dept Clin Biochem, Prenatal Screening Unit, Barking Havering Univ Hosp, Goodmayes IG3 8YB, England
关键词
prenatal screening: trisomy 21; nuchal translucency; free beta-human chorionic gonadotrophin; pregnancy-associated plasma protein-A; HUMAN CHORIONIC-GONADOTROPIN; PLASMA PROTEIN-A; 1ST TRIMESTER; CHROMOSOMAL-ANOMALIES; DOWN-SYNDROME; PAPP-A; PREGNANCY; TRISOMY-21; MOM; GESTATION;
D O I
10.1002/pd.2589
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective To evaluate the influence of maternal insulin-dependent diabetes mellitus (IDDM) on maternal scrum free beta-hCG, pregnancy-associated plasma protein-A (PAPP-A) and fetal nuchal translucency (NT) thickness from 11 weeks to 13 weeks 6 days of gestation in a large cohort of women screened prospectively for chromosomal anomalies Methods Information on maternal IDDM status. maternal serum biochemical marker levels and fetal NT were collected from the prenatal screening computer records. On total, the control group included 83 972 and the IDDM group included 489 pregnancies The median-corrected free beta-hCG and PAPP-A. expressed as MoM. and fetal NT. expressed as delta values, in the IDDM and non-IDDM groups were compared Results There were no significant differences between the IDDM and non-IDDM groups in median-corrected free beta-hCG (IDDM 1 01 MoM, non-IDDM 1 01 MoM, p = 0 970). or mean delta NT (IDDM 0 00 mm, non-IDDM 0 02 mm, p = 0 412) However, the median-corrected PAPP-A was significantly lower (IDDM 0.88 MoM, non-IDDM 1 03 MoM, p < 0 0001) Conclusions In pregnancies with maternal IDDM, first-trimester screening for chromosomal defects does not require adjustments for the measured fetal NT and maternal serum free beta-hCG However, for PAPP-A the 15% reduction is large enough to require correction in the calculation of risks for chromosomal defects Copyright (C) 2010 John Wiley & Sons, Ltd
引用
收藏
页码:937 / 940
页数:4
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