Temporal changes in maternal serum biochemical markers of Trisomy 21 across the first and second trimester of pregnancy

Nix, Arthur Barry John, Aitken, D. A., Crossley, J. A. and Spencer, K. 2002. Temporal changes in maternal serum biochemical markers of Trisomy 21 across the first and second trimester of pregnancy. Annals of Clinical Biochemistry 39 (6) , pp. 567-576. 10.1177/000456320203900604

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Abstract

Background Many maternal serum markers show concentration changes in Down's syndrome pregnancies but the magnitude of the change in median marker levels varies with gestation. To date these changes have not been accurately specified. Methods The trends in marker median levels between 6 and 20 weeks of gestation were examined for alphafetoprotein (AFP), free β human chorionic gonadotrophin (F β-hCG), total human chorionic gonadotrophin (ThCG) and pregnancy-associated plasma protein A (PAPP-A) by a meta-analysis of data obtained from our collaborative studies and routine screening programmes for Down's syndrome over a 10-year period. Data were available from between 709 and 1082 Down's syndrome pregnancies and from between 14 607 and 153 909 unaffected pregnancies for each marker. The median multiple of the median (MoM) and mean log10MoM for each marker at each completed week of gestation were estimated and the trend with gestation smoothed using a weighted least squares regression model. Results The gestational ages at which maximum separation of marker levels occurred, comparing affected and unaffected pregnancies, and the respective regressed median MoMs and mean log10MoMs, were: for AFP at 16 weeks, 0·72 MoM, 0·14288 log10MoM; for F β-hCG at 15 weeks, 2·24 MoM, 0·35034 log10MoM; for ThCG at 16 weeks, 1·93 MoM, 0·28548 log10MoM, as well as before 8 weeks (< 0·65 MoM, 0·18853 log10MoM); and for PAPP-A before 8 weeks, < 0·33 MoM, 0·47727 log10MoM. Conclusion There is significant temporal variation in mean log10MoM values for the screening markers investigated. Screening algorithms, modified to take account of this variation, should allow more accurate gestation-specific risks to be calculated in individual pregnancies.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Schools > Medicine
Subjects:	R Medicine > RG Gynecology and obstetrics
Publisher:	Royal Society of Medicine
ISSN:	0004-5632
Last Modified:	05 Nov 2019 04:10
URI:	https://orca.cardiff.ac.uk/id/eprint/500

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