Dual Analyte Immunoassay in Neural Tube Defect and Down's Syndrome Screening: Results of a Multicentre Clinical Trial

Author(s):  
K Spencer ◽  
J N Macri ◽  
R W Anderson ◽  
D A Aitken ◽  
E Berry ◽  
...  

We report a multicentre clinical field trial of a novel dual analyte enzyme immunoassay method for the simultaneous measurement of alpha-fetoprotein (AFP) and free β-human choriogonadotropin (hCG) in the same microtitre well. The assay was shown to have good technical performance in the hands of all trial centres, with between assay coefficients of variation better than 10% for both analytes across the whole of the assay ranges. The method compared well with single analyte measuring procedures and produced acceptable performance as judged by external quality assurance criteria. Recovery of added analyte and analyte dilution curves also showed acceptable performance. In clinical evaluation of a large set of neural tube defect cases, good clinical discrimination from unaffected cases was observed using APP. With over 150 Down's syndrome cases, the combination of AFP and free (3 hCG confirmed the high detection rates achievable using this marker combination, with detection rates in excess of 70% in early gestation. We conclude that the combination of clinically superior markers coupled with technologically innovative assay design will lead to more efficient Down's screening programmes.

1998 ◽  
Vol 13 (6) ◽  
pp. 367-371 ◽  
Author(s):  
Bojana Brajenović-Milić ◽  
Dubravka Tišlarić ◽  
Josip Bačić ◽  
Jadranka Paravić ◽  
Anatelo Slivar ◽  
...  

Author(s):  
Esther Berry ◽  
David A. Aitken ◽  
Jennifer A. Crossley ◽  
James N. Macri ◽  
J. Michael Connor

Author(s):  
S N Millner

Down's syndrome risks are estimated between 15 and 20 completed weeks' gestation (cGW) using an algorithm involving maternal age and serum x-fetoprotein (AFP), chorionic gonadotrophin and unconjugated oestriol levels, each expressed as a multiple of the median level (MoM) at the cGW. The AFP MoM itself is the basis for screening for open neural tube defects (oNTD). Because medians change during this period, gestational dating must be accurate so that appropriate medians are used. A calculated Down's syndrome risk >1:380 at term is generally considered to indicate a 'high-risk' pregnancy. This study focused on 378 patients with reported risk ≤1:500 based on physician-supplied cGW (and hence considered at 'low risk' for Down's syndrome) to determine the effect of common 1-2-week dating errors on risk estimates. Using the original analytical data, each patient's risk was recalculated for each week over the 15-20 weeks, and classified into three categories: <1:380 'low'; 1:380-1:100 'moderate'; and >1:100 'high'. Advancing originally 'low-risk' patients by one week increased the risk by 1·09-14·1 times (median 3·18, mean 3·60); 46 (12·2%) became 'moderate' and 2 (0·5%) became 'high' risk. Advancing by two weeks increased risks 1·58-60·5 times (median 10·03, mean 12·04); 131 (36·5%) became 'moderate' and 39 (10.9%) became 'high' risk. Predictably, oNTD screening results also were affected. Although 1-2 week differences in AFP medians had little effect on most patients in this study sample, some who originally were oNTD negative became oNTD positive, whereas others who had been oNTD positive became screen negative. Thus, in many cases, a 1-2 week dating error may have only minimal effect on the estimated risks for chromosome or neural tube defects, but in other cases the effect of such an error would be significant.


2000 ◽  
Vol 15 (3) ◽  
pp. 177-181 ◽  
Author(s):  
M Cioffi ◽  
P Gazzerro ◽  
C Di Macchia ◽  
MT Vietri ◽  
A Contursi ◽  
...  

The Lancet ◽  
2003 ◽  
Vol 361 (9366) ◽  
pp. 1316 ◽  
Author(s):  
Jørgen H Olsen ◽  
Jeanette Falck Winther

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