Clinical Articles Maternal serum α-fetoprotein screening for fetal Down syndrome in the United States: Results of a survey

1990 ◽  
Vol 162 (2) ◽  
pp. 317-321 ◽  
Author(s):  
Glenn E. Palomaki ◽  
George J. Knight ◽  
Mary S. Holman ◽  
James E. Haddow
2004 ◽  
Vol 50 (10) ◽  
pp. 1804-1808 ◽  
Author(s):  
Glenn E Palomaki ◽  
Louis M Neveux ◽  
George J Knight ◽  
James E Haddow ◽  
Raj Pandian

Abstract Background: Approximately two million pregnancies in the United States are screened for Down syndrome annually by use of second-trimester maternal serum markers. At present, a combination of four markers can identify 75% of affected pregnancies when 5% of screened women are classified as candidates for amniocentesis. Although not currently included in screening panels, invasive trophoblast antigen (ITA) is a promising screening marker in serum or urine in both the second and first trimesters. This study aims at better defining the screening performance of serum ITA in the second trimester. Methods: In an earlier study, serum samples from an unbiased sampling of 45 Down syndrome (cases) and 238 unaffected (control) pregnancies between 14 and 20 weeks of gestation were collected from various centers in the United States. Samples were aliquoted and stored at −20 °C for 8 years. We measured ITA in these samples and determined the screening performance both univariately and in combination with other screening markers. Results: The median ITA in Down syndrome pregnancies was >3.00 multiples of the median, higher than that found for human chorionic gonadotropin (hCG) or free β-hCG. At a 5% false-positive rate, ITA univariately detected 38% and 40% of Down syndrome pregnancies, respectively, when assigned by date of last menstrual period or ultrasound date. Modeling yielded rates of 45% and 48%. ITA correlated strongly with hCG and free β-hCG. When substituted for either of these in a multiple marker panel, ITA performed comparably. Conclusions: This study indicates that serum ITA is an effective marker for Down syndrome. It is highly correlated with both hCG and free β-hCG and could replace either of them in a multiple marker panel.


1997 ◽  
Vol 176 (5) ◽  
pp. 1046-1051 ◽  
Author(s):  
Glenn E. Palomaki ◽  
George J. Knight ◽  
Jane E. McCarthy ◽  
James E Haddow ◽  
John M Donhowe

2021 ◽  
pp. 096914132110316
Author(s):  
Nathalie Lepage ◽  
Philip Wyatt ◽  
Edward R Ashwood ◽  
Robert G Best ◽  
Thomas Long ◽  
...  

Objective To compile current usage of serum-based prenatal screening for Down syndrome in the United States and compare it with results from a similar 2011/2012 survey. Setting The College of American Pathologists maternal screening proficiency testing survey includes a supplemental question on the first of three yearly distributions. Methods Information regarding tests offered and the monthly number of pregnancies tested for US-based laboratories were reviewed. Results were stratified by size of laboratory, tests offered, and pregnancies tested. Findings were compared to an earlier survey. Results Fifty-six laboratories reported they will have screened 1,131,336 pregnancies in 2020. Of these, 36% are screened by stand-alone first trimester testing, 48% by stand-alone second trimester testing, and 16% using tests that integrate results from both trimesters. Eighty percent of all serum screens were provided by the five laboratories that performed the most screens (at least 50,000). These five performed similar proportions of first or second trimester screens (42.2% and 41.8%, respectively). Compared to eight years earlier, there are now 54% fewer laboratories. Pregnancies screened using the first trimester, second trimester, and integrated protocols were lower by 27%, 69%, and 72%, respectively. The serum screening activity in the US showed a 62% decrease from 2012 levels. During 2012–2020, the number of cell-free DNA tests increased from negligible to 1,492,332. Conclusions Maternal serum screening for common aneuploidies has changed significantly in eight years with fewer laboratories, a shift toward larger laboratories and a 2.5-fold reduction in pregnancies tested, likely due to the introduction of cell-free DNA screening.


1993 ◽  
Vol 169 (6) ◽  
pp. 1558-1562 ◽  
Author(s):  
Glenn E. Palomaki ◽  
George J. Knight ◽  
Jane McCarthy ◽  
James E. Haddow ◽  
John H. Eckfeldt

2022 ◽  
Vol 226 (1) ◽  
pp. S481-S482
Author(s):  
Sarina R. Chaiken ◽  
Marguerite Susich ◽  
Uma Doshi ◽  
Claire H. Packer ◽  
Bharti Garg ◽  
...  

PEDIATRICS ◽  
2012 ◽  
Vol 131 (1) ◽  
pp. e27-e36 ◽  
Author(s):  
J. E. Kucik ◽  
M. Shin ◽  
C. Siffel ◽  
L. Marengo ◽  
A. Correa ◽  
...  

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