Urinary analyte screening: a noninvasive detection method for Down syndrome?

Citation
Ja. Canick et al., Urinary analyte screening: a noninvasive detection method for Down syndrome?, MOL MED TOD, 5(2), 1999, pp. 68-73
Citations number
29
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research General Topics
Journal title
MOLECULAR MEDICINE TODAY
ISSN journal
13574310 → ACNP
Volume
5
Issue
2
Year of publication
1999
Pages
68 - 73
Database
ISI
SICI code
1357-4310(199902)5:2<68:UASAND>2.0.ZU;2-6
Abstract
Prenatal screening for Down syndrome using maternal serum markers achieves detection rates of 60-80% with a 5% false positive rate. Improvement in the accuracy of screening, as well as its ease and safety, will increase the u se of such tests. The most effective of the current serum markers is human chorionic gonadotropin (hCG), Studies on beta core fragment (beta CF), the major urinary metabolite of hCG, have indicated that screening with beta CF and other markers measured in maternal urine might improve the detection o f Down syndrome and provide a less expensive and simpler test. However, rec ent results have been unusually variable, Although it has great potential, the true clinical value of maternal urine screening to detect Down syndrome still remains to be determined.