Incorporating thyroid markers in Down syndrome screening protocols
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F27661989%3A_____%2F17%3AN0000006" target="_blank" >RIV/27661989:_____/17:N0000006 - isvavai.cz</a>
Výsledek na webu
<a href="https://obgyn.onlinelibrary.wiley.com/doi/10.1002/pd.5047" target="_blank" >https://obgyn.onlinelibrary.wiley.com/doi/10.1002/pd.5047</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/pd.5047" target="_blank" >10.1002/pd.5047</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Incorporating thyroid markers in Down syndrome screening protocols
Popis výsledku v původním jazyce
ObjectiveThe article aimed to assess the benefit of incorporating maternal serum thyroid disease marker levels (thyroid-stimulating hormone and free thyroxine) into first trimester Down syndrome screening protocols. MethodsStatistical modelling was used to predict performance with and without the thyroid markers. Two protocols were considered: the combined test and the contingent cell-free DNA (cfDNA) test, where 15-40% women are selected for cfDNA because of increased risk based on combined test results. Published parameters were used for the combined test, cfDNA and the Down syndrome means for thyroid-stimulating hormone and free thyroxine; other parameters were derived from a series of 5230 women screened for both thyroid disease and Down syndrome. ResultsCombined test: For a fixed 85% detection rate, the predicted false positive rate was reduced from 5.3% to 3.6% with the addition of the thyroid markers. Contingent cfDNA test: For a fixed 95% detection rate, the proportion of women selected for cfDNA was reduced from 25.6% to 20.2%. ConclusionsWhen screening simultaneously for maternal thyroid disease and Down syndrome, thyroid marker levels should be used in the calculation of Down syndrome risk. The benefit is modest but can be achieved with no additional cost. (c) 2017 John Wiley & Sons, Ltd.
Název v anglickém jazyce
Incorporating thyroid markers in Down syndrome screening protocols
Popis výsledku anglicky
ObjectiveThe article aimed to assess the benefit of incorporating maternal serum thyroid disease marker levels (thyroid-stimulating hormone and free thyroxine) into first trimester Down syndrome screening protocols. MethodsStatistical modelling was used to predict performance with and without the thyroid markers. Two protocols were considered: the combined test and the contingent cell-free DNA (cfDNA) test, where 15-40% women are selected for cfDNA because of increased risk based on combined test results. Published parameters were used for the combined test, cfDNA and the Down syndrome means for thyroid-stimulating hormone and free thyroxine; other parameters were derived from a series of 5230 women screened for both thyroid disease and Down syndrome. ResultsCombined test: For a fixed 85% detection rate, the predicted false positive rate was reduced from 5.3% to 3.6% with the addition of the thyroid markers. Contingent cfDNA test: For a fixed 95% detection rate, the proportion of women selected for cfDNA was reduced from 25.6% to 20.2%. ConclusionsWhen screening simultaneously for maternal thyroid disease and Down syndrome, thyroid marker levels should be used in the calculation of Down syndrome risk. The benefit is modest but can be achieved with no additional cost. (c) 2017 John Wiley & Sons, Ltd.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30200 - Clinical medicine
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Prenatal Diagnosis
ISSN
0197-3851
e-ISSN
1097-0223
Svazek periodika
37
Číslo periodika v rámci svazku
5
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
5
Strana od-do
510-514
Kód UT WoS článku
000401561200013
EID výsledku v databázi Scopus
2-s2.0-85018935336