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Incorporating thyroid markers in Down syndrome screening protocols
I. Dhaifalah, T. Salek, D. Langova, H. Cuckle,
Jazyk angličtina Země Velká Británie
Typ dokumentu hodnotící studie, časopisecké články
PubMed
28374559
DOI
10.1002/pd.5047
Knihovny.cz E-zdroje
- MeSH
- biologické markery krev MeSH
- dospělí MeSH
- Downův syndrom krev komplikace diagnóza patofyziologie MeSH
- lidé MeSH
- nemoci štítné žlázy krev diagnóza MeSH
- plošný screening metody MeSH
- prediktivní hodnota testů MeSH
- prenatální diagnóza metody MeSH
- první trimestr těhotenství krev MeSH
- senzitivita a specificita MeSH
- štítná žláza patofyziologie MeSH
- těhotenství MeSH
- testy funkce štítné žlázy metody MeSH
- thyreotropin analýza krev MeSH
- thyroxin analýza krev MeSH
- volné cirkulující nukleové kyseliny analýza krev MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
OBJECTIVE: The 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. METHODS: Statistical 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. RESULTS: Combined 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%. CONCLUSIONS: When 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. © 2017 John Wiley & Sons, Ltd.
Department of Clinical Biochemistry Tomas Bata Regional Hospital Zlin Czech Republic
Department of Internal Medicine Clinic Tomas Bata Regional Hospital Zlin Czech Republic
Department of Obstetrics and Gynaecology Columbia University Medical Centre New York NY USA
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- $a OBJECTIVE: The 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. METHODS: Statistical 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. RESULTS: Combined 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%. CONCLUSIONS: When 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. © 2017 John Wiley & Sons, Ltd.
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