Pregled bibliografske jedinice broj: 1201716
Validity and utility of non-invasive prenatal testing for copy number variations and microdeletions: a systematic review
Validity and utility of non-invasive prenatal testing for copy number variations and microdeletions: a systematic review // Journal of clinical medicine, 11 (2022), 12; 3350, 15 doi:10.3390/jcm11123350 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1201716 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Validity and utility of non-invasive prenatal testing for copy number variations
and microdeletions: a systematic review
(Validity and utility of non-invasive prenatal
testing for copy number variations and
microdeletions: a systematic review)
Autori
Zaninović, Luca ; Bašković, Marko ; Ježek, Davor ; Katušić Bojanac, Ana
Izvornik
Journal of clinical medicine (2077-0383) 11
(2022), 12;
3350, 15
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
non-invasive prenatal testing ; microdeletion ; copy number variation ; cell-free DNA ; validity ; screening ; prenatal diagnosis ; molecular method
Sažetak
Valid data on prenatal cell-free DNA-based screening tests for copy number variations and microdeletions are still insufficient. We aimed to compare different methodological approaches concerning the achieved diagnostic accuracy measurements and positive predictive values. For this systematic review, we searched the Scopus and PubMed databases and backward citations for studies published between 2013 and 4 February 2022 and included articles reporting the analytical and clinical performance of cfDNA screening tests for CNVs and microdeletions. Of the 1810 articles identified, 32 met the criteria. The reported sensitivity of the applied tests ranged from 20% to 100%, the specificity from 81.62% to 100%, and the PPV from 3% to 100% for cases with diagnostic or clinical follow-up information. No confirmatory analysis was available in the majority of cases with negative screening results, and, therefore, the NPVs could not be determined. NIPT for CNVs and microdeletions should be used with caution and any developments regarding new technologies should undergo strict evaluation before their implementation into clinical practice. Indications for testing should be in correlation with the application guidelines issued by international organizations in the field of prenatal diagnostics.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
--KK.01.1.1.01.0008 - Znanstveni centar izvrsnosti za reproduktivnu i regenerativnu medicinu – istraživanja novih platormi i potencijala (CERRM) (Ježek, Davor; Vukičević, Slobodan) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb,
Klinika za dječje bolesti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus