4.0 Article

Prenatal diagnosis and socioeconomic status in the non-invasive prenatal testing era: A population-based study

Journal

Publisher

WILEY
DOI: 10.1111/ajo.12778

Keywords

congenital abnormalities; Down syndrome; genetic testing; prenatal diagnosis; social class

Funding

  1. National Health and Medical Research Council [1105603]
  2. National Health and Medical Research Council Senior Research Fellowship [10121252]
  3. National Health and Medical Research Council of Australia [1105603] Funding Source: NHMRC

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BackgroundAdvances in technology can bring great benefits to human health, but their implementation may be influenced by socioeconomic factors, particularly in the field of prenatal screening for Down syndrome. AimTo analyse screening test indications for, and diagnostic yield of, invasive prenatal diagnostic testing (PNDx) according to socioeconomic status. MethodsRetrospective analysis of population-based data on PNDx and karyotype results for 2014-2015 in the Australian state of Victoria. Women having PNDx<25weeks due to combined first trimester screening (CFTS), second trimester serum screening (STSS), or noninvasive prenatal testing (NIPT) results were included. PNDx data were analysed by indication and maternal Index of Relative Socio-economic Advantage and Disadvantage (IRSAD), the latter determined by postcode. ResultsThere were 145206 births in 2014-2015; 1906 women underwent PNDx for the indication of CFTS (70.1%), NIPT (17.8%) or STSS (12.0%). Covariates positively associated with NIPT-indicated PNDx, compared with CFTS-indicated testing, were residence in a region of socioeconomic advantage, metropolitan status and maternal age. Women from the most advantaged regions had higher adjusted odds ratios (aOR) of NIPT-indicated testing compared with women from disadvantaged regions (aOR 5.72, 95% CI: 2.95-11.09). The diagnostic yield of PNDx increased with socioeconomic region, from 14% in the lowest IRSAD quintile to 31.2% in the highest (P<0.0001). ConclusionPopulation-based data reveal significant disparities in screening indications for PNDx and hence, in diagnostic yield, according to socioeconomic region. This finding may have ethical and policy implications for prenatal screening in Australia.

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