AI Article Synopsis

  • - The study investigates the pathophysiological pathways linked to neurodevelopmental disorders (ND) in very preterm (VPTN) and extremely preterm newborns (EPTN), aiming to track ND emergence and factors influencing it from birth to age 6.
  • - It employs a longitudinal, multicenter approach involving two cohorts, assessing over a six-year period to discover urinary metabolomic biomarkers and DNA methylation patterns that could predict ND.
  • - The findings aim to enhance early identification of clinical, environmental, and biological factors related to ND, potentially leading to non-invasive biomarkers for timely and tailored interventions for affected children.

Article Abstract

Background: There are few studies exploring the pathophysiological pathways that may condition differentially the emergence/course of neurodevelopmental disorders (ND) in very preterm and extremely preterm newborns (VPTN/EPTN). Furthermore, there are no established biological markers predictive of ND in this population. The aim of this study is four-fold: in two cohorts of VPTN/EPTN (i) to characterize the emergence/course of ND up to corrected-age 6 years, (ii) to identify those factors (from prenatal stages up to age 6 years) that explain the interindividual differences related to emergence/course of ND, (iii) to identify in the first hours/days of life a urinary metabolomic biomarker profile predictive of ND, and (iv) to determine longitudinally variations in DNA methylation patterns predictive of ND.

Methods: Observational, longitudinal, prospective, six-year follow-up, multicentre collaborative study. Two cohorts are being recruited: the PeriSTRESS-Valencia-cohort (n=26 VPTN, 18 EPTN, and 122 born-at-term controls), and the PremTEA-Madrid-cohort (n=49 EPTN and n=29 controls).

Results: We describe the rationale, objectives and design of the PeriSTRESS-PremTEA project and show a description at birth of the recruited samples.

Conclusions: The PeriSTRESS-PremTEA project could help improve early identification of clinical, environmental and biological variables involved in the physiopathology of ND in VPTN/EPTN. It could also help to improve the early identification of non-invasive ND biomarkers in this population. This may allow early ND detection as well as early and personalised intervention for these children.

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Source
http://dx.doi.org/10.1016/j.rpsm.2021.02.002DOI Listing

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