Study of the pathophysiological mechanisms associated with the onset and course of neurodevelopmental disorders in preterm infants (the PeriSTRESS-PremTEA study): Rationale, objectives, design and sample description

Pablo Navalón , Jéssica Merchan-Naranjo , Farah Ghosn , Belén Almansa , Consuelo Chafer-Pericas , Javier González-Peñas , Elisa Rodríguez-Toscano , Susana Zeballos , María Arriaga , Pedro Castro Castro , Dorotea Blanco Bravo , Máximo Vento , Laura Pina-Camacho , Ana García-Blanco
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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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与早产儿神经发育障碍的发病和病程相关的病理生理机制研究(PeriSTRESS-PremTEA 研究):原理、目标、设计和样本描述
背景很少有研究探讨可能对早产儿和极早产儿(VPTN/EPTN)神经发育障碍(ND)的出现/过程产生不同影响的病理生理途径。此外,在这一人群中还没有可预测 ND 的既定生物标志物。本研究的目的有四个方面:在两组 VPTN/EPTN 中(i)描述 ND 在 6 岁校正前的出现/发展过程;(ii)确定那些因素(从产前阶段到 6 岁)可解释与 ND 出现/发展过程相关的个体间差异;(iii)确定在生命最初几小时/几天内可预测 ND 的尿液代谢组生物标志物特征;以及(iv)确定可预测 ND 的 DNA 甲基化模式的纵向变化。方法观察性、纵向、前瞻性、随访六年的多中心合作研究。目前正在招募两个队列:PeriSTRESS-Valencia队列(n = 26名VPTN、18名EPTN和122名足月儿对照)和PremTEA-Madrid队列(n = 49名EPTN和n = 29名对照)。结果我们介绍了PeriSTRESS-PremTEA项目的原理、目标和设计,并展示了所招募样本的出生描述。结论PeriSTRESS-PremTEA项目有助于改善对VPTN/EPTN玖玖病生理病理相关临床、环境和生物变量的早期识别。该项目还有助于提高对这一人群中非侵入性 ND 生物标志物的早期识别。这样就可以及早发现玖龙病症,并对这些儿童进行早期个性化干预。
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