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
{"title":"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","authors":"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","doi":"10.1016/j.rpsm.2021.02.002","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>Observational, longitudinal, prospective, six-year follow-up, multicentre collaborative study. Two cohorts are being recruited: the PeriSTRESS-Valencia-cohort (<em>n</em> <!-->=<!--> <!-->26 VPTN, 18 EPTN, and 122 born-at-term controls), and the PremTEA-Madrid-cohort (<em>n</em> <!-->=<!--> <!-->49 EPTN and <em>n</em> <!-->=<!--> <!-->29 controls).</p></div><div><h3>Results</h3><p>We describe the rationale, objectives and design of the PeriSTRESS-PremTEA project and show a description at birth of the recruited samples.</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":101179,"journal":{"name":"Spanish Journal of Psychiatry and Mental Health","volume":"17 1","pages":"Pages 19-27"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1888989121000288/pdfft?md5=141d44430ae250cf504ff85f71f2f768&pid=1-s2.0-S1888989121000288-main.pdf","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1016/j.rpsm.2021.02.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>Observational, longitudinal, prospective, six-year follow-up, multicentre collaborative study. Two cohorts are being recruited: the PeriSTRESS-Valencia-cohort (<em>n</em> <!-->=<!--> <!-->26 VPTN, 18 EPTN, and 122 born-at-term controls), and the PremTEA-Madrid-cohort (<em>n</em> <!-->=<!--> <!-->49 EPTN and <em>n</em> <!-->=<!--> <!-->29 controls).</p></div><div><h3>Results</h3><p>We describe the rationale, objectives and design of the PeriSTRESS-PremTEA project and show a description at birth of the recruited samples.</p></div><div><h3>Conclusions</h3><p>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.</p></div>\",\"PeriodicalId\":101179,\"journal\":{\"name\":\"Spanish Journal of Psychiatry and Mental Health\",\"volume\":\"17 1\",\"pages\":\"Pages 19-27\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1888989121000288/pdfft?md5=141d44430ae250cf504ff85f71f2f768&pid=1-s2.0-S1888989121000288-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Spanish Journal of Psychiatry and Mental Health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1888989121000288\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"0\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spanish Journal of Psychiatry and Mental Health","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1888989121000288","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"PSYCHIATRY","Score":null,"Total":0}
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
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.