Intrauterine growth restriction modifies gene expression profiling in cord blood. Issue 4 (17th June 2014)
- Record Type:
- Journal Article
- Title:
- Intrauterine growth restriction modifies gene expression profiling in cord blood. Issue 4 (17th June 2014)
- Main Title:
- Intrauterine growth restriction modifies gene expression profiling in cord blood
- Authors:
- Yoshida, Taketoshi
Takasaki, Ichiro
Kanegane, Hirokazu
Inomata, Satomi
Ito, Yasunori
Tamura, Kentaro
Makimoto, Masami
Saito, Shigeru
Yoshimoto, Yuko
Miyawaki, Toshio - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="ped12324-sec-0001" sec-type="section"> <title>Background</title> <p>Small‐for‐gestational‐age (SGA) newborns are at an increased risk for perinatal morbidity and mortality and development of metabolic syndromes such as cardiovascular disease and type 2 diabetes mellitus (T2DM) in adulthood. The mechanism underlying this increased risk remains unclear. In this study, genetic modifications of cord blood were investigated to characterize fetal change in SGA newborns.</p> </sec> <sec id="ped12324-sec-0002" sec-type="section"> <title>Methods</title> <p>Gene expression in cord blood cells was compared between 10 SGA newborns and 10 appropriate‐for‐gestational‐age (AGA) newborns using microarray analysis. Pathway analysis was conducted using the Ingenuity Pathways Knowledge Base. To confirm the microarray analysis results, quantitative real‐time polymerase chain reaction (RT‐PCR) was performed for upregulated genes in SGA newborns.</p> </sec> <sec id="ped12324-sec-0003" sec-type="section"> <title>Results</title> <p>In total, 775 upregulated and 936 downregulated probes were identified in SGA newborns and compared with those in AGA newborns. Of these probes, 1149 were annotated. Most of these genes have been implicated in the development of cardiovascular disease and T2DM. There was good agreement between the RT‐PCR and microarray analyses results.</p> </sec> <sec id="ped12324-sec-0004" sec-type="section"><abstract abstract-type="main"> <title>Abstract</title> <sec id="ped12324-sec-0001" sec-type="section"> <title>Background</title> <p>Small‐for‐gestational‐age (SGA) newborns are at an increased risk for perinatal morbidity and mortality and development of metabolic syndromes such as cardiovascular disease and type 2 diabetes mellitus (T2DM) in adulthood. The mechanism underlying this increased risk remains unclear. In this study, genetic modifications of cord blood were investigated to characterize fetal change in SGA newborns.</p> </sec> <sec id="ped12324-sec-0002" sec-type="section"> <title>Methods</title> <p>Gene expression in cord blood cells was compared between 10 SGA newborns and 10 appropriate‐for‐gestational‐age (AGA) newborns using microarray analysis. Pathway analysis was conducted using the Ingenuity Pathways Knowledge Base. To confirm the microarray analysis results, quantitative real‐time polymerase chain reaction (RT‐PCR) was performed for upregulated genes in SGA newborns.</p> </sec> <sec id="ped12324-sec-0003" sec-type="section"> <title>Results</title> <p>In total, 775 upregulated and 936 downregulated probes were identified in SGA newborns and compared with those in AGA newborns. Of these probes, 1149 were annotated. Most of these genes have been implicated in the development of cardiovascular disease and T2DM. There was good agreement between the RT‐PCR and microarray analyses results.</p> </sec> <sec id="ped12324-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Expression of certain genes was modified in SGA newborns in the fetal period. These genes have been associated with metabolic syndrome. To clarify the association between modified gene expression in cord blood and individual vulnerability to metabolic syndrome in adulthood, these SGA newborns will be have long‐term follow up for examination of genetic and postnatal environmental factors. Gene expression of cord blood can be a useful and non‐invasive method of investigation of genetic alterations in the fetal period.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatrics international. Volume 56:Issue 4(2014)
- Journal:
- Pediatrics international
- Issue:
- Volume 56:Issue 4(2014)
- Issue Display:
- Volume 56, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 56
- Issue:
- 4
- Issue Sort Value:
- 2014-0056-0004-0000
- Page Start:
- 559
- Page End:
- 565
- Publication Date:
- 2014-06-17
- Subjects:
- Pediatrics -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1442-200X/issues. Subscription to online journal required for access to full text. ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ped.12324 ↗
- Languages:
- English
- ISSNs:
- 1328-8067
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.655800
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4039.xml