scholarly journals Fetal Effects of COVID-19 Infection: Targeted Metabolomic profiling of cord blood

2022 ◽  
Vol 226 (1) ◽  
pp. S36-S37
Author(s):  
Onur Turkoglu ◽  
Ali Alhousseini ◽  
Sonia Sajja ◽  
Jay Idler ◽  
Sean Stuart ◽  
...  
2020 ◽  
Vol 5 ◽  
pp. 264
Author(s):  
Kurt Taylor ◽  
Nancy McBride ◽  
Neil J Goulding ◽  
Kimberley Burrows ◽  
Dan Mason ◽  
...  

Metabolomics is the quantification of small molecules, commonly known as metabolites. Collectively, these metabolites and their interactions within a biological system are known as the metabolome. The metabolome is a unique area of study, capturing influences from both genotype and environment. The availability of high-throughput technologies for quantifying large numbers of metabolites, as well as lipids and lipoprotein particles, has enabled detailed investigation of human metabolism in large-scale epidemiological studies. The Born in Bradford (BiB) cohort includes 12,453 women who experienced 13,776 pregnancies recruited between 2007-2011, their partners and their offspring. In this data note, we describe the metabolomic data available in BiB, profiled during pregnancy, in cord blood and during early life in the offspring. These include two platforms of metabolomic profiling: nuclear magnetic resonance and mass spectrometry. The maternal measures, taken at 26-28 weeks’ gestation, can provide insight into the metabolome during pregnancy and how it relates to maternal and offspring health. The offspring cord blood measurements provide information on the fetal metabolome. These measures, alongside maternal pregnancy measures, can be used to explore how they may influence outcomes. The infant measures (taken around ages 12 and 24 months) provide a snapshot of the early life metabolome during a key phase of nutrition, environmental exposures, growth, and development. These metabolomic data can be examined alongside the BiB cohorts’ extensive phenotype data from questionnaires, medical, educational and social record linkage, and other ‘omics data.


2011 ◽  
Vol 402 (3) ◽  
pp. 1109-1121 ◽  
Author(s):  
Donata Favretto ◽  
Erich Cosmi ◽  
Eugenio Ragazzi ◽  
Silvia Visentin ◽  
Marianna Tucci ◽  
...  

2019 ◽  
Vol 54 (S1) ◽  
pp. 49-49
Author(s):  
L. Youssef ◽  
R.V. Simoes ◽  
J. Miranda ◽  
M. Garcia Martin ◽  
C. Paules ◽  
...  

2020 ◽  
Vol 8 (6) ◽  
pp. 296-296
Author(s):  
Chunchao Zhao ◽  
Jun Ge ◽  
Ruifen Jiao ◽  
Xia Li ◽  
Yuan Li ◽  
...  

2021 ◽  
Vol 5 ◽  
pp. 264
Author(s):  
Kurt Taylor ◽  
Nancy McBride ◽  
Neil J Goulding ◽  
Kimberley Burrows ◽  
Dan Mason ◽  
...  

Metabolomics is the quantification of small molecules, commonly known as metabolites. Collectively, these metabolites and their interactions within a biological system are known as the metabolome. The metabolome is a unique area of study, capturing influences from both genotype and environment. The availability of high-throughput technologies for quantifying large numbers of metabolites, as well as lipids and lipoprotein particles, has enabled detailed investigation of human metabolism in large-scale epidemiological studies. The Born in Bradford (BiB) cohort includes 12,453 women who experienced 13,776 pregnancies recruited between 2007-2011, their partners and their offspring. In this data note, we describe the metabolomic data available in BiB, profiled during pregnancy, in cord blood and during early life in the offspring. These include two platforms of metabolomic profiling: nuclear magnetic resonance and mass spectrometry. The maternal measures, taken at 26-28 weeks’ gestation, can provide insight into the metabolome during pregnancy and how it relates to maternal and offspring health. The offspring cord blood measurements provide information on the fetal metabolome. These measures, alongside maternal pregnancy measures, can be used to explore how they may influence outcomes. The infant measures (taken around ages 12 and 24 months) provide a snapshot of the early life metabolome during a key phase of nutrition, environmental exposures, growth, and development. These metabolomic data can be examined alongside the BiB cohorts’ extensive phenotype data from questionnaires, medical, educational and social record linkage, and other ‘omics data.


2004 ◽  
Vol 10 ◽  
pp. 31
Author(s):  
Florence M. Amorado-Santos ◽  
Maria Honolina S. Gomez ◽  
Maria Victoria R. Olivares ◽  
Zayda N. Gamilla

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