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Abstract P020: 1 H Nmr Metabonomic Profiling Identifies Novel Biomarkers for Cardiovascular Mortality
Abstract only Background Cardiovascular disease (CVD) is the leading cause of death world-wide. Existing tools for identification of CVD risk have modest predictive power and discrimination. New biomarkers for CVD prediction are urgently needed. Hypothesis We have used 1 H NMR metabonomic profiling...
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Published in: | Circulation (New York, N.Y.) N.Y.), 2012-03, Vol.125 (suppl_10) |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract only
Background
Cardiovascular disease (CVD) is the leading cause of death world-wide. Existing tools for identification of CVD risk have modest predictive power and discrimination. New biomarkers for CVD prediction are urgently needed.
Hypothesis
We have used
1
H NMR metabonomic profiling of serum to identify novel biomarkers for incident CVD.
Methods
We investigated 9,179 men and women participating in the London Life Sciences Population study. Participants were recruited between 2002-2008 from the lists of 58 GPs in London UK, and assessed for baseline CVD risk factors, including smoking, body mass index, waist circumference, blood pressure, fasting glucose and lipid profile. Participants were followed for CVD mortality to July 2011 (mean 5.5 years per person).
1
H NMR metabonomic profiling was done on baseline serum sample by 12T Bruker spectrometer, with quantification of 44 fatty acid and low molecular weight markers.
Results
There were 161 CVD deaths. Compared to survivors, people with CVD death were older, had higher prevalence of type-2 diabetes and cigarette smoking, higher blood pressure, body mass index, glucose, and lower total and HDL cholesterol (Table). Framingham risk scores were higher in cases with CVD death than survivors (18.7±0.9% vs. 11.4±0.7%, P=10
-31
). We found six NMR metabolites associated with incident CVD at P |
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ISSN: | 0009-7322 1524-4539 |
DOI: | 10.1161/circ.125.suppl_10.AP020 |