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Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data
MOTIVATION: Biobanks are important infrastructures for life science research. Optimal sample handling regarding e.g. collection and processing of biological samples is highly complex, with many variables that could alter sample integrity and even more complex when considering multiple study centers...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870544/ https://www.ncbi.nlm.nih.gov/pubmed/29036400 http://dx.doi.org/10.1093/bioinformatics/btx442 |
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author | Brunius, Carl Pedersen, Anders Malmodin, Daniel Karlsson, B Göran Andersson, Lars I Tybring, Gunnel Landberg, Rikard |
author_facet | Brunius, Carl Pedersen, Anders Malmodin, Daniel Karlsson, B Göran Andersson, Lars I Tybring, Gunnel Landberg, Rikard |
author_sort | Brunius, Carl |
collection | PubMed |
description | MOTIVATION: Biobanks are important infrastructures for life science research. Optimal sample handling regarding e.g. collection and processing of biological samples is highly complex, with many variables that could alter sample integrity and even more complex when considering multiple study centers or using legacy samples with limited documentation on sample management. Novel means to understand and take into account such variability would enable high-quality research on archived samples. RESULTS: This study investigated whether pre-analytical sample variability could be predicted and reduced by modeling alterations in the plasma metabolome, measured by NMR, as a function of pre-centrifugation conditions (1–36 h pre-centrifugation delay time at 4 °C and 22 °C) in 16 individuals. Pre-centrifugation temperature and delay times were predicted using random forest modeling and performance was validated on independent samples. Alterations in the metabolome were modeled at each temperature using a cluster-based approach, revealing reproducible effects of delay time on energy metabolism intermediates at both temperatures, but more pronounced at 22 °C. Moreover, pre-centrifugation delay at 4 °C resulted in large, specific variability at 3 h, predominantly of lipids. Pre-analytical sample handling error correction resulted in significant improvement of data quality, particularly at 22 °C. This approach offers the possibility to predict pre-centrifugation delay temperature and time in biobanked samples before use in costly downstream applications. Moreover, the results suggest potential to decrease the impact of undesired, delay-induced variability. However, these findings need to be validated in multiple, large sample sets and with analytical techniques covering a wider range of the metabolome, such as LC-MS. AVAILABILITY AND IMPLEMENTATION: The sampleDrift R package is available at https://gitlab.com/CarlBrunius/sampleDrift. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-5870544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58705442018-04-05 Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data Brunius, Carl Pedersen, Anders Malmodin, Daniel Karlsson, B Göran Andersson, Lars I Tybring, Gunnel Landberg, Rikard Bioinformatics Original Papers MOTIVATION: Biobanks are important infrastructures for life science research. Optimal sample handling regarding e.g. collection and processing of biological samples is highly complex, with many variables that could alter sample integrity and even more complex when considering multiple study centers or using legacy samples with limited documentation on sample management. Novel means to understand and take into account such variability would enable high-quality research on archived samples. RESULTS: This study investigated whether pre-analytical sample variability could be predicted and reduced by modeling alterations in the plasma metabolome, measured by NMR, as a function of pre-centrifugation conditions (1–36 h pre-centrifugation delay time at 4 °C and 22 °C) in 16 individuals. Pre-centrifugation temperature and delay times were predicted using random forest modeling and performance was validated on independent samples. Alterations in the metabolome were modeled at each temperature using a cluster-based approach, revealing reproducible effects of delay time on energy metabolism intermediates at both temperatures, but more pronounced at 22 °C. Moreover, pre-centrifugation delay at 4 °C resulted in large, specific variability at 3 h, predominantly of lipids. Pre-analytical sample handling error correction resulted in significant improvement of data quality, particularly at 22 °C. This approach offers the possibility to predict pre-centrifugation delay temperature and time in biobanked samples before use in costly downstream applications. Moreover, the results suggest potential to decrease the impact of undesired, delay-induced variability. However, these findings need to be validated in multiple, large sample sets and with analytical techniques covering a wider range of the metabolome, such as LC-MS. AVAILABILITY AND IMPLEMENTATION: The sampleDrift R package is available at https://gitlab.com/CarlBrunius/sampleDrift. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-11-15 2017-07-14 /pmc/articles/PMC5870544/ /pubmed/29036400 http://dx.doi.org/10.1093/bioinformatics/btx442 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Brunius, Carl Pedersen, Anders Malmodin, Daniel Karlsson, B Göran Andersson, Lars I Tybring, Gunnel Landberg, Rikard Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data |
title | Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data |
title_full | Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data |
title_fullStr | Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data |
title_full_unstemmed | Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data |
title_short | Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data |
title_sort | prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma nmr metabolomics data |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870544/ https://www.ncbi.nlm.nih.gov/pubmed/29036400 http://dx.doi.org/10.1093/bioinformatics/btx442 |
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