4.6 Article

Impact of the pre-examination phase on multicenter metabolomic studies

期刊

NEW BIOTECHNOLOGY
卷 68, 期 -, 页码 37-47

出版社

ELSEVIER
DOI: 10.1016/j.nbt.2022.01.006

关键词

Metabolomics; Pre-analytical procedures; NMR; Biobanks

资金

  1. Gentransmed [2014-2020.4.01.15-0012]
  2. EU Horizon 2020 research and innovation programme under grant SPIDIA4P [733,112]
  3. FP7 project: BBMRI-LPC [313010313010]
  4. FP7 project: SPIDIA [222,916]
  5. AIRC/FIRC fellowship for Italy
  6. Regione Toscana via the COMETA project

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The development of metabolomics in clinical applications is limited by insufficient validation in large multicenter studies. Large population cohorts and biobanks offer valuable resources for understanding molecular disease mechanisms, but their collections are often not tailored for metabolomics and lack specific attention to pre-analytical requirements. This study demonstrates how H-1 NMR-based analyses can differentiate human serum and plasma samples collected from different biobanks within large European cohort studies, highlighting the importance of adhering to evidence-based guidelines for wider-scale application of metabolomics in biomedicine.
The development of metabolomics in clinical applications has been limited by the lack of validation in large multicenter studies. Large population cohorts and their biobanks are a valuable resource for acquiring insights into molecular disease mechanisms. Nevertheless, most of their collections are not tailored for metabolomics and have been created without specific attention to the pre-analytical requirements for high-quality metabolome assessment. Thus, comparing samples obtained by different pre-analytical procedures remains a major challenge. Here, H-1 NMR-based analyses are used to demonstrate how human serum and plasma samples collected with different operating procedures within several large European cohort studies from the Biobanking and Biomolecular Resources Infrastructure - Large Prospective Cohorts (BBMRI-LPC) consortium can be easily revealed by supervised multivariate statistical analyses at the initial stages of the process, to avoid biases in the downstream analysis. The inter-biobank differences are discussed in terms of deviations from the validated CEN/TS 16945:2016 / ISO 23118:2021 norms. It clearly emerges that biobanks must adhere to the evidence-based guidelines in order to support wider-scale application of metabolomics in biomedicine, and that NMR spectroscopy is informative in comparing the quality of different sample sources in multi cohort/center studies.

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