Mary Ni Lochlainn, Nathan J Cheetham, Mario Falchi, Paolo Piazza, Claire J Steves
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引用次数: 0
Abstract
Background: Capillary blood collection has a number of advantages over venous collection, especially in the context of increasing decentralized clinical trials and field-based testing. No studies are available comparing venous versus capillary blood collection for proteomics measurement. The aim of this study was to compare venous versus capillary blood collection methods for proteomic measurement in peripheral blood.
Methods: The expression of 368 different proteins from the Olink Explore 384 Inflammation panel was measured in both venous and capillary blood samples collected from 22 individuals at a single time point. Protein levels from venous and capillary blood samples were compared with descriptive statistics and correlation calculations. Correlations were examined for a subset of proteins identified in recent reports as associated with morbidity and mortality.
Results: Strong positive correlation (r ≥ 0.7) between protein concentrations measured in venous and capillary blood samples was observed for two in three proteins tested (215 of 327, 66%). A further 47 (14%) showed a moderate positive correlation (0.4 ≤ r < 0.7), with weak or very weak correlation (r < 0.4) observed for the remaining 65 (20%). Protein expression was consistently higher in capillary blood samples for proteins with lower correlation (r < 0.6) between sampling methods. Further work is required to understand the underlying reasons why proteins were consistently under-expressed in venous samples/over-expressed in capillary samples in a minority of proteins tested.
Conclusions: Proteomic measurement utilising capillary blood collection provides very similar results to using venous blood collection. This is a promising sign for the validity and reliability of studies using capillary blood collection, including decentralised and remote studies.
期刊介绍:
PROTEOMICS - Clinical Applications has developed into a key source of information in the field of applying proteomics to the study of human disease and translation to the clinic. With 12 issues per year, the journal will publish papers in all relevant areas including:
-basic proteomic research designed to further understand the molecular mechanisms underlying dysfunction in human disease
-the results of proteomic studies dedicated to the discovery and validation of diagnostic and prognostic disease biomarkers
-the use of proteomics for the discovery of novel drug targets
-the application of proteomics in the drug development pipeline
-the use of proteomics as a component of clinical trials.