Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples
Abstract Many emerging technologies are reliant on circulating cell-free DNA (cfDNA) and cell-free RNA (cfRNA) applications in the clinic. However, the impact of diurnal cycles or daily meals on circulating analytes are poorly understood and may be confounding factors when developing diagnostic plat...
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2020-10-01
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Online Access: | https://doi.org/10.1038/s41598-020-73350-3 |
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doaj-98bffb7158944ae683a9bed573a1b3d22021-10-10T11:25:02ZengNature Publishing GroupScientific Reports2045-23222020-10-011011810.1038/s41598-020-73350-3Diurnal stability of cell-free DNA and cell-free RNA in human plasma samplesJosiah T. Wagner0Hyun Ji Kim1Katie C. Johnson-Camacho2Taylor Kelley3Laura F. Newell4Paul T. Spellman5Thuy T. M. Ngo6Knight Cancer Institute, Cancer Early Detection Advanced Research Center (CEDAR), Oregon Health & Science UniversityKnight Cancer Institute, Cancer Early Detection Advanced Research Center (CEDAR), Oregon Health & Science UniversityKnight Cancer Institute, Cancer Early Detection Advanced Research Center (CEDAR), Oregon Health & Science UniversityKnight Cancer Institute, Oregon Health & Science UniversityKnight Cancer Institute, Hematology and Medical Oncology, Oregon Health & Science UniversityKnight Cancer Institute, Cancer Early Detection Advanced Research Center (CEDAR), Oregon Health & Science UniversityKnight Cancer Institute, Cancer Early Detection Advanced Research Center (CEDAR), Oregon Health & Science UniversityAbstract Many emerging technologies are reliant on circulating cell-free DNA (cfDNA) and cell-free RNA (cfRNA) applications in the clinic. However, the impact of diurnal cycles or daily meals on circulating analytes are poorly understood and may be confounding factors when developing diagnostic platforms. To begin addressing this knowledge gap, we obtained plasma from four healthy donors serially sampled five times during 12 h in a single day. For all samples, we measured concentrations of cfDNA and cfRNA using both bulk measurements and gene-specific digital droplet PCR. We found no significant variation attributed to blood draw number for the cfDNA or cfRNA. This indicated that natural diurnal cycles and meal consumption do not appear to significantly affect abundance of total cfDNA, total cfRNA, or our two selected cfRNA transcripts. Conversely, we observed significant variation between individual donors for cfDNA and one of the cfRNA transcripts. The results of this work suggest that it will be important to consider patient-specific baselines when designing reliable circulating cfDNA or cfRNA clinical assays.https://doi.org/10.1038/s41598-020-73350-3 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Josiah T. Wagner Hyun Ji Kim Katie C. Johnson-Camacho Taylor Kelley Laura F. Newell Paul T. Spellman Thuy T. M. Ngo |
spellingShingle |
Josiah T. Wagner Hyun Ji Kim Katie C. Johnson-Camacho Taylor Kelley Laura F. Newell Paul T. Spellman Thuy T. M. Ngo Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples Scientific Reports |
author_facet |
Josiah T. Wagner Hyun Ji Kim Katie C. Johnson-Camacho Taylor Kelley Laura F. Newell Paul T. Spellman Thuy T. M. Ngo |
author_sort |
Josiah T. Wagner |
title |
Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples |
title_short |
Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples |
title_full |
Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples |
title_fullStr |
Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples |
title_full_unstemmed |
Diurnal stability of cell-free DNA and cell-free RNA in human plasma samples |
title_sort |
diurnal stability of cell-free dna and cell-free rna in human plasma samples |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2020-10-01 |
description |
Abstract Many emerging technologies are reliant on circulating cell-free DNA (cfDNA) and cell-free RNA (cfRNA) applications in the clinic. However, the impact of diurnal cycles or daily meals on circulating analytes are poorly understood and may be confounding factors when developing diagnostic platforms. To begin addressing this knowledge gap, we obtained plasma from four healthy donors serially sampled five times during 12 h in a single day. For all samples, we measured concentrations of cfDNA and cfRNA using both bulk measurements and gene-specific digital droplet PCR. We found no significant variation attributed to blood draw number for the cfDNA or cfRNA. This indicated that natural diurnal cycles and meal consumption do not appear to significantly affect abundance of total cfDNA, total cfRNA, or our two selected cfRNA transcripts. Conversely, we observed significant variation between individual donors for cfDNA and one of the cfRNA transcripts. The results of this work suggest that it will be important to consider patient-specific baselines when designing reliable circulating cfDNA or cfRNA clinical assays. |
url |
https://doi.org/10.1038/s41598-020-73350-3 |
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