Cited by 33Advanced Biosensing Techniques and ApplicationsClinical Laboratory Practices and Quality ControlAdvanced Proteomics Techniques and Applications

Correlations Within and Between Highly Multiplexed Proteomic Assays of Human Plasma

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Rooney, Mary R, Chen, Jingsha, Ballantyne, Christie M, Hoogeveen, Ron C, Boerwinkle, Eric, Yu, Bing, Walker, Keenan A, Schlosser, Pascal +5 more·2025·Clinical Chemistry

Abstract

Introduction: The number of assays on proteomic platforms has grown rapidly. The leading platforms, SomaScan and Olink, have strengths and limitations. Comparisons of precision on the latest platforms—SomaScan 11k and Olink Explore HT—have not yet been established. Methods: Among 102 participants in the Atherosclerosis Risk in Communities Study (mean age 74 years, 53% women, 47% Black), we used split plasma samples to measure platform precision. CV and Spearman correlations were calculated for each assay. Cross-platform agreement was assessed for overlapping proteins. Results: SomaScan 11k demonstrated a median correlation of 0.85 for the 10 778 assays and a median CV of 6.8%, similar precision to earlier versions. The 5420 assays on Olink Explore HT exhibited a median correlation of 0.65 and median CV of 35.7%, which was higher than observed in its predecessors (e.g., 19.8% for Olink Explore 3072). Precision of Olink assays was inversely correlated with the percentage of samples above the limit of detection (LOD) (r = −0.77). Upon replacing Olink values below the LOD with values half the LOD, the median correlation for Olink assays measured in duplicate increased to 0.79; the median CV decreased to 13.3%. The distribution of between-platform correlations for the 4443 overlapping proteins had peaks at r approximately 0 and at r approximately 0.8. One-tenth of the protein pairs had cross-platform correlations r ≥ 0.8. Conclusions: Precision of these 2 proteomics platforms in human plasma has diverged as the coverage has increased. These results highlight the need for careful consideration in platform selection based on specific research requirements.

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  • Proteins with >50% measures above LOD were modestly correlated (N = 1361, median Pearson's r = 0.43, SD = 0.32), while proteins with <50% measures above LOD exhibited low inter-platform correlation (N = 796, median Pearson's r = 0.04, SD = 0.32).

    “While proteins with >50% measures above LOD were modestly correlated (N = 1361, median Pearson’s r = 0.43, SD = 0.32), proteins with <50% measures above LOD exhibited low inter-platform correlation (N = 796, median Pearson’s r = 0.04, SD = 0.32), consistent with prior reports (Supplementary Data 15 and 16)26.”

    From Cross-ancestry comparison of aptamer and antibody protein measures (2026) · cites this paper as [26]

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Authors
Rooney, M. R., Chen, J., Ballantyne, C. M., Hoogeveen, R. C., Boerwinkle, E., Yu, B., Walker, K. A., Schlosser, P., Selvin, E., Chatterjee, N., Couper, D., Grams, M. E., & Coresh, J.
Affiliations
  • Johns Hopkins University (US)
  • Baylor College of Medicine (US)
  • The University of Texas Health Science Center at Houston (US)
  • National Institute on Aging (US)
  • University of North Carolina at Chapel Hill (US)
  • New York University (US)
Corresponding author
Coresh, Josef
Venue
Clinical Chemistry
Published
2025-04-02
Volume
71
Issue
6
Pages
677-687
ISSN
  • 0009-9147 (ISSN-L)
  • 1530-8561
OpenAlex
W4409118908
Cited by
33
References
2
Citations by year
2026: 19 · 2025: 14
FWCI
9.86
Type
journal article
Language
en
Open access
Locations
  • Clinical Chemistry (publishedVersion)
  • PubMed (publishedVersion)
  • Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
  • Digital Commons-TMC (Texas Medical Center) (submittedVersion)
  • PubMed Central (submittedVersion)
  • FreiDok plus (Universitätsbibliothek Freiburg) (submittedVersion)
Funders
  • National Heart, Lung, and Blood Institute
  • National Institutes of Health
  • Department of Health and Human Services (75N92022D00001, 75N92022D00002, 75N92022D00003, 75N92022D00004, 75N92022D00005)
  • German Research Foundation (530592017)
  • National Institute on Aging’s Intramural Research Program (AG000348-01, AG000349-01)
  • NIH/NHLBI (K24 HL152440, R01DK108803, K24HL155861)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced Biosensing Techniques and Applications
  • Health Sciences › Medicine › Physiology › Clinical Laboratory Practices and Quality Control
  • Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
Keywords
human plasma, assay precision, detection limit, coefficient of variation, protein biomarkers, platform selection, Atherosclerosis Risk in Communities Study
MeSH terms
Aged, Blood Proteins, Female, Humans, Male, Proteomics

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