Evidence map›Paper›PMID 39088388›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Diagnostic potential of blood plasma longitudinal viscosity measured using Brillouin light scattering.

Jennifer Illibauer, Tamara Clodi-Seitz, Alexander Zoufaly, Judith H Aberle, Wolfgang J Weninger, Manuela Foedinger, Kareem Elsayad

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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  9. Diagnostic potential of blood plasma longitudinal viscosity measured using Brillouin light scattering.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jennifer IllibauerDivision of Anatomy, Center for Anatomy & Cell Biology, Medical University of Vienna, Vienna A-1090, Austria.ORCID 0000-0001-7965-3378
Tamara Clodi-SeitzDepartment of Medicine, Klinik Favoriten, Vienna A-1100, Austria.
Alexander ZoufalyDepartment of Medicine, Klinik Favoriten, Vienna A-1100, Austria.
Judith H AberleCenter for Virology, Medical University of Vienna, Vienna A-1090, Austria.ORCID 0000-0003-1197-3935
Wolfgang J WeningerDivision of Anatomy, Center for Anatomy & Cell Biology, Medical University of Vienna, Vienna A-1090, Austria.ORCID 0000-0003-0575-0073
Manuela FoedingerSigmund Freud Private University, Vienna A-1020, Austria.
Kareem ElsayadDivision of Anatomy, Center for Anatomy & Cell Biology, Medical University of Vienna, Vienna A-1090, Austria.

Funding

Austrian Science Fund (FWF) P34783
6 · The paper itself

Abstract

Blood plasma viscosity (PV) is an established biomarker for numerous diseases. Measurement of the shear PV using conventional rheological techniques is, however, time consuming and requires significant plasma volumes. Here, we show that Brillouin light scattering (BLS) and angle-resolved spectroscopy measurements of the longitudinal PV from microliter-sized plasma volumes can serve as a proxy for the shear PV measured using conventional viscometers. This is not trivial given the distinct frequency regime probed and the longitudinal viscosity, a combination of the shear and bulk viscosity, representing a unique material property on account of the latter. We demonstrate this for plasma from healthy persons and patients suffering from different severities of COVID-19 (CoV), which has been associated with an increased shear PV. We further show that the additional information contained in the BLS-measured effective longitudinal PV and its temperature scaling can provide unique insight into the chemical constituents and physical properties of plasma that can be of diagnostic value. In particular, we find that changes in the effective longitudinal viscosity are consistent with an increased suspension concentration in CoV patient samples at elevated temperatures that is correlated with disease severity and progression. This is supported by results from rapid BLS spatial-mapping, angle-resolved BLS measurements, changes in the elastic scattering, and anomalies in the temperature scaling of the shear viscosity. Finally, we introduce a compact BLS probe to rapidly perform measurements in plastic transport tubes. Our results open a broad avenue for PV diagnostics based on the high-frequency effective longitudinal PV and show that BLS can provide a means for its implementation.

Indexed as

Blood ViscosityCOVID-19HumansLightMalePlasmaRheologySARS-CoV-2Scattering, Radiationblood plasma viscosityBrillouin light scatteringCOVID-19longitudinal viscosity

Identifiers

PMID39088388
PMCPMC11331083

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.