Evidence map›Paper›PMID 38106464›Full record

ArticleInternational journal of tryptophan research : IJTR2023

Stability Studies of Kynurenine Pathway Metabolites in Blood Components Define Optimal Blood Processing Conditions.

Benjamin Heng, Ananda Staats Pires, Sharron Chow, Shivani Krishnamurthy, Brooke Bonnell, Sonia Bustamante, Gilles J Guillemin

Open access · goldAbstract read
In one paragraph

Article in International journal of tryptophan research : IJTR, 2023. 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
0.7field-weighted citation impact, top 34% of its field
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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
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 at 2 institutions in 1 country.

Benjamin HengMacquarie Medical School, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW, Australia.
Ananda Staats PiresMacquarie Medical School, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW, Australia.
Sharron ChowMacquarie Medical School, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW, Australia.
Shivani KrishnamurthyMacquarie Medical School, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW, Australia.
Brooke BonnellMacquarie Medical School, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW, Australia.
Sonia BustamanteBioanalytical Mass Spectrometry Facility, University of New South Wales, Sydney, Australia.
Gilles J GuilleminMacquarie Medical School, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW, Australia.
Macquarie University · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kynurenine pathway (KP) is the main pathway of tryptophan (TRP) metabolism that generates energy for multiple cellular processes. The activity of this pathway has been shown to be dysregulated in multiple human diseases. The resultant modulation of metabolites has been suggested to comprise biomarkers to track disease progression or could identify new therapeutic targets. While metabolite changes can be measured readily in blood, there is limited knowledge on the effect of blood matrices and sample processing time may have on the stability of KP metabolites. Understanding the stability of KP metabolites in blood is integral to obtaining accurate KP data to correlate with clinical pathology. Hence, the aim of this study was to assess the concentration of KP metabolites in matched whole blood, plasma and serum. The impact of pre-analytical sample processing time in the various blood matrices was also analysed. Serum and plasma had the higher concentration of KP metabolites compared to whole blood. Furthermore, concentrations of KP metabolites declined when the collected blood was processed after 24 hours storage at 4°C. Our study shows that that type of blood matrix and the time to processing have an impact on the stability of the KP metabolites. Serum or plasma are the preferred choice of matrix and the isolation of these matrices from whole blood is best performed immediately after collection for optimal analytical KP data.

Indexed as

analytical chemistryBiochemistrykynurenine pathwayserotonintryptophan

Identifiers

PMID38106464
PMCPMC10725091
OpenAlexW4389787208

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.