Evidence map›Paper›PMID 23499573›Full record

ArticleClinica chimica acta; international journal of clinical chemistry2013

Development and validation of an LC-MS/MS assay for the quantification of the trans-methylation pathway intermediates S-adenosylmethionine and S-adenosylhomocysteine in human plasma.

Jacek Klepacki, Nina Brunner, Volker Schmitz, Jelena Klawitter, Uwe Christians, Jost Klawitter

Abstract readValidation Study
In one paragraph

Article in Clinica chimica acta; international journal of clinical chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Endothelial dysfunction and oxidative stress in polycystic kidney disease.American journal of physiology. Renal physiology · 2014
    Trial
  4. Article
  5. Review
  6. Two Novel S-methyltransferases Confer Dimethylsulfide Production in Actinomycetota.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

6 authors at 2 institutions in 2 countries.

Jacek KlepackiDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045-7503, United States. jacek.klepacki@ucdenver.edu
Nina Brunner
Volker Schmitz
Jelena Klawitter
Uwe Christians
Jost Klawitter
University of Colorado Anschutz Medical Campus · USCharité - Universitätsmedizin Berlin · DE

Funding

In Vivo Assessment of Calcineurin Inhibitor Toxicity in ChildrenR01HD070511 · NICHD · UNIVERSITY OF COLORADO DENVER · PI CHRISTIANS, UWE, THURMAN, JOSHUA M · 2011 to 2015
$1.9M
NICHD NIH HHS R01 HD070511NICHD NIH HHS R01HD070511
6 · The paper itself

Abstract

backgroundAlthough increased levels of S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) have been implicated as markers for renal and vascular dysfunction, until now there have been no studies investigating their association with clinical post-transplant events such as organ rejection and immunosuppressant nephrotoxicity.

methodsA newly developed and validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) assay for the quantification of SAM and SAH in human EDTA plasma was used for a clinical proof-of-concept pilot study. Retrospective analysis was performed using samples from a longitudinal clinical study following de novo kidney transplant patients for the first year (n=16).

resultsThe ranges of reliable response were 8 to 1024 nmol/l for SAM and 16 to 1024 nmol/l for SAH. The inter-day accuracies were 96.7-103.9% and 97.9-99.3% for SAM and SAH, respectively. Inter-day imprecisions were 8.1-9.1% and 8.4-9.8%. The total assay run time was 5 min. SAM and SAH concentrations were significantly elevated in renal transplant patients preceding documented acute rejection and nephrotoxicity events when compared to healthy controls (n=8) as well as transplant patients void of allograft dysfunction (n=8).

conclusionThe LC-MS/MS assay will provide the basis for further large-scale clinical studies to explore these thiol metabolites as molecular markers for the management of renal transplant patients.

Indexed as

Kidney TransplantationAdultFemaleGraft RejectionHumansLongitudinal StudiesMaleMiddle AgedPilot ProjectsPredictive Value of TestsPrognosisReference ValuesReproducibility of ResultsRetrospective StudiesS-AdenosylhomocysteineS-AdenosylmethionineS-AdenosylhomocysteineS-Adenosylmethionine

Identifiers

PMID23499573
PMCPMC4033670
OpenAlexW1983789873

What OpenQuestion holds

Textmetadata
LicenceTDM
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.