Evidence map›Paper›PMID 24872406›Full record

Trial reportJournal of lipid research2014

Challenges in accurate quantitation of lysophosphatidic acids in human biofluids.

Joelle M Onorato, Petia Shipkova, Anne Minnich, Anne-Françoise Aubry, John Easter, Adrienne Tymiak

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Journal of lipid research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Lysophospholipid Mediators in Health and Disease.Annual review of pathology · 2022
    Review
  7. Autotaxin-LPA-LPP3 Axis in Energy Metabolism and Metabolic Disease.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Spiroguanidine rhodamines as fluorogenic probes for lysophosphatidic acid.Chemical communications (Cambridge, England) · 2015
    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

6 authors at 2 institutions in 1 country.

Joelle M OnoratoDepartments of Bioanalytical and Discovery Analytical Science, Bristol-Myers Squibb Co., Princeton, NJ.
Petia ShipkovaDepartments of Bioanalytical and Discovery Analytical Science, Bristol-Myers Squibb Co., Princeton, NJ.
Anne MinnichExploratory Clinical and Translational Research, Bristol-Myers Squibb Co., Princeton, NJ.
Anne-Françoise AubryAnalytical and Bioanalytical Development, Bristol-Myers Squibb Co., Princeton, NJ.
John EasterDiscovery Chemistry, Bristol-Myers Squibb Co., Princeton, NJ.
Adrienne TymiakDepartments of Bioanalytical and Discovery Analytical Science, Bristol-Myers Squibb Co., Princeton, NJ.
Bristol-Myers Squibb (United States) · USBioanalytical Systems (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lysophosphatidic acids (LPAs) are biologically active signaling molecules involved in the regulation of many cellular processes and have been implicated as potential mediators of fibroblast recruitment to the pulmonary airspace, pointing to possible involvement of LPA in the pathology of pulmonary fibrosis. LPAs have been measured in various biological matrices and many challenges involved with their analyses have been documented. However, little published information is available describing LPA levels in human bronchoalveolar lavage fluid (BALF). We therefore conducted detailed investigations into the effects of extensive sample handling and sample preparation conditions on LPA levels in human BALF. Further, targeted lipid profiling of human BALF and plasma identified the most abundant lysophospholipids likely to interfere with LPA measurements. We present the findings from these investigations, highlighting the importance of well-controlled sample handling for the accurate quantitation of LPA. Further, we show that chromatographic separation of individual LPA species from their corresponding lysophospholipid species is critical to avoid reporting artificially elevated levels. The optimized sample preparation and LC/MS/MS method was qualified using a stable isotope-labeled LPA as a surrogate calibrant and used to determine LPA levels in human BALF and plasma from a Phase 0 clinical study comparing idiopathic pulmonary fibrosis patients to healthy controls.

Indexed as

Bronchoalveolar Lavage FluidChromatography, LiquidFemaleHumansIdiopathic Pulmonary FibrosisLysophospholipidsMaleMass Spectrometrylysophosphatidic acidLysophospholipidsbronchoalveolar lavage fluidhuman plasmaidiopathic pulmonary fibrosisstability

Identifiers

PMID24872406
PMCPMC4109772
OpenAlexW2320509049

What OpenQuestion holds

Textmetadata
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.