Evidence map›Paper›PMID 35888707›Full record

ArticleMetabolites2022

Ring Trial on Quantitative Assessment of Bile Acids Reveals a Method- and Analyte-Specific Accuracy and Reproducibility.

Sven-Bastiaan Haange, Andreas Till, Per-Olof Bergh, Günter Fauler, Michael Gigl, Anita Löfgren-Sandblom, Frank G Schaap, Thomas Clavel, Christian Trautwein, Wiebke Fenske and 6 more

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Bile Acids in Intrahepatic Cholestasis of Pregnancy.Diagnostics (Basel, Switzerland) · 2022
    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

16 authors at 7 institutions in 4 countries.

Sven-Bastiaan HaangeDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research-UFZ, 04318 Leipzig, Germany.ORCID 0000-0003-2952-1152
Andreas TillDepartment of Internal Medicine I, Division of Endocrinology, Diabetes, and Metabolism, University Medical Center Bonn, 53127 Bonn, Germany.ORCID 0000-0002-0139-9143
Per-Olof BerghWallenberg Laboratory, Department of Molecular and Clinical Medicine, University of Gothenburg, 413 45 Gothenburg, Sweden.ORCID 0000-0001-9993-6965
Günter FaulerClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, 8036 Graz, Austria.
Michael GiglBavarian Center for Biomolecular Mass Spectrometry, TUM School of Life Sciences, Technical University of Munich, 85354 Freising, Germany.ORCID 0000-0002-5617-9236
Anita Löfgren-SandblomDepartment of Laboratory Medicine, Karolinska Institute, 171 77 Stockholm, Sweden.
Frank G SchaapDepartment of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6229 ER Maastricht, The Netherlands.ORCID 0000-0002-1597-572X
Thomas ClavelFunctional Microbiome Research Group, Institute of Medical Microbiology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.
Christian TrautweinMedizinische Klinik III (Gastroenterology, Metabolic Disease and Intensive Care), University Clinic RWTH, 52074 Aachen, Germany.
Wiebke FenskeDepartment of Internal Medicine I, Division of Endocrinology, Diabetes, and Metabolism, University Medical Center Bonn, 53127 Bonn, Germany.
Karin KleigreweBavarian Center for Biomolecular Mass Spectrometry, TUM School of Life Sciences, Technical University of Munich, 85354 Freising, Germany.ORCID 0000-0002-7718-0252
Hanns-Ulrich MarschallWallenberg Laboratory, Department of Molecular and Clinical Medicine, University of Gothenburg, 413 45 Gothenburg, Sweden.ORCID 0000-0001-7347-3085
Steven W M Olde DaminkDepartment of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6229 ER Maastricht, The Netherlands.
Tarek MoustafaDivision of Gastroenterology and Hepatology, Medical University of Graz, 8036 Graz, Austria.
Martin von BergenDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research-UFZ, 04318 Leipzig, Germany.
Ulrike Rolle-KampczykDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research-UFZ, 04318 Leipzig, Germany.ORCID 0000-0002-7728-6284
Helmholtz Centre for Environmental Research · DEMaastricht University · NLMedical University of Graz · ATTechnical University of Munich · DEUniversity of Gothenburg · SEKarolinska Institutet · SERWTH Aachen University · DE

Funding

Deutsche Forschungsgemeinschaft 395357507 - SFB 1371Deutsche Forschungsgemeinschaft 403224013 - SFB 1382Deutsche Forschungsgemeinschaft AOBJ: 450149205Deutsche Forschungsgemeinschaft AOBJ: 624808Deutsche Forschungsgemeinschaft AOBJ: 667675Deutsche Forschungsgemeinschaft AOBJ: 676866Deutsche Forschungsgemeinschaft TRR333/1Federal Ministry of Education and Research FKZ: 01EO1501
6 · The paper itself

Abstract

Bile acids are a key mediator of the molecular microbiome-host interaction, and various mass spectrometry-based assays have been developed in the recent decade to quantify a wide range of bile acids. We compare existing methodologies to harmonize them. Methodology for absolute quantification of bile acids from six laboratories in Europe were compared for the quantification of the primary bile acids cholic acid (CA) and chenodeoxycholic acid (CDCA) and conjugated products glycocholic acid (GCA) and taurocholic acid (TCA). For the bacterially modified secondary bile acids, the quantification of deoxycholic acid (DCA) and lithocholic acid (LCA) was compared. For the murine bile acids, we used the primary muricholic acids (α-MCA and, β-MCA) and the intestinally produced secondary bile acid muricholic (ω-MCA). The standards were spiked into methanol:water (1:1) mix as well as in human and murine serum at either low concentration range (150-3000 nM) or high concentration range (1500-40,000 nM). The precision was better for higher concentrations. Measurements for the hydrophobic unconjugated bile acids LCA and ω-MCA were the most challenging. The quality assessments were generally very similar, and the comprehensive analyses demonstrated that data from chosen locations can be used for comparisons between studies.

Indexed as

absolute quantificationbile acidshuman serumLC-MS/MSmurine serumring trial

Identifiers

PMID35888707
PMCPMC9319092
OpenAlexW4283369733

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.