Evidence map›Paper›PMID 34296888›Full record

ArticleJournal of proteome research2021

Bridging the Polar and Hydrophobic Metabolome in Single-Run Untargeted Liquid Chromatography-Mass Spectrometry Dried Blood Spot Metabolomics for Clinical Purposes.

Hanne Bendiksen Skogvold, Elise Mørk Sandås, Anja Østeby, Camilla Løkken, Helge Rootwelt, Per Ola Rønning, Steven Ray Wilson, Katja Benedikte Prestø Elgstøen

Abstract read
In one paragraph

Article in Journal of proteome research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
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  5. Article
  6. Global Metabolomics Using LC-MS for Clinical Applications.Methods in molecular biology (Clifton, N.J.) · 2025
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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

8 authors.

Hanne Bendiksen SkogvoldNational Unit for Screening and Diagnosis of Congenital Pediatric Metabolic Disorders, Department of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, Oslo 0372, Norway.
Elise Mørk SandåsNational Unit for Screening and Diagnosis of Congenital Pediatric Metabolic Disorders, Department of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, Oslo 0372, Norway.
Anja ØstebyNational Unit for Screening and Diagnosis of Congenital Pediatric Metabolic Disorders, Department of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, Oslo 0372, Norway.
Camilla LøkkenNational Unit for Screening and Diagnosis of Congenital Pediatric Metabolic Disorders, Department of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, Oslo 0372, Norway.
Helge RootweltDepartment of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, Oslo 0372, Norway.
Per Ola RønningDepartment of Mechanical, Electronic and Chemical Engineering, Faculty of Technology, Art and Design, Oslo Metropolitan University, Pilestredet 35, Oslo 0166, Norway.
Steven Ray WilsonDepartment of Chemistry, University of Oslo, Sem Sælands vei 26, Oslo 0371, Norway.ORCID 0000-0002-9755-1188
Katja Benedikte Prestø ElgstøenNational Unit for Screening and Diagnosis of Congenital Pediatric Metabolic Disorders, Department of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, Oslo 0372, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dried blood spot (DBS) metabolite analysis is a central tool for the clinic, e.g., newborn screening. Instead of applying multiple analytical methods, a single liquid chromatography-mass spectrometry (LC-MS) method was developed for metabolites spanning from highly polar glucose to hydrophobic long-chain acylcarnitines. For liquid chromatography, a diphenyl column and a multi-linear solvent gradient operated at elevated flow rates allowed for an even-spread resolution of diverse metabolites. Injecting moderate volumes of DBS organic extracts directly, in contrast to evaporation and reconstitution, provided substantial increases in analyte recovery. Q Exactive MS settings were also tailored for sensitivity increases, and the method allowed for analyte retention time and peak area repeatabilities of 0.1-0.4 and 2-10%, respectively, for a wide polarity range of metabolites (log

Indexed as

MetabolomeMetabolomicsChromatography, LiquidDried Blood Spot TestingHumansInfant, NewbornMass Spectrometrydried blood spotsinborn errors of metabolismLC−MSmetabolomics

Identifiers

PMID34296888
PMCPMC8397434

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Registered trials

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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.