Evidence map›Paper›PMID 36370095›Full record

ArticleBasic & clinical pharmacology & toxicology2023

Falsely low phosphatidylethanol may be associated with biomarkers of haemolytic disease.

Alexander Årving, Thor Hilberg, Michael Sovershaev, Stig Tore Bogstrand, Gudrun Høiseth

Open access · hybridAbstract read
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Article in Basic & clinical pharmacology & toxicology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

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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

3 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Alexander ÅrvingDepartment of Forensic Sciences, Oslo University Hospital, Oslo, Norway.ORCID https://orcid.org/0000-0002-8674-8487
Thor HilbergFürst Medisinsk Laboratorium, Oslo, Norway.
Michael SovershaevFürst Medisinsk Laboratorium, Oslo, Norway.
Stig Tore BogstrandDepartment of Forensic Sciences, Oslo University Hospital, Oslo, Norway.
Gudrun HøisethDepartment of Forensic Sciences, Oslo University Hospital, Oslo, Norway.ORCID https://orcid.org/0000-0003-0872-9536
Oslo University Hospital · NOSkedsmo Medisinske Senter · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsFalsely lower or even negative phosphatidylethanol (PEth) levels may theoretically be seen in patients with haemolytic diseases, and the present study aimed to elucidate this hypothesis.

methodsPEth and carbohydrate-deficient transferrin (CDT) from 9893 serum and whole blood samples were included along with markers of haemolysis (i.e. haptoglobin, HbA1c, reticulocytes, LD and Hb). Cases showing discrepancy between PEth and CDT, that is, a low PEth value and a high CDT value, were considered to be possibly caused by falsely lowered PEth despite high alcohol consumption. These cases (N = 233) were compared to the control group without PEth and CDT mismatch.

resultsThe levels of haptoglobin were significantly lower in the cases showing low PEth and high CDT (estimate = -0.62, p = 0.002). The levels of HbA1c (estimate = -3.26, p = 0.001) and Hb (estimate = -0.507, p < 0.001) were also significantly lower in this group. These findings indicate haemolytic diseases in the low PEth/high CDT group. There were no significant differences for reticulocytes and LD concentrations between the low PEth/high CDT group and the control group.

conclusionsThese results indicate that falsely low PEth values could be associated with markers of haemolytic diseases, although more research is needed to highlight this further.

Indexed as

AlcoholismHematologic DiseasesAlcohol DrinkingBiomarkersGlycated HemoglobinGlycerophospholipidsHaptoglobinsHemolysisHumansBiomarkersGlycated HemoglobinGlycerophospholipidsHaptoglobinsphosphatidylethanolalcohol biomarkercarbohydrate-deficient transferrinhaemolytic diseaseshaptoglobinphosphatidylethanol

Identifiers

PMID36370095
PMCPMC10098851
OpenAlexW4308826756

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.