Evidence map›Paper›PMID 37698748›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2023

Identifying possible biomarkers of lower urinary tract symptoms using metabolomics and partial least square regression.

Florin V Hopland-Nechita, John R Andersen, Tarja Kvalheim Rajalahti, Trygve Andreassen, Christian Beisland

Open access · hybridAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 5 institutions in 2 countries.

Florin V Hopland-NechitaDepartment of Urology, Førde Central Hospital, Førde, Norway. florin.nechita@icloud.com.ORCID 0000-0003-3981-2172
John R AndersenWestern Norway University of Applied Sciences, Førde, Norway.
Tarja Kvalheim RajalahtiDepartment of Chemistry, University of Bergen, Bergen, Norway.
Trygve AndreassenDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
Christian BeislandDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.
Haukeland University Hospital · NONorwegian University of Science and Technology · NOUniversity of Bergen · NOWestern Norway University of Applied Sciences · NOZiauddin Hospital · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe objective of this study was to explore potential novel biomarkers for moderate to severe lower urinary tract symptoms (LUTS) using a metabolomics-based approach, and statistical methods with significant different features than previous reported. MATERIALS AND

methodsThe patients and the controls were selected to participate in the study according to inclusion/exclusion criteria (n = 82). We recorded the following variables: International prostatic symptom score (IPSS), prostate volume, comorbidities, PSA, height, weight, triglycerides, glycemia, HDL cholesterol, and blood pressure. The study of 41 plasma metabolites was done using the nuclear magnetic resonance spectroscopy technique. First, the correlations between the metabolites and the IPSS were done using Pearson. Second, significant biomarkers of LUTS from metabolites were further analysed using a multiple linear regression model. Finally, we validated the findings using partial least square regression (PLS).

resultsSmall to moderate correlations were found between IPSS and methionine (-0.301), threonine (-0.320), lactic acid (0.294), pyruvic acid (0.207) and 2-aminobutyric-acid (0.229). The multiple linear regression model revealed that only threonine (p = 0.022) was significantly associated with IPSS, whereas methionine (p = 0.103), lactic acid (p = 0.093), pyruvic acid (p = 0.847) and 2-aminobutyric-acid (p = 0.244) lost their significance. However, all metabolites lost their significance in the PLS model.

conclusionWhen using the robust PLS-regression method, none of the metabolites in our analysis had a significant association with lower urinary tract symptoms. This highlights the importance of using appropriate statistical methods when exploring new biomarkers in urology.

Indexed as

Lower Urinary Tract SymptomsPyruvic AcidAminobutyratesBiomarkersHumansLactic AcidLeast-Squares AnalysisMaleMetabolomicsMethionineRacemethioninealpha-aminobutyric acidAminobutyratesBiomarkersLactic AcidMethioninePyruvic AcidRacemethionineBiomarkerBPHLUTSMetabolomicsPLS

Identifiers

PMID37698748
PMCPMC10497431
OpenAlexW4386623996

What OpenQuestion holds

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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.