Evidence map›Paper›PMID 33603000›Full record

ArticleScientific reports2021

Plasma lipocalin-2/NGAL is stable over 12 weeks and is not modulated by exercise or dieting.

Michael E Nakai, Joshua Denham, Priscilla R Prestes, Nina Eikelis, Elisabeth A Lambert, Nora E Straznicky, Markus P Schlaich, Murray D Esler, Brendan J O'Brien, Fadi J Charchar and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 13 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

12 authors at 5 institutions in 1 country.

Michael E NakaiHypertension Research Laboratory, School of Biological Sciences, Faculty of Science, Monash University, 25 Rainforest Walk, Melbourne, Clayton, VIC, 3800, Australia.
Joshua DenhamDiscipline of Exercise and Sports Science, School of Health and Biomedical Sciences, RMIT University, Melbourne, VIC, 3083, Australia.
Priscilla R PrestesFaculty of Science and Technology, Federation University Australia, Mount Helen, Australia.
Nina EikelisIverson Health Innovation Research Institute and Faculty of Health, Arts and Design, Swinburne University of Technology, Melbourne, Australia.
Elisabeth A LambertIverson Health Innovation Research Institute and Faculty of Health, Arts and Design, Swinburne University of Technology, Melbourne, Australia.
Nora E StraznickyBaker Heart and Diabetes Institute, Melbourne, Australia.
Markus P SchlaichBaker Heart and Diabetes Institute, Melbourne, Australia.
Murray D EslerBaker Heart and Diabetes Institute, Melbourne, Australia.
Brendan J O'BrienFaculty of Science and Technology, Federation University Australia, Mount Helen, Australia.
Fadi J CharcharFaculty of Science and Technology, Federation University Australia, Mount Helen, Australia.
Gavin W LambertIverson Health Innovation Research Institute and Faculty of Health, Arts and Design, Swinburne University of Technology, Melbourne, Australia.
Francine Z MarquesHypertension Research Laboratory, School of Biological Sciences, Faculty of Science, Monash University, 25 Rainforest Walk, Melbourne, Clayton, VIC, 3800, Australia. Francine.marques@monash.edu.
Baker Heart and Diabetes Institute · AUFederation University · AUMonash University · AUSwinburne University of Technology · AURMIT University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amongst other immune cells, neutrophils play a key role in systemic inflammation leading to cardiovascular disease and can release inflammatory factors, including lipocalin-2 (LCN2). LCN2 drives cardiac hypertrophy and plays a role in maladaptive remodelling of the heart and has been associated with renal injury. While lifestyle factors such as diet and exercise are known to attenuate low-grade inflammation, their ability to modulate plasma LCN2 levels is unknown. Forty-eight endurance athletes and 52 controls (18-55 years) underwent measurement for various cardiovascular health indicators, along with plasma LCN2 concentration. No significant difference in LCN2 concentration was seen between the two groups. LCN2 was a very weak predictor or absent from models describing blood pressures or predicting athlete status. In another cohort, 57 non-diabetic overweight or obese men and post-menopausal women who fulfilled Adult Treatment Panel III metabolic syndrome criteria were randomly allocated into either a control, modified Dietary Approaches to Stop Hypertension (DASH) diet, or DASH and exercise group. Pre- and post-intervention demographic, cardiovascular health indicators, and plasma LCN2 expression were measured in each individual. While BMI fell in intervention groups, LCN2 levels remained unchanged within and between all groups, as illustrated by strong correlations between LCN2 concentrations pre- and 12 weeks post-intervention (r = 0.743, P < 0.0001). This suggests that circulating LCN2 expression are stable over a period of at least 12 weeks and is not modifiable by diet and exercise.

Indexed as

Diet, ReducingAdultAthletesExerciseFemaleHumansLipocalin-2MaleLCN2 protein, humanLipocalin-2

Identifiers

PMID33603000
PMCPMC7893047
OpenAlexW3129386280

What OpenQuestion holds

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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.