Evidence map›Paper›PMID 32456645›Full record

ArticleBMC medicine2020

Serum free thiols predict cardiovascular events and all-cause mortality in the general population: a prospective cohort study.

Amaal E Abdulle, Arno R Bourgonje, Lyanne M Kieneker, Anne M Koning, S la Bastide-van Gemert, Marian L C Bulthuis, Gerard Dijkstra, Klaas Nico Faber, Robin P F Dullaart, Stephan J L Bakker and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 57 citations in OpenAlex.

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  20. Systemic oxidative stress associates with disease severity and outcome in patients with new-onset or worsening heart failure.Clinical research in cardiology : official journal of the German Cardiac Society · 2023
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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

15 authors at 3 institutions in 2 countries.

Amaal E AbdulleDivision of Vascular Medicine, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Arno R BourgonjeDepartment of Gastroenterology and Hepatology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Lyanne M KienekerDivision of Nephrology, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Anne M KoningDepartment of Pathology and Medical Biology, Section Pathology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
S la Bastide-van GemertDepartment of Epidemiology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Marian L C BulthuisDepartment of Pathology and Medical Biology, Section Pathology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Gerard DijkstraDepartment of Gastroenterology and Hepatology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Klaas Nico FaberDepartment of Gastroenterology and Hepatology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Robin P F DullaartDivision of Endocrinology, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Stephan J L BakkerDivision of Nephrology, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Reinold O B GansDivision of Vascular Medicine, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Ron T GansevoortDivision of Nephrology, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Douwe J MulderDivision of Vascular Medicine, Department of Internal Medicine, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands.
Andreas PaschInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Linz, Austria.
Harry van GoorDepartment of Pathology and Medical Biology, Section Pathology, University of Groningen - University Medical Center Groningen, Groningen, the Netherlands. h.van.goor@umcg.nl.
University of Groningen · NLUniversity Medical Center Groningen · NLJohannes Kepler University of Linz · AT

Funding

Dutch Kidney Foundation E.013
6 · The paper itself

Abstract

backgroundSerum free thiols (R-SH, sulfhydryl groups) reliably reflect systemic oxidative stress. Since serum free thiols are rapidly oxidized by reactive species, systemic oxidative stress is generally associated with reduced serum free thiol levels. Free thiols associate with favorable disease outcomes in many patient cohorts, and the current hypothesis is that oxidative stress might also play an important role in cardiovascular disease. In this study, we aimed to establish the role of serum free thiols in the general population by investigating their relationship with the risk of cardiovascular (CV) events and all-cause mortality.

methodsParticipants (n = 5955) of the Prevention of REnal and Vascular ENd-stage Disease (PREVEND) cohort study from the general population were included. At baseline, serum levels of free thiols were quantified and adjusted to total protein levels. Protein-adjusted serum free thiol levels were studied for their associations with clinical and biochemical parameters, as well as with the risk of CV events and all-cause mortality.

resultsThe mean protein-adjusted serum free thiol level was 5.05 ± 1.02 μmol/g of protein. Protein-adjusted serum free thiols significantly predicted the risk of CV events, even after adjustment for potential confounding factors (hazard ratio [HR] per doubling 0.68 [95% confidence interval [CI] 0.47-1.00], P = 0.048). Similarly, protein-adjusted serum free thiols were significantly predictive of the risk of all-cause mortality (HR per doubling 0.66 [95% CI 0.44-1.00], P = 0.050). Stratified analyses revealed lower HRs for subjects with a lower body mass index (BMI), without hypertension, and without diabetes. Conversely, HRs were lower in subjects with albuminuria.

conclusionsIn this large population-based cohort study, serum free thiols significantly predicted the risk of CV events and all-cause mortality. Our results highlight the potential significance and clinical applicability of serum free thiols since they are amendable to therapeutic intervention.

Indexed as

AdultAgedCardiovascular DiseasesCohort StudiesFemaleHumansMaleMiddle AgedOxidative StressProspective StudiesRisk FactorsSulfhydryl CompoundsSurvival AnalysisSulfhydryl CompoundsCardiovascular diseaseFree thiolsMortalityOxidative stressPopulation study

Identifiers

PMID32456645
PMCPMC7251849
OpenAlexW3022635298

What OpenQuestion holds

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LicenceCC BY
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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.