Evidence map›Paper›PMID 30450757›Full record

Observational studyJournal of cellular and molecular medicine2019

Clinical association of metabolic syndrome, C-reactive protein and testosterone levels with clinically significant prostate cancer.

Enrique Gómez-Gómez, Julia Carrasco-Valiente, Juan Pablo Campos-Hernández, Ana Maria Blanca-Pedregosa, Juan Manuel Jiménez-Vacas, Jesus Ruiz-García, Jose Valero-Rosa, Raul Miguel Luque, María José Requena-Tapia

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 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

9 authors at 2 institutions in 2 countries.

Enrique Gómez-GómezMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Julia Carrasco-ValienteMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Juan Pablo Campos-HernándezMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Ana Maria Blanca-PedregosaMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Juan Manuel Jiménez-VacasMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Jesus Ruiz-GarcíaMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Jose Valero-RosaMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Raul Miguel LuqueMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.ORCID 0000-0002-7585-1913
María José Requena-TapiaMaimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Instituto Maimónides de Investigación Biomédica de Córdoba · ESSpanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, the influence that metabolic syndrome (MetS), hormonal alterations and inflammation might have on prostate cancer (PCa) risk has been a subject of controversial debate. Herein, we aimed to investigate the association between MetS-components, C-reactive protein (CRP) and testosterone levels, and the risk of clinically significant PCa (Sig-PCa) at the time of prostate biopsy. For that, men scheduled for transrectal ultrasound guided biopsy of the prostate were studied. Clinical, laboratory parameters and criteria for MetS characterization just before the biopsy were collected. A total of 524 patients were analysed, being 195 (37.2%) subsequently diagnosed with PCa and 240 (45.8%) meet the diagnostic criteria for MetS. Among patients with PCa, MetS-diagnosis was present in 94 (48.2%). Remarkably, a higher risk of Sig-PCa was associated to MetS, greater number of MetS-components and higher CRP levels (odds-ratio: 1.83, 1.30 and 2.00, respectively; P < 0.05). Moreover, higher circulating CRP levels were also associated with a more aggressive Gleason score in PCa patients. Altogether, our data reveal a clear association between the presence of MetS, a greater number of MetS-components or CRP levels >2.5 mg/L with an increased Sig-PCa diagnosis and/or with aggressive features, suggesting that MetS and/or CRP levels might influence PCa pathophysiology.

Indexed as

AgedBiopsyC-Reactive ProteinHumansInflammationMaleMetabolic SyndromeMiddle AgedNeoplasm GradingOdds RatioProspective StudiesProstateProstatic NeoplasmsRisk FactorsTestosteroneC-Reactive ProteinTestosteroneC-reactive proteininflammationmetabolic syndromesignificant prostate cancertestosterone

Identifiers

PMID30450757
PMCPMC6349154
OpenAlexW2901574714

What OpenQuestion holds

Textmetadata
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.