Evidence map›Paper›PMID 23984312›Full record

Trial reportBioMed research international2013

Cardiovascular and renal effects of bromocriptine in diabetic patients with stage 4 chronic kidney disease.

Oliva Mejía-Rodríguez, Jorge E Herrera-Abarca, Guillermo Ceballos-Reyes, Marcela Avila-Diaz, Carmen Prado-Uribe, Francisco Belio-Caro, Antonio Salinas-González, Helios Vega-Gomez, Cleto Alvarez-Aguilar, Bengt Lindholm and 2 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BioMed research international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-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

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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Therapeutic activity of sarpogrelate and dopamine DBMC pharmacology & toxicology · 2021
    Article
  7. Article
  8. Article
  9. Neuroprotective strategies for retinal disease.Progress in retinal and eye research · 2018
    Review
  10. Article
  11. Review
  12. Article
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 4 institutions in 2 countries.

Oliva Mejía-RodríguezCoordinación de Educación e Investigación en Salud, Unidad de Medicina Familiar No 80, Instituto Mexicano del Seguro Social, Morelia, Mich, Mexico. olivamejia@yahoo.com
Jorge E Herrera-Abarca
Guillermo Ceballos-Reyes
Marcela Avila-Diaz
Carmen Prado-Uribe
Francisco Belio-Caro
Antonio Salinas-González
Helios Vega-Gomez
Cleto Alvarez-Aguilar
Bengt Lindholm
Elvia García-López
Ramón Paniagua
Mexican Social Security Institute · MXInstituto Politécnico Nacional · MXBaxter (Sweden) · SEKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective of this study was to investigate the effect of bromocriptine (BEC) on left ventricular mass index (LVMI) and residual renal function (RRF) in chronic kidney disease (CKD) patients with type 2 diabetes (T2D). RESEARCH DESIGN AND

methodsA 6-month double-blind randomized controlled trial was conducted in 28 patients with T2D and stage 4 CKD with increased LVMI. Fourteen patients received BEC (2.5 mg, initially 1 tablet with subsequent increase to three times a day) and 14 received a placebo (PBO; initially 1 tablet with subsequent increase to three times a day). Cardiovascular changes were assessed by monitoring 24 h ambulatory blood pressure, two-dimensional-guided M-mode echocardiography, and N-terminal brain natriuretic peptide (NT-proBNP) plasma levels. RRF was evaluated by creatinine clearance and cystatin-C plasma levels.

resultsBoth BEC and PBO groups decreased blood pressure-but the effect was more pronounced in the BEC group. Average 24 h, diurnal and nocturnal blood pressures, and circadian profile showed improved values compared to the PBO group; LVMI decreased by 14% in BEC and increased by 8% in PBO group. NT-proBNP decreased in BEC (0.54 ± 0.15 to 0.32 ± 0.17 pg/mL) and increased in PBO (0.37 ± 0.15 to 0.64 ± 0.17 pg/mL). Creatinine clearance did not change in the BEC group and decreased in the PBO group.

conclusionsBEC resulted in a decrease on blood pressure and LVMI. BEC also prevented the progression of CKD while maintaining the creatinine clearance unchanged.

Indexed as

Blood PressureBlood Pressure Monitoring, AmbulatoryBromocriptineDemographyDiabetes Mellitus, Type 2EchocardiographyFemaleHeartHeart VentriclesHormone AntagonistsHumansKidneyMaleMiddle AgedOrgan SizePlacebosBromocriptineHormone AntagonistsPlacebos

Identifiers

PMID23984312
PMCPMC3747336
OpenAlexW2146063550

What OpenQuestion holds

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LicenceCC BY
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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.