Evidence map›Paper›PMID 26448944›Full record

ReviewBioMed research international2015

Modulation of Immunity and Inflammation by the Mineralocorticoid Receptor and Aldosterone.

N Muñoz-Durango, A Vecchiola, L M Gonzalez-Gomez, F Simon, C A Riedel, C E Fardella, A M Kalergis

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 58 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

7 authors at 2 institutions in 1 country.

N Muñoz-DurangoInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago de Chile, Chile.
A VecchiolaInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Endocrinología, Pontificia Universidad Católica de Chile, Lira 85, 8330074 Santiago de Chile, Chile.
L M Gonzalez-GomezInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Endocrinología, Pontificia Universidad Católica de Chile, Lira 85, 8330074 Santiago de Chile, Chile.
F SimonInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Ciencias Biológicas, Facultad de Medicina, Universidad Andres Bello, República 217, 8370146 Santiago de Chile, Chile.
C A RiedelInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Ciencias Biológicas, Facultad de Medicina, Universidad Andres Bello, República 217, 8370146 Santiago de Chile, Chile.
C E FardellaInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Endocrinología, Pontificia Universidad Católica de Chile, Lira 85, 8330074 Santiago de Chile, Chile.
A M KalergisInstituto Milenio en Inmunología e Inmunoterapia, Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago de Chile, Chile ; Departamento de Inmunología Clínica y Reumatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago de Chile, Chile.
Pontificia Universidad Católica de Chile · CLUniversidad Andrés Bello · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mineralocorticoid receptor (MR) is a ligand dependent transcription factor. MR has been traditionally associated with the control of water and electrolyte homeostasis in order to keep blood pressure through aldosterone activation. However, there is growing evidence indicating that MR expression is not restricted to vascular and renal tissues, as it can be also expressed by cells of the immune system, where it responds to stimulation or antagonism, controlling immune cell function. On the other hand, aldosterone also has been associated with proinflammatory immune effects, such as the release of proinflammatory cytokines, generating oxidative stress and inducing fibrosis. The inflammatory participation of MR and aldosterone in the cardiovascular disease suggests an association with alterations in the immune system. Hypertensive patients show higher levels of proinflammatory mediators that can be modulated by MR antagonism. Although these proinflammatory properties have been observed in other autoimmune and chronic inflammatory diseases, the cellular and molecular mechanisms that mediate these effects remain unknown. Here we review and discuss the scientific work aimed at determining the immunological role of MR and aldosterone in humans, as well as animal models.

Indexed as

Models, ImmunologicalAdrenal CortexAldosteroneAnimalsHumansImmunologic FactorsImmunomodulationInflammationReceptors, MineralocorticoidAldosteroneImmunologic FactorsReceptors, Mineralocorticoid

Identifiers

PMID26448944
PMCPMC4581510
OpenAlexW1770024411

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.