Evidence map›Paper›PMID 22684104›Full record

ArticleThe Journal of clinical investigation2012

Mineralocorticoid receptor is involved in rat and human ocular chorioretinopathy.

Min Zhao, Isabelle Célérier, Elodie Bousquet, Jean-Claude Jeanny, Laurent Jonet, Michèle Savoldelli, Olivier Offret, Antoine Curan, Nicolette Farman, Frédéric Jaisser and 1 more

3 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 167 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed, 6 pooled it
16.0field-weighted citation impact, top 1% 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.

NCT01822561 phase2completednot on this mapstarted 2013, after this paper: background citation

Eplerenone for Central Serous Chorioretinopathy: A Pilot Study

TypeinterventionalSponsorTufts Medical CenterRan2013 to 2017Enrolled17ConditionsCentral Serous ChorioretinopathyArmsEplerenone 50mg
NCT02153125 phase2unknown statusnot on this mapstarted 2014, after this paper: background citation

Eplerenone For the Treatment of Chronic Central Serous Chorioretinopathy

TypeinterventionalSponsorTel-Aviv Sourasky Medical CenterRan2014Enrolled30ConditionsCentral Serous ChorioretinopathyArmsEplerenone
NCT02354170 phase2completednot on this mapstarted 2015, after this paper: background citation

Short-Term Oral Mifepristone for Central Serous Chorioretinopathy. A Placebo-controlled Dose Ranging Study of Mifepristone in the Treatment of CSC (STOMP-CSC)

TypeinterventionalSponsorRoger Goldberg, M.D., MBARan2015 to 2017Enrolled16ConditionsCentral Serous ChorioretinopathyArmsMifepristone, Placebo
3 · Its place in the literature

Who cites it

167 citing papers in PubMed, 6 syntheses or guidelines pooled it, 378 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Interventions for central serous chorioretinopathy: a network meta-analysis.The Cochrane database of systematic reviews · 2025
    Pooled it
  4. Pooled it
  5. Pooled it
  6. Interventions for central serous chorioretinopathy: a network meta-analysis.The Cochrane database of systematic reviews · 2015
    Pooled it
  7. Trial
  8. Trial
  9. Long-term results and recurrence rates after spironolactone treatment in non-resolving central serous chorio-retinopathy (CSCR).Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2017
    Trial
  10. Trial
  11. Trial
  12. Hormonal factors in the pathophysiology of central serous chorioretinopathy - a systematic review and meta-analysis.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Review
  13. Review
  14. Longitudinal and cross-sectional study of retinal and choroidal changes in primary aldosteronism.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Article
  15. Article
  16. A KBiomolecules · 2026
    Article
  17. Article
  18. Review
  19. Article
  20. Review

107 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Min ZhaoINSERM, U872, Team 17, Centre de Recherche des Cordeliers, Paris, France.
Isabelle Célérier
Elodie Bousquet
Jean-Claude Jeanny
Laurent Jonet
Michèle Savoldelli
Olivier Offret
Antoine Curan
Nicolette Farman
Frédéric Jaisser
Francine Behar-Cohen
Délégation Paris 5 · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Central serous chorioretinopathy (CSCR) is a vision-threatening eye disease with no validated treatment and unknown pathogeny. In CSCR, dilation and leakage of choroid vessels underneath the retina cause subretinal fluid accumulation and retinal detachment. Because glucocorticoids induce and aggravate CSCR and are known to bind to the mineralocorticoid receptor (MR), CSCR may be related to inappropriate MR activation. Our aim was to assess the effect of MR activation on rat choroidal vasculature and translate the results to CSCR patients. Intravitreous injection of the glucocorticoid corticosterone in rat eyes induced choroidal enlargement. Aldosterone, a specific MR activator, elicited the same effect, producing choroid vessel dilation -and leakage. We identified an underlying mechanism of this effect: aldosterone upregulated the endothelial vasodilatory K channel KCa2.3. Its blockade prevented aldosterone-induced thickening. To translate these findings, we treated 2 patients with chronic nonresolved CSCR with oral eplerenone, a specific MR antagonist, for 5 weeks, and observed impressive and rapid resolution of retinal detachment and choroidal vasodilation as well as improved visual acuity. The benefit was maintained 5 months after eplerenone withdrawal. Our results identify MR signaling as a pathway controlling choroidal vascular bed relaxation and provide a pathogenic link with human CSCR, which suggests that blockade of MR could be used therapeutically to reverse choroid vasculopathy.

Indexed as

AdultAldosteroneAnimalsCentral Serous ChorioretinopathyChoroidCorticosteroneEplerenoneHumansMaleMiddle AgedMineralocorticoid Receptor AntagonistsRatsReceptors, MineralocorticoidRetinaSignal TransductionSmall-Conductance Calcium-Activated Potassium ChannelsAldosteroneCorticosteroneEplerenoneKcnn3 protein, ratMineralocorticoid Receptor AntagonistsReceptors, MineralocorticoidSmall-Conductance Calcium-Activated Potassium ChannelsSpironolactoneVasodilator Agents

Identifiers

PMID22684104
PMCPMC3386817
OpenAlexW2151703860

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.