Evidence map›Paper›PMID 31112270›Full record

ArticleThe Journal of clinical endocrinology and metabolism2019

Mifepristone Treatment in Four Cases of Primary Bilateral Macronodular Adrenal Hyperplasia (BMAH).

Pejman Cohan, Honey E East, Sandi-Jo Galati, Jennifer U Mercado, Precious J Lim, Michele Lamerson, James J Smith, Anne L Peters, Kevin C J Yuen

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  7. A NovelJCEM case reports · 2025
    Article
  8. Review
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  10. Review
  11. Review
  12. Management and Medical Therapy of Mild Hypercortisolism.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Mifepristone-Induced Hypothyroidism.Journal of investigative medicine high impact case reports
    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

9 authors at 5 institutions in 1 country.

Pejman CohanSpecialized Endocrine Care Center, Beverly Hills, California.
Honey E EastBaptist Premier Medical Group, Jackson, Mississippi.
Sandi-Jo GalatiEndocrine and Diabetes Specialists of Connecticut, Trumbull, Connecticut.
Jennifer U MercadoSwedish Pituitary Center, Departments of Neuroendocrinology and Neurosurgery, Swedish Neuroscience Institute, Seattle, Washington.
Precious J LimCorcept Therapeutics, Menlo Park, California.
Michele LamersonCorcept Therapeutics, Menlo Park, California.
James J SmithCorcept Therapeutics, Menlo Park, California.
Anne L PetersKeck School of Medicine, University of Southern California, Los Angeles, California.
Kevin C J YuenSwedish Pituitary Center, Departments of Neuroendocrinology and Neurosurgery, Swedish Neuroscience Institute, Seattle, Washington.
Corcept Therapeutics (United States) · USBaptist Medical Center Jacksonville · USBarrow Neurological Institute · USSwedish Medical Center · USUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextPrimary bilateral macronodular adrenal hyperplasia (BMAH) is a rare form of adrenal Cushing syndrome conventionally treated with adrenalectomy. Medical treatment is often reserved for patients not eligible for surgery. However, to date there have been few studies about the efficacy of mifepristone for the treatment of BMAH associated with hypercortisolism.

objectiveTo describe a series of patients with hypercortisolism due to BMAH treated with mifepristone from multiple medical practices.

designWe retrospectively assessed four patients treated with mifepristone for hypercortisolism due to BMAH who had either failed unilateral adrenalectomy, declined surgery, or were poor surgical candidates.

resultsMifepristone induced clinical improvement and remission of the signs and symptoms of hypercortisolism in all described patients with BMAH. The median treatment duration at the time of efficacy response assessment was 5 months (range: 3 to 18 months). Improvement in cardiometabolic parameters was observed as early as 2 weeks after treatment was started. All patients achieved improvements in glycemic control and hypertension and had significant weight loss. The most common adverse event observed with mifepristone therapy was fatigue. Increases in TSH level occurred in two patients.

conclusionMifepristone can be an effective medical alternative to surgery in patients with hypercortisolism due to BMAH.

Indexed as

Adrenal Hyperplasia, CongenitalAdultAgedFemaleHormone AntagonistsHumansMagnetic Resonance ImagingMaleMiddle AgedMifepristonePrognosisHormone AntagonistsMifepristone

Identifiers

PMID31112270
PMCPMC6830498
OpenAlexW2945677948

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.