Evidence map›Paper›PMID 24633761›Full record

Trial reportInternational journal of geriatric psychiatry2014

Antiglucocorticoid therapy for older adults with anxiety and co-occurring cognitive dysfunction: results from a pilot study with mifepristone.

Eric J Lenze, Tamara Hershey, John W Newcomer, Jordan F Karp, Daniel Blumberger, Jennifer Anger, Peter Doré, David Dixon

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of geriatric psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01333098 (Antiglucocorticoid Therapy for Cognitive Impairment in Late-life Anxiety Disorders), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 51% 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.

NCT01333098 phase1 / phase2completednot on this map

Antiglucocorticoid Therapy for Cognitive Impairment in Late-life Anxiety Disorders

TypeinterventionalSponsorWashington University School of MedicineRan2012 to 2013Enrolled15ConditionsAnxiety DisordersArmsMifepristone
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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

8 authors at 4 institutions in 2 countries.

Eric J LenzeSchool of Medicine, Washington University, St Louis, MO, USA.
Tamara Hershey
John W Newcomer
Jordan F Karp
Daniel Blumberger
Jennifer Anger
Peter Doré
David Dixon
Washington University in St. Louis · USFlorida Atlantic University · USUniversity of Pittsburgh · USUniversity of Toronto · CA

Funding

Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
2/3-Incomplete Response in Late-Life Depression: Getting to RemissionR01MH083648 · NIMH · WASHINGTON UNIVERSITY · PI LENZE, ERIC J · 2009 to 2013
$2.0M
MINDFULNESS- BASED STRESS REDUCTION AND COGNITIVE FUNCTION IN STRESS AND AGINGR34AT007064 · NCCIH · WASHINGTON UNIVERSITY · PI LENZE, ERIC J · 2011 to 2013
$636k
NCATS NIH HHS UL1 TR000448NCCIH NIH HHS R34 AT007064NIDDK NIH HHS P30 DK020579NIMH NIH HHS R01 MH083648
6 · The paper itself

Abstract

objectivesIn older adults with anxiety disorders, chronically elevated cortisol may contribute to cognitive impairment and elevated anxiety. We conducted a pilot study with mifepristone, a glucocorticoid receptor antagonist, as a potential treatment for late-life anxiety disorders and co-occurring cognitive dysfunction.

methodsFifteen individuals 60 years and older with an anxiety disorder plus cognitive dysfunction participated in the 12-week study. In the first week, participants were randomly assigned to mifepristone 300 mg daily or placebo. In the subsequent 3 weeks, all participants received mifepristone 300 mg. Mifepristone was then discontinued, and the participants were reassessed 8 weeks later. We examined the following: (1) cognitive changes; (2) worry symptom severity; (3) safety and tolerability; and (4) salivary cortisol before, during, and after mifepristone exposure.

resultsOverall safety, tolerability, and high retention supported the feasibility of this research. Participants with higher baseline cortisol levels (peak cortisol >6.0 ng/ml, n = 5) showed improvements in memory, executive function, and worry severity after 3-4 weeks of mifepristone with persistent memory and worry improvements 8 weeks after mifepristone discontinuation. Individuals with low-to-normal baseline cortisol (n = 8) showed little to no improvement. As expected, cortisol levels rose during mifepristone exposure and returned to pretreatment levels 8 weeks after mifepristone discontinuation. In the first week of treatment, there were no differences between placebo-treated and mifepristone-treated participants.

conclusionThe results of this pilot study warrant further testing of antiglucocorticoid agents in late-life anxiety disorders with co-occurring cognitive dysfunction. Mifepristone is hypothesized to have benefits in patients with evidence of glucocorticoid excess. Directions for further study are discussed.

Indexed as

AgedAged, 80 and overAnxiety DisordersBiomarkersCognitionExecutive FunctionFemaleHormone AntagonistsHumansHydrocortisoneMaleMemoryMifepristonePilot ProjectsReceptors, GlucocorticoidSalivaBiomarkersHormone AntagonistsHydrocortisoneMifepristoneReceptors, Glucocorticoidanxietyglucocorticoidmemorymifepristoneolder adultsstress

Identifiers

PMID24633761
PMCPMC4138285
OpenAlexW2139297944

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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.