Evidence map›Paper›PMID 26209223›Full record

ArticleThe American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry2015

Cognitive Effects of Hormone Therapy Continuation or Discontinuation in a Sample of Women at Risk for Alzheimer Disease.

Tonita E Wroolie, Heather A Kenna, Katherine E Williams, Natalie L Rasgon

Open access · greenAbstract read
In one paragraph

Article in The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. SeXX Matters in Multiple Sclerosis.Frontiers in neurology · 2020
    Review
  11. Article
  12. A heartfelt message, estrogen replacement therapy: use it or lose it.American journal of physiology. Heart and circulatory physiology · 2018
    Review
  13. Article
  14. Sleep and Brain Function at Menopause.Journal of mid-life health
    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

4 authors at 1 institution in 1 country.

Tonita E WroolieDepartment of Psychiatry and Behavioral Sciences, Stanford Center for Neuroscience in Women's Health, Stanford University School of Medicine, Stanford, CA.
Heather A KennaDepartment of Psychiatry and Behavioral Sciences, Stanford Center for Neuroscience in Women's Health, Stanford University School of Medicine, Stanford, CA.
Katherine E WilliamsDepartment of Psychiatry and Behavioral Sciences, Stanford Center for Neuroscience in Women's Health, Stanford University School of Medicine, Stanford, CA.
Natalie L RasgonDepartment of Psychiatry and Behavioral Sciences, Stanford Center for Neuroscience in Women's Health, Stanford University School of Medicine, Stanford, CA. Electronic address: nrasgon@stanford.edu.
Stanford University · US

Funding

XOLAIR IN SUBJECTS WITH MODERATE TO SEVERE ATOPIC DERMATITIS WITH FOOD ALLERGYM01RR000070 · NCRR · STANFORD UNIVERSITY · PI RASGON, NATALIE L · 1985 to 2008
$32.4M
Estrogen Use in Protection from Cognitive DeclineR01AG022008 · NIA · STANFORD UNIVERSITY · PI RASGON, NATALIE L · 2003 to 2010
$2.5M
NCRR NIH HHS M01 RR000070NCRR NIH HHS M01 RR00070NIA NIH HHS R01 AG022008NIA NIH HHS R01 AG22008
6 · The paper itself

Abstract

objectiveUse of estrogen-based hormone therapy (HT) as a protection from cognitive decline and Alzheimer disease (AD) is controversial, although cumulative data support HT use when initiated close to menopause onset with estrogen formulations containing 17β-estradiol preferable to conjugated equine estrogen formulations. Little is known regarding specific populations of women who may derive benefit from HT.

methodsWomen with heightened risk for AD (aged 49-69), all of whom were taking HT for at least 1 year and most of whom initiated HT close to menopause onset, underwent cognitive assessment followed by randomization to continue or discontinue HT. Assessments were repeated at 2 years after randomization.

resultsWomen who continued HT performed better on cognitive domains composed of measures of verbal memory and combined attention, working memory, and processing speed measures. Women who used 17β-estradiol versus conjugated equine estrogen, whether randomized to continue or discontinue HT, showed better verbal memory performance at the 2-year follow-up assessment. An interaction was also found with HT randomization and family history of AD in a first-degree relative. All female offspring of patients with AD declined in verbal memory; however, women who continued HT declined less than women who discontinued HT. Women without a first-degree relative with AD showed verbal memory improvement (likely because of practice effects) with continuance and declined with discontinuance of HT.

conclusionContinuation of HT use appears to protect cognition in women with heightened risk for AD when initiated close to menopause onset.

Indexed as

Estrogen Replacement TherapyAgedAlzheimer DiseaseCognitionEstradiolFemaleHumansMenopauseMiddle AgedRisk FactorsEstradiolAlzheimer diseasecognitionHormone therapypostmenopausal women

Identifiers

PMID26209223
PMCPMC4654994
OpenAlexW1006899190

What OpenQuestion holds

Textmetadata
LicenceTDM
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.