Evidence map›Paper›PMID 21560159›Full record

Trial reportInternational journal of geriatric psychiatry2012

Effects of non-steroidal anti-inflammatory drug treatments on cognitive decline vary by phase of pre-clinical Alzheimer disease: findings from the randomized controlled Alzheimer's Disease Anti-inflammatory Prevention Trial.

Jeannie-Marie S Leoutsakos, Bengt O Muthen, John C S Breitner, Constantine G Lyketsos, ADAPT Research Team

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in International journal of geriatric psychiatry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 105 citations in OpenAlex.

  1. Trial
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  6. Glutamate and GABA in Microglia-Neuron Cross-Talk in Alzheimer's Disease.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Article
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  11. Article
  12. Article
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  15. Review
  16. Microbiota-gut-brain axis and toll-like receptors in Alzheimer's disease.Computational and structural biotechnology journal · 2019
    Review
  17. Innate Immunity Cells and the Neurovascular Unit.International journal of molecular sciences · 2018
    Review
  18. Microglia in Alzheimer's disease.The Journal of clinical investigation · 2017
    Review
  19. Strategies for dementia prevention: latest evidence and implications.Therapeutic advances in chronic disease · 2017
    Review
  20. 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

5 authors at 3 institutions in 1 country.

Jeannie-Marie S LeoutsakosDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA. jeannie-marie@jhu.edu
Bengt O Muthen
John C S Breitner
Constantine G Lyketsos
ADAPT Research Team
Johns Hopkins University · USUniversity of California, Los Angeles · USVA Puget Sound Health Care System · US

Funding

PREVENTION OF ALZHEIMER DEMENTIA &COGNITIVE DECLINEU01AG015477 · NIA · UNIVERSITY OF WASHINGTON · PI BREITNER, JOHN C S · 2000 to 2010
$44.4M
'T V ASSESSMENT - MEMORY DISORDERED PATIENTS'P50AG005146 · NIA · JOHNS HOPKINS UNIVERSITY · PI HUGANIR, RICHARD L · 1985 to 2019
$37.6M
Citalopram Treatment for Agitation in Alzheimer DementiaR01AG031348 · NIA · JOHNS HOPKINS UNIVERSITY · PI LYKETSOS, CONSTANTINE G · 2008 to 2012
$7.9M
Summer Research Training in Aging for Medical StudentsT35AG026778 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STUDENSKI, STEPHANIE A · 2005 to 2009
$460k
NIA NIH HHS P50 AG005146NIA NIH HHS P50‐AG005146NIA NIH HHS R01 AG031348NIA NIH HHS T32‐AG026778NIA NIH HHS T35 AG026778NIA NIH HHS U01 AG015477NIA NIH HHS U01‐AG15477
6 · The paper itself

Abstract

objectiveWe examined the effects of non-steroidal anti-inflammatory drugs on cognitive decline as a function of phase of pre-clinical Alzheimer disease.

methodsGiven recent findings that cognitive decline accelerates as clinical diagnosis is approached, we used rate of decline as a proxy for phase of pre-clinical Alzheimer disease. We fit growth mixture models of Modified Mini-Mental State (3MS) Examination trajectories with data from 2388 participants in the Alzheimer's Disease Anti-inflammatory Prevention Trial and included class-specific effects of naproxen and celecoxib.

resultsWe identified three classes: "no decline", "slow decline", and "fast decline", and examined the effects of celecoxib and naproxen on linear slope and rate of change by class. Inclusion of quadratic terms improved fit of the model (-2 log likelihood difference: 369.23; p < 0.001) but resulted in reversal of effects over time. Over 4 years, participants in the slow-decline class on placebo typically lost 6.6 3MS points, whereas those on naproxen lost 3.1 points (p-value for difference: 0.19). Participants in the fast-decline class on placebo typically lost 11.2 points, but those on celecoxib first declined and then gained points (p-value for difference from placebo: 0.04), whereas those on naproxen showed a typical decline of 24.9 points (p-value for difference from placebo: <0.0001).

conclusionsOur results appeared statistically robust but provided some unexpected contrasts in effects of different treatments at different times. Naproxen may attenuate cognitive decline in slow decliners while accelerating decline in fast decliners. Celecoxib appeared to have similar effects at first but then attenuated change in fast decliners.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAnti-Inflammatory Agents, Non-SteroidalCelecoxibCognitionFemaleHumansLongitudinal StudiesMaleMiddle AgedNaproxenPyrazolesSulfonamidesAnti-Inflammatory Agents, Non-SteroidalCelecoxibNaproxenPyrazolesSulfonamides

Identifiers

PMID21560159
PMCPMC3208130
OpenAlexW2117901796

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.