Evidence map›Paper›PMID 35786652›Full record

ArticleJournal of Alzheimer's disease : JAD2022

Clinical Progression of Baseline Risk States for Mild Cognitive Impairment.

Sarah M Goldberg, Yanji Zhao, Yu Cheng, Andrea M Weinstein, Swathi Gujral, Sarah B Berman, Robert A Sweet, Meryl A Butters, Oscar L Lopez, Beth E Snitz

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Sarah M GoldbergDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, USA.
Yanji ZhaoDepartment of Statistics, University of Pittsburgh, Pittsburgh, PA, USA.
Yu ChengDepartment of Statistics, University of Pittsburgh, Pittsburgh, PA, USA.
Andrea M WeinsteinDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
Swathi GujralDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
Sarah B BermanDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, USA.
Robert A SweetDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
Meryl A ButtersDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
Oscar L LopezDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, USA.
Beth E SnitzDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, USA.

Funding

TREATMENT OF DEPRESSION IN ALZHEIMER'S DISEASEP50AG005133 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SWEET, ROBERT A · 1985 to 2019
$43.0M
Research Education ComponentP30AG066468 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Julia K Kofler · 2020 to 2026
$29.4M
Aerobic Exercise for Optimizing Cognitive and Brain Health In Remitted Late-Life DepressionK23MH125074 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GUJRAL, SWATHI · 2021 to 2025
$828k
NIA NIH HHS P30 AG066468NIA NIH HHS P50 AG005133NIMH NIH HHS K23 MH125074
6 · The paper itself

Abstract

backgroundThis memory-clinic study joins efforts to study earliest clinical signs and symptoms of Alzheimer's disease and related dementias: subjective reports and objective neuropsychological test performance.

objectiveThe memory-clinic denoted two clinical "grey zones": 1) subjective cognitive decline (SCD; n = 107) with normal objective test scores, and 2) isolated low test scores (ILTS; n = 74) without subjective complaints to observe risk for future decline.

methodsInitial and annual follow-up clinical research evaluations and consensus diagnosis were used to evaluate baseline characteristics and clinical progression over 2.7 years, compared to normal controls (NC; n = 117).

resultsThe ILTS group was on average older than the NC and SCD groups. They had a higher proportion of people identifying as belonging to a minoritized racial group. The SCD group had significantly more years of education than the ILTS group. Both ILTS and SCD groups had increased risk of progression to mild cognitive impairment. Older age, minoritized racial identity, and baseline cognitive classification were risk factors for progression.

conclusionThe two baseline risk groups look different from each other, especially with respect to demographic correlates, but both groups predict faster progression than controls, over and above demographic differences. Varied presentations of early risk are important to recognize and may advance cognitive health equity in aging.

Indexed as

Alzheimer DiseaseCognitive DysfunctionDisease ProgressionHumansNeuropsychological TestsRisk FactorsCognitive declinemild cognitive impairmentneurocognitive testsrisk factors

Identifiers

PMID35786652
PMCPMC9661415

What OpenQuestion holds

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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.