Evidence map›Paper›PMID 38621578›Full record

ArticleNeuropsychologia2024

News event memory in amnestic and non-amnestic MCI, heritable risk for dementia, and subjective memory complaints.

Isabel Asp, Andrew T J Cawley-Bennett, Jennifer C Frascino, Shahrokh Golshan, Mark W Bondi, Christine N Smith

Open access · greenAbstract read
In one paragraph

Article in Neuropsychologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 92% 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

2 citing papers in PubMed, 0 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Isabel AspSan Diego Veterans Affairs Medical Center, San Diego, CA, USA.
Andrew T J Cawley-BennettSan Diego Veterans Affairs Medical Center, San Diego, CA, USA.
Jennifer C FrascinoSan Diego Veterans Affairs Medical Center, San Diego, CA, USA; Department of Psychiatry, University of California San Diego, CA, USA.
Shahrokh GolshanSan Diego Veterans Affairs Medical Center, San Diego, CA, USA; Department of Psychiatry, University of California San Diego, CA, USA.
Mark W BondiSan Diego Veterans Affairs Medical Center, San Diego, CA, USA; Department of Psychiatry, University of California San Diego, CA, USA.
Christine N SmithSan Diego Veterans Affairs Medical Center, San Diego, CA, USA; Department of Psychiatry, University of California San Diego, CA, USA; Center for the Neurobiology of Learning and Memory, University of California Irvine, CA, USA. Electronic address: cnsmith@ucsd.edu.
San Francisco VA Medical Center · US

Funding

UCSD Shiley-Marcos Alzheimer's Disease Research Center P30P30AG062429 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DOUGLAS R GALASKO · 2019 to 2026
$34.9M
CSRD VA I01 CX001375CSRD VA I01 CX002626NIA NIH HHS P30 AG062429US Department of Veterans Affairs I01CX001375US Department of Veterans Affairs I01CX002626
6 · The paper itself

Abstract

Robust and sensitive clinical measures are needed for more accurate and earlier detection of Alzheimer's disease (AD), for staging preclinical AD, and for gauging the efficacy of treatments. Mild impairment on episodic memory tests is thought to indicate a cognitive risk of developing AD and mild cognitive impairment (MCI), considered to be a transitional stage between normal aging and AD. Novel tests of semantic memory, such as memory for news events, are also impaired early on but have received little clinical attention even though they may provide a novel way to assess cognitive risk for AD. We examined memory for news events in older adults with normal cognition (NC, N = 34), amnestic MCI (aMCI, N = 27), or non-aMCI (N = 10) using the Retrograde Memory News Events Test (RM-NET). We asked if news event memory was sensitive to 1) aMCI and also non-aMCI, which has rarely been examined, 2) genetic risk for dementia (positive family history of any type of dementia, presence of an APOE-4 allele, or polygenic risk for AD), and 3) subjective memory functioning judgments about the past. We found that both MCI subgroups exhibited impaired RM-NET Lifespan accuracy scores together with temporally-limited retrograde amnesia. For the aMCI group amnesia extended back 45 years prior to testing, but not beyond that time frame. The extent of retrograde amnesia could not be reliably estimated in the small non-aMCI group. The effect sizes of having MCI on the RM-NET were medium for the non-aMCI group and large for the aMCI group, whereas the effect sizes of participant characteristics on RM-NET accuracy scores were small. For the combined MCI group (N = 37), news event memory was significantly related to positive family history of dementia but was not related to the more specific genetic markers of AD risk. For the NC group, news event memory was not related to any measure of genetic risk. Objective measures of past memory from the RM-NET were not related to subjective memory judgements about the present or the recent past in either group. By contrast, when individuals subjectively compared their present versus past memory abilities, there was a significant association between this judgment and objective measures of the past from the RM-NET (direct association for the NC group and inverse for the MCI group). The RM-NET holds significant promise for early identification of those with cognitive and genetic risk factors for AD and non-AD dementias.

Indexed as

Cognitive DysfunctionAgedAged, 80 and overAmnesiaApolipoprotein E4DementiaFemaleGenetic Predisposition to DiseaseHumansMaleMemory DisordersMemory, EpisodicMiddle AgedNeuropsychological TestsApolipoprotein E4Anterograde memoryMild cognitive impairmentNews eventsRetrograde memorySemantic memorySubjective memory complaints

Identifiers

PMID38621578
PMCPMC11925352
OpenAlexW4394823771

What OpenQuestion holds

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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.