Evidence map›Paper›PMID 36490272›Full record

ArticleInternational journal of geriatric psychiatry2023

Are neuropsychiatric symptoms a marker of small vessel disease progression in older adults? Evidence from the Lothian Birth Cohort 1936.

Una Clancy, Ratko Radakovic, Fergus Doubal, Maria Del C Valdés Hernández, Susana Muñoz Maniega, Adele M Taylor, Janie Corley, Francesca M Chappell, Tom C Russ, Simon R Cox and 3 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of geriatric psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
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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

13 authors at 3 institutions in 1 country.

Una ClancyCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0002-8062-7537
Ratko RadakovicDepartment of Clinical Psychology and Psychological Therapies, University of East Anglia, Norwich, UK.
Fergus DoubalCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Maria Del C Valdés HernándezCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Susana Muñoz ManiegaCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Adele M TaylorLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Janie CorleyLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Francesca M ChappellCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Tom C RussLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Simon R CoxLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Mark E BastinCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Ian J DearyLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Joanna M WardlawCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
NHS Lothian · GBUK Dementia Research Institute · GBUniversity of East Anglia · GB

Funding

Evaluating Longitudinal Changes in the Human Structural Connectome in Relation to Cognitive AgingR01AG054628 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI TUCKER-DROB, ELLIOT MAX · 2017 to 2021
$2.7M
Biotechnology and Biological Sciences Research CouncilBritish Heart Foundation RE/18/5/34216Chief Scientist Office CAF/18/08Medical Research Council G0700704Medical Research Council G0701120Medical Research Council G1001245Medical Research Council MR/K026992/1Medical Research Council MR/M013111/1Medical Research Council MR/R024065/1NIA NIH HHS R01 AG054628
6 · The paper itself

Abstract

backgroundNeuropsychiatric symptoms could form part of an early cerebral small vessel disease prodrome that is detectable before stroke or dementia onset. We aimed to identify whether apathy, depression, anxiety, and subjective memory complaints associate with longitudinal white matter hyperintensity (WMH) progression.

methodsCommunity-dwelling older adults from the observational Lothian Birth Cohort 1936 attended three visits at mean ages 73, 76, and 79 years, repeating MRI, Mini-Mental State Examination, neuropsychiatric (Dimensional Apathy Scale, Hospital Anxiety and Depression Scale), and subjective memory symptoms. We ran regression and mixed-effects models for symptoms and normalised WMH volumes (cube root of WMH:ICV × 10).

resultsAt age 73, 76, and 79, m = 672, n = 476, and n = 382 participants attended MRI respectively. Worse apathy at age 79 was associated with WMH volume increase (β = 0.27, p = 0.04) in the preceding 6 years. A 1SD increase in apathy score at age 79 associated with a 0.17 increase in WMH (β = 0.17 normalised WMH percent ICV, p = 0.009). In apathy subscales, executive (β = 0.13, p = 0.05) and emotional (β = 0.13, p = 0.04) scores associated with increasing WMH more than initiation scores (β = 0.11, p = 0.08). Increasing WMH also associated with age (β = 0.40, p = 0.002) but not higher depression (β = -0.01, p = 0.78), anxiety (β = 0.05, p = 0.13) scores, or subjective memory complaints (β = 1.12, p = 0.75).

conclusionsApathy independently associates with preceding longitudinal WMH progression, while depression, anxiety, and subjective memory complaints do not. Patients with apathy should be considered for enrolment to small vessel disease trials.

Indexed as

Cerebral Small Vessel DiseasesWhite MatterAgedBirth CohortDisease ProgressionHumansMagnetic Resonance Imagingageingapathycerebral small vessel diseasecognitionlongitudinal studieswhite matter hyperintensities

Identifiers

PMID36490272
PMCPMC10108049
OpenAlexW4310191218

What OpenQuestion holds

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LicenceCC BY
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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.