Evidence map›Paper›PMID 23552688›Full record

ArticleJAMA neurology2013

Neuropathologic basis of age-associated brain atrophy.

Deniz Erten-Lyons, Hiroko H Dodge, Randall Woltjer, Lisa C Silbert, Diane B Howieson, Patricia Kramer, Jeffrey A Kaye

Abstract read
In one paragraph

Article in JAMA neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

  1. Trial
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  18. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  19. Article
  20. Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease.Journal of neuropathology and experimental neurology · 2022
    Article

9 more citing papers are in PubMed but not listed here.

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

7 authors.

Deniz Erten-LyonsDepartment of Neurology, Oregon Health and Science University, Portland, OR 97239, USA. ertenlyo@ohsu.edu
Hiroko H Dodge
Randall Woltjer
Lisa C Silbert
Diane B Howieson
Patricia Kramer
Jeffrey A Kaye

Funding

Outreach, Recruitment and Education CoreP30AG008017 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI KAYE, JEFFREY A · 1990 to 2019
$27.7M
NIA NIH HHS AG08017NIA NIH HHS P30 AG008017
6 · The paper itself

Abstract

importanceWhile brain volume changes are used as surrogate markers for Alzheimer disease neuropathology in clinical studies, the extent to which these changes are due to pathologic features of Alzheimer disease in the aging brain is not well established. This study aims to clarify the neuropathologic correlates of longitudinal brain atrophy.

objectiveTo examine the association between brain atrophy during life and neuropathology in an elderly population.

designAutopsy study of a cohort of elderly individuals.

settingCommunity-based population.

participantsSeventy-one healthy elderly individuals were selected from participants of the Oregon Brain Aging Study for having an autopsy, more than 1 magnetic resonance imaging scan, and the last magnetic resonance imaging scan within 36 months of death. MAIN OUTCOMES AND MEASURES: The associations between brain volume trajectories (ventricular, total brain, and hippocampal) and time interaction terms for neurofibrillary tangles, neuritic plaques, gross infarcts, microinfarcts, amyloid angiopathy, Lewy bodies, APOE ε4 presence, and clinical diagnosis (no cognitive impairment, mild cognitive impairment, or dementia as time-varying covariates) were examined in mixed-effects models, adjusting for duration of follow-up and age at death.

resultsVentricular volume trajectory was significantly associated with age, presence of infarcts, neurofibrillary tangle and neuritic plaque scores, APOE ε4 allele presence, and dementia diagnosis. Total brain volume trajectory was significantly associated with age and mild cognitive impairment diagnosis. Hippocampal volume trajectory was significantly associated with amyloid angiopathy. CONCLUSIONS AND RELEVANCE: Ventricular volume trajectory is more sensitive than total brain and hippocampal volume trajectories as a marker of accruing Alzheimer disease and vascular pathology in elderly individuals. The association between brain volume trajectories and cognitive impairment (mild cognitive impairment and dementia) remained after controlling for the degree of neuropathology and other covariates. This suggests that there may be other factors not measured in this study that could be contributing to brain atrophy in those with cognitive impairment.

Indexed as

AgedAged, 80 and overAgingAtrophyBrainCerebral VentriclesCognitive DysfunctionDementiaFemaleHumansLewy BodiesMagnetic Resonance ImagingMaleNeurofibrillary TanglesPlaque, Amyloid

Identifiers

PMID23552688
PMCPMC3898525

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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.