Evidence map›Paper›PMID 28856766›Full record

SynthesisHuman brain mapping2017

Gray matter asymmetries in aging and neurodegeneration: A review and meta-analysis.

Lora Minkova, Annegret Habich, Jessica Peter, Christoph P Kaller, Simon B Eickhoff, Stefan Klöppel

Open access · greenAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Human brain mapping, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed, 7 pooled it
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

111 citing papers in PubMed, 7 syntheses or guidelines pooled it, 194 citations in OpenAlex.

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  11. Hippocampal Total, Subregion, and Subfield Volume Alterations in Late-Life Depression.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2026
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  15. Altered topological properties in PD patients with probable REM sleep behavior disorder through fuctional MRI.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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  18. Review
  19. Lifespan Trajectories of Asymmetry in White Matter Tracts.bioRxiv : the preprint server for biology · 2025
    Article
  20. Article

51 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

6 authors at 3 institutions in 2 countries.

Lora MinkovaDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0003-0945-0553
Annegret HabichDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Jessica PeterDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-0817-8431
Christoph P KallerFreiburg Brain Imaging Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Simon B EickhoffInstitute of Systems Neuroscience, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.
Stefan KlöppelDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
University of Bern · CHUniversity of Freiburg · DEHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inter-hemispheric asymmetries are a common phenomenon of the human brain. Some evidence suggests that neurodegeneration related to aging and disease may preferentially affect the left-usually language- and motor-dominant-hemisphere. Here, we used activation likelihood estimation meta-analysis to assess gray matter (GM) loss and its lateralization in healthy aging and in neurodegeneration, namely, mild cognitive impairment (MCI), Alzheimer's dementia (AD), Parkinson's disease (PD), and Huntington's disease (HD). This meta-analysis, comprising 159 voxel-based morphometry publications (enrolling 4,469 patients and 4,307 controls), revealed that GM decline appeared to be asymmetric at trend levels but provided no evidence for increased left-hemisphere vulnerability. Regions with asymmetric GM decline were located in areas primarily affected by neurodegeneration. In HD, the left putamen showed converging evidence for more pronounced atrophy, while no consistent pattern was found in PD. In MCI, the right hippocampus was more atrophic than its left counterpart, a pattern that reversed in AD. The stability of these findings was confirmed using permutation tests. However, due to the lenient threshold used in the asymmetry analysis, further work is needed to confirm our results and to provide a better understanding of the functional role of GM asymmetries, for instance in the context of cognitive reserve and compensation. Hum Brain Mapp 38:5890-5904, 2017. © 2017 Wiley Periodicals, Inc.

Indexed as

AgingBrainFunctional LateralityGray MatterHumansNeurodegenerative DiseasesagingALEdementiaHuntington's diseaseParkinson's diseaseVBM

Identifiers

PMID28856766
PMCPMC6866813
OpenAlexW2751898811

What OpenQuestion holds

Textmetadata
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.