Evidence map›Paper›PMID 30927600›Full record

ArticleNeuroImage. Clinical2019

Relevance of brain lesion location for cognition in vascular mild cognitive impairment.

Antonio Giorgio, Ilaria Di Donato, Alessandro De Leucio, Jian Zhang, Emilia Salvadori, Anna Poggesi, Stefano Diciotti, Mirco Cosottini, Stefano Ciulli, Domenico Inzitari and 6 more

Abstract readMulticenter Study
In one paragraph

Article in NeuroImage. Clinical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Late-life depression accentuates cognitive weaknesses in older adults with small vessel disease.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  5. Article
  6. Mechanisms of cognitive dysfunction in CKD.Nature reviews. Nephrology · 2020
    Review
  7. 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

16 authors.

Antonio GiorgioDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy. Electronic address: giorgio3@unisi.it.
Ilaria Di DonatoDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.
Alessandro De LeucioDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.
Jian ZhangDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.
Emilia SalvadoriNEUROFARBA Department, Neuroscience Section, University of Florence, Florence, Italy. Electronic address: emilia.salvadori@unifi.it.
Anna PoggesiNEUROFARBA Department, Neuroscience Section, University of Florence, Florence, Italy. Electronic address: anna.poggesi@unifi.it.
Stefano DiciottiDepartment of Electrical, Electronic, and Information Engineering "Guglielmo Marconi", University of Bologna, Cesena, Italy. Electronic address: stefano.diciotti@unibo.it.
Mirco CosottiniDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Stefano CiulliDepartment of Clinical and Experimental Biomedical Sciences -"Mario Serio", University of Florence, Florence, Italy.
Domenico InzitariNEUROFARBA Department, Neuroscience Section, University of Florence, Florence, Italy. Electronic address: domenico.inzitari@unifi.it.
Leonardo Pantoni"L. Sacco" Department of Biomedical and Clinical Sciences, University of Milano, Italy. Electronic address: leonardo.pantoni@unimi.it.
Mario MascalchiDepartment of Clinical and Experimental Biomedical Sciences -"Mario Serio", University of Florence, Florence, Italy. Electronic address: mario.mascalchi@unifi.it.
Antonio FedericoDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy. Electronic address: federico@unisi.it.
Maria Teresa DottiDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy. Electronic address: dotti@unisi.it.
Nicola De StefanoDepartment of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy. Electronic address: destefano@unisi.it.
VMCI-Tuscany Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVascular mild cognitive impairment (VMCI) is a potentially transitional state between normal aging and vascular dementia. The presence of macroscopic white matter lesions (WML) of moderate or severe extension on brain MRI is the hallmark of the VMCI.

objectiveTo assess the clinical relevance of the frequency of WML in patients with VMCI independently of total lesion volume (LV).

methodsIn this multicenter study, we included 110 patients with VMCI (age: 74.3 ± 6.6 years; sex: 60 women). Cognitive assessment was performed with the VMCI-Tuscany Neuropsychological Battery, which allowed to identify four VMCI groups: amnestic single (n = 9) and multi-domain (n = 76), non-amnestic single- (n = 10) and multi-domain (n = 15). Distribution and frequency of WML on MRI FLAIR images were evaluated with lesion probability map (LPM). Voxelwise statistics was performed with nonparametric permutation tests, controlling for age, sex, slice thickness, center, magnetic field strength, total LV and head size (p < .01, family-wise error-corrected for multiple comparisons across space).

resultsLPM of the WML had a fairly symmetric and widespread distribution across brain. A higher frequency of WML along association tracts of the WM such as inferior longitudinal fascicle, inferior fronto-occipital fascicle and superior longitudinal fascicle, was correlated with worst cognitive scores at the Trail Making Test Part A and Copy of the Rey-Osterrieth Complex Figure. The non-amnestic groups showed a higher frequency of WML in the anterior cingulum and superior longitudinal fascicle close to the frontal gyrus.

conclusionsOur study showed that in patients with VMCI, independently of total LV, the higher frequency of lesions along association tracts of the WM, which mediate intrahemispheric long-range connectivity, is related with psychomotor speed and constructional praxis. Moreover, a prevalence of lesions in the frontal WM seems to characterize VMCI patients with involvement of non-amnestic domains.

Indexed as

AgedAged, 80 and overCerebral Small Vessel DiseasesCognitive DysfunctionFemaleHumansMagnetic Resonance ImagingMaleNeuroimagingWhite MatterDementiaLesion probability mapLesionsMild cognitive impairmentSmall vessel diseaseWhite matter

Identifiers

PMID30927600
PMCPMC6439281

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Registered trials

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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.