Evidence map›Paper›PMID 31491836›Full record

ArticleNeuroImage. Clinical2019

Hippocampal atrophy has limited usefulness as a diagnostic biomarker on the early onset Alzheimer's disease patients: A comparison between visual and quantitative assessment.

Neus Falgàs, Raquel Sánchez-Valle, Núria Bargalló, Mircea Balasa, Guadalupe Fernández-Villullas, Beatriz Bosch, Jaume Olives, Adrià Tort-Merino, Anna Antonell, Cristina Muñoz-García and 7 more

Registry-linked trialOpen access · goldAbstract readComparative 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. It is linked to trial NCT06304909 (Effect of Intravenous Dexmedetomidine Versus Dexamethasone for Management of Repound Pain After Supraclavicular Brachial Plexus Block), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.6field-weighted citation impact, top 5% 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.

NCT06304909 phase1completednot on this mapstarted 2024, after this paper: background citation

Effect of Intravenous Dexmedetomidine Versus Dexamethasone for Management of Repound Pain After Supraclavicular Brachial Plexus Block

TypeinterventionalSponsorAssiut UniversityRan2024 to 2025Enrolled111ConditionsTrauma InjuryArmsDexmedetomidine injection, Dexamethasone, Saline
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  3. Review
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  10. The Association Between Brain Metabolic Biomarkers UsingJournal of Alzheimer's disease reports · 2024
    Article
  11. Article
  12. The Role of Clinical Assessment in the Era of Biomarkers.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  13. Review
  14. Article
  15. Article
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  17. Review
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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

17 authors at 3 institutions in 4 countries.

Neus FalgàsAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Raquel Sánchez-ValleAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Núria BargallóImaging Diagnostic Center, Hospital Clínic, Barcelona, Spain; Magnetic Resonance Image Core Facility, IDIBAPS, Spain.
Mircea BalasaAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain; Atlantic Fellow for Equity in Brain Health, Global Brain Health Institute, Trinity College Dublin, Ireland.
Guadalupe Fernández-VillullasAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Beatriz BoschAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Jaume OlivesAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Adrià Tort-MerinoAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Anna AntonellAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Cristina Muñoz-GarcíaAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
María LeónAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Oriol GrauAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Magdalena CastellvíAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Nina Coll-PadrósAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Lorena RamiAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain.
Alberto RedolfiLaboratory of Alzheimer's Neuroimaging and Epidemiology - LANE, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.
Albert LladóAlzheimer's disease and other cognitive disorders Unit, Neurology department, IDIBAPS, Hospital Clínic, Barcelona, Spain. Electronic address: allado@clinic.cat.
Hospital Clínic de Barcelona · ESCentro San Giovanni di Dio Fatebenefratelli · ITTrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NIA-AA diagnostic criteria include volumetric or visual rating measures of hippocampal atrophy (HA) as a diagnostic biomarker of Alzheimer's disease (AD). We aimed to determine its utility as a diagnostic biomarker for early onset Alzheimer's disease (EOAD) by assessing Medial Temporal Atrophy (MTA) and hippocampal volume (HV) determination. MTA score and HV quantified by FreeSurfer were assessed in 140 (aged ≤65) subjects with biomarker supported diagnosis: 38 amnesic (A-EOAD), 20 non-amnesic (NA-EOAD), 30 late onset AD (LOAD), 20 fronto-temporal dementia (FTD) and 32 healthy controls (HC). The results showed that the proportion of MTA ≥ 1.5 was higher on LOAD and FTD than EOAD and HC but none of the MTA thresholds (≥1, ≥1.5 and ≥ 2) showed acceptable diagnostic accuracy. LOAD had lower HV than the other groups. A-EOAD HV was lower than NA-EOAD and HC but equal to FTD. The 6258 mm3 cut-off showed good diagnostic accuracy between A-EOAD and HC. Both tools showed a moderate inverse correlation. In conclusion, MTA has a limited diagnostic utility as an EOAD biomarker as it does not discriminate AD from FTD or HC in initial symptomatic stages. HV may discriminate A-EOAD from HC but not from FTD.

Indexed as

AgedAge of OnsetAlzheimer DiseaseAmnesiaAtrophyBiomarkersFemaleFrontotemporal DementiaHippocampusHumansMagnetic Resonance ImagingMaleMiddle AgedNeuroimagingBiomarkersAlzheimer's diseaseAtrophyFrontotemporal dementiaMagnetic resonance imaging

Identifiers

PMID31491836
PMCPMC6627030
OpenAlexW2955233086

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.