Evidence map›Paper›PMID 35888023›Full record

ArticleLife (Basel, Switzerland)2022

Logogenic Primary Progressive Aphasia or Alzheimer Disease: Contribution of Acoustic Markers in Early Differential Diagnosis.

Eloïse Da Cunha, Alexandra Plonka, Seçkin Arslan, Aurélie Mouton, Tess Meyer, Philippe Robert, Fanny Meunier, Valeria Manera, Auriane Gros

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 1 country.

Eloïse Da CunhaSpeech Therapy Department of Nice, Faculty of medicine, Université Côte d'Azur, 06000 Nice, France.
Alexandra PlonkaSpeech Therapy Department of Nice, Faculty of medicine, Université Côte d'Azur, 06000 Nice, France.
Seçkin ArslanBCL, CNRS UMR7320, Campus Saint Jean d'Angely-SJA3/MSHS-SE, Université Côte d'Azur, 06300 Nice, France.
Aurélie MoutonSpeech Therapy Department of Nice, Faculty of medicine, Université Côte d'Azur, 06000 Nice, France.
Tess MeyerSpeech Therapy Department of Nice, Faculty of medicine, Université Côte d'Azur, 06000 Nice, France.
Philippe RobertSpeech Therapy Department of Nice, Faculty of medicine, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0002-0963-1728
Fanny MeunierBCL, CNRS UMR7320, Campus Saint Jean d'Angely-SJA3/MSHS-SE, Université Côte d'Azur, 06300 Nice, France.
Valeria ManeraLaboratoire CoBTeK (Cognition Behaviour Technology), Université Côte d'Azur, 06000 Nice, France.
Auriane GrosSpeech Therapy Department of Nice, Faculty of medicine, Université Côte d'Azur, 06000 Nice, France.
Université Côte d'Azur · FRCentre National de la Recherche Scientifique · FRCognition Behaviour Technology · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The logopenic variant of Primary Progressive Aphasia (lvPPA), a syndromic disorder centered on language impairment, often presents variable underlying neurodegenerative pathologies such as Alzheimer Disease (AD). Actual language assessment tests and lumbar puncture, focused on AD diagnosis, cannot precisely distinguish the symptoms, or predict their progression at onset time. We analyzed acoustic markers, aiming to discriminate lvPPA and AD as well as the influence of AD biomarkers on acoustic profiles at the beginning of the disease. We recruited people with AD (n = 8) and with lvPPA (n = 8), with cerebrospinal fluid biomarker profiles determined by lumbar puncture. The participants performed a sentence repetition task that allows assessing potential lvPPA phonological loop deficits. We found that temporal and prosodic markers significantly differentiate the lvPPA and AD group at an early stage of the disease. Biomarker and acoustic profile comparisons discriminated the two lvPPA subgroups according to their biomarkers. For lvPPA with AD biomarkers, acoustic profile equivalent to an atypical AD form with a specific alteration of the phonological loop is shown. However, lvPPA without AD biomarkers has an acoustic profile approximating the one for DLFT. Therefore, these results allow us to classify lvPPA differentially from AD based on acoustic markers from a sentence repetition task. Furthermore, our results suggest that acoustic analysis would constitute a clinically efficient alternative to refused lumbar punctures. It offers the possibility to facilitate early, specific, and accessible neurodegenerative diagnosis and may ease early care with speech therapy, preventing the progression of symptoms.

Indexed as

acoustic markersAlzheimer’s diseasediagnosisearly markerslogopenic variantprimary progressive aphasiaprosody

Identifiers

PMID35888023
PMCPMC9316974
OpenAlexW4283387170

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.