Evidence map›Paper›PMID 28264768›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2017

Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy.

Rosa Capozzo, Celeste Sassi, Monia B Hammer, Simona Arcuti, Chiara Zecca, Maria R Barulli, Rosanna Tortelli, J Raphael Gibbs, Cynthia Crews, Davide Seripa and 9 more

Open access · greenAbstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  7. Article
  8. Regenerative Stem Cell Therapy for Neurodegenerative Diseases: An Overview.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Review
  11. Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohort.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2020
    Article
  12. Heritability in frontotemporal tauopathies.Alzheimer's & dementia (Amsterdam, Netherlands) · 2019
    Article
  13. Article
  14. Frontotemporal dementia: latest evidence and clinical implications.Therapeutic advances in psychopharmacology · 2018
    Review
  15. Letter.Alzheimer's & dementia (Amsterdam, Netherlands) · 2017
    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

19 authors at 9 institutions in 3 countries.

Rosa CapozzoDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy.
Celeste SassiNeurogenetics Laboratory, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA; Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Monia B HammerDepartment of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Simona ArcutiDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy.
Chiara ZeccaDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy.
Maria R BarulliDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy.
Rosanna TortelliDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy.
J Raphael GibbsNeurogenetics Laboratory, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Cynthia CrewsNeurogenetics Laboratory, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Davide SeripaDepartment of Medical Sciences, Gerontology-Geriatrics Research Laboratory, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy.
Francesco CarnicellaDepartment of Neurology, "Bonomo" Hospital, Andria, Italy.
Claudia Dell'AquilaDepartment of Neurology, "Bonomo" Hospital, Andria, Italy.
Marco RossiDepartment of Neurology, "Miulli" Hospital, Bari, Italy.
Filippo TammaDepartment of Neurology, "Miulli" Hospital, Bari, Italy.
Francesco ValluzziUnit of Neurology, "S. Giacomo" Hospital, Bari, Italy.
Bruno BrancasiDepartment of Basic Medical Science, Neuroscience and Sense Organs, University of Bari, Bari, Italy.
Francesco PanzaDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy; Department of Medical Sciences, Gerontology-Geriatrics Research Laboratory, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy; Neurodegenerative Diseases Unit, Department of Basic Medical Science, Neuroscience and Sense Organs, University of Bari, Bari, Italy.
Andrew B SingletonNeurogenetics Laboratory, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Giancarlo LogroscinoDepartment of Clinical Research in Neurology, University of Bari, "Pia Fondazione Cardinale G. Panico", Lecce, Italy; Neurodegenerative Diseases Unit, Department of Basic Medical Science, Neuroscience and Sense Organs, University of Bari, Bari, Italy. Electronic address: giancarlo.logroscino@uniba.it.
National Institute on Aging · USInnovation Engineering (Italy) · ITUniversity of Bari Aldo Moro · ITFerioli & Gianotti (Italy) · ITOspedale Generale Regionale Francesco Miulli · ITOspedale L. Bonomo · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale San Giacomo Apostolo · ITUniversity College London · GB

Funding

Genome wide SNP analysis in Parkinson's diseaseZIAAG000949 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW · 2009 to 2024
$12.6M
Genetic Analysis Of Non- Alzheimer's disease DementiasZIAAG000951 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW · 2009 to 2020
$5.6M
Genome wide SNP analysis in Parkinson's diseaseZ01AG000949 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW B · 2006 to 2008
$2.6M
Intramural NIH HHS Z01 AG000949
6 · The paper itself

Abstract

introductionWe investigated the clinical differences between familial and sporadic frontotemporal dementia (FTD), screening for mutations in known FTD genes.

methodsWe diagnosed 22 affected individuals belonging to eight families and 43 sporadic cases with FTD in Apulia, Southern Italy, in 2 years. Mutations in common causative FTD genes (GRN, MAPT, VCP, and TARDBP) and C9ORF72 expansions were screened.

resultsBehavioral variant of FTD was the most common clinical subtype (50% and 69% in familial and sporadic cases, respectively). Social conduct impairment/disinhibition, loss of insight, and inflexibility were the most frequent clinical features observed at onset. One new mutation was identified in GRN in family A. DISCUSSION: Disease onset in sporadic FTD was more frequently characterized by a clustering of behavioral symptoms with apathy and loss of personal hygiene. Mutations in common causative FTD genes are not a major cause of familial and sporadic FTD in the Southern Italian population.

Indexed as

AgedAge of OnsetC9orf72 ProteinDNA-Binding ProteinsFamilyFemaleFrontotemporal DementiaGenetic Predisposition to DiseaseHumansIntercellular Signaling Peptides and ProteinsItalyMaleMiddle AgedMutationProgranulinsRegistriesC9orf72 ProteinC9orf72 protein, humanDNA-Binding ProteinsGRN protein, humanIntercellular Signaling Peptides and ProteinsMAPT protein, humanProgranulinsTARDBP protein, humantau ProteinsValosin Containing ProteinVCP protein, humanBehavioral variant of FTDFrontotemporal dementiaPrimary progressive aphasia: familialSemantic dementiaSporadic

Identifiers

PMID28264768
PMCPMC6232845
OpenAlexW2594636964

What OpenQuestion holds

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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.