Evidence map›Paper›PMID 26401709›Full record

ArticleJournal of Alzheimer's disease : JAD2015

Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?

Paola Caroppo, Marie-Odile Habert, Stanley Durrleman, Aurélie Funkiewiez, Vincent Perlbarg, Valérie Hahn, Hugo Bertin, Malo Gaubert, Alexandre Routier, Didier Hannequin and 16 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04014673 (Natural History Characterization in Symptomatic and Asymptomatic Progranuline Gene Mutation Carriers), which is not on this map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 14% 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.

NCT04014673 nacompletednot on this map

Natural History Characterization in Symptomatic and Asymptomatic Progranuline Gene Mutation Carriers

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2010 to 2022Enrolled78ConditionsFrontotemporal Lobar DegenerationArmsBehavioral : Characterization
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Composite grey matter fingerprints for genetic frontotemporal dementia.Journal of neurology, neurosurgery, and psychiatry · 2026
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  9. Plasma NfL levels and longitudinal change rates inJournal of neurology, neurosurgery, and psychiatry · 2021
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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

26 authors at 3 institutions in 2 countries.

Paola CaroppoSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Marie-Odile HabertSorbonne Universités, UPMC Univ Paris 06, UMR 7371, UMR_S 1146, Laboratoire d'Imagerie Biomédicale, Paris, France.
Stanley DurrlemanSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Aurélie FunkiewiezInserm, U1127, ICM, Paris, France.
Vincent PerlbargSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Valérie HahnAP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Centre de Référence des Démences Rares, Paris, France.
Hugo BertinSorbonne Universités, UPMC Univ Paris 06, UMR 7371, UMR_S 1146, Laboratoire d'Imagerie Biomédicale, Paris, France.
Malo GaubertSorbonne Universités, UPMC Univ Paris 06, UMR 7371, UMR_S 1146, Laboratoire d'Imagerie Biomédicale, Paris, France.
Alexandre RoutierSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Didier HannequinService de Neurologie et CMRR, Inserm U1079, Centre Hospitalier Universitaire, Rouen, France.
Vincent DeramecourtInserm U1171, Université de Lille, Lille, France.
Florence PasquierInserm U1171, Université de Lille, Lille, France.
Sophie Rivaud-PechouxSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Martine VercellettoService de Neurologie, CHU Guillaume et René Laënnec, Nantes, France.
Geoffrey EdouartSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Romain ValabregueSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Pascal LejeuneService de neurologie, CHD La Roche sur Yon, France.
Mira DidicService de Neurologie et Neuropsychologie, APHM, CHU Timone et Aix Marseille Université, Inserm, INS UMR_S 1106, 13005 Marseille, France.
Jean-Christophe CorvolSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Habib BenaliSorbonne Universités, UPMC Univ Paris 06, UMR 7371, UMR_S 1146, Laboratoire d'Imagerie Biomédicale, Paris, France.
Stephane LehericySorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Bruno DuboisSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Olivier ColliotSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Alexis BriceSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Isabelle Le BerSorbonne Universités, UPMC Université Paris 06, UMR S 1127, ICM, Paris, France.
Predict-PGRN study group
Centre National de la Recherche Scientifique · FRInserm · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The preclinical stage of frontotemporal lobar degeneration (FTLD) is not well characterized. We conducted a brain metabolism (FDG-PET) and structural (cortical thickness) study to detect early changes in asymptomatic GRN mutation carriers (aGRN+) that were evaluated longitudinally over a 20-month period. At baseline, a left lateral temporal lobe hypometabolism was present in aGRN+ without any structural changes. Importantly, this is the first longitudinal study and, across time, the metabolism more rapidly decreased in aGRN+ in lateral temporal and frontal regions. The main structural change observed in the longitudinal study was a reduction of cortical thickness in the left lateral temporal lobe in carriers. A limit of this study is the relatively small sample (n = 16); nevertheless, it provides important results. First, it evidences that the pathological processes develop a long time before clinical onset, and that early neuroimaging changes might be detected approximately 20 years before the clinical onset of disease. Second, it suggests that metabolic changes are detectable before structural modifications and cognitive deficits. Third, both the baseline and longitudinal studies provide converging results implicating lateral temporal lobe as early involved in GRN disease. Finally, our study demonstrates that structural and metabolic changes could represent possible biomarkers to monitor the progression of disease in the presymptomatic stage toward clinical onset.

Indexed as

MutationAdultAsymptomatic DiseasesDisease ProgressionFemaleFluorodeoxyglucose F18Frontal LobeFrontotemporal Lobar DegenerationHumansIntercellular Signaling Peptides and ProteinsLongitudinal StudiesMagnetic Resonance ImagingMaleOrgan SizePositron-Emission TomographyProgranulinsFluorodeoxyglucose F18GRN protein, humanIntercellular Signaling Peptides and ProteinsProgranulinsRadiopharmaceuticalsCortical thicknessdementiafrontotemporal dementiafrontotemporal lobar degenerationGRNlongitudinalPETpreclinical studypresymptomaticprogranulin

Identifiers

PMID26401709
PMCPMC4923734
OpenAlexW2262171011

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.