Amygdalar nuclei and hippocampal subfields on MRI: Test‐retest reliability of automated segmentation in old and young healthy volunteers: Neuroimaging / Normal brain aging. (7th December 2020)
- Record Type:
- Journal Article
- Title:
- Amygdalar nuclei and hippocampal subfields on MRI: Test‐retest reliability of automated segmentation in old and young healthy volunteers: Neuroimaging / Normal brain aging. (7th December 2020)
- Main Title:
- Amygdalar nuclei and hippocampal subfields on MRI: Test‐retest reliability of automated segmentation in old and young healthy volunteers
- Authors:
- Quattrini, Giulia
Pievani, Michela
Jovicich, Jorge
Aiello, Marco
Bargalló, Nuria
Barkhof, Frederik
Bartrés‐Faz, David
Beltramello, Alberto
Pizzini, Francesca B
Blin, Olivier
Bordet, Régis
Caulo, Massimo
Constantinides, Manos
Didic, Mira
Drevelegas, Antonios
Ferretti, Antonio
Fiedler, Ute
Floridi, Piero
Gros‐Dagnac, Helene
Hensch, Tilman
Hoffmann, Karl‐Titus
Kuijer, Joost
Lopes, Renaud
Marra, Camillo
Müller, Bernhard W.
Nobili, Flavio
Parnetti, Lucilla
Payoux, Pierre
Picco, Agnese
Ranjeva, Jean‐Philippe
Roccatagliata, Luca
Rossini, Paolo Maria
Salvatore, Marco
Schonknecht, Peter
Schott, Björn H
Sein, Julien
Soricelli, Andrea
Tarducci, Roberto
Tsolaki, Magda
Visser, Pieter Jelle
Wiltfang, Jens
Richardson, Jill
Frisoni, Giovanni B
Marizzoni, Moira
Consortium, PharmaCog
… (more) - Abstract:
- Abstract: Background: The amygdala and the hippocampus are two limbic structures that play a critical role in cognition and behaviour but their small size hampers their manual segmentation in multicenter datasets. Here, we assessed the reliability of the automated segmentation of amygdalar nuclei and hippocampal subfields across sites and vendors. We applied a new high‐resolution atlas in two independent cohorts of older and younger healthy adults. Method: Sixty‐four older (PharmaCog study; age range: 50‐78 years) and 67 younger subjects (CoRR consortium; age range: 18‐43 years) underwent repeated 3D‐T1 MRI at two different time points between 1 and 90 days. Amygdala and hippocampus segmentation was performed using FreeSurfer v6.0. Reliability of functional parcellations was assessed using volume reproducibility error (ε) and spatial overlapping coefficient (DICE) between test and retest session. Nuclei/subfields were considered as single structures and grouped into relevant subregions (for the amygdala, basolateral and the centromedial complexes; for the hippocampus, head, body, and tail subdivisions). Result: Differences in MRI site/vendor had a significant impact ( p <.05) for the ε of few subfields/nuclei, while extensively impacted DICE of most structures. The effect on DICE was limited by the functional parcellation only in the younger cohort. Reliability was strongly influenced by volume, as ε correlated negatively and DICE correlated positively with volume size ofAbstract: Background: The amygdala and the hippocampus are two limbic structures that play a critical role in cognition and behaviour but their small size hampers their manual segmentation in multicenter datasets. Here, we assessed the reliability of the automated segmentation of amygdalar nuclei and hippocampal subfields across sites and vendors. We applied a new high‐resolution atlas in two independent cohorts of older and younger healthy adults. Method: Sixty‐four older (PharmaCog study; age range: 50‐78 years) and 67 younger subjects (CoRR consortium; age range: 18‐43 years) underwent repeated 3D‐T1 MRI at two different time points between 1 and 90 days. Amygdala and hippocampus segmentation was performed using FreeSurfer v6.0. Reliability of functional parcellations was assessed using volume reproducibility error (ε) and spatial overlapping coefficient (DICE) between test and retest session. Nuclei/subfields were considered as single structures and grouped into relevant subregions (for the amygdala, basolateral and the centromedial complexes; for the hippocampus, head, body, and tail subdivisions). Result: Differences in MRI site/vendor had a significant impact ( p <.05) for the ε of few subfields/nuclei, while extensively impacted DICE of most structures. The effect on DICE was limited by the functional parcellation only in the younger cohort. Reliability was strongly influenced by volume, as ε correlated negatively and DICE correlated positively with volume size of structures (| rs| >.43, p <.001). In line, nuclei larger than 200 mm 3 and subfields larger than 300 mm 3 (except for molecular layer) had the best test‐retest reproducibility (ε<5% and DICE>0.80). Conclusion: Our results support the use of volumetric measures derived automatically from larger amygdalar nuclei and hippocampal subfields as reliable measures in multisite longitudinal MRI studies. These measures could be useful for studies evaluating disease progression and treatment response. … (more)
- Is Part Of:
- Alzheimer's & dementia. Volume 16(2020)Supplement 5
- Journal:
- Alzheimer's & dementia
- Issue:
- Volume 16(2020)Supplement 5
- Issue Display:
- Volume 16, Issue 5 (2020)
- Year:
- 2020
- Volume:
- 16
- Issue:
- 5
- Issue Sort Value:
- 2020-0016-0005-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-12-07
- Subjects:
- Alzheimer's disease -- Periodicals
Alzheimer Disease -- Periodicals
Dementia -- Periodicals
Démence
Maladie d'Alzheimer
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
616.83 - Journal URLs:
- http://www.sciencedirect.com/science/journal/15525260 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1002/alz.040322 ↗
- Languages:
- English
- ISSNs:
- 1552-5260
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 0806.255333
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