Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers

Simon F Eskildsen; Lasse R Østergaard; Anders B Rodell; Leif Østergaard; Jørgen E Nielsen; Adrian M Isaacs; Peter Johannsen

doi:10.1016/j.neuroimage.2008.12.024

Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers

Simon F Eskildsen, Lasse R Østergaard, Anders B Rodell, Leif Østergaard, Jørgen E Nielsen, Adrian M Isaacs, Peter Johannsen

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

24 Citationer (Scopus)

Abstract

Udgivelsesdato: 2009-Apr-15

Originalsprog	Engelsk
Tidsskrift	NeuroImage
Vol/bind	45
Udgave nummer	3
Sider (fra-til)	713-21
Antal sider	8
ISSN	1053-8119
DOI	https://doi.org/10.1016/j.neuroimage.2008.12.024
Status	Udgivet - 2008

Bibliografisk note

Keywords: Aged; Atrophy; Cerebral Cortex; Dementia; Endosomal Sorting Complexes Required for Transport; Family; Female; Humans; Image Interpretation, Computer-Assisted; Magnetic Resonance Imaging; Male; Middle Aged; Nerve Tissue Proteins

Adgang til dokumentet

10.1016/j.neuroimage.2008.12.024

Citationsformater

@article{47d7944068a411df928f000ea68e967b,

title = "Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers",

abstract = "Frontotemporal dementia constitutes the third most prevalent neurodegenerative disease with dementia. We compared cortical structural changes in nine presymptomatic CHMP2B frontotemporal dementia mutation positive individuals with seven mutation negative family members. Using serial MRI scans with a mean interval of 16 months and surface based cortical segmentation we measured cortical thickness and volume, and quantified atrophy rates. Cortical thickness and atrophy rates were averaged within major lobes and focal effects were determined by parametric statistical maps. The volumetric atrophy rates in the presymptomatic CHMP2B mutation carriers were statistically significant, though of a lower magnitude than those previously reported in patients of other types of frontotemporal dementia. Cortical thickness measurements revealed cortical thinning in mutation carriers bilaterally in the frontal and occipital lobes, and in the left temporal lobe. Results indicated that cortical thickness has a higher sensitivity for detecting small changes than whole-brain volumetric measures. Comparing mutation carriers with non-carriers revealed increased atrophy rates in mutation carriers bilaterally in the inferio-temporal cortex, the superior frontal cortex, and the insular cortex. These findings indicated impairment of regions involved in both behaviour and language. The symptoms previously reported in clinical CHMP2B frontotemporal dementia patients are associated with the anatomically affected regions here found in the presymptomatic mutation carriers.",

author = "Eskildsen, {Simon F} and {\O}stergaard, {Lasse R} and Rodell, {Anders B} and Leif {\O}stergaard and Nielsen, {J{\o}rgen E} and Isaacs, {Adrian M} and Peter Johannsen",

note = "Keywords: Aged; Atrophy; Cerebral Cortex; Dementia; Endosomal Sorting Complexes Required for Transport; Family; Female; Humans; Image Interpretation, Computer-Assisted; Magnetic Resonance Imaging; Male; Middle Aged; Nerve Tissue Proteins",

year = "2008",

doi = "10.1016/j.neuroimage.2008.12.024",

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T1 - Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers

AU - Eskildsen, Simon F

AU - Østergaard, Lasse R

AU - Rodell, Anders B

AU - Østergaard, Leif

AU - Nielsen, Jørgen E

AU - Isaacs, Adrian M

AU - Johannsen, Peter

N1 - Keywords: Aged; Atrophy; Cerebral Cortex; Dementia; Endosomal Sorting Complexes Required for Transport; Family; Female; Humans; Image Interpretation, Computer-Assisted; Magnetic Resonance Imaging; Male; Middle Aged; Nerve Tissue Proteins

PY - 2008

Y1 - 2008

N2 - Frontotemporal dementia constitutes the third most prevalent neurodegenerative disease with dementia. We compared cortical structural changes in nine presymptomatic CHMP2B frontotemporal dementia mutation positive individuals with seven mutation negative family members. Using serial MRI scans with a mean interval of 16 months and surface based cortical segmentation we measured cortical thickness and volume, and quantified atrophy rates. Cortical thickness and atrophy rates were averaged within major lobes and focal effects were determined by parametric statistical maps. The volumetric atrophy rates in the presymptomatic CHMP2B mutation carriers were statistically significant, though of a lower magnitude than those previously reported in patients of other types of frontotemporal dementia. Cortical thickness measurements revealed cortical thinning in mutation carriers bilaterally in the frontal and occipital lobes, and in the left temporal lobe. Results indicated that cortical thickness has a higher sensitivity for detecting small changes than whole-brain volumetric measures. Comparing mutation carriers with non-carriers revealed increased atrophy rates in mutation carriers bilaterally in the inferio-temporal cortex, the superior frontal cortex, and the insular cortex. These findings indicated impairment of regions involved in both behaviour and language. The symptoms previously reported in clinical CHMP2B frontotemporal dementia patients are associated with the anatomically affected regions here found in the presymptomatic mutation carriers.

AB - Frontotemporal dementia constitutes the third most prevalent neurodegenerative disease with dementia. We compared cortical structural changes in nine presymptomatic CHMP2B frontotemporal dementia mutation positive individuals with seven mutation negative family members. Using serial MRI scans with a mean interval of 16 months and surface based cortical segmentation we measured cortical thickness and volume, and quantified atrophy rates. Cortical thickness and atrophy rates were averaged within major lobes and focal effects were determined by parametric statistical maps. The volumetric atrophy rates in the presymptomatic CHMP2B mutation carriers were statistically significant, though of a lower magnitude than those previously reported in patients of other types of frontotemporal dementia. Cortical thickness measurements revealed cortical thinning in mutation carriers bilaterally in the frontal and occipital lobes, and in the left temporal lobe. Results indicated that cortical thickness has a higher sensitivity for detecting small changes than whole-brain volumetric measures. Comparing mutation carriers with non-carriers revealed increased atrophy rates in mutation carriers bilaterally in the inferio-temporal cortex, the superior frontal cortex, and the insular cortex. These findings indicated impairment of regions involved in both behaviour and language. The symptoms previously reported in clinical CHMP2B frontotemporal dementia patients are associated with the anatomically affected regions here found in the presymptomatic mutation carriers.

U2 - 10.1016/j.neuroimage.2008.12.024

DO - 10.1016/j.neuroimage.2008.12.024

M3 - Journal article

C2 - 19150504

VL - 45

SP - 713

EP - 721

JO - NeuroImage

JF - NeuroImage

SN - 1053-8119

IS - 3

ER -