Structural brain abnormalities in adolescent patients with anorexia nervosa at both the acute and weight-recovered phase

Author(s):  
Takeshi Asami ◽  
Masao Takaishi ◽  
Ryota Nakamura ◽  
Asuka Yoshimi ◽  
Jun Konishi ◽  
...  
2012 ◽  
Vol 74 (6) ◽  
pp. 574-582 ◽  
Author(s):  
Verena Mainz ◽  
Martin Schulte-Rüther ◽  
Gereon R. Fink ◽  
Beate Herpertz-Dahlmann ◽  
Kerstin Konrad

2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Melissa J Dreier ◽  
Avery L. Van De Water ◽  
Danielle L. Kahn ◽  
Kendra R. Becker ◽  
Kamryn T. Eddy ◽  
...  

Abstract Background Anorexia nervosa (AN) is associated with structural brain abnormalities. Studies have reported less cerebral tissue and more cerebrospinal fluid (CSF) in individuals with AN relative to healthy controls, although findings are variable and inconsistent due to variations in sample size, age, and disease state (e.g., active AN, weight-recovered AN). Further, it remains unclear if structural brain abnormalities observed in AN are a consequence of specific brain pathologies or malnutrition, as very few longitudinal neuroimaging studies in AN have been completed. Methods To overcome this issue, this comprehensive meta-analysis will combine region-of-interest (ROI) and voxel-based morphometry (VBM) approaches to understand how regional and global structural brain abnormalities differ among individuals with AN and healthy controls (HCs). Additionally, we aim to understand how clinical characteristics and physiological changes during the course of illness, including acute illness vs. weight recovery, may moderate these structural abnormalities. We will create an online database of studies that have investigated structural brain abnormalities in AN. Data will be reviewed independently by two members of our team using MEDLINE databases, Web of Science, PsycINFO, EMBASE, and CINAHL. We will conduct ROI and VBM meta-analysis using seed-based d mapping in AN and HCs. We will include all studies that include structural neuroimaging of individuals with AN (both acute and weight-recovered) and HCs between January 1997 and 2020. Discussion This systematic review will assess the effects of AN compared to HC on brain structure. Futhermore, it will explore the role of acute AN and weight-recovered AN on brain structure. Findings will help researchers and clinicians to better understand the course of illness in AN and the nature of recovery, in terms of weight, malnutrition, and the state of the brain. Systematic review registration PROSPERO CRD42020180921


2008 ◽  
Vol 23 ◽  
pp. S119-S120
Author(s):  
R. Herold ◽  
A. Feldmann ◽  
T. Tenyi ◽  
F. Kover ◽  
S. Fekete

The Lancet ◽  
1998 ◽  
Vol 352 (9130) ◽  
pp. 784-785 ◽  
Author(s):  
AL Madsen ◽  
N Keiding ◽  
A Karle ◽  
S Esbjerg ◽  
R Hemmingsen ◽  
...  

2021 ◽  
pp. 106771
Author(s):  
Solange Denervaud ◽  
Christian Korff ◽  
Joël Fluss ◽  
Judith Kalser ◽  
Eliane Roulet-Perez ◽  
...  

Cell Reports ◽  
2012 ◽  
Vol 2 (6) ◽  
pp. 1554-1562 ◽  
Author(s):  
Martin Breuss ◽  
Julian Ik-Tsen Heng ◽  
Karine Poirier ◽  
Guoling Tian ◽  
Xavier Hubert Jaglin ◽  
...  

2014 ◽  
Vol 20 (9) ◽  
pp. 1189-1197 ◽  
Author(s):  
Felipe von Glehn ◽  
Sven Jarius ◽  
Rodrigo Pessoa Cavalcanti Lira ◽  
Maria Carolina Alves Ferreira ◽  
Fadua H Ribeiro von Glehn ◽  
...  

Background: Although aquaporin-4 (AQP4) is widely expressed in the human brain cortex, lesions are rare in neuromyelitis optica (NMO) spectrum disorders (NMOSD). Recently, however, several studies have demonstrated occult structural brain atrophy in NMO. Objective: This study aims to investigate magnetic resonance imaging (MRI) patterns of gray matter (GM) and white matter (WM) abnormalities in patients with NMOSD and to assess the visual pathway integrity during disease duration correlation of the retinal nerve fiber layer (RNFL) and pericalcarine cortex thickness. Methods: Twenty-one patients with NMOSD and 34 matched healthy controls underwent both high-field MRI (3T) high-resolution T1-weighted and diffusion-tensor MRI. Voxel-based morphometry, cortical analyses (Freesurfer) and diffusion-tensor imaging (DTI) analyses (TBSS-FSL) were used to investigate brain abnormalities. In addition, RNFL measurement by optic-coherence tomography (OCT) was performed. Results: We demonstrate that NMOSD is associated with GM and WM atrophy, encompassing more frequently the motor, sensory and visual pathways, and that the extent of GM atrophy correlates with disease duration. Furthermore, we demonstrate for the first time a correlation between RNFL and pericalcarine cortical thickness, with cortical atrophy evolving over the course of disease. Conclusions: Our findings indicate a role for retrograde and anterograde neurodegeneration in GM atrophy in NMOSD. However, the presence atrophy encompassing almost all lobes suggests that additional pathomechanisms might also be involved.


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