» Articles » PMID: 30994310

Altered Thalamo–cortical and Occipital–parietal– Temporal–frontal White Matter Connections in Patients with Anorexia and Bulimia Nervosa: a Systematic Review of Diffusion Tensor Imaging Studies

Overview
Specialty Psychiatry
Date 2019 Apr 18
PMID 30994310
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Anorexia nervosa and bulimia nervosa are complex mental disorders, and their etiology is still not fully understood. This paper reviews the literature on diffusion tensor imaging studies in patients with anorexia nervosa and bulimia nervosa to explore the usefulness of white matter microstructural analysis in understanding the pathophysiology of eating disorders.

Methods: We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines to identify diffusion tensor imaging studies that compared patients with an eating disorder to control groups. We searched relevant databases for studies published from database inception to August 2018, using combinations of select keywords. We categorized white matter tracts according to their 3 main classes: projection (i.e., thalamo–cortical), association (i.e., occipital–parietal–temporal–frontal) and commissural (e.g., corpus callosum).

Results: We included 19 papers that investigated a total of 427 participants with current or previous eating disorders and 444 controls. Overall, the studies used different diffusion tensor imaging approaches and showed widespread white matter abnormalities in patients with eating disorders. Despite differences among the studies, patients with anorexia nervosa showed mainly white matter microstructural abnormalities of thalamo–cortical tracts (i.e., corona radiata, thalamic radiations) and occipital–parietal–temporal–frontal tracts (i.e., left superior longitudinal and inferior fronto-occipital fasciculi). It was less clear whether white matter alterations persist after recovery from anorexia nervosa. Available data on bulimia nervosa were partially similar to those for anorexia nervosa.

Limitations: Study sample composition and diffusion tensor imaging analysis techniques were heterogeneous. The number of studies on bulimia nervosa was too limited to be conclusive.

Conclusion: White matter microstructure appears to be affected in anorexia nervosa, and these alterations may play a role in the pathophysiology of this eating disorder. Although we found white matter alterations in bulimia nervosa that were similar to those in anorexia nervosa, white matter changes in bulimia nervosa remain poorly investigated, and these findings were less conclusive. Further studies with longitudinal designs and multi-approach analyses are needed to better understand the role of white matter changes in eating disorders.

Citing Articles

Mendelian randomization analyses uncover causal relationships between brain structural connectome and risk of psychiatric disorders.

Xiao K, Chang X, Ye C, Zhang Z, Ma T, Su J medRxiv. 2025; .

PMID: 40034754 PMC: 11875323. DOI: 10.1101/2025.02.20.25322606.


Exploring the neurobiological correlates of psilocybin-assisted psychotherapy in eating disorders: a review of potential methodologies and implications for the psychedelic study design.

Koning E, Chaves C, Kirkpatrick R, Brietzke E J Eat Disord. 2024; 12(1):214.

PMID: 39731144 PMC: 11673730. DOI: 10.1186/s40337-024-01185-8.


Structural connectivity modifications following deep brain stimulation of the subcallosal cingulate and nucleus accumbens in severe anorexia nervosa.

Abellaneda-Perez K, Delgado-Martinez I, Salgado P, Gines J, Guardiola R, Vaque-Alcazar L Acta Neurochir (Wien). 2024; 166(1):364.

PMID: 39261306 DOI: 10.1007/s00701-024-06258-w.


Appearance-related cyberbullying and its association with the desire to alter physical appearance among adolescent females.

Prince T, Mulgrew K, Driver C, Mills L, Loza J, Hermens D J Eat Disord. 2024; 12(1):125.

PMID: 39215341 PMC: 11365200. DOI: 10.1186/s40337-024-01083-z.


Effects of repetitive transcranial magnetic stimulation of the right inferior parietal lobe on the body image perception in anorexia nervosa: A pilot randomized controlled study.

Chastan N, Achamrah N, Etard O, Nathou C, Piquet M, Guillaume S Brain Behav. 2024; 14(7):e3617.

PMID: 38970216 PMC: 11226536. DOI: 10.1002/brb3.3617.


References
1.
Boghi A, Sterpone S, Sales S, DAgata F, Bradac G, Zullo G . In vivo evidence of global and focal brain alterations in anorexia nervosa. Psychiatry Res. 2011; 192(3):154-9. DOI: 10.1016/j.pscychresns.2010.12.008. View

2.
Brooks S, ODaly O, Uher R, Friederich H, Giampietro V, Brammer M . Thinking about eating food activates visual cortex with reduced bilateral cerebellar activation in females with anorexia nervosa: an fMRI study. PLoS One. 2012; 7(3):e34000. PMC: 3313953. DOI: 10.1371/journal.pone.0034000. View

3.
Yau W, Bischoff-Grethe A, Theilmann R, Torres L, Wagner A, Kaye W . Alterations in white matter microstructure in women recovered from anorexia nervosa. Int J Eat Disord. 2013; 46(7):701-8. PMC: 3812403. DOI: 10.1002/eat.22154. View

4.
Philippi C, Mehta S, Grabowski T, Adolphs R, Rudrauf D . Damage to association fiber tracts impairs recognition of the facial expression of emotion. J Neurosci. 2009; 29(48):15089-99. PMC: 2819193. DOI: 10.1523/JNEUROSCI.0796-09.2009. View

5.
Mori S, Oishi K, Jiang H, Jiang L, Li X, Akhter K . Stereotaxic white matter atlas based on diffusion tensor imaging in an ICBM template. Neuroimage. 2008; 40(2):570-582. PMC: 2478641. DOI: 10.1016/j.neuroimage.2007.12.035. View