Brain age estimation in subjects with anxiety/depression reliant on occipital cortex.

Poster No:

690 

Submission Type:

Abstract Submission 

Authors:

Owen Vega1, Nahian Chowdhury1, Nikhil Chaudhari2,1, Anar Amgalan1, Andrei Irimia2,3,1

Institutions:

1Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California, Los Angeles, USA, 2Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles, USA, 3Department of Quantitative and Computational Biology, Dana and David Dornsife College of Letters, Arts and Sciences, University of Southern California, Los Angeles, USA

First Author:

Owen Vega  
Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California
Los Angeles, USA

Co-Author(s):

Nahian Chowdhury  
Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California
Los Angeles, USA
Nikhil Chaudhari  
Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California|Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California
Los Angeles, USA|Los Angeles, USA
Anar Amgalan, PhD  
Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California
Los Angeles, USA
Andrei Irimia  
Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California|Department of Quantitative and Computational Biology, Dana and David Dornsife College of Letters, Arts and Sciences, University of Southern California|Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California
Los Angeles, USA|Los Angeles, USA|Los Angeles, USA

Introduction:

Depression is a highly prevalent psychiatric disorder. It is the 19th most common disease in the world and the most diagnosed psychiatric disorder in adults - 1 in 5 people in the U.S. in any 6-month period suffers from depression. Depression can persist throughout life, with a 14.9-16.2% lifelong prevalence in the U.S. adult population (Kessler et al., 2015) (Richards, 2011). It can be fatal, as it increases suicide risk by 20.9-27 times, and it is a risk factor for cardiac disease (Lépine & Briley, 2011). Depression is also co-morbid with anxiety, another common psychiatric disorder. 85% of people with depression have anxiety, and 90% of people with anxiety have depression. Difficulties arise as both illnesses require different treatments (Tiller, 2013). Furthermore, the burden and prevalence of both anxiety and depression have increased following the 2020 COVID pandemic (COVID-19 Mental Disorders Collaborators, 2021). As anxiety and depression are both potentially lifelong disorders, age has been seen as a factor regarding both disorders (Gao et al., 2023). The interactions between aging and anxiety or depression remain understudied.

Our lab has developed a convolutional neural network that predicts a person's age from their T1-weighted magnetic resonance imaging (MRI) volume. The model outputs saliency maps that capture the contribution of each brain voxel to the age prediction. Here we investigate the interaction of anxiety and depression with aging by comparing patterns of saliency between subjects with these disorders and healthy controls.

Methods:

Subject MRIs were obtained from the UK Biobank (UKBB). UKBB codes F32-33 and F40-43 were used to select subjects with primary or secondary diagnoses of depression and anxiety. Subjects with both anxiety and depression were excluded from the study. Subjects without MRI and subjects who had already been used to train the age prediction model were also excluded.

Sets of healthy control subjects were age-, sex-, and sample size-matched to each case group. As such, the data was separated into four groups: anxiety (N=700), anxiety-control (N=700), depression (N=940), and depression-control (N=940). Age prediction and saliency map generation were performed for each subject using the trained model. Each subject's saliency map was normalized using min-max scaling and projected onto a shared cortical surface space. Saliency maps were averaged within-group across subjects. Maps of group differences were acquired by subtracting the mean saliency of each control cohort by the mean saliency of the corresponding case cohort and dividing the difference by the average saliency of the case group.

All difference plots were smoothed using FreeSurfer 'fs_smooth.m' function with 5 iterations. Figures were plotted using MATLAB.

Results:

Saliency differences were largely symmetrical across hemispheres in both the control/anxiety (Fig. 1) and control/depression (Fig. 2) comparisons. Both anxiety and depression groups showed roughly 6% higher saliency than controls in occipital regions. Meanwhile, controls exhibited ~6% higher saliency in pre/postcentral gyri and in the central sulcus.
Supporting Image: AnxietySal_Diff_sm.png
   ·Figure 1. Saliency differences between anxiety group and anxiety-control group. Red indicates higher saliency in control group, while Blue indicates higher saliency in patients.
Supporting Image: DepressionSal_Diff_sm.png
   ·Figure 2. Saliency differences between depression group and depression-control group. Red indicates higher saliency in control group, while Blue indicates higher saliency in patients.
 

Conclusions:

The two maps of saliency differences exhibit spatial overlap, suggesting that anxiety and depression influence the aging process in similar ways. Previous research has highlighted the occipital lobe as an affected area in anxiety/depression. Increased saliency at the occipital lobe in anxiety/depression subjects may relate to decreased function, which has been observed bilaterally in the occipital lobe in both task-based (Li et al., 2013) and resting-state fMRI (Peng et al., 2011) studies. A CT study also demonstrated early atrophy of the occipital lobe in subjects with depression (Tanaka et al., 1982). Grey matter volume in the right occipital region was found to be negatively correlated with anxious traits (Yin et al., 2016). Further research on how anxiety and depression influence the aging of the occipital lobe is recommended.

Disorders of the Nervous System:

Psychiatric (eg. Depression, Anxiety, Schizophrenia) 1

Lifespan Development:

Aging 2

Modeling and Analysis Methods:

Image Registration and Computational Anatomy

Neuroanatomy, Physiology, Metabolism and Neurotransmission:

Anatomy and Functional Systems

Novel Imaging Acquisition Methods:

Anatomical MRI

Keywords:

Affective Disorders
Aging
Anxiety
Computing
Data analysis
MRI
Psychiatric Disorders
STRUCTURAL MRI

1|2Indicates the priority used for review

Provide references using author date format

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Gao, X. (2023). ‘Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants’. Nature Communications, vol. 14, no. 1, pp. 2277.
Kessler, R. C. (2015). ‘Anxious and non-anxious major depressive disorder in the World Health Organization World Mental Health Surveys’. Epidemiology and Psychiatric Sciences, vol. 24, no. 3, pp. 210–226.

Lépine, J. P. (2011). ‘The increasing burden of depression’. Neuropsychiatric Disease and Treatment, vol. 7, no. Suppl 1, pp. 3–7.
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