Gray and white matter volume changes and the correlation with depression and anxiety in obese patients revealed by voxel-based morphometry
Jun-Cheng Weng1,2, Chi-Ju Lai1, Hse-Huang Chao3, Ming-Chou Ho4, and Vincent Chin-Hung Chen5

1Department of Medical Imaging and Radiological Sciences, Chung Shan Medical University, Taichung, Taiwan, 2Department of Medical Imaging, Chung Shan Medical University Hospital, Taichung, Taiwan, 3Tiawan Center for Metabolic and Bariatric Surgery, Jen-Ai Hospital, Taichung, Taiwan, 4Department of Psychology, Chung Shan Medical University, Taichung, Taiwan, 5Department of Psychiatry, Chang Gung Memorial Hospital, Chiayi, Taiwan

Synopsis

Obesity is an important health issue in modern society. The prevalence of obesity has been increasing in these years and morbid obesity is related to cardiovascular disease and overall mortality. Past reviews regarded binge eating as a manifestation of dysfunctional reward system and disinhibition. Some authors considered binge eating as a kind of addiction. Recent study demonstrated the more extensive involvement of brain pathways other than reward system. The mechanism of change is not clear. There is scanty of research regarding correlation between change of activation pattern in brain areas in functional MRI, binge eating and psychiatric illness. To gain insight into the correlation of physiological alteration and psychiatric illness and to develop subsequent detectable biomarker are crucial. The goal of our study was to investigate the morphological changes in gray and white matter between obese patients and healthy subjects using voxel-based morphometry (VBM). Our results suggested the changes of the volume in the brain structures may closely linked to the symptom and behavior of obese patients. Apply these novel markers to monitoring and improving cormorbid psychiatric illness will be an essential part of multidiscipline integral care for obese patients.

Purpose

Obesity is an important health issue in modern society. The prevalence of obesity has been increasing in these years [1, 2] and morbid obesity is related to cardiovascular disease and overall mortality [3]. Past reviews regarded binge eating as a manifestation of dysfunctional reward system and disinhibition. Some authors considered binge eating as a kind of addiction. Recent study demonstrated the more extensive involvement of brain pathways other than reward system [4]. The mechanism of change is not clear. There is scanty of research regarding correlation between change of activation pattern in brain areas in functional MRI, binge eating and psychiatric illness. To gain insight into the correlation of physiological alteration and psychiatric illness and to develop subsequent detectable biomarker are crucial. The goal of our study was to investigate the morphological changes in gray and white matter between obese patients and healthy subjects using voxel-based morphometry (VBM). Apply these novel markers to monitoring and improving comorbid psychiatric illness will be an essential part of multidiscipline integral care for obese patients.

Materials and Methods

Twenty morbid obese participants (BMI = 37.9 ± 5.2)aged between 20 and 65 years-old who are preparing to undergo bariatric surgery will be recruited from an obesity clinic in a single regional teaching hospital. The participants meet the criteria of severe binge eating defined by scores > 27 on Binge Eating Scale [5]. The control group as comparison objects for the cross sectional study includes 30 subjects (BMI = 22.6 ± 3.4) who are morbid obese, preparing to undergo bariatric surgery and scores < 17 on Binge Eating Scale. The control group will be recruited from the same clinic. All participants are not taking psychotropic agents during the study period and are not in need of immediate psychiatric intervention, such as suicidal ideation. The participants receive neuropsychological tests, including anxiety and depression test, and MRI before the bariatric surgery. All participants were scanned to obtain 3D gradient echo T1-weighted images (T1WI) using 1.5T MRI (Ingenia, Philips, Netherlands) with an 8-channel head coil. All images were acquired with TR/TE= 7.6/3.5 ms, Flip angle= 8°, voxel resolution = 1 x 1 x 1 mm3.

In data analysis, all structural data were processed using Statistical Parametric Mapping software package (SPM8, http://www.fil.ion.ucl.ac.uk/spm) with VBM toolbox (VBM8, http://dbm.neuro.uni-jena.de/vbm). A segmentation approach was used to perform tissue classification after brain extraction, image registration and normalization. Then gray and white matter images were smoothed for statistical analysis. The gray and white matter images were also calculated to find the correlation between the brain regions and body mass index (BMI), anxiety and depression scores.

Results

In our results, we found the significant increased volume in the amygdala of obese patients compared to healthy subjects, and the significant decreased volume in the premotor cortex of obese patients was also found (p < 0.001) (Fig. 1a, b). We also found the significant increased volume in the inferior frontal gyrus and the thalamus of obese patients compared to healthy subjects (p < 0.001) (Fig. 1c, d). In the correlation analysis, as shown in Fig. 2, the positive correlation was found between amygdala and BMI; the positive correlation was found between thalamus and anxiety score; the positive correlation was found between amygdala and depression (p < 0.001).

Discussion

Previous reports in animal and human showed deficiency in reward system might be related to eating disorder [6]. The reward system is composed by the mesolimbic pathway which projecting from the ventral tegmental area to the nucleus accumbens. The amygdala and the hippocampus were also regarded as part of the system. Besides the reward system, the prefrontal cortex is implicated in initiating behavioral responses based on hedonic appraisals of food cues.

Conclusion

Our study used neuroimaging and neuropsychological test for evaluation the difference in obese patients and healthy subjects, and we explored the possible neuromarker in obese patients. Our results suggested the changes of the volume in the brain structures may closely linked to the symptom and behavior of obese patients. The finding in this study confirmed the potential psychobiological biomarkers (neuroimaging and neuropsychological test results) for binge eating among obese patients.

Acknowledgements

This study was supported in part by the research program NSC103-2420-H-040-003, which was sponsored by the Ministry of Science and Technology, Taipei, Taiwan.

References

1. Karnieli E, et al. The growing prevalence of obesity worldwide is an increasing concern. Preface. Endocrinol Metab Clin North Am, 2008; 37(3): xvii-xviii.

2. Wyatt SB, et al. Overweight and obesity: prevalence, consequences, and causes of a growing public health problem. Am J Med Sci. 2006; 331(4): 166-174.

3. Pontiroli AE, et al. Long-term prevention of mortality in morbid obesity through bariatric surgery. a systematic review and meta-analysis of trials performed with gastric banding and gastric bypass. Ann Surg. 2011; 253(3): 484-487.

4. Tomasi D, et al. Striatocortical pathway dysfunction in addiction and obesity: differences and similarities. Crit Rev Biochem Mol Biol. 2013; 48(1): 1-19.

5. Freitas SR, et al. The assessment of binge eating disorder in obese women: a comparison of the binge eating scale with the structured clinical interview for the DSM-IV. Eat Behav. 2006; 7(3): 282-289.

6. Halpern CH, et al. Amelioration of binge eating by nucleus accumbens shell deep brain stimulation in mice involves D2 receptor modulation. J Neurosci. 2013; 33(17): 7122-7129.

Figures

Fig. 1 (a) amygdala of obese patients was greater than control; (b) premotor cortex of obese patients was smaller than control (p<0.001); (c) inferior frontal gyrus and (d) thalamus of obese patients were greater than control (p<0.001).

Fig. 2 (a) The positive correlation was found between amygdala and BMI; (b) the positive correlation was found between thalamus and anxiety score; (c) the positive correlation was found between amygdala and depression (p < 0.001).



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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