Literature DB >> 27373590

Analysis of glucose metabolism of (18)F-FDG in major depression patients using PET imaging: Correlation of salivary cortisol and α-amylase.

Kai Wei1, Hong-Li Xue1, Yi-Hui Guan2, Chuan-Tao Zuo2, Jing-Jie Ge2, Hong-Ying Zhang1, Bao-Jun Liu1, Yu-Xue Cao1, Jing-Cheng Dong3, Yi-Jie Du4.   

Abstract

Current diagnosis of Major depressive disorder (MDD) depends on its clinical symptoms, not on the results of any laboratory examinations. Establishing biological markers for diagnosis of MDD is one of the most important problems to be solved in psychiatry practice. MDD patients (n=8) and a healthy control group (n=8) were recruited in this study. Hamilton Depression Rating Scale (HAM-D) assessments were completed and saliva samples were collected for assessments of salivary cortisol and salivary α-amylase (sAA). PET examination was performed. Salivary cortisol and sAA in the MDD patients group were significantly higher than the healthy control group (P<0.001). MDD patients showed lower glucose metabolism of 18F-FDG in Cingulate Gyrus (BA24), Superior Frontal Gyrus (BA6), Rectal Gyrus (BA11) and Orbital Gyrus (BA11/47) compared with the healthy control group. The severity of depression, salivary cortisol and sAA correlated negatively with regional glucose metabolism in Cingulate Gyrus (BA 24), Superior Frontal Gyrus (BA 6), Rectal Gyrus (BA 11) and Orbital Gyrus (BA 11/47). The combination of salivary cortisol, sAA, superior frontal gyrus and rectal gyrus was the potential predictor of depression for MDD patients (ΔR(2)=0.981, p<0.001). The present study showed that, MDD patients group showed higher salivary cortisol, sAA levels and lower glucose metabolism of (18)F-FDG in several brain areas compared with the healthy control group. The combination of salivary cortisol, sAA, glucose metabolism of (18)F-FDG of superior frontal gyrus and rectal gyrus may serve as a simple clinical tool for the early diagnosis of MDD.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Glucose metabolism of 18F-FDG; Major depression; PET imaging; Salivary cortisol; Salivary α-amylase

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Year:  2016        PMID: 27373590     DOI: 10.1016/j.neulet.2016.06.039

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  4 in total

1.  Functional assessment of prefrontal lobes in patients with major depression disorder using a dual-mode technique of 3D-arterial spin labeling and 18F-fluorodeoxyglucose positron emission tomography/computed tomography.

Authors:  Chang Fu; Dapeng Shi; Yongju Gao; Junling Xu
Journal:  Exp Ther Med       Date:  2017-06-13       Impact factor: 2.447

2.  Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study.

Authors:  Paula Kopschina Feltes; Erik Fj de Vries; Luis E Juarez-Orozco; Ewelina Kurtys; Rudi Ajo Dierckx; Cristina M Moriguchi-Jeckel; Janine Doorduin
Journal:  J Cereb Blood Flow Metab       Date:  2017-12-22       Impact factor: 6.200

3.  Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder.

Authors:  Sarah C Hellewell; Thomas Welton; Jerome J Maller; Matthew Lyon; Mayuresh S Korgaonkar; Stephen H Koslow; Leanne M Williams; A John Rush; Evian Gordon; Stuart M Grieve
Journal:  Transl Psychiatry       Date:  2019-07-24       Impact factor: 6.222

Review 4.  Steps Towards Developing Effective Treatments for Neuropsychiatric Disturbances in Alzheimer's Disease: Insights From Preclinical Models, Clinical Data, and Future Directions.

Authors:  Amalie Clement; Ove Wiborg; Ayodeji A Asuni
Journal:  Front Aging Neurosci       Date:  2020-03-06       Impact factor: 5.750

  4 in total

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