Relationship between Inflammation and Diurnal Cortisol Secretion in Patients with Major Depression: Role of Tumor Necrosis Factor Alpha Public

Koch, Jennifer (2014)

Permanent URL: https://etd.library.emory.edu/concern/etds/ft848q70w?locale=fr
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Abstract

Major Depressive Disorder (MDD) has been shown to be associated with high inflammation, including high levels of inflammatory cytokines such as tumor necrosis factor (TNF), as well as glucocorticoid resistance and disrupted diurnal cortisol secretion. It is believed that cortisol feedback inhibition is suppressed by inflammatory cytokines such as TNF. A double blind, clinical trial was conducted in which 60 patients, who met the criteria for MDD, were enrolled and either administered a placebo or the TNF antagonist infliximab over a period of 8 weeks. Blood samples were collected at weeks 1 and 8 and these samples were analyzed via ELISA assays for cortisol and TNF levels and were used to determine gene expression. This study determined that the administration of infliximab was able to restore natural diurnal cortisol rhythms and that TNF antagonists may be useful in lessening depressive symptoms.

Table of Contents

Table of Contents:

Introduction....................................................................................................................1-9

Methods......................................................................................................................10-15

Results........................................................................................................................16-22

Discussion....................................................................................................................23-27

References...................................................................................................................28-33

Tables............................................................................................................................34

Figure 1............................................................................................................................3

Figure 2............................................................................................................................4

Figure 3............................................................................................................................7

Figure 4...........................................................................................................................11

Figure 5...........................................................................................................................13

Figure 6...........................................................................................................................17

Figure 7...........................................................................................................................17

Figure 8...........................................................................................................................18

Figure 9...........................................................................................................................19

Figure 10..........................................................................................................................19

Figure 11..........................................................................................................................20

Figure 12..........................................................................................................................20

Figure 13..........................................................................................................................21

Figure 14..........................................................................................................................22

Table 1............................................................................................................................34

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