Literature DB >> 12759553

Depressed patients have higher body temperature: 5-HT transporter long promoter region effects.

J L Rausch1, M E Johnson, K M Corley, H M Hobby, N Shendarkar, Y Fei, V Ganapathy, F H Leibach.   

Abstract

BACKGROUND: Depression has been associated with a decrease in intracellular serotonin (5-HT) reuptake through its transporter, SERT. The 5-HT transporter long promoter region (5-HTTLPR) deletion in the SERT gene has also been associated with a decrease in 5-HT reuptake. Conversely, increases in extracellular 5-HT have been associated with increased temperature. It has not been established, however, whether body temperature in depressed patients is different from controls. Here, we hypothesized that temperature would be increased in depressed patients as well as in those with the 5-HTTLPR deletion.
METHODS: A strict oral temperature protocol employed single, cross-sectional, naturalistic time-of-day temperature measures in 125 subjects (46 normal controls, 79 outpatients with major depression). Controls and depressed patients were free of psychotropic medication and classified by the Structured Clinical Interview for Psychiatric Diagnoses. Eighty-one of the subjects (68 depressed, 13 normal) were additionally genotyped for 5-HTTLPR polymorphisms.
RESULTS: Depressed patients had a significantly higher uncorrected body temperature (mean +/- SD 98.38 +/- 0.61 degrees F) than controls (mean +/- SD 98.13 +/- 0.59 degrees F; F = 4.8, p = 0.03). An age (F = 14.09, p < 0.001) and time-of-day (11.4, p = 0.001) correction revealed a more robust (F = 14.02, p < 0.001) difference between depressed patients (mean +/- SD 98.44 +/- 0.55 degrees F) and controls (mean +/- SD 98.02 +/- 0.56 degrees F). When normalized for age and circadian differences between subjects, random, outpatient oral temperatures had a sensitivity of 63% and a specificity of 76% in identifying the depressed subjects from the controls. Independent of depression, subjects with the 5-HTTLPR deletion (short SERT allele) were warmer (mean +/- SD 98.33 +/- 0.65 degrees F) than those lacking the short allele on either chromosome (mean +/- SD 97.91 +/- 0.69 degrees F; F = 7.0, p = 0.01). However, the genotype did not explain the temperature differences between controls and depressed patients.
CONCLUSION: This is the first demonstration of an increased daytime body temperature in cases with major depression. Subjects with a corrected temperature above 98.3 degrees F were 2.6-fold more likely to be depressed. The results may strengthen the hypothesis of an inflammatory component of depression. In addition, the findings suggest a potential link between genetic differences in 5-HT transport and body temperature. Copyright 2003 S. Karger AG, Basel

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12759553     DOI: 10.1159/000070579

Source DB:  PubMed          Journal:  Neuropsychobiology        ISSN: 0302-282X            Impact factor:   2.328


  15 in total

1.  Altered expression of circadian rhythm genes among individuals with a history of depression.

Authors:  Jean-Philippe Gouin; James Connors; Janice K Kiecolt-Glaser; Ronald Glaser; William B Malarkey; Cathie Atkinson; David Beversdorf; Ning Quan
Journal:  J Affect Disord       Date:  2010-05-14       Impact factor: 4.839

2.  Chronic non-invasive corticosterone administration abolishes the diurnal pattern of tph2 expression.

Authors:  Nina C Donner; Christian D Montoya; Jodi L Lukkes; Christopher A Lowry
Journal:  Psychoneuroendocrinology       Date:  2011-09-15       Impact factor: 4.905

Review 3.  Can body temperature dysregulation explain the co-occurrence between overweight/obesity, sleep impairment, late-night eating, and a sedentary lifestyle?

Authors:  Rhonda F Brown; Einar B Thorsteinsson; Michael Smithson; C Laird Birmingham; Hessah Aljarallah; Christopher Nolan
Journal:  Eat Weight Disord       Date:  2017-09-19       Impact factor: 4.652

4.  Proinflammatory cytokine responses correspond with subjective side effects after influenza virus vaccination.

Authors:  Lisa M Christian; Kyle Porter; Erik Karlsson; Stacey Schultz-Cherry
Journal:  Vaccine       Date:  2015-05-28       Impact factor: 3.641

Review 5.  How the serotonin story is being rewritten by new gene-based discoveries principally related to SLC6A4, the serotonin transporter gene, which functions to influence all cellular serotonin systems.

Authors:  Dennis L Murphy; Meredith A Fox; Kiara R Timpano; Pablo R Moya; Renee Ren-Patterson; Anne M Andrews; Andrew Holmes; Klaus-Peter Lesch; Jens R Wendland
Journal:  Neuropharmacology       Date:  2008-09-11       Impact factor: 5.250

6.  The relationship between depression and chronotype: A longitudinal assessment during childhood and adolescence.

Authors:  Dustin A Haraden; Benjamin C Mullin; Benjamin L Hankin
Journal:  Depress Anxiety       Date:  2017-09-08       Impact factor: 6.505

7.  The evolutionary significance of depression in Pathogen Host Defense (PATHOS-D).

Authors:  C L Raison; A H Miller
Journal:  Mol Psychiatry       Date:  2012-01-31       Impact factor: 15.992

8.  Ketamine influences CLOCK:BMAL1 function leading to altered circadian gene expression.

Authors:  Marina M Bellet; Marquis P Vawter; Blynn G Bunney; William E Bunney; Paolo Sassone-Corsi
Journal:  PLoS One       Date:  2011-08-24       Impact factor: 3.240

9.  Serotonin-mediated modulation of Na+/K+ pump current in rat hippocampal CA1 pyramidal neurons.

Authors:  Li Nan Zhang; Su Wen Su; Fang Guo; Hui Cai Guo; Xiao Lu Shi; Wen Ya Li; Xu Liu; Yong Li Wang
Journal:  BMC Neurosci       Date:  2012-01-19       Impact factor: 3.288

Review 10.  Current Advances in Wearable Devices and Their Sensors in Patients With Depression.

Authors:  Seunggyu Lee; Hyewon Kim; Mi Jin Park; Hong Jin Jeon
Journal:  Front Psychiatry       Date:  2021-06-17       Impact factor: 4.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.