Tumor necrosis factor antagonism normalizes rapid eye movement sleep in alcohol dependence.

TitleTumor necrosis factor antagonism normalizes rapid eye movement sleep in alcohol dependence.
Publication TypeJournal Article
Year of Publication2009
AuthorsIrwin MR, Olmstead R, Valladares EM, Breen ECrabb, Ehlers CL
JournalBiol Psychiatry
Volume66
Issue2
Pagination191-5
Date Published2009 Jul 15
ISSN1873-2402
KeywordsAdult, Alcoholism, Cross-Over Studies, Double-Blind Method, Etanercept, Female, Humans, Immunoglobulin G, Immunologic Factors, Male, Polysomnography, Receptors, Tumor Necrosis Factor, Sleep, REM, Temperance, Tumor Necrosis Factors
Abstract

BACKGROUND: In alcohol dependence, markers of inflammation are associated with increases in rapid eye movement (REM) sleep, which is thought to be a prognostic indicator of alcohol relapse. This study was undertaken to test whether blockade of biologically active tumor necrosis factor-alpha (TNF-alpha) normalizes REM sleep in alcohol-dependent adults.

METHODS: In a randomized, placebo-controlled, double-blind, crossover trial, 18 abstinent alcohol-dependent male adults received a single dose of etanercept (25 mg) versus placebo in a counterbalanced order. Polysomnographic sleep was measured at baseline and for 3 nights after the acute dose of etanercept or placebo.

RESULTS: Compared with placebo, administration of etanercept produced significant decreases in the amount and percentage of REM sleep. Decreases in REM sleep were robust and approached low levels typically found in age-comparable control subjects. Individual differences in biologically active drug as indexed by circulating levels of soluble tumor necrosis factor receptor II negatively correlated with the percentage of REM sleep.

CONCLUSIONS: Pharmacologic neutralization of TNF-alpha activity is associated with significant reductions in REM sleep in abstinent alcohol-dependent patients. These data suggest that circulating levels of TNF-alpha may have a physiologic role in the regulation of REM sleep in humans.

DOI10.1016/j.biopsych.2008.12.004
Alternate JournalBiol. Psychiatry
PubMed ID19185287
PubMed Central IDPMC2761725
Grant ListAA 13239 / AA / NIAAA NIH HHS / United States
AG 026364 / AG / NIA NIH HHS / United States
CA 10014152 / CA / NCI NIH HHS / United States
CA116778 / CA / NCI NIH HHS / United States
HL 079955 / HL / NHLBI NIH HHS / United States
M01 RR000865 / RR / NCRR NIH HHS / United States
M01 RR000865-310740 / RR / NCRR NIH HHS / United States
M01 RR000865-320782 / RR / NCRR NIH HHS / United States
M01 RR000865-328456 / RR / NCRR NIH HHS / United States
P30 AG028748 / AG / NIA NIH HHS / United States
P30 AG028748-049004 / AG / NIA NIH HHS / United States
P30-AG028748 / AG / NIA NIH HHS / United States
R01 AA013239 / AA / NIAAA NIH HHS / United States
R01 AA013239-06 / AA / NIAAA NIH HHS / United States
R01 AG026364 / AG / NIA NIH HHS / United States
R01 DA016541 / DA / NIDA NIH HHS / United States
R01 DA016541-04 / DA / NIDA NIH HHS / United States
RR00827 / RR / NCRR NIH HHS / United States
T32 MH019925 / MH / NIMH NIH HHS / United States
T32 MH019925-12 / MH / NIMH NIH HHS / United States
T32-MH19925 / MH / NIMH NIH HHS / United States