Effects of Acamprosate on Sleep During Alcohol Withdrawal: A Double-Blind Placebo-Controlled Polysomnographic Study in Alcohol-Dependent Subjects
Background: Sleep disturbances are frequently encountered in alcohol‐dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process. Methods: In the present study, the effects of acamprosate, a drug successfully used in maintaining abstine...
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Published in | Alcoholism, clinical and experimental research Vol. 30; no. 9; pp. 1492 - 1499 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Malden, USA
Blackwell Publishing Inc
01.09.2006
Lippincott Williams & Wilkins |
Subjects | |
Online Access | Get full text |
ISSN | 0145-6008 1530-0277 |
DOI | 10.1111/j.1530-0277.2006.00180.x |
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Abstract | Background: Sleep disturbances are frequently encountered in alcohol‐dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process.
Methods: In the present study, the effects of acamprosate, a drug successfully used in maintaining abstinence following alcohol withdrawal, were assessed by polysomnographic recordings. A parallel double‐blind placebo‐controlled study was conducted in 24 male DSM‐IV alcohol‐dependent subjects aged 35.9±1.2 years. Treatments (2 tablets of 333 mg acamprosate vs placebo t.i.d.) were initiated 8 days before alcohol withdrawal and continued during the 15 days following alcohol withdrawal. Polysomnographic assessments were recorded during acute withdrawal (the first 2 nights following withdrawal) and during postwithdrawal abstinence (the last 2 nights of the trial).
Results: Results show that, compared with placebo, acamprosate decreased wake time after sleep onset and increased stage 3 and REM sleep latency (all treatment effects with a p<0.05 significance). Withdrawal effects themselves were also demonstrated as sleep efficiency (p<0.01) and total sleep time (p<0.05) were lower in abstinence nights versus withdrawal nights, whereas no significant treatment × withdrawal effect could be evidenced. Acamprosate was well tolerated during the entire course of the study.
Conclusions: The present study shows that acamprosate ameliorates both sleep continuity and sleep architecture parameters classically described as disturbed in alcohol‐dependent patients. From a clinical perspective, it suggests that an 8‐day acamprosate prewithdrawal treatment is well tolerated and can attenuate the sleep disturbances engendered by alcohol withdrawal in alcohol‐dependent subjects. |
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AbstractList | Background:
Sleep disturbances are frequently encountered in alcohol‐dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process.
Methods:
In the present study, the effects of acamprosate, a drug successfully used in maintaining abstinence following alcohol withdrawal, were assessed by polysomnographic recordings. A parallel double‐blind placebo‐controlled study was conducted in 24 male DSM‐IV alcohol‐dependent subjects aged 35.9±1.2 years. Treatments (2 tablets of 333 mg acamprosate vs placebo t.i.d.) were initiated 8 days before alcohol withdrawal and continued during the 15 days following alcohol withdrawal. Polysomnographic assessments were recorded during acute withdrawal (the first 2 nights following withdrawal) and during postwithdrawal abstinence (the last 2 nights of the trial).
Results:
Results show that, compared with placebo, acamprosate decreased wake time after sleep onset and increased stage 3 and REM sleep latency (all treatment effects with a
p
<0.05 significance). Withdrawal effects themselves were also demonstrated as sleep efficiency (
p
<0.01) and total sleep time (
p
<0.05) were lower in abstinence nights versus withdrawal nights, whereas no significant treatment × withdrawal effect could be evidenced. Acamprosate was well tolerated during the entire course of the study.
Conclusions:
The present study shows that acamprosate ameliorates both sleep continuity and sleep architecture parameters classically described as disturbed in alcohol‐dependent patients. From a clinical perspective, it suggests that an 8‐day acamprosate prewithdrawal treatment is well tolerated and can attenuate the sleep disturbances engendered by alcohol withdrawal in alcohol‐dependent subjects. Sleep disturbances are frequently encountered in alcohol-dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process.BACKGROUNDSleep disturbances are frequently encountered in alcohol-dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process.In the present study, the effects of acamprosate, a drug successfully used in maintaining abstinence following alcohol withdrawal, were assessed by polysomnographic recordings. A parallel double-blind placebo-controlled study was conducted in 24 male DSM-IV alcohol-dependent subjects aged 35.9+/-1.2 years. Treatments (2 tablets of 333 mg acamprosate vs placebo t.i.d.) were initiated 8 days before alcohol withdrawal and continued during the 15 days following alcohol withdrawal. Polysomnographic assessments were recorded during acute withdrawal (the first 2 nights following withdrawal) and during postwithdrawal abstinence (the last 2 nights of the trial).METHODSIn the present study, the effects of acamprosate, a drug successfully used in maintaining abstinence following alcohol withdrawal, were assessed by polysomnographic recordings. A parallel double-blind placebo-controlled study was conducted in 24 male DSM-IV alcohol-dependent subjects aged 35.9+/-1.2 years. Treatments (2 tablets of 333 mg acamprosate vs placebo t.i.d.) were initiated 8 days before alcohol withdrawal and continued during the 15 days following alcohol withdrawal. Polysomnographic assessments were recorded during acute withdrawal (the first 2 nights following withdrawal) and during postwithdrawal abstinence (the last 2 nights of the trial).Results show that, compared with placebo, acamprosate decreased wake time after sleep onset and increased stage 3 and REM sleep latency (all treatment effects with a p < 0.05 significance). Withdrawal effects themselves were also demonstrated as sleep efficiency (p < 0.01) and total sleep time (p < 0.05) were lower in abstinence nights versus withdrawal nights, whereas no significant treatment x withdrawal effect could be evidenced. Acamprosate was well tolerated during the entire course of the study.RESULTSResults show that, compared with placebo, acamprosate decreased wake time after sleep onset and increased stage 3 and REM sleep latency (all treatment effects with a p < 0.05 significance). Withdrawal effects themselves were also demonstrated as sleep efficiency (p < 0.01) and total sleep time (p < 0.05) were lower in abstinence nights versus withdrawal nights, whereas no significant treatment x withdrawal effect could be evidenced. Acamprosate was well tolerated during the entire course of the study.The present study shows that acamprosate ameliorates both sleep continuity and sleep architecture parameters classically described as disturbed in alcohol-dependent patients. From a clinical perspective, it suggests that an 8-day acamprosate prewithdrawal treatment is well tolerated and can attenuate the sleep disturbances engendered by alcohol withdrawal in alcohol-dependent subjects.CONCLUSIONSThe present study shows that acamprosate ameliorates both sleep continuity and sleep architecture parameters classically described as disturbed in alcohol-dependent patients. From a clinical perspective, it suggests that an 8-day acamprosate prewithdrawal treatment is well tolerated and can attenuate the sleep disturbances engendered by alcohol withdrawal in alcohol-dependent subjects. Sleep disturbances are frequently encountered in alcohol-dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process. In the present study, the effects of acamprosate, a drug successfully used in maintaining abstinence following alcohol withdrawal, were assessed by polysomnographic recordings. A parallel double-blind placebo-controlled study was conducted in 24 male DSM-IV alcohol-dependent subjects aged 35.9+/-1.2 years. Treatments (2 tablets of 333 mg acamprosate vs placebo t.i.d.) were initiated 8 days before alcohol withdrawal and continued during the 15 days following alcohol withdrawal. Polysomnographic assessments were recorded during acute withdrawal (the first 2 nights following withdrawal) and during postwithdrawal abstinence (the last 2 nights of the trial). Results show that, compared with placebo, acamprosate decreased wake time after sleep onset and increased stage 3 and REM sleep latency (all treatment effects with a p < 0.05 significance). Withdrawal effects themselves were also demonstrated as sleep efficiency (p < 0.01) and total sleep time (p < 0.05) were lower in abstinence nights versus withdrawal nights, whereas no significant treatment x withdrawal effect could be evidenced. Acamprosate was well tolerated during the entire course of the study. The present study shows that acamprosate ameliorates both sleep continuity and sleep architecture parameters classically described as disturbed in alcohol-dependent patients. From a clinical perspective, it suggests that an 8-day acamprosate prewithdrawal treatment is well tolerated and can attenuate the sleep disturbances engendered by alcohol withdrawal in alcohol-dependent subjects. Background: Sleep disturbances are frequently encountered in alcohol‐dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in the recovery process. Methods: In the present study, the effects of acamprosate, a drug successfully used in maintaining abstinence following alcohol withdrawal, were assessed by polysomnographic recordings. A parallel double‐blind placebo‐controlled study was conducted in 24 male DSM‐IV alcohol‐dependent subjects aged 35.9±1.2 years. Treatments (2 tablets of 333 mg acamprosate vs placebo t.i.d.) were initiated 8 days before alcohol withdrawal and continued during the 15 days following alcohol withdrawal. Polysomnographic assessments were recorded during acute withdrawal (the first 2 nights following withdrawal) and during postwithdrawal abstinence (the last 2 nights of the trial). Results: Results show that, compared with placebo, acamprosate decreased wake time after sleep onset and increased stage 3 and REM sleep latency (all treatment effects with a p<0.05 significance). Withdrawal effects themselves were also demonstrated as sleep efficiency (p<0.01) and total sleep time (p<0.05) were lower in abstinence nights versus withdrawal nights, whereas no significant treatment × withdrawal effect could be evidenced. Acamprosate was well tolerated during the entire course of the study. Conclusions: The present study shows that acamprosate ameliorates both sleep continuity and sleep architecture parameters classically described as disturbed in alcohol‐dependent patients. From a clinical perspective, it suggests that an 8‐day acamprosate prewithdrawal treatment is well tolerated and can attenuate the sleep disturbances engendered by alcohol withdrawal in alcohol‐dependent subjects. |
Author | Rémy, Luthringer Luc, Staner Thierry, Danel Muriel, Muzet Peter, Boeijinga Isabelle, Gendre Frédéric, Landron |
Author_xml | – sequence: 1 givenname: Staner surname: Luc fullname: Luc, Staner organization: FORENAP, Centre Hospitalier de Rouffach, Rouffach, France – sequence: 2 givenname: Boeijinga surname: Peter fullname: Peter, Boeijinga organization: FORENAP, Centre Hospitalier de Rouffach, Rouffach, France – sequence: 3 givenname: Danel surname: Thierry fullname: Thierry, Danel organization: Unité de Psychopathologie et Alcoologie Clinique de l'Anxiété, Lille, France – sequence: 4 givenname: Gendre surname: Isabelle fullname: Isabelle, Gendre organization: FORENAP, Centre Hospitalier de Rouffach, Rouffach, France – sequence: 5 givenname: Muzet surname: Muriel fullname: Muriel, Muzet organization: FORENAP, Centre Hospitalier de Rouffach, Rouffach, France – sequence: 6 givenname: Landron surname: Frédéric fullname: Frédéric, Landron organization: MERCK Santé, Lyon, France – sequence: 7 givenname: Luthringer surname: Rémy fullname: Rémy, Luthringer organization: FORENAP, Centre Hospitalier de Rouffach, Rouffach, France |
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Keywords | Human Antialcohol drug Poison withdrawal Acamprosate Ethanol Alcohol Withdrawal Alcoholism Glutamate Alcoholic beverage Sleep Placebo Excitatory aminoacid Neurotransmitter Disintoxication Double blind study Sleep wake cycle |
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Notes | ArticleID:ACER180 ark:/67375/WNG-6WCQMW01-J istex:97138F7B7E76BCC52196408A427794C0742FA8AA This work was supported by an unrestricted grant of Merck Santé, France. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
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JAMA 278:144-151. 2004; 65 1997; 278 1989; 84 2000; 6 2004; 29 1984; 21 1976 2000; 292 1999; 84 1970 1998; 82 1998; 155 1998; 43 2001; 40 1996; 305 1994; 62 2003; 54 2003; 99 1998; 59 2000; 14 2000; 54 2003; 7 1999; 12 2001; 15 1999; 93 1998; 287 1985; 9 1981; 5 1994; 45 2000; 394 1994 2000; 275 2002 1995; 18 2001; 25 1995; 3 2001; 62 1998; 22 1994; 9 1989; 50 2004; 50 1991; 26 2000; 149 1973; 28 1999; 35 1998; 31 1994; 51 1968 1996; 314 2003; 23 1998; 35 Williams HL (e_1_2_5_55_1) 1981; 5 e_1_2_5_23_1 Ansseau M (e_1_2_5_6_1) 2000; 6 Holter SM (e_1_2_5_24_1) 2000; 292 e_1_2_5_44_1 James SP (e_1_2_5_25_1) 2004; 65 American Psychiatric Association (APA) (e_1_2_5_4_1) 1994 Drummond SP (e_1_2_5_18_1) 1998; 22 Miyakawa T (e_1_2_5_36_1) 1997; 278 e_1_2_5_29_1 Brower KJ (e_1_2_5_11_1) 2001; 25 e_1_2_5_42_1 Spielberger CD (e_1_2_5_46_1) 1970 Rechtschaffen A (e_1_2_5_39_1) 1968 e_1_2_5_15_1 e_1_2_5_38_1 e_1_2_5_17_1 Krystal JH (e_1_2_5_28_1) 2002 e_1_2_5_34_1 Roehrs T (e_1_2_5_40_1) 2001; 25 e_1_2_5_57_1 e_1_2_5_7_1 Meyer RE (e_1_2_5_35_1) 1989; 50 e_1_2_5_13_1 e_1_2_5_32_1 e_1_2_5_5_1 e_1_2_5_19_1 Johnson BA (e_1_2_5_26_1) 2000; 149 e_1_2_5_30_1 Sullivan JT (e_1_2_5_48_1) 1989; 84 e_1_2_5_51_1 Spanagel R (e_1_2_5_45_1) 1996; 305 Bolo N (e_1_2_5_10_1) 1998; 82 Mason BJ (e_1_2_5_33_1) 2001; 62 e_1_2_5_47_1 Al Qatari M (e_1_2_5_3_1) 1998; 22 e_1_2_5_43_1 Thomas MP (e_1_2_5_49_1) 1998; 287 Krystal JH (e_1_2_5_27_1) 2003; 99 e_1_2_5_20_1 e_1_2_5_41_1 e_1_2_5_14_1 e_1_2_5_16_1 e_1_2_5_37_1 e_1_2_5_8_1 e_1_2_5_56_1 Boismare F (e_1_2_5_9_1) 1984; 21 e_1_2_5_12_1 e_1_2_5_54_1 e_1_2_5_2_1 Grant KA (e_1_2_5_21_1) 1995; 3 Tsai GE (e_1_2_5_53_1) 1998; 155 e_1_2_5_31_1 e_1_2_5_52_1 Gross MM (e_1_2_5_22_1) 1976 e_1_2_5_50_1 |
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Snippet | Background: Sleep disturbances are frequently encountered in alcohol‐dependent patients. Drugs improving sleep during abstinence from alcohol may play an... Background: Sleep disturbances are frequently encountered in alcohol‐dependent patients. Drugs improving sleep during abstinence from alcohol may play an... Sleep disturbances are frequently encountered in alcohol-dependent patients. Drugs improving sleep during abstinence from alcohol may play an important role in... |
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SubjectTerms | Acamprosate Adult Alcohol Deterrents - adverse effects Alcohol Deterrents - therapeutic use Alcohol Withdrawal Alcoholism Alcoholism - psychology Alcoholism and acute alcohol poisoning Biological and medical sciences Central Nervous System Depressants - adverse effects Compulsive Personality Disorder - psychology Double-Blind Method Electrophysiology Ethanol - adverse effects Glutamate Humans Male Medical sciences Polysomnography - drug effects Psychiatric Status Rating Scales Sleep Sleep - drug effects Sleep, REM - drug effects Substance Withdrawal Syndrome - drug therapy Substance Withdrawal Syndrome - psychology Taurine - adverse effects Taurine - analogs & derivatives Taurine - therapeutic use Toxicology |
Title | Effects of Acamprosate on Sleep During Alcohol Withdrawal: A Double-Blind Placebo-Controlled Polysomnographic Study in Alcohol-Dependent Subjects |
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