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1.
J Clin Psychopharmacol ; 32(1): 75-82, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22198453

ABSTRACT

The objective of the present naturalistic study was to assess the differential effects of opioid detoxification with methadone or buprenorphine on activity, circadian rhythm, and sleep. Forty-two consecutive inpatients with opiate addiction were switched to either methadone or buprenorphine and gradually tapered down over the course of 2 to 3 weeks. There were no significant differences in comedication (lofexidine, quetiapine, and valproic acid) between the methadone and buprenorphine groups. Patients in the methadone group showed 11% lower activity and were 24 minutes phase delayed as compared with buprenorphine-treated patients, whereas the latter had 2.5% lower sleep efficiency and 9% shorter actual sleep time. These significant group differences were most pronounced for the lowest doses (≤20% of maximum individual daily dose, ie, at the end of withdrawal representing late withdrawal effects). Furthermore, for the total sample, we found a significant decrease in the relative amplitude of the sleep-wake cycle and worsening of all actigraphic sleep parameters from the higher (100% to 20%) to the lowest doses (20% to 0%). The acrophase of the circadian rhythm displayed a phase advance (-88 minutes) from the highest (100% to 80%) to the lower doses (80% to 0%) in methadone-treated patients. Opioid tapering with methadone or buprenorphine leads to characteristic changes of the rest-activity cycle, but further study is required to validate these results.


Subject(s)
Actigraphy , Buprenorphine/therapeutic use , Methadone/therapeutic use , Opiate Substitution Treatment , Adult , Austria , Buprenorphine/adverse effects , Circadian Rhythm/drug effects , Dose-Response Relationship, Drug , Female , Humans , Length of Stay , Male , Methadone/adverse effects , Sleep/drug effects
2.
Nord J Psychiatry ; 65(3): 203-7, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21047193

ABSTRACT

BACKGROUND: Genetic factors likely contribute to the biological vulnerability of eating disorders. AIMS: Case-control association study on one neuropeptide Y gene (Leu7Pro) polymorphism and three ghrelin gene (Arg51Gln, Leu72Met and Gln90Leu) polymorphisms. METHODS: 114 eating disorder patients (46 with anorexia nervosa, 30 with bulimia nervosa, 38 with binge eating disorder) and 164 healthy controls were genotyped. RESULTS: No differences were detected between patients and controls for any of the four polymorphisms in allele frequency and genotype distribution (P > 0.05). Allele frequencies and genotypes had no significant influence on body mass index (P > 0.05) in eating disorder patients. CONCLUSION: Positive findings of former case-control studies of associations between ghrelin gene polymorphisms and eating disorders could not be replicated. Neuropeptide Y gene polymorphisms have not been investigated in eating disorders before.


Subject(s)
Feeding and Eating Disorders/genetics , Genetic Association Studies , Ghrelin/genetics , Neuropeptide Y/genetics , Polymorphism, Single Nucleotide/genetics , Adolescent , Adult , Anorexia Nervosa/genetics , Binge-Eating Disorder/genetics , Body Mass Index , Bulimia Nervosa/genetics , Case-Control Studies , Female , Gene Frequency , Genotype , Humans , Male , Middle Aged , Young Adult
3.
Aust N Z J Psychiatry ; 40(6-7): 554-60, 2006.
Article in English | MEDLINE | ID: mdl-16756580

ABSTRACT

OBJECTIVE: Environmental influences have been reported to play a role in the genesis of both schizophrenia and violent behaviour. METHOD: We studied the central features of the family and social influences of 103 healthy non-offenders, 103 non-schizophrenic offenders, 103 schizophrenic non-offenders, and 103 schizophrenic offenders, using a semistructured instrument. RESULTS: Lower social class of origin, offending behaviour in the parental generation, loss of the father, a new partnership of the remaining parent, growing up in blended families, larger sibships and stays in foster homes during childhood and adolescence, promoted the development of offending behaviour in general. Schizophrenic patients were more likely to have relatives with schizophrenia, a finding which was more marked among offenders than non-offenders. CONCLUSIONS: We were able to identify characteristic unfavourable family and social influences which were associated in schizophrenic patients with a high risk of offending behaviour. This offers the prospect of early detection of those with schizophrenia who will go on to offend.


Subject(s)
Crime/statistics & numerical data , Family/psychology , Interpersonal Relations , Schizophrenia/epidemiology , Social Behavior , Adult , Antisocial Personality Disorder/diagnosis , Antisocial Personality Disorder/epidemiology , Antisocial Personality Disorder/psychology , Comorbidity , Demography , Humans , Male , Parent-Child Relations , Prisoners/psychology , Prisoners/statistics & numerical data , Risk Factors , Schizophrenia/diagnosis , Schizophrenic Psychology , Socioeconomic Factors , Violence/psychology , Violence/statistics & numerical data
5.
Int J Eat Disord ; 35(4): 522-37, 2004 May.
Article in English | MEDLINE | ID: mdl-15101068

ABSTRACT

OBJECTIVE: The aim of the current study was to evaluate whether guided self-help was effective in the short and long term in the treatment of bulimia nervosa. METHOD: Eighty-one patients with bulimia nervosa were randomly assigned to either a self-help manual with a maximum of 18 short weekly visits (guided self-help) or to 18 weekly 1.5-h sessions of cognitive-behavioral group therapy (CBT). The primary outcome variables were monthly frequencies of self-reported binge eating and vomiting episodes. Secondary outcome variables were eating disorder-related psychopathology (assessed with the Eating Disorders Inventory [EDI]) and depression (assessed by the Beck Depression Inventory [BDI]). Patients were followed up 1 year after the end of treatment. RESULTS: A mixed-effects linear regression analysis indicated that subjects in both treatment conditions showed a significant decrease over time in binge eating and vomiting frequencies, in the scores of the EDI subscales, and in the BDI. Both treatment modalities led to a sustained improvement at follow-up. A separate analysis of the completer sample showed significantly higher remission rates in the self-help condition (74%) compared with the CBT condition (44%) at follow-up. CONCLUSIONS: Guided self-help incorporating the use of a self-help manual offers an approach that can be effective in the short and long-term treatment of bulimia nervosa.


Subject(s)
Bulimia/psychology , Bulimia/therapy , Cognitive Behavioral Therapy/methods , Self-Help Groups , Adolescent , Adult , Bulimia/diagnosis , Female , Humans , Patient Compliance , Surveys and Questionnaires
6.
Eur Neuropsychopharmacol ; 13(2): 73-9, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12650949

ABSTRACT

Controlled trials in patients with bulimia nervosa have demonstrated efficacy of antidepressant medications with serotonergic function (e.g. fluoxetine) as well as noradrenergic function (e.g. desipramine). Sixteen out-patients with bulimia nervosa according to DSM-IV criteria were treated in a drug surveillance with 100 mg of milnacipran, a specific serotonin and noradrenaline reuptake inhibitor (SNRI). Ten patients completed the 8-week observation period. The reasons for premature attrition were improvement in one patient (no. 12), a generalized exanthema in one patient (no. 7), severe nausea in one patient (no. 8) and non-compliance due to non-drug-related reasons in three patients (no. 1, 2, and 16). An intent-to-treat analysis exhibited a significant reduction in weekly binge eating and vomiting frequency from baseline to the end of treatment. Three patients stopped binge eating and purging completely during the last week of treatment. Furthermore, there was a concomitant decrease of depression ratings (HAMD, BDI). Our preliminary data give rise to the notion that milnacipran may be promising in the treatment of bulimia nervosa.


Subject(s)
Bulimia/drug therapy , Bulimia/psychology , Cyclopropanes/therapeutic use , Adult , Antidepressive Agents/adverse effects , Antidepressive Agents/pharmacology , Antidepressive Agents/therapeutic use , Cyclopropanes/adverse effects , Cyclopropanes/pharmacology , Feeding Behavior/drug effects , Feeding Behavior/psychology , Female , Humans , Milnacipran , Statistics, Nonparametric
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