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1.
Eur Eat Disord Rev ; 23(2): 163-9, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25448409

RESUMO

OBJECTIVE: Technology assisted guided self-help has been proven to be effective in the treatment of bulimia nervosa (BN). The aim of this study was to determine predictors of good long-term outcome as well as drop-out, in order to identify patients for whom these interventions are most suitable. METHODS: One hundred and fifty six patients with BN were assigned to either 7 months internet-based guided self-help (INT-GSH) or to conventional guided bibliotherapy (BIB-GSH), both guided by e-mail support. Evaluations were taken at baseline, after 4, 7, and 18 months. As potential predictors, psychiatric comorbidity, personality features, and eating disorder psychopathology were considered. RESULTS: Higher motivation, lower frequency of binge eating, and lower body dissatisfaction at baseline predicted good outcome after the end of treatment. Lower frequency of binge eating predicted good outcome at long-term follow-up. Factors prediciting drop-out were higher depression and lower self-directedness at baseline. CONCLUSION: Technology assisted self-help can be recommended for patients with a high motivation to change, lower binge-eating frequency and lower depression scores.


Assuntos
Transtorno da Compulsão Alimentar/terapia , Bulimia Nervosa/terapia , Bulimia/terapia , Terapia Cognitivo-Comportamental/métodos , Avaliação de Resultados em Cuidados de Saúde/estatística & dados numéricos , Autocuidado/métodos , Terapia Assistida por Computador , Adulto , Biblioterapia , Transtorno da Compulsão Alimentar/psicologia , Imagem Corporal , Bulimia/psicologia , Bulimia Nervosa/psicologia , Depressão/psicologia , Depressão/terapia , Correio Eletrônico , Feminino , Humanos , Internet , Masculino , Pessoa de Meia-Idade , Motivação , Pacientes Desistentes do Tratamento , Fenótipo , Psicopatologia , Inquéritos e Questionários
2.
Br J Psychiatry ; 202: 135-41, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23222037

RESUMO

BACKGROUND: Cognitive-behavioural therapy (CBT)-based guided self-help is recommended as a first step in the treatment of bulimia nervosa. AIMS: To evaluate in a randomised controlled trial (Clinicaltrials.gov registration number: NCT00461071) the long-term effectiveness of internet-based guided self-help (INT-GSH) compared with conventional guided bibliotherapy (BIB-GSH) in females with bulimia nervosa. METHOD: A total of 155 participants were randomly assigned to INT-GSH or BIB-GSH for 7 months. Outcomes were assessed at baseline, month 4, month 7 and month 18. RESULTS: The greatest improvement was reported after 4 months with a continued reduction in eating disorder symptomatology reported at month 7 and 18. After 18 months, 14.6% (n = 7/48) of the participants in the INT-GSH group and 25% (n = 7/28) in the BIB-GSH group were abstinent from binge eating and compensatory measures, 43.8% (n = 21/48) and 39.2% (n = 11/28) respectively were in remission. No differences regarding outcome between the two groups were found. CONCLUSIONS: Internet-based guided self-help for bulimia nervosa was not superior compared with bibliotherapy, the gold standard of self-help. Improvements remain stable in the long term.


Assuntos
Bulimia Nervosa/terapia , Terapia Cognitivo-Comportamental/métodos , Avaliação de Resultados em Cuidados de Saúde/estatística & dados numéricos , Autocuidado/métodos , Terapia Assistida por Computador , Adolescente , Adulto , Biblioterapia , Bulimia/prevenção & controle , Bulimia Nervosa/psicologia , Feminino , Seguimentos , Humanos , Internet , Modelos Lineares , Pacientes Desistentes do Tratamento , Indução de Remissão/métodos , Vômito/prevenção & controle , Adulto Jovem
3.
Addict Biol ; 14(2): 227-37, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19291011

RESUMO

Hepatitis C viral (HCV) infection is present in 30 to 98% of intravenous drug users. Intravenous substance abuse represents the main route of HCV transmission in industrialized countries. A multi-centre, randomized, controlled, prospective study assessed sustained virological response (SVR), adverse events such as depressive episodes and retention rate of HCV treatment in opioid-dependent patients. Stabilized, opioid-dependent patients with chronic HCV infection (genotype 2 or 3) received pegylated interferon alpha-2a in combination with ribavirin 800 mg/day (Group A) or 400 mg/day (Group B). Participants were randomized, blocked and stratified by genotype and viral load. A standardized psychiatric assessment, Beck Depression Inventory (BDI) and Van Zerssen's list of complaints were administered at each study visit. In 31 months, 300 opioid-dependent patients were screened; 190 (63.3%) were hepatitis C antibody positive. According to study protocol, out of 75 'potential-to-treat' patients with genotype 2 or 3, 17 stable patients (22.6%) were included in the study. All participants completed the study. Significant haemoglobin decreases occurred in both Groups A (P = 0.001) and B (P = 0.011). All the patients had an end-of-treatment (week 24) HCV RNA negativity. Fifteen (88.2%) achieved SVR at week 48. Overall, 52.9% developed depressive symptoms during treatment. Because of the prompt initiation of antidepressant medication at first appearance of depressive symptoms, no severe depressive episodes occurred. Our data show a high retention rate and reliability, and good viral response for both treatments. Hepatitis C treatment in stable opioid-dependent patients was efficacious, suggesting that addiction clinics can offer antiviral therapy in combination with agonistic treatment as part of multi-disciplinary treatment.


Assuntos
Antivirais/uso terapêutico , Hepatite C/tratamento farmacológico , Hepatite C/epidemiologia , Interferon-alfa/uso terapêutico , Transtornos Relacionados ao Uso de Opioides/epidemiologia , Polietilenoglicóis/uso terapêutico , Retenção Psicológica , Ribavirina/uso terapêutico , Adolescente , Adulto , Idoso , Doença Crônica , Feminino , Genótipo , Hepatite C/genética , Humanos , Interferon alfa-2 , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Proteínas Recombinantes , Adulto Jovem
4.
Ann Neurol ; 61(6): 574-8, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17474108

RESUMO

OBJECTIVE: As dopamine plays an important role in the pathophysiology of migraine and antimigraine drugs have an effect on the dopamine system, the objective of this study was to examine the dopamine D4 receptor gene for involvement in the cause of migraine. METHODS: We tested a VNTR-polymorphism in the dopamine D4 receptor gene, the exon 3 VNTR, in a sample of 190 family trios each with a proband with childhood migraine by using transmission disequilibrium test tests. RESULTS: We found a trend for transmission distortion of this marker in migraine, with the common seven-repeat allele of the VNTR transmitted 58 times and not transmitted 82 times (global likelihood ratio score (LRS) = 12.27, degress of freedom (DF) = 6, p = 0.06; for the 7-repeat allele: chi(2) = 5.1, p = 0.02). This effect came only from migraine without aura (145 trios), with the common 7-repeat allele transmitted 45 times and not transmitted 69 times (global LRS = 15.18; DF = 6, p = 0.019; for the 7-repeat allele: chi(2) = 6.4, p = 0.01; odds ratio, 0.47), whereas in migraine with aura (45 trios) there was no transmission distortion of the 7-repeat allele. INTERPRETATION: We conclude that seven-repeat allele of the dopamine D4 receptor VNTR is a protective factor for migraine without aura. Because migraine is a common disorder, this protective effect may have contributed to the positive selection acting on the dopamine D4 receptor exon 3 VNTR seven-repeat allele in recent human history. We speculate that dopamine function in the lateral parabrachial nucleus is involved in migraine without aura.


Assuntos
Alelos , Predisposição Genética para Doença , Enxaqueca sem Aura/genética , Repetições Minissatélites/genética , Receptores de Dopamina D4/genética , Adolescente , Adulto , Criança , Éxons/genética , Feminino , Frequência do Gene , Humanos , Masculino
5.
J Bacteriol ; 184(11): 3114-21, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12003954

RESUMO

The archaeon Haloferax volcanii was previously shown to contain and transcribe the genes for a 2-oxo acid dehydrogenase (OADH) complex, but their presence remained a mystery because no enzymatic activity with any of the known OADH substrates could be found, and an inactivation of one of the genes did not lead to any phenotype. Here we report the identification of an additional oadh gene cluster in the genome of H. volcanii. In contrast to previously known oadh loci, it contains three genes, oadh2A1, oadh2A2, and oadh2ld, with coding capacity for the E1alpha and E1beta subunits and an unattached lipoyl domain, but it is devoid of the genes for a complete E2 and an E3. The genes were isolated by complementation of a nitrate respiration-deficient mutant of H. volcanii and therefore were shown to be functional in vivo. Phylogenetic analyses revealed that the deduced E1alpha and E1beta subunits of OADH2 group with bacterial acetoin dehydrogenases but not with the OADH1 subunits, and thus, H. volcanii has obtained the two gene groups independently. Comparison of the wild type and the mutant allowed us to exclude a function of OADH2 in the aerobic or anaerobic degradation of acetoin or glucose. Instead, it could be shown that OADH2 is important during nitrate-respirative growth on Casamino Acids. Many physiological and biochemical experiments failed to indicate that OADH2 uses any of the previously known OADH substrates. Growth potentials of the mutant were markedly different in media with a single carbon source versus media with mixed carbon sources.


Assuntos
Haloferax volcanii/enzimologia , Cetona Oxirredutases/metabolismo , Complexos Multienzimáticos/metabolismo , 3-Metil-2-Oxobutanoato Desidrogenase (Lipoamida) , Acetoína/metabolismo , Aminoácidos/metabolismo , Sequência de Bases , Glucose/metabolismo , Haloferax volcanii/crescimento & desenvolvimento , Cetona Oxirredutases/classificação , Cetona Oxirredutases/genética , Dados de Sequência Molecular , Complexos Multienzimáticos/classificação , Complexos Multienzimáticos/genética , Família Multigênica , Mutação , Nitratos/metabolismo , Oxirredução , Filogenia
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