Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Int J Obes (Lond) ; 31(12): 1859-63, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17684509

RESUMO

BACKGROUND: The mechanisms underlying food choices are complex and involve neuroendocrine and biochemical signaling. Among neuroendocrine signals, leptin may play a prominent role in food preference. OBJECTIVE: This study was designed to obtain an understanding of the effects of leptin replacement on macro- and micronutrient preferences in leptin-deficient adults. DESIGN: We studied the effects of leptin replacement on three adults with genetic leptin deficiency during the initial 12 months of treatment. Dietary intake was measured in our study by weighed food consumption records. Nutrient intake was calculated using a nutrition analysis software. RESULTS: After leptin replacement was started, all patients had initially a marked reduction in food intake. The reduction in caloric intake differentially affected intake of macro- and micronutrients. There was an initial shift toward a higher percentage consumption of fats and a decrease in the intake of carbohydrates. Significant differences also occurred in 7 distinct types of macronutrients, 12 vitamins, 11 minerals and 1 amino acid. CONCLUSIONS: We documented several specific leptin-induced changes in macro- and micronutrients intake during the course of leptin-replacement treatment, the majority of which were not related to the decrease in total caloric consumption.


Assuntos
Carboidratos da Dieta/administração & dosagem , Gorduras na Dieta/administração & dosagem , Proteínas Alimentares/administração & dosagem , Preferências Alimentares/fisiologia , Leptina/deficiência , Micronutrientes/administração & dosagem , Análise de Variância , Registros de Dieta , Ingestão de Energia , Feminino , Humanos , Leptina/genética , Leptina/metabolismo , Masculino , Valor Nutritivo , Saciação/efeitos dos fármacos , Fatores de Tempo
2.
Braz J Med Biol Res ; 34(10): 1303-7, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11593305

RESUMO

Mirtazapine is an antidepressant whose side effect profile differs from that of first-line agents (selective serotonin reuptake inhibitors) used in the treatment of panic disorder. The present study compared the effect of mirtazapine and fluoxetine in the treatment of panic disorder in a double-blind, randomized, flexible-dose trial conducted with outpatients. After a 1-week single-blind placebo run-in, 27 patients entered an 8-week double-blind phase in which they were randomly assigned to treatment with either mirtazapine or fluoxetine. Both groups improved significantly in all but one efficacy measure (P < or = 0.01). ANOVA showed no significant differences between the two treatment groups in number of panic attacks, Hamilton Anxiety Scale or Sheehan Phobic Scale, whereas measures of patient global evaluation of phobic anxiety were significantly different between groups (F1,20 = 6.91, P = 0.016) favoring mirtazapine. For the 22 patients who completed the study, the mean daily dose of mirtazapine was 18.3 +/- 1.3 vs 14.0 +/- 1.0 mg for fluoxetine at the endpoint. Weight gain occurred more frequently in the mirtazapine group (50 vs 7.7%, P = 0.04) and nausea and paresthesia occurred more often in the fluoxetine group (P = 0.01). Results suggest that mirtazapine has properties that make it attractive for the treatment of panic disorder.


Assuntos
Antidepressivos Tricíclicos/uso terapêutico , Fluoxetina/uso terapêutico , Mianserina/análogos & derivados , Mianserina/uso terapêutico , Transtorno de Pânico/tratamento farmacológico , Inibidores Seletivos de Recaptação de Serotonina/uso terapêutico , Adolescente , Adulto , Análise de Variância , Antidepressivos Tricíclicos/efeitos adversos , Método Duplo-Cego , Feminino , Fluoxetina/efeitos adversos , Humanos , Masculino , Mianserina/efeitos adversos , Mirtazapina , Inibidores Seletivos de Recaptação de Serotonina/efeitos adversos
3.
Braz. j. med. biol. res ; 34(10): 1303-1307, Oct. 2001. tab
Artigo em Inglês | LILACS | ID: lil-299844

RESUMO

Mirtazapine is an antidepressant whose side effect profile differs from that of first-line agents (selective serotonin reuptake inhibitors) used in the treatment of panic disorder. The present study compared the effect of mirtazapine and fluoxetine in the treatment of panic disorder in a double-blind, randomized, flexible-dose trial conducted with outpatients. After a 1-week single-blind placebo run-in, 27 patients entered an 8-week double-blind phase in which they were randomly assigned to treatment with either mirtazapine or fluoxetine. Both groups improved significantly in all but one efficacy measure (P<=0.01). ANOVA showed no significant differences between the two treatment groups in number of panic attacks, Hamilton Anxiety Scale or Sheehan Phobic Scale, whereas measures of patient global evaluation of phobic anxiety were significantly different between groups (F1,20 = 6.91, P = 0.016) favoring mirtazapine. For the 22 patients who completed the study, the mean daily dose of mirtazapine was 18.3 + or - 1.3 vs 14.0 + or - 1.0 mg for fluoxetine at the endpoint. Weight gain occurred more frequently in the mirtazapine group (50 vs 7.7 percent, P = 0.04) and nausea and paresthesia occurred more often in the fluoxetine group (P = 0.01). Results suggest that mirtazapine has properties that make it attractive for the treatment of panic disorder


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Antidepressivos Tricíclicos , Fluoxetina , Mianserina , Transtorno de Pânico , Inibidores Seletivos de Recaptação de Serotonina , Análise de Variância , Antidepressivos Tricíclicos , Método Duplo-Cego , Fluoxetina , Mianserina , Inibidores Seletivos de Recaptação de Serotonina
4.
Subst Use Misuse ; 36(8): 1053-69, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11504152

RESUMO

Benzodiazepines are among the most prescribed and consumed medication groups in the world. Although benzodiazepines are used in the treatment of several psychiatric and non-psychiatric disorders, and are generally safe and well-tolerated, the potential for misuse and abuse is considerable. This makes the study and regulation of benzodiazepine prescription and consumption an item of concern in public health around the world. Most developed countries have consistent data of benzodiazepine sales and consumption; however, data from developing countries is scarce, making health policies on the use of benzodiazepines a much tougher issue in these countries. This article aims to review the epidemiology of benzodiazepine use in Brazil, as well as to analyze how legislation, physician misinformation and economic factors might contribute to making benzodiazepine abuse a problem in the country.


Assuntos
Ansiolíticos/efeitos adversos , Ansiolíticos/uso terapêutico , Medicamentos sem Prescrição/efeitos adversos , Medicamentos sem Prescrição/uso terapêutico , Transtornos Relacionados ao Uso de Substâncias/psicologia , Benzodiazepinas , Brasil , Países em Desenvolvimento , Monitoramento de Medicamentos/psicologia , Prescrições de Medicamentos , Feminino , Humanos , Masculino , Fatores de Tempo
5.
J Pediatr Gastroenterol Nutr ; 31(4): 371-6, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11045832

RESUMO

BACKGROUND: Visual evoked potentials (VEPs) and brain stem auditory evoked potentials (BAEPs) have been proposed as tools in the diagnosis of subclinical hepatic encephalopathy (HE). However, little information exists to determine their usefulness in pediatric patients. This study was undertaken to evaluate both methods in the detection of subclinical HE in pediatric liver transplant candidates. METHODS: VEPs and BAEPs were recorded in 15 pediatric liver transplant candidates with no clinical signs of HE. The wave latencies found in these examinations were then compared with those in 16 healthy controls of similar age. Laboratory data on liver function and electroencephalographic data from the patients were also recorded to examine their correlation with the evoked potentials results. RESULTS: No differences were found in the BAEP results between patients and controls. However, in the VEPs, the liver transplant candidates had significantly prolonged N1 (N75) latencies when compared with controls; no significant delay was found in the other waves. In contrast, among the children with liver disease, higher BAEP peak latencies correlated positively with electroencephalographic abnormalities, but this correlation was not observed in VEPs. CONCLUSIONS: Evoked potentials might be of use in detecting alterations related to HE in children. However, further studies are necessary to determine their sensitivity and specificity in this situation.


Assuntos
Potenciais Evocados Auditivos do Tronco Encefálico , Potenciais Evocados Visuais , Encefalopatia Hepática/diagnóstico , Transplante de Fígado , Adolescente , Criança , Pré-Escolar , Eletroencefalografia/métodos , Potenciais Evocados Auditivos do Tronco Encefálico/fisiologia , Potenciais Evocados Visuais/fisiologia , Feminino , Encefalopatia Hepática/fisiopatologia , Humanos , Testes de Função Hepática , Masculino
6.
Am J Gastroenterol ; 95(7): 1661-8, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10925965

RESUMO

OBJECTIVE: The term Barrett's esophagus refers to a premalignant condition that is characterized by the replacement of the esophageal squamous mucosa by a columnar-lined one. Preliminary studies have demonstrated reversal of Barrett's mucosa after endoscopic coagulation with different techniques associated with acid inhibition. However, most of these studies have shown that residual Barrett's glands are found underneath the new squamous epithelium in up to 40% of patients. The goal of our study is to verify whether complete restoration of Barrett's mucosa can be achieved by the combination of high power setting argon plasma coagulation and omeprazole. METHODS: A total of 33 patients (mean age: 55.2 yr, range: 21-84 yr; 21 men and 12 women) with histologically demonstrated Barrett's esophagus (mean length: 4.05 cm, range: 0.5-7 cm) were treated. Fourteen cases presented with low-grade dysplasia and one with high-grade dysplasia. All of the extent, or until a maximum of 4 cm, of the Barrett's mucosa was cauterized in each session using argon beam coagulation at a power setting of 65-70 W. All patients received 60 mg omeprazole during the treatment period. RESULTS: Complete restoration of squamous mucosa was obtained in all 33 cases after a mean of 1.96 sessions (range, 1-4). Endoscopic results were histologically confirmed. Nineteen (57.5%) patients experienced moderate to severe chest pain and odyno-dysphagia lasting for 3-10 days after the procedure. Five of these cases experienced high fever and a small volume of pleural effusion, and three patients developed esophageal strictures that needed to be dilated. Another patient developed pneumomediastinum and subcutaneous emphysema without evidences of perforation. After a mean follow-up of 10.6 months there was one endoscopic, as well as histological, recurrence of Barrett's mucosa in a patient with an ineffective laparoscopic fundoplication. CONCLUSIONS: High power setting argon plasma coagulation combined with intensive acid suppression is an effective treatment for the total endoscopic ablation of Barrett's esophagus, at least in the short term. Long-term follow-up of treated patients in whom gastroesophageal reflux is surgically or medically alleviated seems mandatory before drawing definitive conclusions about this therapy.


Assuntos
Esôfago de Barrett/cirurgia , Fotocoagulação a Laser/métodos , Adulto , Idoso , Idoso de 80 Anos ou mais , Antiulcerosos/uso terapêutico , Argônio , Esôfago de Barrett/tratamento farmacológico , Esôfago de Barrett/patologia , Terapia Combinada , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Omeprazol/uso terapêutico , Cuidados Pós-Operatórios , Complicações Pós-Operatórias/epidemiologia
7.
J Psychopharmacol ; 14(2): 157-63, 2000 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10890310

RESUMO

Acute tryptophan depletion (ATD) studies have been used to assess the role of the serotonergic system in various aspects of human behaviour. Changes in mood have already been described in selected groups of individuals submitted to ATD. The present study was a randomized, double-blind, cross-over trial designed to evaluate the effects of ATD on mood, memory, attention and induced anxiety in normal male volunteers. Twelve healthy male volunteers were submitted to two separate sessions of ATD, 1 week apart. Drinks containing either a balanced mixture of amino acids (B) or a similar mixture devoid of tryptophan (T-) were administered in each session. Mood was assessed using self-rating scales. Attention and memory were assessed using a battery of psychological tests. Anxiety induction was carried out using a simulation of public speaking. Blood levels of tryptophan were assessed before and after the B and T- drinks. Results showed that ATD markedly decreased plasma tryptophan (p < 0.0001). Mood ratings, memory and attention were not changed by the T- drink. There was no difference among the anxiety levels measured under T- or B mixtures. These data supports the notion that ATD does not change mood and cognitive function in healthy subjects.


Assuntos
Comportamento/fisiologia , Triptofano/fisiologia , Adulto , Afeto/efeitos dos fármacos , Ansiedade/psicologia , Atenção/efeitos dos fármacos , Estudos Cross-Over , Dieta , Método Duplo-Cego , Emoções/efeitos dos fármacos , Humanos , Masculino , Memória/efeitos dos fármacos , Escalas de Graduação Psiquiátrica , Triptofano/sangue
8.
Behav Pharmacol ; 11(2): 169-73, 2000 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-10877122

RESUMO

This report describes the effects of the antiepileptic agent gabapentin on anxiety and memory. Male Wistar rats received intraperitoneal administrations of gabapentin (10, 30 and 100mg/kg), diazepam (1 mg/kg), saline or diazepam vehicle 30 minutes prior to experimental procedures. Animals were: (1) tested on step-down inhibitory avoidance (footshock 0.3 mA) and habituation to an open-field for memory assessment; and (2) submitted to the elevated plus-maze to evaluate the potential anxiolytic effects of gabapentin. Animals treated with gabapentin showed a reduction in anxiety similar to that observed in animals treated with diazepam. Memory was not affected by gabapentin in any of the tests, but was impaired by diazepam. The lack of effects of gabapentin on memory suggest a potential advantage of this drug over compounds with previously known anxiolytic property, which have amnesic effects at doses used for the treatment of anxiety disorders.


Assuntos
Acetatos/farmacologia , Aminas , Amnésia/induzido quimicamente , Ansiolíticos/farmacologia , Anticonvulsivantes/farmacologia , Ácidos Cicloexanocarboxílicos , Ácido gama-Aminobutírico , Amnésia/psicologia , Animais , Aprendizagem da Esquiva/efeitos dos fármacos , Gabapentina , Masculino , Memória/efeitos dos fármacos , Ratos , Ratos Wistar
9.
Hepatogastroenterology ; 47(36): 1522-5, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11148992

RESUMO

BACKGROUND/AIMS: The introduction of laparoscopic cholecystectomy has increased the need for preoperative diagnosis of common bile duct stones. The purpose of this study is to verify the sensitivity of the liver function tests in the detection of duct stones. METHODOLOGY: We evaluated 438 patients (223 retrospectively and 215 prospectively) who underwent endoscopic papillotomy for bile duct stones in two different services. In every case, blood samples for liver function tests levels were collected prior to endoscopic retrograde cholangiopancreatography. RESULTS: The most sensitive test was gamma-glutamyl transpeptidase, that was abnormal in 92.2% of the cases. Alkaline phosphatase was elevated in 74.7% of the patients with choledocholithiasis. The least sensitive parameter was AST, altered in only 50.8% of times. The sensitivity of all liver tests for the diagnosis of choledochal stones taken together was 94.3%. CONCLUSIONS: Liver function tests are very sensitive in the detection of common bile duct stones, however these blood tests are in the normal range of about 5% of endoscopically treated patients.


Assuntos
Ensaios Enzimáticos Clínicos , Cálculos Biliares/diagnóstico , Cálculos Biliares/enzimologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Fosfatase Alcalina/sangue , Biomarcadores/sangue , Feminino , Cálculos Biliares/sangue , Cálculos Biliares/cirurgia , Humanos , Fígado/enzimologia , Testes de Função Hepática , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Sensibilidade e Especificidade , Esfinterotomia Endoscópica , gama-Glutamiltransferase/sangue
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA