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2.
Acta Psychiatr Scand ; 140(2): 158-168, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31155713

RESUMO

OBJECTIVE: To evaluate the incidence of suicidal outcomes and risk factors for short- and long-term recurrence of suicidal behavior (SB) among high-risk borderline personality disorder (BPD) patients during a 24-month prospective follow-up period. METHODS: A multicenter prospective cohort study was designed to compare data obtained from 136 patients admitted to the emergency department for current suicidal ideation (SI) or a recent suicide attempt (SA). Subjects were clinically evaluated and monitored for a new SA or suicide. RESULTS: The incidence of a new SA was 25.63 events/100 persons-year, and one patient died by suicide. Child sexual abuse (CSA) was the only significant predictor throughout the complete follow-up period. The absence of prior psychiatric treatment predicts the recurrence of SB in the first 6 months of follow-up. Patient age, poor psychosocial functioning before hospitalization, age at first SA, and having multiple suicide attempts increased risk of SB recurrence at the long-term period (24th months). In addition, there was an interaction between CSA and poor psychosocial functioning that increased risk of SB. CONCLUSION: The risk of recurrence was higher during the first 6 months. Risk factors at 6 and 24 months vary. These findings are important for implementing suicide strategies.


Assuntos
Transtorno da Personalidade Borderline/psicologia , Abuso Sexual na Infância/psicologia , Tentativa de Suicídio/psicologia , Adulto , Argentina/epidemiologia , Transtorno da Personalidade Borderline/epidemiologia , Transtorno da Personalidade Borderline/mortalidade , Estudos de Casos e Controles , Criança , Abuso Sexual na Infância/estatística & dados numéricos , Feminino , Seguimentos , Hospitalização/estatística & dados numéricos , Humanos , Incidência , Estudos Longitudinais , Masculino , Valor Preditivo dos Testes , Estudos Prospectivos , Recidiva , Fatores de Risco , Ideação Suicida
3.
J Affect Disord ; 220: 15-23, 2017 10 01.
Artigo em Inglês | MEDLINE | ID: mdl-28575715

RESUMO

BACKGROUND: Depression is one of the major contributors to the global burden of diseases; however, population-based data in South America are limited. METHODS: We conducted a population-based cross sectional study with 7524 participants, aged 35-74 years old, recruited between February 2010 and December 2011 from randomly selected samples in 4 cities (Bariloche and Marcos Paz, Argentina; Temuco, Chile; and Pando-Barros Blancos, Uruguay). Major Depressive Episode (MDE) was assessed using the Patient Health Questionnaire (PHQ) - 9. RESULTS: The overall prevalence of MDE was 14.6% (95% CI: 13.6, 15.6). However, there was a geographical variability of up to 3.7 folds between different cities being 5.6% (95% CI: 4.6, 6.7) in Marcos Paz, Argentina; 9.5% (95% CI: 8.2, 10.9) in Bariloche, Argentina; 18.1% (95% CI: 16.3, 20.0) in Temuco, Chile, and 18.2 (95% CI: 16.3, 20.2) in Pando-Barros Blancos, Uruguay. The multivariate model showed that, adjusted by location, being female, being between 35 and 44 years old, having experienced at least one stressful life event, currently smoking, and having a history of chronic medical diseases were independently associated with an increased risk of MDE, while having higher education and being married or living with a partner reduced the risk of MDE. LIMITATIONS: These results are representative of the selected cities included in the study. As such extrapolation to the general populations of Argentina, Chile, and Uruguay should be done with caution CONCLUSIONS: This study showed a high prevalence and variability of MDE in the Southern Cone of Latin America.


Assuntos
Transtorno Depressivo Maior/epidemiologia , Adulto , Idoso , Argentina/epidemiologia , Chile/epidemiologia , Doença Crônica , Cidades , Estudos Transversais , Feminino , Geografia , Inquéritos Epidemiológicos , Humanos , América Latina , Masculino , Pessoa de Meia-Idade , Prevalência , Inquéritos e Questionários , Uruguai/epidemiologia
4.
Compr Psychiatry ; 70: 25-31, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27624420

RESUMO

BACKGROUND: Family history of suicidal behavior and suicide are both risk factors for suicide. However, the effects of family history of suicide versus suicide attempts on patient suicidal behavior remain unclear. The aim of the present study was to understand if family history of suicide as compared to family history of suicide attempts or no family history of suicidal behavior evidences different associations with suicidal behavior among psychiatric patients. METHOD: Participants included 157 female patients between the ages of 18 and 65years admitted at the Dr. Braulio A. Moyano Neuropsychiatric Women's Hospital. RESULTS: Seventy-nine patients (50.3%) reported no family history of suicidal behavior (NFHSB), while 78 patients (49.7%) reported a family history of suicidal behavior. Specifically, 41 patients (26.1%) reported a family history of suicide attempt (FHSA) and 37 patients (23.6%) reported a family history of suicide (FHS). These groups showed significant differences between family history of psychopathology and number of previous suicide attempts. Patients with an FHSA were more likely to present with a greater number of previous suicide attempts as compared to patients with NFHSB and FHS. CONCLUSION: There is an association between the number of suicide attempts and family history of suicide attempts in female patients hospitalized for suicidal behavior.


Assuntos
Saúde da Família , Ideação Suicida , Tentativa de Suicídio/psicologia , Suicídio/psicologia , Adolescente , Adulto , Idoso , Feminino , Humanos , Pessoa de Meia-Idade , Fatores de Risco , Adulto Jovem
5.
Naunyn Schmiedebergs Arch Pharmacol ; 364(2): 149-56, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11534854

RESUMO

In isolated human umbilical vein (HUV), the contractile response to des-Arg9-bradykinin (des-Arg9-BK), selective BK B1 receptor agonist, increases as a function of the incubation time. Here, we evaluated whether cyclooxygenase (COX) pathway is involved in BK B1-sensitized response obtained in 5-h incubated HUV rings. The effect of different concentrations of indomethacin, sodium salicylate, ibuprofen, meloxicam, lysine clonixinate or NS-398 administrated 30 min before concentration-response curves (CRC) was studied. All treatments produced a significant rightward shift of the CRC to des-Arg9-BK in a concentration-dependent manner, which provides pharmacological evidence that COX pathway is involved in the BK B1 responses. Moreover, in this tissue, the NS-398 pKb (5.2) observed suggests that COX-2 pathway is the most relevant. The strong correlation between published pIC50 for COX-2 and the NSAIDs' pKbs estimated further supports the hypothesis that COX-2 metabolites are involved in BK B1 receptor-mediated responses. In other rings, indomethacin (30, 100 micromol/l) or NS-398 (10, 30 micromol/l) produced a significant rightward shift of the CRC to BK, selective BK B2 agonist, and its pKbs were similar to the values to inhibit BK B1 receptor responses, suggesting that COX-2 pathway also is involved in BK B2 receptor responses. Western blot analysis shows that COX-1 and COX-2 isoenzymes are present before and after 5-h in vitro incubation and apparently COX-2 does not suffer additional induction.


Assuntos
Bradicinina/análogos & derivados , Isoenzimas/fisiologia , Prostaglandina-Endoperóxido Sintases/fisiologia , Receptores da Bradicinina/fisiologia , Transdução de Sinais/fisiologia , Veias Umbilicais/enzimologia , Anti-Inflamatórios não Esteroides/farmacologia , Bradicinina/farmacologia , Ciclo-Oxigenase 2 , Relação Dose-Resposta a Droga , Humanos , Contração Isométrica/efeitos dos fármacos , Contração Isométrica/fisiologia , Proteínas de Membrana , Técnicas de Cultura de Órgãos , Receptor B1 da Bradicinina , Receptor B2 da Bradicinina , Receptores da Bradicinina/agonistas , Transdução de Sinais/efeitos dos fármacos , Veias Umbilicais/efeitos dos fármacos , Veias Umbilicais/metabolismo , Vasoconstrição/efeitos dos fármacos , Vasoconstrição/fisiologia
6.
J Pharmacol Exp Ther ; 290(3): 1019-25, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10454473

RESUMO

Previous reports have provided evidence to support the view that the de novo synthesis of bradykinin (BK) B(1) receptor is involved in the induction of vascular responses in human umbilical vein (HUV). In the present study, we evaluated different pharmacological tools to further analyze this up-regulation process in HUV. Concentration-response curves to des-Arg(9)-BK, a selective BK B(1) receptor agonist, were performed after 5 h of incubation. Tumor necrosis factor-alpha potentiated BK B(1) receptor responses at 5 h without modifying the maximal response to des-Arg(9)-BK. Pyrrolidine dithiocarbamate, an inhibitor of nuclear factor-kappaB activation, produced a concentration-dependent decrease of the BK B(1) receptor sensitization. When tissues were continuously exposed to actinomycin D, a transcription inhibitor, or cycloheximide, a protein synthesis inhibitor, concentration-response curves to des-Arg(9)-BK were markedly diminished. On the other hand, transitory exposure to cycloheximide allowed the full recovery of BK B(1) receptor-sensitized responses at 5 h. Finally, continuous incubation with the N-linked glycosylation inhibitor, tunicamycin, almost completely abolished des-Arg(9)-BK-mediated responses. In summary, this sensitization process is potentiated by tumor necrosis factor-alpha and is selectively inhibited by pyrrolidine dithiocarbamate, suggesting that BK B(1) receptor up-regulation in HUV involves nuclear factor-kappaB activation. The effects of actinomycin D and tunicamycin provide evidence that the de novo synthesis of a transmembrane glycoprotein has an obligatory role in the BK B(1) up-regulation. The reversion of the cycloheximide effect on BK B(1) response indicates that the time necessary for synthesis, trafficking, and functional membrane expression of this receptor would be less than 1 h.


Assuntos
Receptores da Bradicinina/biossíntese , Veias Umbilicais/efeitos dos fármacos , Veias Umbilicais/metabolismo , Antineoplásicos/farmacologia , Cicloeximida/farmacologia , Dactinomicina/análogos & derivados , Dactinomicina/farmacologia , Relação Dose-Resposta a Droga , Sinergismo Farmacológico , Feminino , Humanos , Técnicas In Vitro , Gravidez , Pirrolidinas/farmacologia , Receptor B1 da Bradicinina , Receptores da Bradicinina/agonistas , Receptores da Bradicinina/metabolismo , Proteínas Recombinantes/farmacologia , Tiocarbamatos/farmacologia , Fator de Necrose Tumoral alfa/farmacologia , Tunicamicina/farmacologia , Regulação para Cima/efeitos dos fármacos
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