Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 14 de 14
Filtrar
1.
Int. braz. j. urol ; 40(4): 463-473, Jul-Aug/2014. tab, graf
Artigo em Inglês | LILACS | ID: lil-723962

RESUMO

Objective To evaluate the influence of polymorphisms in GSTA1, GSTM1, GSTT1, and GSTP1 in the risk of developing Prostate Cancer (PCa) in a population of Rio de Janeiro and compare the distribution of allele and genotype frequencies of the polymorphisms analyzed in the present study population with other regions in the country and different ethnic groups. Materials and Methods We analyzed a sample of the Brazilian population, comprising 196 patients with PCa treated by the urology services of the Brazilian National Cancer Institute (INCA) and Mario Kroeff Hospital (HMK), and 208 male blood donors from the Clementino Fraga Filho Hospital, Federal University of Rio de Janeiro (UFRJ). The polymorphisms were determined in DNA, extracted from peripheral blood leucocytes using the Polymerase Chain Reaction and Restriction Fragment Length Polymorphism (PCR-RFLP). Results Our results showed that the distribution of polymorphisms can vary significantly according to the Brazilian region and ethnic groups. The distribution of allele and genotype frequencies of the polymorphism GSTA1 was statistically different between cases and controls. Genotypes (A / B + B / B) were associated with protection (OR = 0.61, 95 % CI = 0.40-0.92) for PCa in comparison to genotype A / A. Conclusion The distribution of genotype frequencies of the polymorphism GSTA1 was statistically different between the case and control groups (p = 0.023), and the presence of genotypes A / B and B / B suggests a protective role against the risk of PCa compared to genotype A / A. This is the first study that reports the genotypic frequency of this polymorphism and its association with PCa in a Brazilian population sample. .


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Glutationa Transferase/genética , Polimorfismo Genético/genética , Neoplasias da Próstata/genética , Brasil/etnologia , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , Frequência do Gene , Predisposição Genética para Doença , Glutationa S-Transferase pi/genética , Isoenzimas/genética , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Fatores de Risco
2.
Mem. Inst. Oswaldo Cruz ; 107(2): 224-230, Mar. 2012. tab
Artigo em Inglês | LILACS | ID: lil-617069

RESUMO

Severe forms of dengue, such as dengue haemorrhagic fever (DHF) and dengue shock syndrome, are examples of a complex pathogenic mechanism in which the virus, environment and host immune response interact. The influence of the host's genetic predisposition to susceptibility or resistance to infectious diseases has been evidenced in several studies. The association of the human leukocyte antigen gene (HLA) class I alleles with DHF susceptibility or resistance has been reported in ethnically and geographically distinct populations. Due to these ethnic and viral strain differences, associations occur in each population, independently with a specific allele, which most likely explains the associations of several alleles with DHF. As the potential role of HLA alleles in the progression of DHF in Brazilian patients remains unknown, we then identified HLA-A alleles in 67 patients with dengue fever and 42 with DHF from Rio de Janeiro, Brazil, selected from 2002-2008 by the sequence-based typing technique. Statistical analysis revealed an association between the HLA-A*01 allele and DHF [odds ratio (OR) = 2.7, p = 0.01], while analysis of the HLA-A*31 allele (OR = 0.5, p = 0.11) suggested a potential protective role in DHF that should be further investigated. This study provides evidence that HLA class I alleles might be important risk factors for DHF in Brazilian patients.


Assuntos
Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Dengue Grave/genética , Predisposição Genética para Doença/genética , Antígeno HLA-A1/genética , Alelos , Brasil , Estudos de Casos e Controles , Fatores de Risco
3.
Mem. Inst. Oswaldo Cruz ; 106(6): 716-724, Sept. 2011. ilus, tab
Artigo em Inglês | LILACS | ID: lil-602055

RESUMO

Isoniazid (INH), one of the most important drugs used in antituberculosis (anti-TB) treatment, is also the major drug involved in hepatotoxicity. Differences in INH-induced toxicity have been attributed to genetic variability at several loci, such as NAT2, CYP2E1, GSTM1 and GSTT1, that code for drug-metabolising enzymes. Our goal was to examine the polymorphisms in these enzymes as susceptibility factors to anti-TB drug-induced hepatitis in Brazilian individuals. In a case-control design, 167 unrelated active tuberculosis patients from the University Hospital of the Federal University of Rio de Janeiro, Brazil, were enrolled in this study. Patients with a history of anti-TB drug-induced acute hepatitis (cases with an increase to 3 times the upper limit of normal serum transaminases and symptoms of hepatitis) and patients with no evidence of anti-TB hepatic side effects (controls) were genotyped for NAT2, CYP2E1, GSTM1 and GSTT1 polymorphisms. Slow acetylators had a higher incidence of hepatitis than intermediate/rapid acetylators [22 percent (18/82) vs. 9.8 percent (6/61), odds ratio (OR), 2.86, 95 percent confidence interval (CI), 1.06-7.68, p = 0.04). Logistic regression showed that slow acetylation status was the only independent risk factor (OR 3.59, 95 percent CI, 2.53-4.64, p = 0.02) for the occurrence of anti-TB drug-induced hepatitis during anti-TB treatment with INH-containing schemes in Brazilian individuals.


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Antituberculosos/efeitos adversos , Arilamina N-Acetiltransferase/genética , /genética , Doença Hepática Induzida por Substâncias e Drogas/genética , Glutationa Transferase/genética , Isoniazida/efeitos adversos , Polimorfismo Genético , Acetilação , Brasil/etnologia , Estudos de Casos e Controles , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Predisposição Genética para Doença , Genótipo , Fenótipo , Fatores de Risco , Tuberculose Pulmonar/tratamento farmacológico
4.
Arq. bras. cardiol ; 88(4): 447-451, abr. 2007.
Artigo em Português | LILACS | ID: lil-451836

RESUMO

OBJETIVO: Este estudo avaliou a contribuição de seis polimorfismos genéticos presentes em genes do sistema renina-angiotensina-aldosterona (SRAA) e fatores de risco clínicos para o desenvolvimento da hipertensão arterial essencial em um município da região Amazônica. MÉTODOS: Oitenta e dois indivíduos hipertensos e setenta e oito indivíduos normotensos foram genotipados quanto à presença de polimorfismos REN-G1051A (renina), AGT-M235T (angiotensinogênio), ECA-Alu I/D (enzima conversora de angiotensina I), AGTR1-A1166C (receptor tipo 1 da angiotensina II) e CYP11B2-C344T (aldosterona sintetase) pela técnica de reação em cadeia da polimerase (PCR), com análise de restrição quando necessário. A influência de polimorfismos genéticos e fatores de risco clínicos na variação da pressão arterial foi avaliada por meio de regressão linear stepwise. RESULTADOS: Relatamos a co-ocorrência de fatores de risco clínicos e polimorfismo do gene da enzima conversora de angiotensina (ECA) na população de um município da região amazônica. Nossos resultados mostram que a elevação da pressão arterial sistólica é favorecida pelo alelo D do polimorfismo de inserção/deleção do gene da ECA e pelo aumento da idade, enquanto consumo de bebida alcoólica e envelhecimento estão associados ao aumento da pressão arterial diastólica (PAD). CONCLUSÃO: Esses achados indicam que os moradores de Santa Isabel do Rio Negro que possuem o alelo D da ECA ou têm o hábito de beber apresentam valores mais elevados de PAS e PAD, respectivamente, com o passar dos anos.


OBJECTIVE: In the present study, we evaluated the contribution of six genetic polymorphisms of the Renin-Angiotensis-Aldosterone system (RAAS) and clinical risk factors in the development of essential hypertension in a Brazilian rural population in the Amazon region. METHODS: Eighty-two hypertensive patients and seventy-eight normotensive individuals were evaluated. Genotyping for renin (REN G1051A), angiotensinogen (AGT) M235T, insertion/deletion of angiotensin-converting enzyme (ACE I/D), angiotensin II type 1 receptor (AGTR1) A1166C and aldosterone synthase (CYP11B2) C344T polymorphisms were performed using polymerase chain reaction, with further restriction analysis when required. The influence of genetic polymorphisms and clinical risk factors on blood pressure variation was assessed by stepwise linear regression. RESULTS: We report the co-occurrence of clinical risk factors and angiotensin-converting enzyme (ACE) gene polymorphism in a Brazilian rural population in the Amazon region. Our results indicate that increase of systolic blood pressure (SBP) is favored by ACE I/D- D allele and advanced age, while alcohol consumption and aging are associated with high diastolic blood pressure (DBP). CONCLUSION: These findings suggest that in the Santa Isabel do Rio Negro population, the residents that carry ACE-D allele or have an alcohol consumption habit present higher values of SBP and DBP, respectively, with the passing of years.


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Hipertensão/genética , Polimorfismo Genético , Sistema Renina-Angiotensina/genética , Alelos , Brasil , Meio Ambiente , Marcadores Genéticos/genética , Hipertensão/etiologia , Reação em Cadeia da Polimerase , Fatores de Risco , População Rural
5.
Mem. Inst. Oswaldo Cruz ; 102(1): 53-57, Feb. 2007. tab, graf
Artigo em Inglês | LILACS | ID: lil-440632

RESUMO

Campylobacteriosis is an extremely important zoonosis, circulating freely in the environment. In nonhuman primates kept in open facilities and bred for experimental purposes, the presence of Campylobacter spp. could cause severe damage to the production and interfere with the results of scientific research. In this paper, we assessed the circulation of Campylobacter spp. in a colony of clinically healthy rhesus monkeys (Macaca mulatta) destined to research. The analysis was carried out during seven non-consecutive years. Data showed that despite several changes made in animal management along the studied years in order to control this zoonosis, reduction of bacterial charge did not occur. Significant differences among the age groups and sex were observed. Infants showed higher susceptibility than adult animals. In general males were more infected than females. Modifications adopted in the handling techniques need to be reviewed with the intent of improving the production, reducing bacterial infection of the stock and avoiding undesirable cross reactions in the research carried out with these animals. Therefore, this paper alerts professionals that work directly with captive rhesus monkeys about the risks of Campylobacter spp. infection and possible interference on the experimental procedures.


Assuntos
Animais , Masculino , Feminino , Animais de Laboratório/microbiologia , Infecções por Campylobacter/veterinária , Campylobacter/isolamento & purificação , Macaca mulatta/microbiologia , Doenças dos Macacos/microbiologia , Infecções por Campylobacter/diagnóstico , Campylobacter/classificação , Campylobacter/efeitos dos fármacos , Estudos Longitudinais , Testes de Sensibilidade Microbiana , Doenças dos Macacos/diagnóstico
6.
Genet. mol. biol ; 30(1): 1-5, 2007. tab
Artigo em Inglês | LILACS | ID: lil-445674

RESUMO

The enzymes encoded by the polymorphic genes CYP1A1 and CYP2E1 play an important role in the activation and inactivation of xenobiotics. These enzymes have been associated with xenobiotic-induced diseases, such as cancer, therapeutic failure and adverse effects of drugs. The aim of the present study was to determine the allelic and genotypic frequencies of these polymorphisms in a large, ethnically mixed Brazilian population sample from Rio de Janeiro. Polymorphisms CYP1A1 and CYP2E1 were determined in 870 unrelated individuals by PCR-RFLP analysis in peripheral blood DNA. The observed allelic frequencies were 0.90 for CYP1A1*1A and 0.95 for CYP2E1*1A, in the total sample. The allelic frequency of CYP1A1*2C in "pardos" (0.13) and Brazilian whites (0.11) was higher than in Caucasians (0.05), which may be a result of the Amerindian genetic component, that presents the highest frequency of this allele observed up to now. The genotype distributions for both polymorphisms were in Hardy-Weinberg equilibrium and were statistically different between males and females, and among ethnic groups.


Assuntos
Humanos , Masculino , Feminino , Citocromo P-450 CYP1A1 , Citocromo P-450 CYP2E1 , Citocromos a1 , Esteroide 17-alfa-Hidroxilase
7.
Mem. Inst. Oswaldo Cruz ; 101(2): 143-147, Mar. 2006. mapas, tab
Artigo em Inglês | LILACS | ID: lil-430890

RESUMO

Artificial ecotopes of 121 peridomiciliary environments in four rural localities in the state of Ceará, Brazil, were studied and the type of material of the ecotopes was identified as triatomine infestation. Two thousand two hundred and four Triatoma brasiliensis Neiva, 340 Triatoma pseudomaculata Corrêa and Espínola, 121 Rhodnius nasutus Stall, and 5 Panstrongylus lutzi (Neiva and Pinto) were captured. Out of the 323 ecotopes found (X =2.0 ± 1.8 per dwelling) such as pigpens, henhouses, corrals, perches, dovecotes, piles of roofing tiles, bricks, wood, and straw 30.3 percent were infested by triatomines in all different developmental stages, including eggs. A substantial number of triatomines were found in perches, however the largest infestation took place in roofing materials used in the construction of goat/sheep corrals, henhouses, and pigpens, where 98 percent of them were captured: 1372 triatomines were located in the roofing tile covers, 285 in the straw, 187 in the perches, 77 in the coverings of roofing tiles and straw, and 13 in the straw and wood. Among all the different pile of materials, roofing tiles were the most infested (50 percent) followed by bricks (38.9 percent) and woods (36.1 percent). T. brasiliensis colonized mainly brick piles (chi2=16.539; p < 0.05) and roofing tiles (chi2=5,090.58; p < 0.05); T. pseudomaculata preferred wood perches (chi2= 472.39; p < 0.05) and woodpiles (chi2=126.0 p < 0.05), and R. nasutus was principally found in roofing straw (chi2=384.43; p < 0.05). These findings suggest that triatomines tend to colonize peridomiciliary ecotopes similar to their original habitats.


Assuntos
Humanos , Animais , Animais Domésticos/parasitologia , Insetos Vetores/fisiologia , Triatominae/fisiologia , Brasil , Doença de Chagas/transmissão , Insetos Vetores/classificação , População Rural , Triatominae/classificação
8.
Arq. neuropsiquiatr ; 63(1): 145-149, Mar. 2005. tab
Artigo em Português | LILACS | ID: lil-398806

RESUMO

OBJETIVO: Descrever o perfil clínico e laboratorial de pacientes com atrofia muscular espinhal (AME) com deleção no gene da proteína sobrevivência do neurônio motor (SMN). MÉTODO: Estudo descritivo de uma série de casos confirmados pela presença da deleção no gene SMN. Determinação da freqüência da positividade dos critérios clínicos e laboratoriais revisados. RESULTADOS: Foram incluídos no estudo 22 casos. Em todos havia paresia simétrica, sendo a localização difusa predominante nos casos de início antes de 6 meses (75 por cento), enquanto nos demais havia predominância de localização proximal e/ou em membros inferiores (67 por cento). Fasciculações e atrofia foram freqüentes (82 por cento). Os exames complementares tiveram resultados variáveis, sendo a positividade da eletroneuromiografia (ENMG) de 57 por cento e da biopsia muscular de 58 por cento. CONCLUSÃO: A presença de deleção no gene SMN pode ajudar a confirmar o diagnóstico de casos indefinidos .


Assuntos
Feminino , Humanos , Lactente , Masculino , Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/genética , Deleção de Genes , Atrofia Muscular Espinal/diagnóstico , Proteínas do Tecido Nervoso/genética , Proteínas de Ligação a RNA/genética , Idade de Início , Biópsia , Estudos Transversais , Eletromiografia , Atrofia Muscular Espinal/genética , Atrofia Muscular Espinal/patologia
9.
Mem. Inst. Oswaldo Cruz ; 99(6): 584-589, Oct. 2004. tab, graf
Artigo em Inglês | LILACS | ID: lil-387906

RESUMO

Physiological parameters of laboratory animals used for biomedical research is crucial for following several experimental procedures. With the intent to establish baseline biologic parameters for non-human primates held in closed colonies, hematological and morphometric data of captive monkeys were determined. Data of clinically healthy rhesus macaques (Macaca mulatta), cynomolgus monkeys (Macaca fascicularis), and squirrel monkeys (Saimiri sciureus) were collected over a period of five years. Animals were separated according to sex and divided into five age groups. Hematological data were compared with those in the literature by Student's t test. Discrepancies with significance levels of 0.1, 1 or 5 percent were found in the hematological studies. Growth curves showed that the sexual dimorphism of rhesus monkeys appeared at an age of four years. In earlier ages, the differences between sexes could not be distinguished (p < 0.05). Sexual dimorphism in both squirrel monkeys and cynomolgus monkeys occurred at an age of about 32 months. Data presented in this paper could be useful for comparative studies using primates under similar conditions.


Assuntos
Animais , Masculino , Feminino , Macaca fascicularis , Macaca mulatta , Saimiri , Caracteres Sexuais , Biometria
10.
Mem. Inst. Oswaldo Cruz ; 99(3): 263-270, May 2004. mapas, tab
Artigo em Inglês | LILACS | ID: lil-361992

RESUMO

In order to assay the triatomine infestation and domiciliation in the rural area of Jaguaruana district, state of Ceará, Brazil, we studied, from November 2000 to April 2002, 4 localities comprising 158 domiciles as a whole, with an average of 4 inhabitants/house, who are dwelling in there for more than 7 years. Most houses have tile-covered roofs and the walls built with plaster-covered bricks (57 percent), followed by bricks without plaster (33 percent), and mud walls (7.5 percent). A total of 3082 triatomines were captured from different locations, according to the following capture plan: (a) intradomiciles: 238 Triatoma brasiliensis, 6 T. pseudomaculata, 9 Rhodnius nasutus, and 2 Panstrongylus lutzi; (b) peridomiciles (annexes): 2069 T. brasiliensis, 223 T. pseudomaculata, 121 R. nasutus, and 1 P. lutzi; (c) wild, in carnauba palms (Copernicia prunifera): 413 R. nasutus. From the captured triatomines, 1773 (57.5 percent) were examined. The natural index of Trypanosoma cruzi infection ranged from 10.8 percent to 30.2 percent (average of 17 percent), depending on the species and the location from where the triatomines were captured.


Assuntos
Animais , Humanos , Doença de Chagas , Doenças Endêmicas , Habitação , Insetos Vetores , Triatominae , Trypanosoma cruzi , Brasil , Doença de Chagas , Insetos Vetores , Densidade Demográfica , População Rural , Triatominae
11.
Mem. Inst. Oswaldo Cruz ; 97(6): 909-913, Sept. 2002. tab, graf
Artigo em Inglês | LILACS, SES-SP | ID: lil-320153

RESUMO

Samples from 20 lots of diphtheria-tetanus (adult use dT) vaccine and from 20 lots of diphtheria-tetanus-pertussis (DTP) vaccine were used to standardize and validate the in vitro toxin binding inhibition (ToBI) test for the immunogenicity test of the tetanus component. The levels of tetanus antitoxin obtained by ToBI test were compared to those obtained using the toxin neutralization (TN) test in mice routinely employed to perform the quality control of the tetanus component in adsorbed vaccines. The results ranged from 1.8 to 3.5 IU/ml for dT and 2 to 4 IU/ml for DTP by ToBI test and 1.4 to 3 IU/ml for dT and 1.8 to 3.5 IU/ml for DTP by TN in mice. These results were significantly correlated. From this study, it is concluded that the ToBI test is an alternative to the in vivo neutralization procedure in the immunogenicity test of the tetanus component in adsorbed vaccines. A substantial refinement and a reduction in use of animals can be achieved


Assuntos
Animais , Cobaias , Camundongos , Antitoxina Tetânica , Vacina contra Difteria, Tétano e Coqueluche , Vacina contra Difteria e Tétano , Controle de Qualidade , Toxina Tetânica , Testes de Neutralização , Toxoide Diftérico , Antitoxina Tetânica , Toxoide Tetânico , Camundongos Endogâmicos BALB C
12.
Genet. mol. biol ; 23(4): 709-713, Dec. 2000. tab
Artigo em Inglês | LILACS | ID: lil-303636

RESUMO

A distribuiçäo das freqüências fenotípicas do gene GSTM1 de duas amostras brasileiras, compostas de doadores sanguíneos de ambos os sexos com idade entre 18 e 61 anos, foi estudada. A primeira amostra é composta de 658 indivíduos provenientes do Rio de Janeiro e a segunda de 179 indivíduos de Brasília. Os fenótipos da GSTM1 foram determinados utilizando-se a técnica da reaçäo em cadeia da polimerase e subsequente digestäo com a enzima de restriçäo HaeII. As freqüências observadas para o fenótipo GSTM1 nulo foram de 46,4 por cento e 48,6 por cento para as amostras do Rio de Janeiro e Brasília, respectivamente. Os resultados também mostram que a distribuiçäo fenotípica da GSTM1 näo está em equilíbrio de Hardy-Weinberg para ambas as amostras: X²1 = 11,49 (P < 0,001) para o Rio de Janeiro e X²1 = 6,77 (P < 0,01) para Brasília. Este desequilíbrio pode ser atribuído a fatores como seleçäo, erros na determinaçäo fenotípica ou panmixia ainda incompleta da populaçäo brasileira, cujos componentes raciais säo caucasóides, africanos e índios.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Glutationa Transferase , Polimorfismo Genético , Reação em Cadeia da Polimerase , Brasil , Mutação , Fenótipo
13.
Ciênc. cult. (Säo Paulo) ; 38(5): 776-82, maio 1986. tab, ilus
Artigo em Português | LILACS | ID: lil-33972

RESUMO

Uma amostra de 1806 famílias do Nordeste brasileiro foi examinada para se estudar o efeito de diversos parâmetros sócio-econômicos sobre a estrutura reprodutiva dessa populaçäo. Uma análise comparativa dos dados encontrados em relaçäo aos verificados em países de maior desenvolvimento sócio-econômico nos mostra que as condiçöes médico-sanitárias da populaçäo em estudo säo extremamente precárias, e isto se reflete na estrutura da mortalidade, sobretudo na pós-natal. Assim, verificou-se que as taxas de mortalidade pós-natal aumentam na direçäo Sul-Norte, acompanhando a deterioraçäo sócio-econômica que segue o mesmo sentido


Assuntos
Humanos , Mortalidade , Saúde da População Rural , População Rural , Brasil , Fatores Socioeconômicos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA