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1.
J Appl Microbiol ; 111(1): 224-32, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21496189

RESUMO

AIMS: To investigate the distribution of the genes that encode enterotoxins and the colonization factors (CF) types as well as the antibiotic susceptibility profile of enterotoxigenic Escherichia coli (ETEC) isolated from children from the Brazilian Northeast. METHODS AND RESULTS: We conducted a 3·5-year prospective study that involved 250 children with and 150 without diarrhoea, aged 1-60 months, from low-income families in Teresina/Brazilian Northeast. All samples were assayed for E. coli, enterotoxin and CF genes and antimicrobial susceptibility by microbiological methods and PCR. ETEC strains were isolated from 9·2% children with and 4·0% without diarrhoea. Infection was more common in children aged 6-24 months in rainy months. elt⁺ /CFA/IV⁺ and elt⁺ /CS14⁺ were the most frequent genotypes. Susceptibility to nalidixic acid, ciprofloxacin and gentamicin and resistance to ampicillin, cephalothin and sulfamethoxazole-trimethoprim were common. CONCLUSIONS: elt ⁺isolates and ETEC strains harbouring genes encoding CFA/IV and CS/14 were the most common ETEC found in Brazilian Northeast. SIGNIFICANCE AND IMPACT OF THE STUDY: Our data, the first generated for north-eastern Brazilian children, may be important for the development of an effective vaccine and for facilitation of an empirical choice of antibiotic treatment or prophylaxis for traveller's diarrhoea in the area studied.


Assuntos
Diarreia/microbiologia , Escherichia coli Enterotoxigênica/isolamento & purificação , Infecções por Escherichia coli/microbiologia , Toxinas Bacterianas/genética , Brasil , Pré-Escolar , Diarreia/tratamento farmacológico , Diarreia Infantil/tratamento farmacológico , Diarreia Infantil/microbiologia , Escherichia coli Enterotoxigênica/efeitos dos fármacos , Escherichia coli Enterotoxigênica/genética , Escherichia coli Enterotoxigênica/patogenicidade , Infecções por Escherichia coli/tratamento farmacológico , Proteínas de Escherichia coli/genética , Feminino , Humanos , Lactente , Masculino , Estudos Prospectivos , Combinação Trimetoprima e Sulfametoxazol/uso terapêutico , Fatores de Virulência/genética
2.
Braz. j. med. biol. res ; 35(1): 31-38, Jan. 2002. ilus, tab
Artigo em Inglês | LILACS | ID: lil-304190

RESUMO

The objective of the present study was to determine the possible prognostic factors which may explain the difference in the survival of patients with cystic fibrosis (CF) with and without meconium ileus. Over a period of 20 years, 127 patients with CF, whose diagnosis was confirmed by typical clinical characteristics and altered sweat chloride levels, were studied retrospectively. The patients were divided into two groups: group 1 consisted of patients who presented CF and meconium ileus (N = 9), and group 2 consisted of patients with CF without meconium ileus (N = 118). The characteristics studied were based on data obtained upon admission of the patients using a specific protocol. Demographic, clinical, nutritional and laboratory data were obtained. The genotype was determined in 106 patients by PCR. Survival was analyzed using the Kaplan-Meier method. The median follow-up period was 44 months. A statistically significant difference was observed between the groups studied regarding the following variables: age at diagnosis and weight and height z scores. The presence of meconium ileus was associated with an earlier diagnosis; these patients had greater deficits in height and weight at the time of diagnosis and at the end of the study. The estimated probability of survival for patients with CF without meconium ileus was 62 ± 14 percent and for those with meconium ileus 32 ± 18 percent. Patients with CF and meconium ileus presented a poor nutritional status at diagnosis and a lower survival rate compared to the general CF population


Assuntos
Humanos , Feminino , Masculino , Recém-Nascido , Lactente , Fibrose Cística/complicações , Mecônio , Obstrução Intestinal/etiologia , Distribuição de Qui-Quadrado , Fibrose Cística/genética , Fibrose Cística/mortalidade , Seguimentos , Prognóstico , Estudos Retrospectivos
3.
Braz J Med Biol Res ; 35(1): 31-8, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11743612

RESUMO

The objective of the present study was to determine the possible prognostic factors which may explain the difference in the survival of patients with cystic fibrosis (CF) with and without meconium ileus. Over a period of 20 years, 127 patients with CF, whose diagnosis was confirmed by typical clinical characteristics and altered sweat chloride levels, were studied retrospectively. The patients were divided into two groups: group 1 consisted of patients who presented CF and meconium ileus (N = 9), and group 2 consisted of patients with CF without meconium ileus (N = 118). The characteristics studied were based on data obtained upon admission of the patients using a specific protocol. Demographic, clinical, nutritional and laboratory data were obtained. The genotype was determined in 106 patients by PCR. Survival was analyzed using the Kaplan-Meier method. The median follow-up period was 44 months. A statistically significant difference was observed between the groups studied regarding the following variables: age at diagnosis and weight and height z scores. The presence of meconium ileus was associated with an earlier diagnosis; these patients had greater deficits in height and weight at the time of diagnosis and at the end of the study. The estimated probability of survival for patients with CF without meconium ileus was 62 +/- 14% and for those with meconium ileus 32 +/- 18%. Patients with CF and meconium ileus presented a poor nutritional status at diagnosis and a lower survival rate compared to the general CF population.


Assuntos
Fibrose Cística/complicações , Obstrução Intestinal/etiologia , Mecônio , Distribuição de Qui-Quadrado , Fibrose Cística/genética , Fibrose Cística/mortalidade , Feminino , Seguimentos , Humanos , Lactente , Recém-Nascido , Masculino , Prognóstico , Estudos Retrospectivos , Taxa de Sobrevida
4.
Braz. j. med. biol. res ; 34(11): 1415-1420, Nov. 2001. ilus, tab
Artigo em Inglês | LILACS | ID: lil-303311

RESUMO

The objective of the present study was to determine the efficacy of detection of antigliadin immunoglobulins G and A (IgG and IgA) for the diagnosis of celiac disease in a developing country, since other enteropathies might alter the levels of these antibodies. Three groups were studied: 22 patients with celiac disease (mean age: 30.6 months), 61 patients with other enteropathies (mean age: 43.3 months), and 46 patients without enteropathies (mean age: 96.9 months). Antigliadin IgG and IgA ELISA showed sensitivity of 90.9 and 95.5 percent, respectively. With the hypothetical values of prevalence ranging from 1:500 to 1:2000 liveborns, the positive predictive value varied from 8.5 to 2.3 percent for IgG and from 4.8 to 1.1 percent for IgA. Considering the patients without enteropathies, specificity was 97.8 and 95.7 percent for IgG and IgA, respectively. In patients with other enteropathies, specificity was 82.0 and 84.1 percent, respectively. When patients with and without other enteropathies were considered as a whole, specificity was 88.8 and 91.6 percent, respectively. The specificity of positive IgG or IgA was 93.5 percent in children without enteropathies and 78.7 percent in the presence of other enteropathies. The negative predictive value for hypothetical prevalences varying from 1:500 to 1:2000 liveborns was 99.9 percent. Thus, even in developing countries where the prevalence of non-celiac enteropathies is high, the determination of serum antigliadin antibody levels is a useful screening test prior to the jejunal biopsy in the investigation of intestinal malabsorption


Assuntos
Criança , Pré-Escolar , Lactente , Feminino , Humanos , Masculino , Autoanticorpos , Doença Celíaca/diagnóstico , Imunoglobulina A , Imunoglobulina G , Análise de Variância , Autoanticorpos , Biópsia , Estudos de Casos e Controles , Países em Desenvolvimento , Doença Celíaca/imunologia , Ensaio de Imunoadsorção Enzimática , Imunoglobulina A , Imunoglobulina G , Enteropatias , Jejuno , Biomarcadores , Estudos de Casos Organizacionais , Valor Preditivo dos Testes , Sensibilidade e Especificidade , Estatísticas não Paramétricas
5.
Braz J Med Biol Res ; 34(11): 1415-20, 2001 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11668350

RESUMO

The objective of the present study was to determine the efficacy of detection of antigliadin immunoglobulins G and A (IgG and IgA) for the diagnosis of celiac disease in a developing country, since other enteropathies might alter the levels of these antibodies. Three groups were studied: 22 patients with celiac disease (mean age: 30.6 months), 61 patients with other enteropathies (mean age: 43.3 months), and 46 patients without enteropathies (mean age: 96.9 months). Antigliadin IgG and IgA ELISA showed sensitivity of 90.9 and 95.5%, respectively. With the hypothetical values of prevalence ranging from 1:500 to 1:2000 liveborns, the positive predictive value varied from 8.5 to 2.3% for IgG and from 4.8 to 1.1% for IgA. Considering the patients without enteropathies, specificity was 97.8 and 95.7% for IgG and IgA, respectively. In patients with other enteropathies, specificity was 82.0 and 84.1%, respectively. When patients with and without other enteropathies were considered as a whole, specificity was 88.8 and 91.6%, respectively. The specificity of positive IgG or IgA was 93.5% in children without enteropathies and 78.7% in the presence of other enteropathies. The negative predictive value for hypothetical prevalences varying from 1:500 to 1:2000 liveborns was 99.9%. Thus, even in developing countries where the prevalence of non-celiac enteropathies is high, the determination of serum antigliadin antibody levels is a useful screening test prior to the jejunal biopsy in the investigation of intestinal malabsorption.


Assuntos
Autoanticorpos/sangue , Doença Celíaca/diagnóstico , Imunoglobulina A/sangue , Imunoglobulina G/sangue , Análise de Variância , Autoanticorpos/imunologia , Biomarcadores/sangue , Biópsia , Estudos de Casos e Controles , Doença Celíaca/sangue , Doença Celíaca/imunologia , Criança , Pré-Escolar , Países em Desenvolvimento , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Imunoglobulina A/imunologia , Imunoglobulina G/imunologia , Lactente , Enteropatias/sangue , Enteropatias/diagnóstico , Enteropatias/imunologia , Jejuno/patologia , Masculino , Valor Preditivo dos Testes , Sensibilidade e Especificidade , Estatísticas não Paramétricas
6.
Braz. j. med. biol. res ; 34(9): 1147-1153, Sept. 2001. tab, graf
Artigo em Inglês | LILACS | ID: lil-290398

RESUMO

The objective of the present study was to evaluate associations between fiber intake, colonic transit time and stool frequency. Thirty-eight patients aged 4 to 14 years were submitted to alimentary evaluation and to measurement of colonic transit time. The median fiber intake of the total sample was age + 10.3 g/day. Only 18.4 percent of the subjects presented a daily dietary fiber intake below the levels recommended by the American Health Foundation. In this group, the median left colonic transit time was shorter than in the group with higher dietary fiber intake (11 vs 17 h, P = 0.067). The correlation between stool frequency and colonic transit time was negative and weak for left colon (r = -0.3, P = 0.04), and negative and moderate for rectosigmoid and total colon (r = -0.5, P<0.001 and r = -0.5, P<0.001, respectively). The stool frequency was lower in the group with slow transit time (0.8 vs 2.3 per week, P = 0.014). In conclusion, most patients with chronic functional constipation had adequate dietary fiber intake. The negative correlation between stool frequency and colonic transit time increased progressively from proximal segments to distal segments of the colon. Patients with normal and prolonged colonic transit time differ in terms of stool frequency


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Adolescente , Colo/fisiologia , Constipação Intestinal/fisiopatologia , Fibras na Dieta , Ingestão de Alimentos , Fezes , Trânsito Gastrointestinal/fisiologia , Doença Crônica , Ingestão de Energia , Reto/fisiologia
7.
J Pediatr Gastroenterol Nutr ; 33(1): 70-4, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11479411

RESUMO

BACKGROUND: This study was carried out to determine whether early inoculation of the plasmid-free human Escherichia coli into human newborns would reduce the frequency of acute diarrhea during a 1-year period. The plasmid-free E. coli strain isolated from the fecal microbiota of a healthy adult was nontoxigenic in vivo and in vitro and sensitive to all usual antibiotics. METHODS: In the experimental group, 51 healthy newborns were inoculated orally with 106 viable cells of the bacteria within 2 hours after birth. In the control group, the same number of newborns received the heat-killed bacteria. The clinical trial was double blind, and the newborns were randomly assigned to the experimental and control groups. RESULTS: Six months and 1 year after bacterial inoculation, infants in the experimental group showed a higher mean body weight (7.59 +/- 1.15 kg and 9.88 +/- 1.31 kg, respectively; P < 0.05) when compared with the control group (7.03 +/- 1.09 kg and 8.92 +/- 1.38 kg, respectively). At the end of the clinical trial, 48% (23/48) of the infants in the experimental group had shown at least one diarrhea episode during the 1-year period, as opposed to 71% (34/48) in the control group. These values were significantly different (P = 0.037), showing a 32.3% protective effect of inoculation. CONCLUSIONS: The present study shows that protection against diarrhea was obtained by oral inoculation with a single dose of plasmid-free human E. coli soon after birth.


Assuntos
Diarreia Infantil/prevenção & controle , Infecções por Escherichia coli/prevenção & controle , Escherichia coli , Plasmídeos , Administração Oral , Peso Corporal , Diarreia Infantil/epidemiologia , Método Duplo-Cego , Infecções por Escherichia coli/epidemiologia , Fezes/microbiologia , Feminino , Humanos , Incidência , Lactente , Recém-Nascido , Masculino
8.
Braz J Med Biol Res ; 34(9): 1147-53, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11514838

RESUMO

The objective of the present study was to evaluate associations between fiber intake, colonic transit time and stool frequency. Thirty-eight patients aged 4 to 14 years were submitted to alimentary evaluation and to measurement of colonic transit time. The median fiber intake of the total sample was age + 10.3 g/day. Only 18.4% of the subjects presented a daily dietary fiber intake below the levels recommended by the American Health Foundation. In this group, the median left colonic transit time was shorter than in the group with higher dietary fiber intake (11 vs 17 h, P = 0.067). The correlation between stool frequency and colonic transit time was negative and weak for left colon (r = -0.3, P = 0.04), and negative and moderate for rectosigmoid and total colon (r = -0.5, P<0.001 and r = -0.5, P<0.001, respectively). The stool frequency was lower in the group with slow transit time (0.8 vs 2.3 per week, P = 0.014). In conclusion, most patients with chronic functional constipation had adequate dietary fiber intake. The negative correlation between stool frequency and colonic transit time increased progressively from proximal segments to distal segments of the colon. Patients with normal and prolonged colonic transit time differ in terms of stool frequency.


Assuntos
Colo/fisiologia , Constipação Intestinal/fisiopatologia , Defecação , Fibras na Dieta/administração & dosagem , Ingestão de Alimentos , Trânsito Gastrointestinal/fisiologia , Adolescente , Criança , Pré-Escolar , Doença Crônica , Ingestão de Energia , Feminino , Humanos , Masculino
10.
Rev. Assoc. Med. Bras. (1992, Impr.) ; 46(4): 325-330, out.-dez. 2000. ilus
Artigo em Português | LILACS | ID: lil-277315

RESUMO

OBJETIVOS: A fibrose cística (FC) é a doença genética letal, de herança autossômica recessiva, mais comum entre pacientes de cor branca. O presente estudo foi realizado com o objetivo de identificar o quadro clínico e nutricional à admissäo dos pacientes no Centro de Tratamento de FC do HC-UFMG e avaliar a sobrevida a longo prazo. PACIENTES E MÉTODOS: Em um período de 20 anos, 127 pacientes portadores de FC foram acompanhados longitudinalmente e submetidos a protocolo previamente estabelecido, após confirmaçäo do diagnóstico pelo teste do suo...


Assuntos
Humanos , Recém-Nascido , Lactente , Pré-Escolar , Masculino , Feminino , Adolescente , Criança , Estado Nutricional , Fibrose Cística/mortalidade , Suor/química , Brasil/epidemiologia , Análise de Sobrevida , Cloro/análise , Seguimentos , Estudos Longitudinais , Idade de Início , Fibrose Cística/diagnóstico , Fibrose Cística/genética , Genótipo , Distúrbios Nutricionais/epidemiologia
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