Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
1.
J Pediatr Endocrinol Metab ; 36(8): 719-725, 2023 Aug 28.
Artigo em Inglês | MEDLINE | ID: mdl-37422722

RESUMO

OBJECTIVES: Metabolic syndrome (MetS) is a cluster of conditions linked to obesity that increases cardiovascular risk. We evaluated the frequency of clinical abnormalities associated with overweight and obesity in childhood, to determine whether a diagnosis of MetS is appropriate in this population. METHODS: Cross-sectional study with 116 pubertal and prepubertal children with a mean age (SD) of 10.9 (2.5) years, with overweight and obesity. We defined MetS using the International Diabetes Federation criteria, regardless of the age. RESULTS: 45 patients met the criteria, 20 had at least one metabolic abnormality in addition to a high waist circumference (WC), and seven with WC below percentile 90th, had at least one metabolic abnormality. The prepubertal had higher zBMI [3.1 (2.6-3.8) vs. 2.8 (2.4-3.3); p=0.037], less lean body mass (kg) [27.13 (7.3) vs. 34.13 (9.8); p=0.005] and a similar frequency of non-alcoholic fatty liver disease (NAFLD) compared to the pubertal [44.7 vs. 35.9; p=0.323]. Prepubertal with NAFLD had higher zBMI, lower HDL levels, higher TG/HDL ratios and higher fat percentages; while pubertal with NAFLD had higher WC/height, aspartate aminotransferase and oxaloacetic transaminase. CONCLUSIONS: The diagnosis of MetS in childhood is not fundamental. Individualized management, focusing on the earliest age groups, in which we identified a more severe degree of obesity, should be done. We also recommend screening for NAFLD in all ages, due to the high prevalence observed.


Assuntos
Síndrome Metabólica , Hepatopatia Gordurosa não Alcoólica , Obesidade Pediátrica , Criança , Humanos , Sobrepeso/complicações , Sobrepeso/epidemiologia , Hepatopatia Gordurosa não Alcoólica/epidemiologia , Obesidade Pediátrica/complicações , Obesidade Pediátrica/epidemiologia , Estudos Transversais , Fatores de Risco , Síndrome Metabólica/etiologia , Síndrome Metabólica/complicações , Índice de Massa Corporal
5.
Rev Paul Pediatr ; 40: e2020447, 2021.
Artigo em Inglês, Português | MEDLINE | ID: mdl-34495279

RESUMO

OBJECTIVE: To evaluate changes in peripheral immunological response (decrease in blood proinflammatory cytokines) and fecal microbiota (especially Bacteroidetes and Firmicutes) after administration of probiotics in children with celiac disease on a gluten-free diet. DATA SOURCE: The databases MEDLINE, LILACS, Springer and SciELO were used for this review, with the descriptors "celiac disease AND probiotics". At the end of the search, 168 articles were retrieved, four of which were included in the final qualitative synthesis, having as inclusion criteria randomized clinical trials and pediatric population (1-19 years) and, as exclusion criteria, interventions other than probiotics, studies with patients with other diseases associated with celiac disease, or patients who did not meet the diagnostic criteria. All elected studies were published until September 2020, without language restriction, with patients receiving strains of Bifidobacterium breve or B. longum and on a gluten-free diet. DATA SYNTHESIS: The studies show that the administration of probiotics along with a gluten-free diet, can approximate the fecal microbiota of celiac patients to typical conditions of healthy individuals, by restoring the abundance of some microbial communities that characterize the typical physiological condition. In addition, the administration of probiotics can reduce serum proinflammatory cytokines (mainly TNF-alpha). CONCLUSIONS: Despite the positive correlation between probiotics and fecal microbiota/serological markers in pediatric patients with celiac disease, we emphasize the need for future multicentric studies that should include a larger number of patients and a longer follow up period.


Assuntos
Doença Celíaca , Microbioma Gastrointestinal , Probióticos , Doença Celíaca/terapia , Criança , Dieta Livre de Glúten , Humanos , Imunidade
7.
Rev Paul Pediatr ; 39: e2019226, 2021.
Artigo em Português, Inglês | MEDLINE | ID: mdl-32876312

RESUMO

OBJECTIVE: Evaluate the effects of probiotics use, compared with placebo, in pediatric patients with non-alcoholic fatty liver disease (NAFLD), using laboratorial and ultrasonographic parameters as outcomes. METHODS: A systematic review of the literature was performed through MEDLINE and Lilacs databases. The articles selected were randomized controlled clinical trials published until November 2018, without any language restriction, dealing with pediatric patients with NAFLD. Patients were divided into 2 groups. One group received probiotic therapy and the other group, only received placebo. The primary outcome evaluated was the difference between the serum levels of alanine aminotransferase (ALT) before and after receiving probiotics or placebo. The secondary outcomes evaluated were the serum aspartate aminotransferase levels, body mass index, serum triglycerides, waist circumference and level of liver steatosis on the ultrasonography. RESULTS: A total of 46 articles were recovered, and 3 articles were included in the qualitative analysis, totaling 128 patients. Two trials revealed a significant decrease of alanine aminotransferase levels after treatment with probiotics (Lactobacillus rhamnosus for 8 weeks; Bifidobacterium+Lactobacillus for 12 weeks), when compared to the placebo. The other variables did not show a statistically significant difference between both groups. CONCLUSIONS: Probiotic therapy has contributed to the reduction of ALT serum levels in pediatric patients with nonalcoholic fatty liver disease, which is in line with results found by other authors in scientific literature. Regarding the secondary outcomes, the use of probiotics did not show benefits or damages compared to placebo.


Assuntos
Hepatopatia Gordurosa não Alcoólica/terapia , Probióticos/administração & dosagem , Alanina Transaminase/sangue , Estudos de Casos e Controles , Criança , Feminino , Humanos , Masculino , Hepatopatia Gordurosa não Alcoólica/sangue , Hepatopatia Gordurosa não Alcoólica/diagnóstico por imagem , Ensaios Clínicos Controlados Aleatórios como Assunto , Ultrassonografia
8.
Rev. Paul. Pediatr. (Ed. Port., Online) ; 39: e2019226, 2021. tab, graf
Artigo em Inglês, Português | LILACS, Sec. Est. Saúde SP | ID: biblio-1136784

RESUMO

ABSTRACT Objective: Evaluate the effects of probiotics use, compared with placebo, in pediatric patients with non-alcoholic fatty liver disease (NAFLD), using laboratorial and ultrasonographic parameters as outcomes. Methods: A systematic review of the literature was performed through MEDLINE and Lilacs databases. The articles selected were randomized controlled clinical trials published until November 2018, without any language restriction, dealing with pediatric patients with NAFLD. Patients were divided into 2 groups. One group received probiotic therapy and the other group, only received placebo. The primary outcome evaluated was the difference between the serum levels of alanine aminotransferase (ALT) before and after receiving probiotics or placebo. The secondary outcomes evaluated were the serum aspartate aminotransferase levels, body mass index, serum triglycerides, waist circumference and level of liver steatosis on the ultrasonography. Results: A total of 46 articles were recovered, and 3 articles were included in the qualitative analysis, totaling 128 patients. Two trials revealed a significant decrease of alanine aminotransferase levels after treatment with probiotics (Lactobacillus rhamnosus for 8 weeks; Bifidobacterium+Lactobacillus for 12 weeks), when compared to the placebo. The other variables did not show a statistically significant difference between both groups. Conclusions: Probiotic therapy has contributed to the reduction of ALT serum levels in pediatric patients with nonalcoholic fatty liver disease, which is in line with results found by other authors in scientific literature. Regarding the secondary outcomes, the use of probiotics did not show benefits or damages compared to placebo.


RESUMO Objetivo: Avaliar os efeitos do uso de probióticos em comparação com placebo, em pacientes pediátricos portadores de doença hepática gordurosa não alcoólica (DHGNA), utilizando parâmetros laboratoriais e ultrassonográficos como desfecho. Métodos: Revisão sistemática da literatura por meio das bases de dados Sistema Online de Busca e Análise de Literatura Médica (MEDLINE) e Literatura Latino-Americana e do Caribe em Ciências da Saúde (Lilacs). Foram selecionados ensaios clínicos controlados randomizados publicados até novembro de 2018, sem restrição de língua, com pacientes pediátricos portadores de DHGNA, divididos em dois grupos. Um grupo foi submetido à terapia probiótica e outro grupo recebeu somente placebo. O desfecho primário avaliado foi a comparação dos níveis de alanina aminotransferase (ALT) ao início e no fim do seguimento entre os grupos probiótico e placebo. Os desfechos secundários avaliados foram os níveis de aspartato aminotransferase sérico, índice de massa corpórea, triglicerídeos totais séricos, circunferência abdominal e grau de esteatose hepática à ultrassonografia abdominal. Resultados: Foram recuperados 46 artigos, sendo três incluídos na análise qualitativa, totalizando 128 pacientes. Dois estudos demonstraram redução significativa dos níveis de ALT com o uso de probiótico (Lactobacillus rhamnosus, por oito semanas; Bifidobacterium+Lactobacillus, por 12 semanas), em comparação ao placebo. As demais variáveis avaliadas não evidenciaram diferença estatisticamente significante ente os dois grupos. Conclusões: O uso de probióticos representou redução nos níveis séricos de ALT na esteatose hepática na infância, indo ao encontro dos resultados obtidos por outros autores da literatura científica vigente. No que se refere às variáveis de desfecho secundário, não foi demonstrado benefício ou dano do tratamento de probióticos em relação ao placebo.


Assuntos
Humanos , Masculino , Feminino , Criança , Probióticos/administração & dosagem , Hepatopatia Gordurosa não Alcoólica/terapia , Estudos de Casos e Controles , Ensaios Clínicos Controlados Aleatórios como Assunto , Ultrassonografia , Alanina Transaminase/sangue , Hepatopatia Gordurosa não Alcoólica/sangue , Hepatopatia Gordurosa não Alcoólica/diagnóstico por imagem
9.
Arq. Asma, Alerg. Imunol ; 4(2): 181-189, abr.jun.2020. ilus
Artigo em Português | LILACS | ID: biblio-1381905

RESUMO

O objetivo deste estudo foi encontrar a relação do uso de probióticos e/ou prebióticos na prevenção do desenvolvimento de eczema atópico em crianças com alto risco. Foram utilizadas para esta revisão as bases de dados MEDLINE, via PubMed, SciELO e LILACS, com os seguintes descritores "(probiotics OR prebiotics) AND (allergy) AND (eczema)". Foram selecionados ensaios clínicos randomizados publicados até janeiro de 2020, sem restrição de idioma, em humanos, desde o nascimento até os 18 anos de idade. Foram recuperados 247 artigos, sendo cinco utilizados para análise. Quatro estudos não demonstraram relação entre o uso de probióticos e/ou prebióticos e a prevenção de eczema atópico em crianças de alto risco. Em contrapartida, um dos trabalhos obteve associação positiva, porém restrito a crianças com alergia à proteína do leite de vaca. Foi concluído nesta revisão que não existe relação entre o uso de probiótico e/ ou prebióticos em crianças de alto risco de atopia na prevenção de eczema, com possível exceção em crianças com alergia ao leite da vaca, com o desenvolvimento de eczema. É necessário a realização de mais estudos em longo prazo para a confirmação de real associação.


The aim of this study was to assess the relationship between the use of probiotics and/or prebiotics and the onset of eczema in children with high risk of atopy. PubMed, SciELO, and LILACS databases were used with the following descriptors: "(probiotics OR prebiotics) AND (allergy) AND (eczema)." Randomized clinical trials published up to January 2020, with no language restriction, involving humans from birth to 18 years of age were included. In total, 247 articles were found, and five were included in the analysis. Four trials did not show a relationship between the use of probiotics and/or prebiotics and the prevention of atopic eczema in high-risk children. In contrast, one clinical trial reported a positive association, but restricted to children with cow's milk allergy. In conclusion, there is no relationship between the use of probiotics and/or prebiotics and the onset of eczema in children with high risk of atopy, with a possible exception for children with cow's milk allergy. Additional long-term studies are necessary to confirm whether this association is true.


Assuntos
Humanos , Recém-Nascido , Lactente , Pré-Escolar , Criança , Adolescente , Hipersensibilidade a Leite , Probióticos , Dermatite Atópica , Eczema , Prebióticos , PubMed , LILACS
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...