RESUMO
Objetivo. Determinar el contenido de vitamina A en la leche materna y evaluar si cubre las recomendaciones para lactantes. Material y métodos. Estudio observacional, prospectivo, de corte transversal. Se analizaron muestras de leche de madres asistidas en el hospital público, obtenidas entre los 30 y los 90 días posparto. Se determinó la concentración de vitamina A por cromatografía y su adecuación a la ingesta dietética recomendada. Se utilizó el coeficiente de Spearman para estudiar la correlación entre variables. Resultados. Participaron 79 madres. La concentración de vitamina A en las leches fue 1,80 µmol/L (1,36-2,30); el tiempo medio de lactancia, de 57 días. No se encontró correlación significativa entre días de lactancia y contenido de vitamina A. El contenido en 50% de las muestras no cubrió las recomendaciones de vitamina A para los lactantes. Conclusión. El contenido de vitamina A fue insuficiente para cubrir las recomendaciones en la mitad de los casos.
Objective. To determine vitamin A content in breast milk and evaluate whether it satisfies the recommendations for infants. Material and methods. Observational, prospective, cross sectional study. Milk samples were obtained between 30 and 90 days postpartum from mothers seen in public hospitals, and analyzed. Vitamin A concentration was determined by chromatography and its adequacy to the recommended dietary intake. The correlation between outcome measures was analyzed using Spearman's correlation coefficient. Results. A total of 79 mothers participated. Vitamin A concentration in milk samples was 1.80 umol/L (1.36-2.30) and the mean breastfeeding time was 57 days. No significant correlation between breastfeeding days and vitamin A content was observed. In 50% of the samples, vitamin A content did not satisfy the recommendations for infants. Conclusion. Vitamin A content was not enough to satisfy the recommendations in half of the cases.
Assuntos
Humanos , Lactente , Vitamina A , Aleitamento Materno , Leite Humano , Necessidades NutricionaisRESUMO
OBJECTIVE: To determine vitamin A content in breast milk and evaluate whether it satisfies the recommendations for infants. MATERIAL AND METHODS: Observational, prospective, cross sectional study. Milk samples were obtained between 30 and 90 days postpartum from mothers seen in public hospitals, and analyzed. Vitamin A concentration was determined by chromatography and its adequacy to the recommended dietary intake. The correlation between outcome measures was analyzed using Spearman's correlation coefficient. RESULTS: A total of 79 mothers participated. Vitamin A concentration in milk samples was 1.80 umol/L (1.36-2.30) and the mean breastfeeding time was 57 days. No significant correlation between breastfeeding days and vitamin A content was observed. In 50% of the samples, vitamin A content did not satisfy the recommendations for infants. CONCLUSION: Vitamin A content was not enough to satisfy the recommendations in half of the cases.
OBJETIVO: Determinar el contenido de vitamina A en la leche materna y evaluar si cubre las recomendaciones para lactantes. MATERIAL Y MÉTODOS: Estudio observacional, prospectivo, de corte transversal. Se analizaron muestras de leche de madres asistidas en el hospital público, obtenidas entre los 30 y los 90 días posparto. Se determinó la concentración de vitamina A por cromatografía y su adecuación a la ingesta dietética recomendada. Se utilizó el coeficiente de Spearman para estudiar la correlación entre variables. RESULTADOS: Participaron 79 madres. La concentración de vitamina A en las leches fue 1,80 µmol/L (1,36-2,30); el tiempo medio de lactancia, de 57 días. No se encontró correlación significativa entre días de lactancia y contenido de vitamina A. El contenido en 50% de las muestras no cubrió las recomendaciones de vitamina A para los lactantes. CONCLUSIÓN: El contenido de vitamina A fue insuficiente para cubrir las recomendaciones en la mitad de los casos.
Assuntos
Fenômenos Fisiológicos da Nutrição do Lactente , Leite Humano/química , Recomendações Nutricionais , Vitamina A/análise , Adulto , Biomarcadores/análise , Aleitamento Materno , Estudos Transversais , Feminino , Humanos , Lactente , Estudos ProspectivosRESUMO
This study was conducted to evaluate the impact of a food aid program (Plan Más Vida, PMV) on the micronutrient nutritional condition of lactating mothers 1 year after its implementation. The food program provided supplementary diets (wheat- and maize-fortified flour, rice or sugar, and fortified soup) to low-income families from the province of Buenos Aires, Argentina. A prospective, non-experimental study was carried out to evaluate the micronutrient nutritional status of lactating mothers (n = 178 at baseline and n = 151 after 1 year). Biochemical tests (hemoglobin, ferritin, zinc, vitamin A, and folic acid), anthropometric assessments (weight and height) and dietary surveys (24-h recall) were performed. We found no significant changes in anthropometric values 1 year after the intervention. The risk for vitamin A (retinol 20-30 µg/dl) and folate deficiency significantly decreased 1 year after PMV implementation (56.3 vs. 29.9 and 50.3 vs. 3.4 %, respectively; p < 0.001). Anemia was seen in 25.8 % of lactating mothers at baseline, without statistically significant differences 1 year after (p = 0.439). The nutritional data obtained after assessing the early impact of PMV actions may be useful to provincial health authorities to perform periodic evaluations in the future.
Assuntos
Assistência Alimentar , Implementação de Plano de Saúde , Lactação , Micronutrientes/deficiência , Estado Nutricional , Adolescente , Adulto , Argentina/epidemiologia , Estudos Transversais , Feminino , Deficiência de Ácido Fólico/epidemiologia , Deficiência de Ácido Fólico/prevenção & controle , Alimentos Fortificados , Humanos , Micronutrientes/administração & dosagem , Micronutrientes/sangue , Pessoa de Meia-Idade , Prevalência , Avaliação de Programas e Projetos de Saúde , Estudos Prospectivos , Risco , Deficiência de Vitamina A/epidemiologia , Deficiência de Vitamina A/prevenção & controle , Adulto JovemRESUMO
AIM: To determine the incidence of peripheral fractures in patients with celiac disease (CD) and the effect of treatment on fracture risk. METHODS: We compared the incidence and risk of peripheral fractures before and after diagnosis between a cohort of 265 patients who had been diagnosed with CD at least 5 years before study entry and a cohort of 530 age- and sex-matched controls who had been diagnosed with functional gastrointestinal disorders. Data were collected through in-person interviews with an investigator. The overall assessment window for patients was 9843 patient-years (2815 patient-years after diagnosis). RESULTS: Compared with the control group, the CD cohort showed significantly higher incidence rate and risk of first peripheral fracture before diagnosis [adjusted hazard ratio (HR): 1.78, 95% CI: 1.23-2.56, P < 0.002] and in men (HR: 2.67, 95% CI: 1.37-5.22, P < 0.004). Fracture risk was significantly associated with the classic CD presentation with gastrointestinal symptoms (P < 0.003). In the time period after diagnosis, the risk of fractures was comparable between the CD cohort and controls in both sexes (HR: 1.08, 95% CI: 0.55-2.10 for women; HR: 1.57, 95% CI: 0.57-4.26 for men). CONCLUSION: CD patients have higher prevalence of fractures in the peripheral skeleton before diagnosis. This is associated with male sex and classic clinical presentation. The fracture risk was reduced after the treatment.