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1.
Birth Defects Res ; 112(1): 40-53, 2020 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-31486292

RESUMO

BACKGROUND: Few studies have examined the effects of low-dose alcohol consumption on the "lipid peroxidation-antioxidant defense" (LPO-AOD) system of mothers and infants, and on infant growth and development. This study examined effects of alcohol consumption on the LPO-AOD system of pregnant women and newborns and infant development. METHODS: A total of 209 pregnant women were recruited for this prospective study at the first prenatal visit and followed until delivery: 112 consumed alcohol and 97 reported no alcohol use during pregnancy. Infants were evaluated at birth, and at 6 and 12 months of age. The study controlled for the confounding effect of maternal smoking. RESULTS: Biomarkers of lipid peroxidation, for example, thiobarbituric acid reactants, were higher and the activity of the antioxidant defense system was lower in drinkers and their infants. Higher rates of pathological conditions and slower postnatal growth were observed among infants who were prenatally exposed to alcohol. Low-dose alcohol use and tobacco smoking were associated with lower postnatal infant growth trajectories, resulting in restricted growth at 6 and 12 months among infants born to mothers who drank or smoked during pregnancy. Alcohol had a broad effect on the infant and maternal LPO-AOD system, while the effect of smoking was limited in this study to maternal glutathione peroxidase. CONCLUSIONS: Small amounts of alcohol consumed during pregnancy are associated with dysfunction of the LPO-AOD system and development of oxidative stress in women and their children. Identification and preventive interventions are needed for pregnant women who use alcohol in any amount.


Assuntos
Consumo de Bebidas Alcoólicas/efeitos adversos , Desenvolvimento Infantil/efeitos dos fármacos , Peroxidação de Lipídeos/efeitos dos fármacos , Adulto , Antioxidantes , Etanol , Feminino , Humanos , Lactente , Recém-Nascido , Estresse Oxidativo , Gravidez , Complicações na Gravidez , Cuidado Pré-Natal , Estudos Prospectivos
2.
J Pediatr Hematol Oncol ; 39(1): 42-45, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27879543

RESUMO

Type I congenital methemoglobinemia is an autosomal recessive disorder. A high frequency of congenital methemoglobinemia has been reported among Native Americans inhabiting the Yukon-Kuskokwim Delta. Other rare cases of congenital methemoglobinemia of types I and II have been reported in Japan and other countries. In Russia-namely, in Yakutia-a high frequency of type I congenital methemoglobinemia has been reported. In 2009, the Consultation Polyclinic of the Pediatric Center in Yakutsk city established a registry of children with congenital methemoglobinemia. In total, 43 patients were registered between 2005 and 2009. The median methemoglobin level was 13.5% (ranging between 4.2% and 33.9%) and physical examination revealed cyanosis of the skin and mucus membranes. There were significant positive relationships between percentage of methemoglobin and erythrocyte count, hemoglobin concentration, and hematocrit among male patients, consistent with an upregulation of the hypoxic response. The prevalence per 100,000 children ranged from 12.7 to 47.0 in 3 geographic regions of Yakutia. Further research is needed to clarify the clinical consequences of congenital methemoglobinemia in the children of Yakutia and the reasons for the high variability in the prevalence of the condition.


Assuntos
Citocromo-B(5) Redutase/deficiência , Metemoglobinemia/genética , Adolescente , Processamento Alternativo , Criança , Pré-Escolar , Citocromo-B(5) Redutase/sangue , Citocromo-B(5) Redutase/genética , Contagem de Eritrócitos , Etnicidade/genética , Feminino , Hemoglobinas/análise , Humanos , Lactente , Masculino , Metemoglobina/análise , Metemoglobinemia/sangue , Metemoglobinemia/epidemiologia , Prevalência , Estudos Retrospectivos , Fatores Sexuais , Sibéria/epidemiologia
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