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2.
East Mediterr Health J ; 8(2-3): 290-7, 2002.
Article in English | MEDLINE | ID: mdl-15339116

ABSTRACT

To assess the role of enzymatic antioxidants in the pathogenesis of protein energy malnutrition (PEM) and the effect of nutritional rehabilitation, we studied 30 infants with PEM (mean age 10.63 +/- 4.39 months: 10 marasmic; 8 with kwashiorkor; 12 with marasmic kwashiorkor) and 15 controls. All underwent clinical examination and laboratory investigations, including superoxide dismutase (SOD) and glutathione peroxidase (GPx) estimation before and after nutrition rehabilitation. SOD and GPx were significantly lower in all malnourished infants compared to controls, and significantly increased after nutritional rehabilitation. These significant correlations suggest that antioxidants could be introduced during PEM nutritional rehabilitation to decrease morbidity and mortality.


Subject(s)
Antioxidants/metabolism , Infant Nutrition Disorders/enzymology , Infant Nutrition Disorders/rehabilitation , Kwashiorkor/enzymology , Kwashiorkor/rehabilitation , Protein-Energy Malnutrition/enzymology , Protein-Energy Malnutrition/rehabilitation , Anthropometry , Antioxidants/therapeutic use , Case-Control Studies , Egypt/epidemiology , Female , Free Radical Scavengers/blood , Free Radical Scavengers/therapeutic use , Glutathione Peroxidase/blood , Glutathione Peroxidase/deficiency , Glutathione Peroxidase/therapeutic use , Hospitals, Pediatric , Hospitals, University , Humans , Infant , Infant Nutrition Disorders/classification , Infant Nutrition Disorders/epidemiology , Kwashiorkor/classification , Kwashiorkor/epidemiology , Male , Morbidity , Nutrition Assessment , Nutritional Requirements , Nutritional Status , Nutritional Support/methods , Nutritional Support/standards , Practice Guidelines as Topic , Protein-Energy Malnutrition/classification , Protein-Energy Malnutrition/epidemiology , Severity of Illness Index , Superoxide Dismutase/blood , Superoxide Dismutase/deficiency , Superoxide Dismutase/therapeutic use , Treatment Outcome
3.
Afr J Med Med Sci ; 28(1-2): 81-5, 1999.
Article in English | MEDLINE | ID: mdl-12953993

ABSTRACT

Golden and Ramdath proposed the free radical theory of kwashiorkor, suggesting that the changes seen in kwashiorkor may be the result of an imbalance between the production and safe disposal of free radicals. In malnourished children, mineral metabolism and antioxidant status need renewed attention especially in relation to cause and functional significance of the changes in concentration of these substances. In the present study, the modified Wellcome classification was used to classify the protein energy malnourished children into kwashiorkor marasmic-kwashiorkor, marasmus and underweight. Twenty-six healthy and normal children were used as controls. Standard procedures were used for the analyses of the biochemical parameters. Our results showed that plasma total cholesterol, sodium, potassium and bicarbonate, beta-carotene, retinol and uric acid were significantly lower in the malnourished group than the control group (P < 0.05), while transaminases were significantly increased in the malnourished group (P < 0.05). These findings suggest an altered electrolyte and antioxidant status in protein energy malnutrition.


Subject(s)
Alanine Transaminase/blood , Antioxidants/metabolism , Aspartate Aminotransferases/blood , Child Nutrition Disorders/metabolism , Cholesterol/blood , Electrolytes/blood , Kwashiorkor/metabolism , Protein-Energy Malnutrition/metabolism , Analysis of Variance , Bicarbonates/blood , Case-Control Studies , Child Nutrition Disorders/classification , Child Nutrition Disorders/complications , Child Nutrition Disorders/diagnosis , Child, Preschool , Hematocrit , Humans , Infant , Kwashiorkor/classification , Kwashiorkor/complications , Kwashiorkor/diagnosis , Nigeria/epidemiology , Nutrition Assessment , Nutritional Status , Potassium/blood , Prevalence , Protein-Energy Malnutrition/classification , Protein-Energy Malnutrition/complications , Protein-Energy Malnutrition/diagnosis , Respiratory Tract Infections/epidemiology , Respiratory Tract Infections/etiology , Sodium/blood , Thinness/metabolism , Uric Acid/blood , Vitamin A/blood , beta Carotene/blood
4.
Eur J Clin Nutr ; 47(9): 658-65, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8243432

ABSTRACT

Glutathione S-transferases (GSTs) are principally involved in detoxification. These enzymes can be induced by an increased flux of substrate, such as occurs during pro-oxidative stress or antioxidant deficiency. We tested the hypothesis that the postulated oxidative stress in severe malnutrition would result in induction of GSTs in erythrocytes. Erythrocyte GST activity towards 1-chloro-2,4-dinitrobenzene (CDNB) was measured in 271 malnourished children (22 undernourished; 92 marasmic; 82 kwashiorkor; 75 marasmic-kwashiorkor) and 48 healthy children. GST activity in the malnourished children was significantly higher than the control group (P < 0.01). The GST activity in the four classes of malnutrition did not differ. There was a weak relationship between GST activity and the height deficit, but not with the weight deficit, or the clinical features displayed by the children. The 11 children that died had a higher value than the survivors. There was no change in GST with anthropometric recovery. We conclude that erythrocyte GST has been induced in children with malnutrition. Induction of erythrocyte GST may be the result of exposure of the children to oxidative stress during the months prior to their presentation with severe malnutrition.


Subject(s)
Child Nutrition Disorders/enzymology , Erythrocytes/enzymology , Glutathione Transferase/metabolism , Kwashiorkor/enzymology , Protein-Energy Malnutrition/enzymology , Age Factors , Body Height , Body Weight , Case-Control Studies , Child Nutrition Disorders/blood , Child Nutrition Disorders/classification , Child Nutrition Disorders/mortality , Child, Preschool , Chronic Disease , Erythrocytes/chemistry , Glutathione Transferase/analysis , Glutathione Transferase/physiology , Humans , Infant , Kwashiorkor/blood , Kwashiorkor/classification , Kwashiorkor/mortality , Oxidants/adverse effects , Patient Admission , Patient Discharge , Protein-Energy Malnutrition/blood , Protein-Energy Malnutrition/classification , Protein-Energy Malnutrition/mortality , Severity of Illness Index , Stress, Physiological/chemically induced , Survival Rate
5.
Eur J Clin Nutr ; 47(9): 658-65, Sept. 1993.
Article in English | MedCarib | ID: med-8344

ABSTRACT

Glutathione S-transferases (GSTs) are principally involved in detoxication. These enzymes can be induced by an increased flux of substrate, such as occurs during pro-oxidative stress or antioxidant deficiency. We tested the hypothesis that the postulated oxidative stress in severe malnutrition would result in induction of GSTs in erythocytes. Erythrocyte GST activity towards 1-chloro-2, 4-dinitrobenzene (CDNB) was measured in 271 malnourished children (22 undernourished; 92 marasmic; 82 kwashiorkor; 75 marasmic-kwashiorkor) and 48 healthy children. GST activity in the malnourished children was significnatly higher than the control group (p < 0.01). The GST activity in the four classes of malnutrition did not differ. There was a weak relationship between GST activity and the height deficit, but not with the weight deficit, or the clinical features displayed by the children. The 11 children that died had a higher value than the survivors. There was no change in GST with anthropometric recovery. We conclude that erythrocyte GST has been induced in children with malnutrition. Induction of erythrocyte GST may be the result of exposure of the children to oxidative stress during the months prior to their presentation with severe malnutrition (AU)


Subject(s)
Humans , Infant , Child, Preschool , Child Nutrition Disorders/enzymology , Erythrocytes/enzymology , Protein-Energy Malnutrition/enzymology , Glutathione Transferase/metabolism , Kwashiorkor/enzymology , Age Factors , Body Height , Body Weight , Case-Control Studies , Child Nutrition Disorders/blood , Child Nutrition Disorders/classification , Child Nutrition Disorders/mortality , Chronic Disease , Erythrocytes , Chemistry , Glutathione Transferase/analysis , Glutathione Transferase/physiology , Kwashiorkor/blood , Kwashiorkor/classification , Kwashiorkor/mortality , Oxidants, Photochemical/adverse effects , Patient Admission , Patient Discharge , Protein-Energy Malnutrition/blood , Protein-Energy Malnutrition/classification , Protein-Energy Malnutrition/mortality , Severity of Illness Index , Stress, Physiological/chemically induced , Survival Rate
6.
Arch Dis Child ; 67(8): 1030-2, 1992 Aug.
Article in English | MEDLINE | ID: mdl-1520007

ABSTRACT

Protein energy malnutrition is associated with cerebral atrophy which may be detrimental to intellectual development. The aim of this study was to document the anatomical abnormalities which lead to the appearance of cerebral atrophy using magnetic resonance imaging (MRI) in the acute stage of kwashiorkor and to monitor changes during nutritional rehabilitation. Twelve children aged 6 to 37 months requiring admission to hospital for the treatment of kwashiorkor were studied. The children were evaluated clinically, biochemically, and by MRI of their brains on admission and 30 and 90 days later. Brain shrinkage was present in every child on admission. White and grey matter appeared equally affected and the myelination was normal for age. At 90 days, the cerebral changes had resolved in nine and improved substantially in the remainder, by which time serum proteins and weight for age were within the normal range. The findings of this study suggest that brain shrinkage associated with kwashiorkor reverses rapidly with nutritional rehabilitation.


Subject(s)
Brain/pathology , Kwashiorkor/diagnosis , Magnetic Resonance Imaging , Atrophy/classification , Atrophy/diagnosis , Atrophy/diet therapy , Child, Preschool , Female , Humans , Infant , Kwashiorkor/classification , Kwashiorkor/diet therapy , Male , Remission Induction , Time Factors
9.
10.
Nutr Rev ; 26(8): 256, 1968 Aug.
Article in English | MEDLINE | ID: mdl-5666198
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