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1.
Compr Psychiatry ; 30(6): 505-11, 1989.
Article in English | MEDLINE | ID: mdl-2510966

ABSTRACT

These are the results of a retrospective study in which we reviewed the charts of 38 consecutive aggressive mentally retarded persons who were treated with lithium carbonate. All subjects were residents of a university operated program that serves mentally retarded persons with behavioral disorders. Over 63% of these subjects evidenced a greater than 30% reduction in the frequency of aggressiveness subsequent to the start of lithium therapy. Subjects with higher serum lithium levels had a more favorable response to lithium, along with those exhibiting higher levels of hyperactivity and violence before treatment.


Subject(s)
Aggression/drug effects , Intellectual Disability/drug therapy , Lithium/therapeutic use , Adult , Behavior Therapy , Combined Modality Therapy , Female , Hospitals, Psychiatric , Humans , Intellectual Disability/psychology , Lithium Carbonate , Male , Middle Aged , Retrospective Studies , Social Adjustment
2.
Clin Nutr ; 4(4): 249-53, 1985 Nov.
Article in English | MEDLINE | ID: mdl-16831740

ABSTRACT

The reason branched chain aminoacids are decreased and aromatic aminoacids increased in chronic liver failure is unclear. Branched chain aminoacids are mainly catabolised in muscles, and it is known that protein energy malnutrition may decrease the concentration of these aminoacids in plasma. In this study we have evaluated the nutritional status of a group of cirrhotics and compared it with their plasma aminoacid imbalance. Fourteen patients were considered as well-nourished and nine as malnourished. Plasma levels of branched chain aminoacids were significantly decreased and the phenylalanine increased in the malnourished group. Arm muscle circumference was significantly correlated with branched chain aminoacids. In conclusion our data suggest that malnutrition may contribute to the low levels of these aminoacids in patients with liver cirrhosis.

3.
Metabolism ; 33(7): 646-51, 1984 Jul.
Article in English | MEDLINE | ID: mdl-6738366

ABSTRACT

The finding of high plasma free fatty acid (FFA) levels in cirrhotic patients has been attributed either to decreased hepatic clearance or to enhanced fat mobilization. To better clarify these hypotheses, total and individual FFA and glycerol levels were determined in 21 cirrhotic patients with different degrees of hepatocellular damage (evaluated by liver function tests), portal hypertension (evaluated by endoscopy and clinical signs), and nutritional status (evaluated by anthropometric and biohumoral parameters) and in 10 age- and sex-matched healthy subjects. Glucose tolerance and insulin and glucagon levels were determined in all individuals. Well-nourished and malnourished patients were identified within the cirrhotic group. Plasma FFA and glycerol concentrations were well correlated (r = 0.47, P less than 0.05), levels being significantly higher in cirrhotic individuals than in controls (746.6 +/- 46.29 SE v 359.22 +/- 40.82 mumol/L, P less than 0.001 for plasma FFA; 150.1 +/- 3.12 v 82.5 +/- 9.2 mumol/L, P less than 0.01 for glycerol). Plasma FFA and glycerol showed no correlation with the liver function test results or portal hypertension parameters. Interestingly, plasma levels of FFA and glycerol were influenced by the nutritional status, significantly higher FFA levels being observed in the well-nourished than in the malnourished patients (842.5 +/- 47.5 v 563.4 +/- 78 mumol/L, P less than 0.005). Furthermore, a positive correlation was found between plasma glycerol level and percentage of triceps skinfold (r = 0.45, P less than 0.05). No correlation was found between plasma levels of FFA or glycerol and glucose tolerance, insulin and glucagon.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Fatty Acids, Nonesterified/blood , Liver Cirrhosis/metabolism , Adult , Aged , Carbohydrate Metabolism , Female , Glycerol/blood , Humans , Hypertension, Portal/blood , Hypertension, Portal/etiology , Liver Cirrhosis/complications , Male , Middle Aged , Nutrition Disorders/blood , Nutrition Disorders/etiology
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