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1.
Article in English | MEDLINE | ID: mdl-22658981

ABSTRACT

This study aimed to explore the relationship between antioxidant enzyme activities and neurological soft signs (NSS) in a sample of patients with schizophrenia. Sixty clinically stable patients with schizophrenia treated mostly by first-generation antipsychotics and 30 matched healthy controls were recruited. NSS were assessed in two groups by a standardized neurological examination (Krebs et al., 2000). The red blood cell (RBC) antioxidant activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT) were measured by spectrophotometry. RBC activities of all enzymes studied: SOD, GSH-Px and CAT, were significantly lower in the patients compared to control group. All NSS scores were significantly higher in the patients compared to healthy controls' scores. In the patients, a negative correlation was found between RBC SOD activity and NSS total score and motor coordination and motor integration sub-scores. The association between low SOD activity as a marker of oxidative stress and NSS in schizophrenic patients suggests a common pathological process of these abnormalities.


Subject(s)
Nervous System Diseases/enzymology , Schizophrenia/enzymology , Superoxide Dismutase/blood , Adult , Case-Control Studies , Catalase/blood , Female , Glutathione Peroxidase/blood , Humans , Male , Nervous System Diseases/blood , Nervous System Diseases/complications , Nervous System Diseases/diagnosis , Neurologic Examination/methods , Schizophrenia/blood , Schizophrenia/complications , Schizophrenia/diagnosis , Severity of Illness Index
2.
Ann Biol Clin (Paris) ; 68(5): 595-7, 2010.
Article in French | MEDLINE | ID: mdl-20870582

ABSTRACT

The deficiency in factor I or fibrinogen is a largely unknown genetic disease. It is a rare condition inherited as an autosomal recessive, whose clinical events are variable, ranging from moderate to minimal bleeding or cataclysmic hemorrhage. We report a case of congenital afibrinogenemia in a 17 years-old patient hospitalized in surgical ICU for hemoperitoneum medium abundance discovered by abdominal ultrasound performed before a picture of abdominopelvic pain lasting for 24 hours. Exploration led to the diagnosis of congenital afibrinogenemia with favorable evolution with a contribution of factor deficient. Through this case we raise the problem of congenital afibrinogenemia in diagnosis and the peculiarities of its management.


Subject(s)
Afibrinogenemia/congenital , Hemoperitoneum/genetics , Adolescent , Afibrinogenemia/genetics , Afibrinogenemia/therapy , Blood Transfusion , Female , Hemoperitoneum/diagnosis , Hemoperitoneum/therapy , Humans
3.
Prog Neuropsychopharmacol Biol Psychiatry ; 32(1): 155-9, 2008 Jan 01.
Article in English | MEDLINE | ID: mdl-17804133

ABSTRACT

OBJECTIVE: To determine Red Blood Cell (RBC) antioxidant enzyme activities and plasma Thiobarbituric Acid Reactive Substances (TBARS) in clinically stable patients with schizophrenia and their unaffected siblings. METHODS: A case-control study carried out on three groups: 60 schizophrenic patients treated with neuroleptics, 33 of their unaffected siblings and 30 healthy controls with no family psychiatric history. Biological markers were measured on fasting patients after a period of tobacco abstinence: RBC antioxidant enzyme activities - superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) - by spectrophotometry and plasma levels of TBARS by spectrofluorimetry. RESULTS: RBC SOD and CAT activities were significantly lower in schizophrenic patients and their unaffected siblings compared to the control group (P<0.001). Schizophrenic patients also had significantly lower RBC GSH-Px activity than controls (P=0.03), whereas their unaffected siblings had significantly higher RBC GSH-Px activity than controls (P=0.04). Plasma TBARS were higher in schizophrenic patients than their unaffected siblings: 2.1+/-0.8 micromol/l vs. 1.7+/-0.6 micromol/l (P=0.06). CONCLUSIONS: Our results showed a decrease in antioxidant enzyme activities and an increase in lipid peroxidation confirming the existence of oxidative stress in schizophrenic patients treated with neuroleptics. Additionally, this suggests that the increase in GSH-Px activity in unaffected siblings would be a protective mechanism against oxidative stress and damage. Other studies are necessary to confirm these findings.


Subject(s)
Erythrocytes/enzymology , Schizophrenia/blood , Schizophrenia/enzymology , Siblings , Thiobarbituric Acid Reactive Substances/metabolism , Adult , Analysis of Variance , Catalase/metabolism , Female , Glutathione Peroxidase/metabolism , Humans , Male , Middle Aged , Schizophrenia/genetics , Spectrophotometry/methods , Superoxide Dismutase/metabolism
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