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1.
Psychiatr Pol ; 44(3): 415-26, 2010.
Article in Polish | MEDLINE | ID: mdl-20672520

ABSTRACT

INTRODUCTION: The influence of antipsychotic medication on brain alterations in proton magnetic resonance spectroscopy (1H MRS) in schizophrenia can be the explanation of many discrepancies observed in the previous papers. AIM: The aim of this study was the evaluation of antipsychotic medication effect on the metabolite levels in the brain of schizophrenic patients based on 1H MRS examination. METHODS: The group of 32 patients with a diagnosis of schizophrenia according to DSM-IV and 26 healthy controls were included into the study. The patients were examined twice--once after the period of at least 7 days without neuroleptics (baseline) and for the second time at least 4 weeks after stable doses ofneuroleptics (follow-up). 21 patients were receiving risperidone and 11--olanzapine. Proton resonance spectroscopy was performed on a 1.5 MR scanner. Each volume element (voxel) was localised in the left frontal lobe, in the left temporal lobe and in the left thalamus. Metabolite ratios: N-acetylaspartate (NAA) to creatine (Cr) and unsupressed water signal were analysed. Results. We found the significant increase of the NAA/Cr level in the thalamus in the group of patients treated with risperidone, we didn't observe similar changes in the olanzapine group. CONCLUSIONS: Our results confirm that the neuroleptic drugs, especially atypicals, modify brain metabolism measured by 1H MRS. The pattern of the changes suggest a possible neuroprotective influence of the antipsychototic treatment in schizophrenic patients. The small group of the olanzapine treated patients doses not allow to make any conclusions regarding this type of medication.


Subject(s)
Antipsychotic Agents/administration & dosage , Benzodiazepines/administration & dosage , Brain/metabolism , Risperidone/administration & dosage , Schizophrenia/drug therapy , Adult , Brain/drug effects , Female , Humans , Magnetic Resonance Imaging , Magnetic Resonance Spectroscopy , Male , Olanzapine , Reference Values , Schizophrenia/metabolism , Temporal Lobe/drug effects , Young Adult
2.
Psychiatr Pol ; 44(1): 137-46, 2010.
Article in Polish | MEDLINE | ID: mdl-20449987

ABSTRACT

An increasing number of new biomarkers of alcohol abuse appear in the literature. The most commonly used biomarkers (5-hydroxytryptophol, fatty acid ethyl esters, ethyl glucuronide, phosphatidyl ethanol, ethyl sulphate, mitochondrial aspartate aminotransferase, carbohydrate deficient transferrin, acetaldehyde adducts, beta-hexosaminidase, and sialic acid) were described. Then other known and less known biomarkers associated with alcohol abuse were described in brief (e.g. acetaldehyde, acetate, methanol, alpha-amino-n-butyric acid, dolichol, proteomics). Their sensitivity and specificity is generally higher than that of traditional biomarkers. The time of detection in biological fluids occur from one day to few months after alcohol consumption. Hence, their usefulness in clinical practice as well as in experimental studies is increasing.


Subject(s)
Alcohol-Induced Disorders/metabolism , Alcoholism/diagnosis , Substance Abuse Detection/methods , Acetaldehyde/analysis , Alcoholism/blood , Alcoholism/enzymology , Alcoholism/urine , Aminobutyrates/analysis , Biomarkers/blood , Biomarkers/urine , Dolichols/analysis , Humans , Methanol/analysis , Reference Values , Sensitivity and Specificity
3.
Psychiatr Pol ; 44(1): 127-36, 2010.
Article in Polish | MEDLINE | ID: mdl-20449986

ABSTRACT

Approximately 15% of the Polish population abuse alcohol. Early detection of alcohol problems may prevent their further development and progression. The study reviews traditional biomarkers associated with alcohol abuse. The nature of biomarkers, their practical application and limitations in alcohol abuse detection, in assessment and monitoring of drinking, are reviewed. Despite the limited sensitivity and specificity in alcohol abuse detection, traditional biomarkers remain useful in alcohol abuse detection. They are widely available and relatively inexpensive, providing valuable data on complications of drinking and prognosis as well as on concurrent conditions affected by drinking.


Subject(s)
Alcoholism/blood , Alcoholism/diagnosis , Substance Abuse Detection/methods , Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Biomarkers/blood , D-Alanine Transaminase/blood , Humans , gamma-Glutamyltransferase/blood
4.
Psychoneuroendocrinology ; 34(1): 129-39, 2009 Jan.
Article in English | MEDLINE | ID: mdl-18838228

ABSTRACT

OBJECTIVE: To study the effect of drugs on the hypothalamo-pituitary-gonadal (HPG) axis we compared the endocrine actions of two neuroleptics with different receptor affinity profiles-risperidone and olanzapine in male schizophrenic patients. METHODS: We investigated the levels of prolactin, estradiol, testosterone, LH, FSH and testicular peptide hormone-inhibin B, and we assessed psychopathology (PANSS), sexual function (ASEX) and treatment adherence (DAI-10) in 89 male schizophrenic inpatients treated with olanzapine or risperidone administered orally. The initial and final evaluations were carried out at weeks 3 and 8 after the onset of treatment, respectively. RESULTS: At initial evaluation the mean serum prolactin and inhibin B levels were markedly higher, whereas testosterone level was lower in patients treated with risperidone, than in those treated with olanzapine. In 5 out of 50 subjects from risperidone group (10%) and in 1 from olanzapine group (2.6%) testosterone levels were below the lower limit (<241ng/ml), which reflected Leydig's cell impairment. In one patient receiving risperidone and in three receiving olanzapine, inhibin B level was below 80pg/ml, indicating Sertoli's cell dysfunction. At the final evaluation the mean serum prolactin level was markedly higher in patients taking risperidone, whereas their FSH levels were lower than in patients receiving olanzapine. In all investigated groups, except for the risperidone-hyperprolactinemic group inhibin B levels were negatively correlated with serum FSH. The mean LH, FSH, testosterone and estradiol levels were within the normal reference range at initial and final evaluation. The non-adherence to medications and ASEX scores were significantly higher in risperidone groups. Sexual dysfunction and medication non-adherence was not related to prolactin or gonadal hormone levels. CONCLUSIONS: Risperidone elicited higher PRL elevation than olanzapine. Treatment with this medication can be associated with disturbances in reproductive hormones (testosterone) and gonadotropins (FSH). The cause of olanzapine-elicited reduction of inhibin B level and the lack of negative correlation between FSH and inhibin B in patients with risperidone-induced hyperprolactinemia require further investigation. Patients receiving risperidone showed higher level of sexual dysfunction and treatment non-adherence than those treated with olanzapine.


Subject(s)
Antipsychotic Agents/pharmacology , Benzodiazepines/pharmacology , Hormones/metabolism , Risperidone/pharmacology , Schizophrenia/physiopathology , Schizophrenic Psychology , Sexual Dysfunction, Physiological/chemically induced , Adult , Antipsychotic Agents/adverse effects , Antipsychotic Agents/metabolism , Antipsychotic Agents/therapeutic use , Benzodiazepines/adverse effects , Benzodiazepines/metabolism , Benzodiazepines/therapeutic use , Estradiol/blood , Gonadotropins, Pituitary/blood , Humans , Hyperprolactinemia/chemically induced , Hyperprolactinemia/metabolism , Inhibins/blood , Male , Olanzapine , Patient Compliance , Prolactin/blood , Risperidone/adverse effects , Risperidone/metabolism , Risperidone/therapeutic use , Schizophrenia/drug therapy , Severity of Illness Index , Testosterone/blood
5.
Psychiatr Pol ; 42(1): 87-95, 2008.
Article in Polish | MEDLINE | ID: mdl-18567406

ABSTRACT

Human sexual function is complex and effected in many different ways by schizophrenia and the antipsychotic drugs used in its treatment. Although not extensively researched, sexual dysfunction seems to be frequent in patients with schizophrenia, especially in men. They appear, in significant part, to be a direct consequence of dopamine antagonism, combined with indirect effects due to increased serum prolactin (PRL) concentration. All of the typical antipsychotics and risperidone can cause substantial PRL elevation. Hyperprolactinemia in male schizophrenics might decrease libido, cause anorgasmia and lead to erectile dysfunction. These sexual side effects are closely associated with the patients' willingness to take antipsychotics, and can affect compliance.


Subject(s)
Antipsychotic Agents/adverse effects , Hyperprolactinemia/chemically induced , Risperidone/adverse effects , Schizophrenia/drug therapy , Sexual Dysfunctions, Psychological/chemically induced , Antipsychotic Agents/therapeutic use , Ejaculation/drug effects , Humans , Libido/drug effects , Male , Orgasm/drug effects , Risperidone/therapeutic use
6.
Med Sci Monit ; 13 Suppl 1: 17-22, 2007 May.
Article in English | MEDLINE | ID: mdl-17507880

ABSTRACT

BACKGROUND: NAA, marker of neurons integrity and viability, is one of the most important brain metabolites visible in 1H MRS. In most studies of schizophrenia, the decrease of NAA level was observed in the temporal, frontal lobes and in the thalamus. This finding was observed more often among chronic patients, what suggests the influence of disease duration or the effect of neuroleptic treatment. The aim of the present study was the comparison of NAA levels in brain of schizophrenic patients taking typical and atypical neuroleptics. MATERIAL/METHODS: We analyzed the NAA levels in selected brain areas in 58 schizophrenic patients and 21 healthy controls. 10 patients were treated with typical neuroleptics, 10 patients with clozapine, 17 received olanzapine and 21 - risperidone. 1H MRS was performed on a 1,5 MR scanner with PRESS sequence. Voxels of 2x2x2 cm were localized in the left frontal, left temporal lobe and left thalamus. RESULTS: There were no differences in NAA levels between patients on typical and atypical medications analyzed together and separately (olanzapine, clozapine and risperidone groups). We also did not find any differences between patients taking selected atypical neuroleptics and controls. The NAA level in the thalamus in the group of patients receiving typical antipsychotics was the lowest among all groups and differed significantly from healthy controls. CONCLUSIONS: The results of our study suggest that atypical neuroleptics may have favorable effect on NAA concentration in brain of schizophrenic patients. Decrease in NAA level in patients taking typical medication may be caused by the progression of the disease or by the direct action of these drugs.


Subject(s)
Antipsychotic Agents/therapeutic use , Aspartic Acid/analogs & derivatives , Brain/anatomy & histology , Brain/metabolism , Schizophrenia/drug therapy , Schizophrenia/metabolism , Adult , Aspartic Acid/metabolism , Brain/pathology , Female , Humans , Magnetic Resonance Imaging , Male , Schizophrenia/pathology , Schizophrenia/physiopathology
7.
Psychiatr Pol ; 41(5): 715-26, 2007.
Article in Polish | MEDLINE | ID: mdl-18421926

ABSTRACT

AIM: The study was undertaken to investigate possible influence of alcoholism on the course and psychopathology of schizophrenia. METHOD: A representative sample of 61 subjects was selected from schizophrenic patients with a history of alcohol dependence (dual diagnosis) registered in the period of 1997-2000. They were compared with 60 control patients with a single diagnosis of schizophrenia. In two groups, with the interview and clinical scales, the onset, course and psychopathology of schizophrenia were assessed. RESULTS: Male patients with schizophrenia and alcohol dependence had a later mean age at onset of mental illness, women--a higher rate of alcohol abuse in the family compared to the control groups. In men with dual diagnosis, the negative symptoms were less prominent. Women with schizophrenia and alcohol dependence reported more depressive symptomatology.


Subject(s)
Alcoholism/epidemiology , Schizophrenia/epidemiology , Severity of Illness Index , Adult , Age of Onset , Case-Control Studies , Causality , Comorbidity , Depression/epidemiology , Diagnosis, Dual (Psychiatry) , Female , Humans , Male , Middle Aged , Multivariate Analysis , Schizophrenic Psychology , Sex Factors
8.
Psychiatr Pol ; 38(3): 433-42, 2004.
Article in Polish | MEDLINE | ID: mdl-15199653

ABSTRACT

UNLABELLED: Earlier studies suggest that psychoeducation as a form of psychosocial care is of value in improving the patient's attitude towards mental illness as well as in reducing and delaying the relapse rates of both--psychotic and depressive disorders. AIM: The aim of this study was the evaluation of influence of psychoeducation on clinical symptoms, quality of life and drug attitude in schizophrenic and depressive patients. METHOD: 52 patients, aged 18-50 years, hospitalized in the Department of Psychiatry of Medical Academy in Bialystok, were involved in the study. They were randomly assigned into 2 groups: on medication without psychoeducation (12 schizophrenics, 12 depressive patients) and on medication and psychoeducation (16 schizophrenics and 12 depressive patients). The patients were assessed by means of BPRS, BNS, IMHC 2000, Raskin/Covi Scale, DAI-10. The assessment was performed twice--shortly after admission and before discharge from the hospital. RESULTS: The patients in both groups showed improvement in symptoms and in quality of life. Patients on psychoeducation changed their drug attitude positively significantly more often. CONCLUSION: Knowledge about the positive influence of medication on psychiatric symptoms helps to improve compliance and improves the course of disease.


Subject(s)
Cognitive Behavioral Therapy , Depressive Disorder/rehabilitation , Patient Education as Topic , Quality of Life , Schizophrenia/rehabilitation , Adult , Antidepressive Agents/therapeutic use , Antipsychotic Agents/therapeutic use , Cognitive Behavioral Therapy/methods , Depressive Disorder/drug therapy , Depressive Disorder/psychology , Female , Humans , Male , Middle Aged , Patient Compliance , Patient Education as Topic/methods , Patient Satisfaction , Poland , Psychiatric Status Rating Scales , Schizophrenia/drug therapy , Schizophrenic Psychology , Surveys and Questionnaires , Time Factors , Treatment Outcome
9.
Pol Merkur Lekarski ; 15(86): 161-4, 2003 Aug.
Article in Polish | MEDLINE | ID: mdl-14648983

ABSTRACT

North-East of Poland is an area endemic for borreliosis. Psychiatric disorders, the most common for the late stage, are more and more frequent manifestations of Lyme disease. The aim of this study is to assess the incidence of different psychiatric complications and identify the spectrum of symptoms and psychopathological syndromes associated with Borrelia burgdorferi infection. Lyme disease causes a variety of psychiatric symptoms. They are less common in skin type of borreliosis manifested by skin erythema.


Subject(s)
Lyme Disease/psychology , Mental Disorders/etiology , Adult , Female , Humans , Incidence , Lyme Disease/epidemiology , Male , Mental Disorders/epidemiology , Middle Aged
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