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1.
Acta Psychiatr Scand ; 138(3): 253-266, 2018 09.
Article in English | MEDLINE | ID: mdl-29984409

ABSTRACT

OBJECTIVE: The study aimed to explore premorbid academic and social functioning in patients with schizophrenia, and its associations with the severity of negative symptoms and neurocognitive impairment. METHOD: Premorbid adjustment (PA) in patients with schizophrenia was compared to early adjustment in unaffected first-degree relatives and healthy controls. Its associations with psychopathology, cognition, and real-life functioning were investigated. The associations of PA with primary negative symptoms and their two factors were explored. RESULTS: We found an impairment of academic and social PA in patients (P ≤ 0.000001) and an impairment of academic aspects of early adjustment in relatives (P ≤ 0.01). Patients with poor PA showed greater severity of negative symptoms (limited to avolition after excluding the effect of depression/parkinsonism), working memory, social cognition, and real-life functioning (P ≤ 0.01 to ≤0.000001). Worse academic and social PA were associated with greater severity of psychopathology, cognitive impairment, and real-life functioning impairment (P ≤ 0.000001). Regression analyses showed that worse PA in the academic domain was mainly associated to the impairment of working memory, whereas worse PA in the social domain to avolition (P ≤ 0.000001). CONCLUSION: Our findings suggest that poor early adjustment may represent a marker of vulnerability to schizophrenia and highlight the need for preventive/early interventions based on psychosocial and/or cognitive programs.


Subject(s)
Academic Performance/psychology , Cognition Disorders/psychology , Cognitive Dysfunction/psychology , Schizophrenia/diagnosis , Academic Performance/trends , Adult , Aged , Cognition/physiology , Cognition Disorders/diagnosis , Cognitive Dysfunction/diagnosis , Depression/epidemiology , Depression/psychology , Female , Humans , Male , Memory, Short-Term/physiology , Middle Aged , Motivation , Psychiatric Status Rating Scales/standards , Psychopathology , Schizophrenia/epidemiology , Schizophrenia/therapy , Schizophrenic Psychology , Severity of Illness Index , Social Adjustment , Social Behavior
2.
Int J Immunopathol Pharmacol ; 24(3): 673-81, 2011.
Article in English | MEDLINE | ID: mdl-21978699

ABSTRACT

Severe fatigue and a significantly reduced health-related quality of life (HRQoL) have been described in patients with chronic fatigue syndrome (CFS) in comparison with patients affected by chronic hepatitis C (CHC) and other chronic medical conditions. We examined 39 CFS and 49 CHC patients to explore whether fatigue and a poor HRQoL represent a greater medical and social problem in CFS than in CHC. The severity of fatigue and the HRQoL were assessed using the Fatigue Impact Scale (FIS) and the Health Status Questionnaire Short Form-36 (SF-36), respectively. The statistical analysis showed both a higher score of fatigue and a lower HRQoL in CFS than in CHC patients. Furthermore, in CHC patients the FIS evaluation showed a significantly reduced score of the psychosocial domain in comparison with the other domains. Multivariate linear regression analysis revealed female gender as the most important positive variable in chronic hepatitis C patients for total score of FIS. In conclusion, CFS was associated with a severe and disabling fatigue and an impaired HRQOL. In particular, both fatigue and all aspects of HRQOL perceived by CFS patients were significantly impaired compared to CHC patients. Consequently, management of fatigue should be considered a priority in order to improve HRQOL in CFS patients. In CHC patients the impact of fatigue on HRQoL was less significant than in CFS patients, even though the FIS evaluation showed a significant impairment of the psychosocial domain.


Subject(s)
Fatigue Syndrome, Chronic/physiopathology , Fatigue Syndrome, Chronic/psychology , Hepatitis C, Chronic/physiopathology , Hepatitis C, Chronic/psychology , Muscle Fatigue/physiology , Quality of Life/psychology , Adult , Aged , Fatigue Syndrome, Chronic/epidemiology , Female , Health Status , Hepatitis C, Chronic/epidemiology , Humans , Linear Models , Male , Middle Aged , Sex Factors , Socioeconomic Factors , Surveys and Questionnaires , Young Adult
3.
Int J Immunopathol Pharmacol ; 24(4): 1017-25, 2011.
Article in English | MEDLINE | ID: mdl-22230407

ABSTRACT

Patients with chronic fatigue syndrome (CFS) often report a comorbid depressive disorder. Comorbid depression may negatively influence the long-term outcome of CFS therefore it must be correctly diagnosed and treated. The aim of the present study is to provide a clinical and psychometric assessment of CFS patients with and without depressive features. A comparative analysis between 57 CFS subjects (CDC, 1994), 17 of whom with a comorbid depression, and 55 matched healthy volunteers was assessed to evaluate the presence of any psychophysical distress and alexithymic traits, by means of Symptom Checklist-90-R (SCL-90R) and Toronto Alexithymia Scale (TAS-20). The severity of fatigue was also assessed in all CFS patients using the Fatigue Impact Scale (FIS). With regard to psychiatric comorbidity, the SCL-90R scores showed higher levels of somatic complaints in CFS patients than in healthy subjects, whereas augmented depressive and obsessive-compulsive symptoms were observed only in the depressed CFS subgroup. When comparing the TAS-20 scores, we observed a selective impairment in the capacity to identify feelings and emotions, as measured by the Difficulty in Identifying Feelings subscale (DIF), non-depressed CFS patients showing an intermediate score between depressed CFS and healthy controls. Finally, in terms of FIS scores, a statistical trend versus a higher fatigue severity in depressed CFS patients, with respect to non-depressed ones, was observed. In conclusion, comorbid depression in CFS significantly increased the level of psychophysical distress and the severity of alexithymic traits. These findings suggest an urgent need to address and treat depressive disorders in the clinical care of CFS cases, to improve social functioning and quality of life in such patients.


Subject(s)
Affective Symptoms/psychology , Depressive Disorder/psychology , Fatigue Syndrome, Chronic/psychology , Stress, Psychological/psychology , Adult , Affective Symptoms/diagnosis , Affective Symptoms/epidemiology , Analysis of Variance , Case-Control Studies , Checklist , Chi-Square Distribution , Comorbidity , Depressive Disorder/diagnosis , Depressive Disorder/epidemiology , Fatigue Syndrome, Chronic/diagnosis , Fatigue Syndrome, Chronic/epidemiology , Female , Hospitalization , Humans , Italy/epidemiology , Male , Middle Aged , Predictive Value of Tests , Psychiatric Status Rating Scales , Psychometrics , Severity of Illness Index , Stress, Psychological/diagnosis , Stress, Psychological/epidemiology
4.
Neurophysiol Clin ; 40(5-6): 255-65, 2010.
Article in English | MEDLINE | ID: mdl-21093797

ABSTRACT

AIMS OF THE STUDY: Earlier P300 studies were conducted when the prevalence of dementia with Lewy Bodies (DLB) was unknown. Our study aims to examine whether P300 abnormalities are present in DLB and to evidence possible differences between DLB and Alzheimer's disease (AD). A second aim of this study is to look for correlations between P300 recordings and EEG, as abnormal EEG variability has been described in DLB. PATIENTS AND METHODS: Auditory P300 responses were recorded by a classic oddball paradigm in 50 controls, in 36 DLB patients, and in 40 AD patients with MMSE>20. RESULTS: Reliable auditory P300 responses were obtained in 26 DLB (72%), 33 AD (82.5%), and 46 controls (92%). P300 was more delayed and had lower amplitude in DLB compared to AD groups. P300 topography was also different as the anterior-to-posterior scalp amplitude gradient was reversed in DLB. P300 latency correlated with neuropsychological test scores and with EEG variables. Gradient inversion and delayed P300 responses in frontal derivations evidenced differences between DLB and AD patients with a sensitivity of 70% and a specificity of 97%. CONCLUSIONS: P300 recordings are abnormal in DLB and can be useful to distinguish DLB from AD.


Subject(s)
Alzheimer Disease/diagnosis , Alzheimer Disease/physiopathology , Cognition/physiology , Electroencephalography/methods , Event-Related Potentials, P300/physiology , Lewy Body Disease/diagnosis , Lewy Body Disease/physiopathology , Aged , Alzheimer Disease/psychology , Cognition Disorders/diagnosis , Female , Humans , Lewy Body Disease/psychology , Male , Middle Aged , Neuropsychological Tests , Psychiatric Status Rating Scales , Reproducibility of Results , Socioeconomic Factors
5.
J Biol Regul Homeost Agents ; 22(3): 195-200, 2008.
Article in English | MEDLINE | ID: mdl-18842173

ABSTRACT

The aim of the present study is to evaluate role of plasma antioxidants (albumin, bilirubin and uric acid) in patients suffering from type I Bipolar Disorder (BD-I) during different phases of illness: acute mania, euthymia and bipolar depression. Medical records of consecutive 110 BD-I patients (38 patients with acute mania, 35 in euthymic state, full remission, and 37 in depressive phase) were reviewed to evaluate plasma antioxidant levels. Laboratory data of 40 healthy controls were also obtained. The scores of Young Mania Rating Scale (YMRS), Bech-Rafaelsen Manic Rating Scale (BRMRS) and Hamilton Rating Scale for Depression (HAM-D) were evaluated. Serum uric acid levels were higher in acute mania than other patient subgroups and healthy controls. Serum uric acid levels directly correlated with BRMRS and YMRS scores. No differences were found between clinical groups during different phases and healthy controls concerning albumin and bilirubin. In conclusion, the results of the present study support the notion that serum uric acid levels may be higher in patients with BP-I (especially during manic phases) which may suggest a dysregulation of the purinergic system. However, limitations should be considered and further studies are needed.


Subject(s)
Antioxidants/metabolism , Bipolar Disorder/blood , Bipolar Disorder/psychology , Adult , Bipolar Disorder/classification , Female , Humans , Male
6.
Int J Immunopathol Pharmacol ; 21(2): 319-24, 2008.
Article in English | MEDLINE | ID: mdl-18547475

ABSTRACT

The aim of the present study is to evaluate the role of CRP and Total Cholesterol (TC) in patients suffering from type I Bipolar Disorder (BD-I). Moreover, the goal is to elucidate possible CRP and TC differences in different phases of BD-I: acute mania, euthymia and bipolar depression. Medical records of 90 BD-I patients (30 patients with acute mania, 30 in euthymic state, full remission, and 30 in depressive phase) were reviewed to evaluate serum CRP and TC levels. Laboratory data of 30 healthy controls were also obtained. The scores of Young Mania Rating Scale (YMRS), Bech-Rafaelsen Manic Rating Scale (BRMRS) and Hamilton Rating Scale for Depression (HAM-D) were evaluated. CRP levels were higher in acute mania and depressive phase subgroups when compared to healthy controls. CRP was positively associated with BRMRS and YMRS scores in acute mania and with HAM-D in depressive phase subgroups. TC levels were lower in all clinical groups compared to controls. TC levels were negatively correlated to BRMRS, YMRS and HAM-D. In conclusion, the results of the present study support the notion that CRP and TC may be altered in patients with BP-I.


Subject(s)
Bipolar Disorder/blood , C-Reactive Protein/metabolism , Cholesterol/blood , Adiposity , Adolescent , Adult , Bipolar Disorder/psychology , Female , Humans , Male , Middle Aged , Psychiatric Status Rating Scales , Retrospective Studies
7.
Int J Immunopathol Pharmacol ; 21(1): 23-33, 2008.
Article in English | MEDLINE | ID: mdl-18336728

ABSTRACT

The protein kinase C (PKC) family of enzymes is a regulator of transmembrane signal transduction. There is evidence demonstrating altered activity of some PKC isoforms (PKC-alpha, PKC-delta and PKC-zeta) in the neurons of brains of Alzheimers Disease (AD) sufferers, but little is known about their involvement in the intracellular machinery of amyloid beta protein-reactive T lymphocytes in AD. By applying a modified, split-well culture system, for Abeta(1-42) reactivity, we carried out flow cytometry analysis and biochemical investigations on the possible involvement of PKC-alpha, PKC-delta and PKC-zeta in the signalling system activated in Abeta-reactive T cells purified from peripheral blood mononucleate cells (PBMC) from healthy subjects and patients with AD. Flow cytometry analysis of Abeta(1-42) activated T lymphocytes in the majority of AD patients highlighted a distinct cellular cluster highly expressing phospho-PKC-delta (P-PKC-delta), while most full-blown AD patients highly expressed two distinct P-PKC-delta and phospho-PKC-zeta (P-PKC-zeta) bright sub-populations. The same investigation performed in freshly purified peripheral T lymphocytes, did not highlight any subpopulation, suggesting that the detection of P-PKC-delta and P-PKC-zeta bright subpopulations is specifically linked to Abeta(1-42) activated T lymphocytes. The data presented here, therefore, suggest possible novel hallmarks to discriminate between healthy elderly subjects and beginning or full-blown Alzheimers Disease patients.


Subject(s)
Alzheimer Disease/immunology , Amyloid beta-Peptides/pharmacology , Isoenzymes/metabolism , Lymphocyte Activation , Peptide Fragments/pharmacology , Protein Kinase C/metabolism , T-Lymphocytes/enzymology , Adult , Aged , Aged, 80 and over , Alzheimer Disease/enzymology , Cells, Cultured , Flow Cytometry , Humans , Middle Aged , Phosphorylation , Signal Transduction
8.
Int J Immunopathol Pharmacol ; 19(4): 721-5, 2006.
Article in English | MEDLINE | ID: mdl-17166394

ABSTRACT

Recently, a possible relationship between C-Reactive Protein (CRP), a marker of underlying low-grade inflammation, and mood disorders has been proposed by some researchers. The aim of this review is to elucidate the current facts and views about CRP in mood disorders such as Depressive and Bipolar Disorders. Several studies have examined the relationship between affective disorders and CRP, but the majority of the studies in literature have been limited by retrospective, case-controlled study design, and very few studies have examined the relationship between depression and CRP in large study samples. In conclusion, the role of CRP in mood disorders is, to date, intriguing but somewhat unclear. Further prospective studies are needed to introduce the CRP in clinical settings as a marker of affective states and suicidability.


Subject(s)
C-Reactive Protein/physiology , Mood Disorders/physiopathology , Humans
9.
Int J Immunopathol Pharmacol ; 18(1): 15-9, 2005.
Article in English | MEDLINE | ID: mdl-15698507

ABSTRACT

Cannabinoids are the constituents of the marijuana plants. The central effects of exogenous cannabinoids are implicated in enhancing mood, altering emotional states, and interfering in the formation of short-term memory. Cannabinoid receptors are G protein-coupled receptors with seven transmembrane domains that are expressed on the cell surface with their binding domain exposed to the extracellular space. To date, two cannabinoid receptors have been cloned, CB1 and CB2. Recent evidence suggests that a third CB3 receptor is out there, waiting to be cloned. The endocannabinoids may represent the first members of a new classes of neuromodulators, that are not stored in cell vesicles, but rather synthesised by the cell on demand. The endogenous cannabinoid system could play a central role in several neuropsychiatric disorders and is also involved in other conditions such as pain, spasticity and neuroprotection. Implication of cannabinoid system in the pathogenesis and development of schizophrenia is also discussed.


Subject(s)
Mental Disorders/metabolism , Nervous System Diseases/metabolism , Receptors, Cannabinoid/metabolism , Humans , Mental Disorders/psychology , Nervous System Diseases/psychology , Receptors, Cannabinoid/genetics , Receptors, Cannabinoid/physiology , Schizophrenia/etiology
10.
Int J Immunopathol Pharmacol ; 18(4): 737-44, 2005.
Article in English | MEDLINE | ID: mdl-16388723

ABSTRACT

Hypothalamic pituitary thyroid (HPT) axis abnormalities and alterations in major depression are reported in the literature. The aim of our study was to evaluate the effect of mirtazapine on thyroid hormones after 6 months of therapy in a sample of adult outpatients with Major Depression (MD). 17 adult outpatients (7 men, 10 women) with MD according to DSM-IV criteria, were included in the study. All participants had to have met criteria for a major depressive episode with a score of at least 15 on the Hamilton Depression Rating Scale (HAM-D). Fasting venous blood samples were obtained for determination of serum Thyroid Stimulating Hormone (TSH), Free T3 (FT3) and Free T4 (FT4) concentrations both at baseline and after 6 months of therapy. HAM-D scores decreased significantly from the first day of treatment to the end of the treatment period (P<0.001) and twelve patients (70.6%) were classified as responders. A significant increase in FT3 concentrations was found between baseline and the end of the treatment period (P=0.015), whereas FT4 concentrations decreased (P=0.046). No significant changes were found in TSH levels. Higher FT4 concentrations at baseline predicted higher HAM-D scorers both at baseline and at the end of the treatment period. Furthermore, higher FT3 concentrations at endpoint were found to be predictors of lower HAM-D scores. Long-term treatment with mirtazapine increases FT3 levels and decreases FT4 maybe involving the deiodination process of T4 into T3.


Subject(s)
Antidepressive Agents, Tricyclic/adverse effects , Depressive Disorder, Major/blood , Mianserin/analogs & derivatives , Thyroid Hormones/blood , Adult , Antidepressive Agents, Tricyclic/therapeutic use , Depressive Disorder, Major/drug therapy , Female , Humans , Hypothalamo-Hypophyseal System/drug effects , Male , Mianserin/adverse effects , Mianserin/therapeutic use , Middle Aged , Mirtazapine , Psychiatric Status Rating Scales , Regression Analysis , Thyroid Gland/drug effects , Thyrotropin/blood , Thyroxine/blood , Treatment Outcome , Triiodothyronine/blood
12.
Neurol Sci ; 21(4): 209-15, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11214659

ABSTRACT

Four patients affected by severe Parkinson's disease developed leucopenia (900-1200 WBC) during treatment of psychosis (3) or untreatable insomnia (1) with clozapine (37.5-75 mg/day). Clozapine withdrawal was followed by recovery of leucopenia (4000-6000 WBC) in two weeks with no need for the administration of leucokines. After 1-6 months olanzapine was administered (increasing the dose from 2.5 to 10 mg/day) to treat persisting disturbances, but the drug induced severe worsening of parkinsonism and also this drug had to be withdrawn.


Subject(s)
Antipsychotic Agents/adverse effects , Clozapine/adverse effects , Leukopenia/chemically induced , Parkinson Disease/drug therapy , Pirenzepine/analogs & derivatives , Pirenzepine/adverse effects , Aged , Aged, 80 and over , Antipsychotic Agents/administration & dosage , Benzodiazepines , Clozapine/administration & dosage , Dose-Response Relationship, Drug , Female , Hallucinations/drug therapy , Hallucinations/etiology , Hallucinations/physiopathology , Humans , Leukopenia/physiopathology , Male , Olanzapine , Parkinson Disease/physiopathology , Parkinson Disease/psychology , Pirenzepine/administration & dosage , Psychotic Disorders/drug therapy , Psychotic Disorders/etiology , Psychotic Disorders/physiopathology , Sexual Dysfunctions, Psychological/drug therapy , Sexual Dysfunctions, Psychological/etiology , Sexual Dysfunctions, Psychological/physiopathology , Sleep Initiation and Maintenance Disorders/drug therapy , Sleep Initiation and Maintenance Disorders/etiology , Sleep Initiation and Maintenance Disorders/physiopathology
13.
Int J Immunopathol Pharmacol ; 12(3): 157-159, 1999.
Article in English | MEDLINE | ID: mdl-12783645

ABSTRACT

Flunitrazepam (FZ) is a sedative/hypnotic nitro-benzodiazepine. This drug has been accepted by both patients and physicians and in the last 20 years flunitrazepam has been included and studied in many clinical trials so, in many countries, flunitrazepam is one of the most prescribed hypnotic. Since 1980 it has been found that FZ began to be a popular drug among drug abusers all over the word. However, little is known about the difference between Fz and other Benzodiazepines in capacity to produce physiologic dependence or in ability to produce drug taking or drug seeking behaviour. Flunitrazepam has little risk of abuse by the vast majority of patients; however when the drug is taken i. v. or intranasally, its effect is much faster and risk of abuse is much greater. In this report we examine the reasons why some populations of drug abusers prefer flunitrazepam over the other benzodiazepines.

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