Publications by authors named "Simona Tomassi"

Article Synopsis
  • The COVID-19 pandemic led to an increase in the use of telepsychiatry, prompting a study to assess the opinions and preferences of service users, carers, and clinicians about its effectiveness.
  • The study involved surveys and focus groups across four sites in the UK and Italy, revealing that telepsychiatry is convenient for specific follow-ups but lacks effectiveness in building therapeutic relationships and assessing acute mental states.
  • Results indicated differing perceptions between clinicians and service users/carers about the quality of telepsychiatry during the pandemic, highlighting the need for a tailored hybrid care model that includes stakeholder preferences and further training for clinicians on telepsychiatry.
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Background: Although it has been proposed that childhood adversities (CAs) may affect the hypothalamic-pituitary-adrenal (HPA) axis activity and psychotic symptoms severity, these associations have not been fully confirmed in first-episode psychosis (FEP). This study explored the association between CA, cortisol and psychotic symptoms in FEP patients.

Methods: 81 FEP patients were enrolled.

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Article Synopsis
  • The study investigates the impact of COVID-19 on the use of telepsychiatry, comparing data from 2020 with two previous years (2018 and 2019) across two UK mental health trusts.
  • Findings show a significant increase in mental health service activity during 2020, with remote consultations surging by 3.5 to 6 times from February to June.
  • For patients with dementia, remote consultations had lower non-attendance rates compared to in-person visits, while the overall health outcomes improved only in patients with organic conditions.
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Introduction: Depression is a quite common comorbidity in patients with rheumatoid arthritis (RA) and is thought to influence its severity. This study aims to estimate, in a large cohort of Italian patients with RA, the prevalence of depression and to investigate the clinical correlates of depression in terms of disease activity and disability.

Methods: This is a cross-sectional study enrolling 490 outpatients with RA (80% female, mean age 59.

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No study investigated the association between stress exposure in different stages of life and metabolic dysfunction. We explore the association between stress exposure and several biomarkers related to glucose metabolism (insulin, c-peptide, GIP, GLP-1, glucagon) in a group of 72 healthy individuals. We used the Childhood Experience of Care and Abuse-Questionnaire (CECA-Q) and a modified version of the Life Events Scale to define exposure to stress, according to four categories: no exposure to childhood trauma (CT) nor to stressful life events (SLEs) (46%), only to CT (25%), only to SLEs (21%), to both (8%).

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Article Synopsis
  • The endocannabinoid (eCB) system is involved in regulating immune responses and has been linked to depressive behaviors, especially after treatments like IFN-α for hepatitis C.
  • Researchers conducted a study to examine how endocannabinoids (anandamide and 2-arachidonoylglycerol) were affected by IFN-α treatment and their potential role in depression among hepatitis C patients.
  • Findings showed that while 2-AG levels increased early during treatment, AEA levels rose later and remained elevated, and HCV patients had lower baseline AEA levels compared to healthy individuals, linking AEA changes to depressive symptoms.
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Although the associations between first-episode psychosis (FEP) and metabolic abnormalities on one side, and childhood trauma (CT) and risk of developing psychosis on the other are both well established, evidence on the relationship between CT and metabolic dysregulation in terms of abnormal glucose metabolism is very limited. We tested whether, already at illness onset, FEP patients with a history of CT show dysregulation of a broad range of glucose metabolism markers. In particular, in 148 FEP patients we evaluated serum concentrations of c-peptide, insulin, plasminogen-activator-inhibitor-1 (PAI-1), resistin, visfatin, glucagon, glucagon-like peptide-1 (GLP-1), gastric-inhibitor-peptide (GIP), leptin, and ghrelin.

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Despite the growing interest in the prodromes of psychosis, the proper identification of those Ultra High Risk (UHR) subjects who will convert to psychosis remains an unresolved issue. It remains to be fully understood whether the risk of transition to psychosis is incremented by the concomitant presence of non-psychotic symptoms. We performed a systematic review in order to estimate: prevalence rates of non-psychotic disorders in UHR individuals and whether any comorbid disorder impacts on the risk of transition to frank psychosis.

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Childhood Trauma (CT) mediation of the epigenome and its impact on gene expression profile could provide a mechanism for the gene-environment interaction underling psychosis. We reviewed the evidence concerning epigenetic and gene expression modifications associated with CT in both First-Episode Psychosis (FEP) and healthy subjects. In order to explore the relative role of psychosis itself in determining these modifications, evidence about FEP and epigenetics/gene expression was also summarized.

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Literature has documented the role of family in the outcome of chronic schizophrenia. In the light of this, family interventions (FIs) are becoming an integral component of treatment for psychosis. The First Episode of Psychosis (FEP) is the period when most of the changes in family atmosphere are observed; unfortunately, few studies on the relatives are available.

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Objective: To summarize risks related to (1) illness and (2) second-generation antipsychotic (SGA) treatment in pregnant women and their offspring. Concerning illness-related risks, we focused on bipolar disorder and schizophrenia, psychiatric disorders for which SGAs are preferentially prescribed.

Data Sources: PubMed, Ovid, Scopus, PsycINFO, and Cochrane Library were searched from the date of the first available article to October 2015 using the following key terms: pregnancy OR gestation OR bipolar disorder OR schizophrenia.

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There is an increasing interest in understanding the biological mechanism underpinning fibromyalgia (FM) and chronic fatigue syndrome (CFS). Despite the presence of mixed findings in this area, a few biological systems have been consistently involved, and the increasing number of studies in the field is encouraging. This chapter will focus on inflammatory and oxidative stress pathways and on the neuroendocrine system, which have been more commonly examined.

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Neuregulin 1 (NRG1) and v-erb-a erythroblastic leukemia viral oncogene homolog 4 (ErbB4) have been extensively studied in schizophrenia susceptibility because of their pivotal role in key neurodevelopmental processes. One of the reasons for the inconsistencies in results could be the fact that the phenotype investigated has mostly the diagnosis of schizophrenia per se, which is widely heterogeneous, both clinically and biologically. In the present study we tested, in a large cohort of 461 schizophrenia patients recruited in Scotland, whether several SNPs in NRG1 and/or ErbB4 are associated with schizophrenia symptom dimensions as evaluated by the Positive and Negative Syndrome Scale (PANSS).

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