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Dive into the research topics where Fabiola Sarchione is active.

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Featured researches published by Fabiola Sarchione.


Current Pharmaceutical Design | 2013

The potential of pregabalin in neurology, psychiatry and addiction: a qualitative overview.

Giovanni Martinotti; M. Lupi; Fabiola Sarchione; Rita Santacroce; Anatolia Salone; Domenico De Berardis; Nicola Serroni; Marilde Cavuto; Maria Salvina Signorelli; Eugenio Aguglia; Alessandro Valchera; Felice Iasevoli; Massimo Di Giannantonio

Pregabalin is an anticonvulsant drug that binds to the α₂δ (alpha2delta) subunit of the voltage-dependent calcium channel in central nervous system (CNS). Pregabalin decreases the release of neurotransmitters, including glutamate, norepinephrine, substance P and calcitonin gene-related peptide. Purpose of this paper is to offer a qualitative overview of the studies currently available in literature about this drug, examining the effectiveness of pregabalin in its various fields of application. Our analysis, conducted on a final selection of 349 scientific papers, shows that pregabalin may help to reduce pain in diabetic neuropathy, in post-herpetic neuralgia and in some patients affected by fibromyalgia. It is also effective for the treatment of diverse types of seizures and has similar efficacy to benzodiazepines and venlafaxine in anxiety disorder. Moreover, pregabalin may be a therapeutic agent for the treatment of alcohol abuse, in both withdrawal phase and relapse prevention. Possible implications in the treatment of benzodiazepines dependence are emerging, but a potential abuse or misuse of the drug has also been reported. Range of dosage may fluctuate considerably, from 75 mg to 600 mg per day. Further studies are needed to completely understand pregabalin mechanism of action in the different diseases.


international journal high risk behaviors & addiction | 2013

The Endocannabinoid System: A Putative Role in Neurodegenerative Diseases

Giuseppe Di Iorio; M. Lupi; Fabiola Sarchione; Ilaria Matarazzo; Rita Santacroce; Filippo Petruccelli; Giovanni Martinotti; Massimo Di Giannantonio

Background: Following the characterization of the chemical structure of D9-tetrahydrocannabinol (THC), the main psychoactive constituent of marijuana, researchers have moved on with scientific valuable explorations. Objectives: The aim of this review is to highlight the role of endocannabinoid system in neurodegenerative diseases. Materials and Methods: The article is a critical analysis of the most recent data currently present in scientific literature on the subject; a qualitative synthesis of only the most significant articles has been performed. Results: In central nervous system, endocannabinoids show a neuromodulatory function, often of retrograde type. This way, they play an important role in synaptic plasticity and in cognitive, motor, sensory and affective processes. In addition, in some acute or chronic pathologies of central nervous system, such as neurodegenerative and neuroinflammatory diseases, endocannabinoids can perform a pro-homeostatic and neuroprotective function, through the activation of CB1 and CB2 receptors. Scientific evidence shows that an hypofunction or a dysregulation of the endocannabinoid system may be responsible for some of the symptoms of diseases such as multiple sclerosis, amyotrophic lateral sclerosis, Huntington’s, Parkinson’s and Alzheimer’s diseases. Conclusions: The important role played by endocannabinoid system promises interesting developments, in particular to evaluate the effectiveness of new drugs in both psychiatry and neurology.


Journal of Health Psychology | 2017

Alcohol drinking patterns in young people: A survey-based study:

Giovanni Martinotti; M. Lupi; Leonardo Carlucci; Rita Santacroce; E. Cinosi; T. Acciavatti; Fabiola Sarchione; Valeria Verrastro; Pierluigi Diotaiuti; Irene Petruccelli; S. Ferrari; Maria Giulia Nanni; Federica Pinna; Umberto Volpe; Aristide Saggino; Luigi Janiri; Lorenzo Leggio; Massimo Di Giannantonio

Binge drinking represents a major clinical and public health concern. Here, we investigated the prevalence of binge drinking and its related consequences, in a population of young adults. A questionnaire was administered to a sample of 4275 healthy subjects. In the overall sample, the percentage of binge drinkers was 67.6 per cent; among regular alcohol users, 79.5 per cent reported episodes of binge drinking. Among binge drinkers, several serious consequences were identified (staggering and stuttering, amnesia, loss of control, aggressiveness, sexual disinhibition). Raising awareness about the seriousness of binge drinking may help health care providers to identify cases early on and provide appropriate treatments.


Clinical Neuropharmacology | 2014

Bupropion as an add-on therapy in depressed bipolar disorder type I patients with comorbid cocaine dependence.

Gianna Sepede; Giuseppe Di lorio; M. Lupi; Fabiola Sarchione; T. Acciavatti; F. Fiori; Rita Santacroce; Giovanni Martinotti; Francesco Gambi; Massimo Di Giannantonio

ObjectivesThe treatment of bipolar disorder type I (BD-I) with a comorbid cocaine dependence disorder (CDD) is a challenge in current psychiatric practice. Drugs with proven efficacy in manic/mixed episodes, such as atypical antipsychotics and mood stabilizers, sometimes do not prevent depressive relapses; on the other hand, the use of antidepressants during acute depressive episodes may increase the risk of a manic switch. The aim of the present study was to investigate the short-term efficacy of bupropion augmentation in acutely depressed BD-I patients with co-occurring CDD. MethodsTwelve depressed BD-I patients, with a comorbid CDD, treated with valproate 1000 to 1500 mg/d and aripiprazole 10 mg/d, were randomly assigned to receive bupropion 150 mg/d as an open-label add-on therapy (n = 5) or to continue their previous treatment (n = 7). ResultsAfter 4 weeks of observation, patients receiving add-on therapy with bupropion have improved in terms of Hamilton Depression Rating Scale scores and Drug Abuse Screening Test scores, with respect to those of the comparison group, whereas no significant increase of Young Mania Rating Scale scores over time was observed. ConclusionsOur preliminary findings suggest that combining bupropion with mood stabilizers and atypical antipsychotics may be a good therapeutic option in short-term treatment of depressed BD-I patients with comorbid CDD.


Human Psychopharmacology-clinical and Experimental | 2017

Substance-related psychopathology and aggressiveness in a nightlife holiday resort: Results from a pilot study in a psychiatric inpatient unit in Ibiza

Giovanni Martinotti; E. Cinosi; Rita Santacroce; Duccio Papanti; Anna Pasquini; Valerio Mancini; M. Corbo; F. Fiori; Fabiola Sarchione; Daniela Marchetti; M.C. Verrocchio; Massimo Di Giannantonio; Marta Torrens; Fabrizio Schifano; Maria Jose Morlan Coarasa; Cristina Merino del Villar

We aimed to describe a sample of subjects admitted to a psychiatric unit after the intake of psychoactive substances for recreational purposes.


European Psychiatry | 2015

Prevalence of Orthorexia Nervosa in a Population of Young Italian Adults

E. Cinosi; Ilaria Matarazzo; Stefano Marini; T. Acciavatti; M. Lupi; M. Corbo; Rita Santacroce; Federica Vellante; Fabiola Sarchione; Domenico De Berardis; Alessandro Carano; G. Di Iorio; G. Martinotti; M. Di Giannantonio

Introduction Orthorexia nervosa (ON) is an alleged eating disorder in which the person is excessively preoccupied with healthy food. First described by Bratman in 1997, ON entails a fixation on healthy food or a health food dependence. The term orthorexia nervosa arises from the Greek words orthos (=accurate) and orexis (=hunger) meaning obsession with healthy food and proper nutrition. Fears and worries about health, eating, and the quality of food are significant. Objectives We investigated the prevalence of ON in a a population of young Italian adults by using a validated questionnaire (ORTO-15). Aims We aimed to assess the prevalence of ON in a large sample of general population and to identify some possible specific correlation such as gender and Body Mass Index (BMI). Methods 1453 adult subjects from the general population were administered the ORTO-15 test and investigated for gender, age and BMI. Statistical analyses were performed referring to diagnostic threshold (40). Results Orthorexia had a 10,9% prevalence in our sample, with a female prevalence statistically significant (female vs male= 72,8% vs 27,2%). Moreover, age and Body Mass Index did not seem to be significant factors. Conclusions ON is not currently considered as a full-fledged and discrete mental disorder. Again, the definition and diagnostic criteria of ON remain unclear. Further studies are needed to clarify appropriate diagnostic methods and the place of ON among psychopathological categories. This should be accompanied by a vigorous research effort aimed at understanding the core nature of this condition.


Clinical Neuropharmacology | 2016

Premenstrual Dysphoric Disorder Without Comorbid Psychiatric Conditions: A Systematic Review of Therapeutic Options.

Gianna Sepede; Fabiola Sarchione; Ilaria Matarazzo; Massimo Di Giannantonio; Rosa Maria Salerno

ObjectivesPremenstrual dysphoric disorder (PMDD) is a disabling condition affecting approximately 2% to 8% of women during reproductive age. It has been recently included in the mood disorder section of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, but its treatment as a primary psychiatric illness is still debated, because of the high prevalence of other mental disturbances in PMDD patients. On the other hand, clear clinical guidelines for PMDD patients not suffering from comorbid mental conditions are not yet available. The aim of the present study was therefore to systematically review the original articles pertaining to the treatment of PMDD in adult women free of any current or previous psychiatric comorbidity. MethodsWe searched PubMed to identify published studies on PMDD, including randomized controlled trials, open-label trials, and case series or case reports involving adult women with no history of comorbid mental conditions. The search was conducted in April 2015. ResultsWe found 55 studies fulfilling our inclusion criteria, 49 of them focused on pharmacological/chemical agents and the remaining 6 on nonpharmacological interventions. ConclusionsBased on the results of our qualitative synthesis, the best therapeutic option in the treatment of adult PMDD patients free of other mental disorders are selective serotonin reuptake inhibitor antidepressants (especially paroxetine and fluoxetine) and low doses of oral estroprogestins. Other interventions, such as light therapy, cognitive behavioral therapy, food supplements, and herbal medicines, showed promising effects, but other investigations are needed to confirm their efficacy.


Progress in Neuro-psychopharmacology & Biological Psychiatry | 2018

Creativity and psychiatric illness: A functional perspective beyond chaos

Federica Vellante; Fabiola Sarchione; Sjoerd J. H. Ebisch; Anatolia Salone; Laura Orsolini; Stefano Marini; Alessandro Valchera; Michele Fornaro; Alessandro Carano; Felice Iasevoli; Giovanni Martinotti; Domenico De Berardis; Massimo Di Giannantonio

HIGHLIGHTSCreativity may be proposed as a bridge between free association and psychiatric disorders in a perspective in which creativity could have neural biomarkers linked one side to free association and to psychiatric diseases too.Literature data report association between creativity and psychiatric illness otherwise. It would be thought that creativity could be canalized in a productive way if passing from a pathological perspective to a free associated one.Free associations have been found having neural basis although many studies are needed.There are, among others, Self‐related brain regions that could be studied in a functional dynamic connectivity perspective to highlight both free association and psychiatric disorders if the focus is creativity.


Human Psychopharmacology-clinical and Experimental | 2017

A matter of life and death: substance-caused and substance-related fatalities in Ibiza in 2015

Rita Santacroce; Claudia Ruiz Bennasar; Juan Ramon Sancho Jaraiz; F. Fiori; Fabiola Sarchione; Federica Angelini; Gabriella Catalano; Maria Luisa Carenti; John Corkery; Fabrizio Schifano; Massimo Di Giannantonio; Giovanni Martinotti

In the framework of the EU‐funded project “EU‐Madness,” we collected and analysed all the reports of fatalities directly or indirectly related to substances of abuse registered in Ibiza from January to September 2015, in order to analyse the characteristics of the sample, the identified substances, and the nature of deaths associated with their consumption.


Clinical Neuropharmacology | 2016

A Case of Resistant Schizophrenia Successfully Treated With Clozapine/long-acting Injectable Aripiprazole Combination

Gianna Sepede; Giuseppe Di Iorio; Maria Chiara Spano; Marco Lorusso; Fabiola Sarchione; Rita Santacroce; Rosa Maria Salerno; Massimo Di Giannantonio

BackgroundTreatment-resistant schizophrenia (TRS) is a condition characterized by intense symptom severity and poor response to different antipsychotic agents. The first therapeutic option in TRS is clozapine, but often high/medium doses are not tolerated. Adding an oral antipsychotic to low doses of clozapine is a promising strategy in the management of TRS. On the contrary, there are few data on combined clozapine/long-acting injectable (LAI) medications, and none on clozapine/LAI-aripiprazole. CaseA 21-year-old male schizophrenic patient, resistant to several oral and LAI medications, partially improved after clozapine 300 mg/d treatment. Unfortunately, he also reported excessive sedation and an episode of myoclonus, so clozapine was reduced to 150 mg/d, but no additional benefits were observed. Subsequently, LAI-aripiprazole (first 200 mg/mo, then 400 mg/mo) was added, and the patients conditions dramatically improved over time. After 1 year of observation, symptoms reduction was 50% or greater, without significant adverse events. ConclusionsClozapine use in TRS is often reduced or delayed due to the fear of serious adverse effects. Adding LAI-aripiprazole to low doses of clozapine may be a useful therapeutic option to obtain a good efficacy/tolerability balance.

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Rita Santacroce

University of Hertfordshire

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M. Di Giannantonio

The Catholic University of America

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Federica Vellante

University of Chieti-Pescara

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E. Cinosi

University of Hertfordshire

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Gianna Sepede

University of Chieti-Pescara

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Stefano Marini

University of Chieti-Pescara

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Laura Orsolini

University of Hertfordshire

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