Davide Arillotta

Dr. Davide Arillotta

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 October 2023 in Brain Sciences
Verified
Journal Article
Open access
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DADavide Arillotta
Davide Arillotta
Giuseppe FlorestaGiuseppe Floresta
Giuseppe Floresta
Amira GuirguisAmira Guirguis
Amira Guirguis
John Martin CorkeryJohn Martin Corkery
John Martin Corkery
VCValeria Catalani
Valeria Catalani
Fabrizio SchifanoFabrizio Schifano
Fabrizio Schifano
The emergence of glucagon-like peptide-1 receptor agonists (GLP-1 RAs; semaglutide and others) now promises effective, non-invasive treatment of obesity for individuals with and without diabetes. Social media platforms’ users started promoting semaglutide/Ozempic as a weight-loss treatment, and the associated increase in demand has contributed to an ongoing worldwide shortage of the drug associated with levels of non-prescribed semaglutide intake. Furthermore, recent reports emphasized some GLP-1 RA-associated risks of triggering depression and suicidal thoughts. Consistent with the above, we aimed to assess the possible impact of GLP-1 RAs on mental health as being perceived and discussed in popular open platforms with the help of a mixed-methods approach. Reddit posts yielded 12,136 comments, YouTube videos 14,515, and TikTok videos 17,059, respectively. Out of these posts/entries, most represented matches related to sleep-related issues, including insomnia (n = 620 matches); anxiety (n = 353); depression (n = 204); and mental health issues in general (n = 165). After the initiation of GLP-1 RAs, losing weight was associated with either a marked improvement or, in some cases, a deterioration, in mood; increase/decrease in anxiety/insomnia; and better control of a range of addictive behaviors. The challenges of accessing these medications were a hot topic as well. To the best of our knowledge, this is the first study documenting if and how GLP-1 RAs are perceived as affecting mood, mental health, and behaviors. Establishing a clear cause-and-effect link between metabolic diseases, depression and medications is difficult because of their possible reciprocal relationship, shared underlying mechanisms and individual differences. Further research is needed to better understand the safety profile of these molecules and their putative impact on behavioral and non-behavioral addictions.

2 April 2022 in Drugs
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Journal Article
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Fabrizio SchifanoFabrizio Schifano
Fabrizio Schifano
VCValeria Catalani
Valeria Catalani
Safia SharifSafia Sharif
Safia Sharif
FNFlavia Napoletano
Flavia Napoletano
John Martin CorkeryJohn Martin Corkery
John Martin Corkery
Amira GuirguisAmira Guirguis
Amira Guirguis

19 March 2024 in European Neuropsychopharmacology
Verified
Journal Article
Open access
Amira GuirguisAmira Guirguis
Amira Guirguis
SCStefania Chiappini
Stefania Chiappini
GPGd Papanti P
Gd Papanti P
RVRachel Vickers-Smith
Rachel Vickers-Smith
DHDaniel Harris
Daniel Harris
FSF Schifano
F Schifano
The study addresses concerns about potential psychiatric side effects of Glucagon-like peptide-1 receptor agonists (GLP-1 RA). The aim of this work was to analyse adverse drug reports (ADRs) from the Food and Drug Administration Adverse Events Reporting System (FAERS) using metformin and orlistat as comparators. Descriptive and pharmacovigilance disproportionality analyses was performed. A total of 209,354 ADRs were reported, including 59,300 serious cases. Of those, a total of 5378 psychiatric disorder cases, including 383 'serious' cases related to selected ADRs were registered during 2005-2023. After unmasking, 271 cases where individual GLP-1 RA were implicated showing liraglutide (n = 90; Reported Odds Ratio (ROR) = 1.64), exenatide (n = 67; ROR = 0.80), semaglutide (n = 61; ROR = 2.03), dulaglutide (n = 45; ROR = 0.84), tirzepatide (n = 5; ROR = 1.76) and albiglutide (n = 2; ROR = 0.04). A greater association between these ADRs with metformin was observed, but not orlistat. With regards to selected preferred terms (PTs), 42 deaths including 13 completed suicides were recorded. Suicidal ideation was recorded in n = 236 cases for 6/7 GLP-1 RA (excluding lixisenatide). Suicide/self-injury reports pertaining to semaglutide; tirzepatide; and liraglutide were characterised, although lower than metformin. It is postulated that rapid weight loss achieved with GLP-1 RA can trigger significant emotional, biological, and psychological responses, hence possibly impacting on suicidal and self-injurious ideations. With the current pharmacovigilance approach, no causality link between suicidal ideation and use of any GLP-1 RA can be inferred. There is a need for further research and vigilance in GLP-1 RA prescribing, particularly in patients with co-existing psychiatric disorders.

20 June 2024 in Brain Sciences
Verified
Journal Article
Open access
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DADavide Arillotta
Davide Arillotta
Giuseppe FlorestaGiuseppe Floresta
Giuseppe Floresta
GPGabriele Duccio Papanti Pelletier
Gabriele Duccio Papanti Pelletier
Amira GuirguisAmira Guirguis
Amira Guirguis
John Martin CorkeryJohn Martin Corkery
John Martin Corkery
Fabrizio SchifanoFabrizio Schifano
Fabrizio Schifano
Glucagon-like peptide-1 (GLP-1) is involved in a range of central and peripheral pathways related to appetitive behavior. Hence, this study explored the effects of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) on substance and behavioral addictions, including alcohol, caffeine, nicotine, cannabis, psychostimulants, compulsive shopping, and sex drive/libido. Data were collected from various social platforms. Keywords related to GLP-1 RAs and substance/behavioral addiction were used to extract relevant comments. The study employed a mixed-methods approach to analyze online discussions posted from December 2019 to June 2023 and collected using a specialized web application. Reddit entries were the focus here due to limited data from other platforms, such as TikTok and YouTube. A total of 5859 threads and related comments were extracted from six subreddits, which included threads about GLP-1 RAs drugs and associated brand names. To obtain relevant posts, keywords related to potential substance use and compulsive behavior were selected. Further analysis involved two main steps: (1) manually coding posts based on users’ references to the potential impact of GLP-1 RAs on substance use and non-substance habits, excluding irrelevant or unclear comments; (2) performing a thematic analysis on the dataset of keywords, using AI-assisted techniques followed by the manual revision of the generated themes. Second, a thematic analysis was performed on the keyword-related dataset, using AI-assisted techniques followed by the manual revision of the generated themes. In total, 29.75% of alcohol-related; 22.22% of caffeine-related; and 23.08% of nicotine-related comments clearly stated a cessation of the intake of these substances following the start of GLP-1 RAs prescription. Conversely, mixed results were found for cannabis intake, and only limited, anecdotal data were made available for cocaine, entactogens, and dissociative drugs’ misuse. Regarding behavioral addictions, 21.35% of comments reported a compulsive shopping interruption, whilst the sexual drive/libido elements reportedly increased in several users. The current mixed-methods approach appeared to be a useful tool in gaining insight into complex topics such as the effects of GLP-1 RAs on substance and non-substance addiction-related disorders; some GLP-1 RA-related mental health benefits could also be inferred from here. Overall, it appeared that GLP-1 RAs may show the potential to target both substance craving and maladaptive/addictive behaviors, although further empirical research is needed.

28 February 2021 in Clinical Psychopharmacology and Neuroscience
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Journal Article
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LFLaura Fusar-Poli
Laura Fusar-Poli
ARAlessandro Rodolico
Alessandro Rodolico
SSSerena Sturiale
Serena Sturiale
BCBianca Carotenuto
Bianca Carotenuto
ANAntimo Natale
Antimo Natale
Eugenio AgugliaEugenio Aguglia
Eugenio Aguglia
Laura Fusar-Poli*, Alessandro Rodolico*, Serena Sturiale, Bianca Carotenuto, Antimo Natale, Davide Arillotta, Spyridon Siafis, Maria Salvina Signorelli, Eugenio Aguglia. Clin Psychopharmacol Neurosci 2021;19:26-45. https://doi.org/10.9758/cpn.2021.19.1.26

18 March 2020 in Frontiers in Neuroscience
Verified
Journal Article
Open access
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DADavide Arillotta
Davide Arillotta
Fabrizio SchifanoFabrizio Schifano
Fabrizio Schifano
FNFlavia Napoletano
Flavia Napoletano
CZCaroline Zangani
Caroline Zangani
LGLiam Gilgar
Liam Gilgar
AVAlessandro Vento
Alessandro Vento
Background: A wide range of novel psychoactive substances (NPSs) are regularly searched and discussed online by e-psychonauts. Among NPSs, the range of prescription/non-prescription opioids (fentanyl and non-fentanyl analogs) and herbal derivatives currently represents a challenge for governments and clinicians. Methods: Using a web crawler (i.e., NPS.Finder®), the present study aimed at assessing psychonaut fora/platforms to better understand the online situation regarding opioids. Results: The open-web crawling/navigating software identified some 426 opioids, including 234 fentanyl analogs. Of these, 176 substances (162 were very potent fentanyls, including two ohmefentanyl and seven carfentanyl analogs) were not listed in either international or European NPS databases. Conclusion: A web crawling approach helped in identifying a large number, indeed higher than that listed by European/international agencies, of unknown opioids likely to possess a significant misuse potential. Most of these novel/emerging substances are still relatively unknown. This is a reason of concern; each of these analogs potentially presents with different toxicodynamic profiles, and there is a lack of docking, preclinical, and clinical observations. Strengthening multidisciplinary collaboration between clinicians and bioinformatics may prove useful in better assessing public health risks associated with opioids.