Monitoring the psychopathological profile of inflammatory bowel disease patients treated with biological agents: a pilot study.


Journal

Minerva gastroenterology
ISSN: 2724-5365
Titre abrégé: Minerva Gastroenterol (Torino)
Pays: Italy
ID NLM: 101777280

Informations de publication

Date de publication:
18 Sep 2024
Historique:
medline: 18 9 2024
pubmed: 18 9 2024
entrez: 18 9 2024
Statut: aheadofprint

Résumé

Biological agents were found to alter the psychopathological profile of a small subgroup of patients treated for a variety of conditions, including inflammatory bowel disease (IBD) and psychiatric disorders. The association between the administration of biological agents and psychopathology needs to be further investigated. In this naturalistic prospective cohort study, patients with IBD were assigned to two treatment groups, i.e., a biological agent (which also included tofacitinib) or conventional therapy. Clinician-administered scales were used to assess psychosomatic symptoms (Hamilton Depression Rating Scale [Ham-D], Hamilton Anxiety Rating Scale [Ham-A], Young Mania Rating Scale [YMRS], and Brief Psychiatric Rating Scale [BPRS]) and disease activity (Mayo Score and Harvey-Bradshaw Index [HBI]) at baseline, after one, three, and six months of treatment. Each group was assessed for the course of their scores during the observation period at each assessment point. Patients on biological drugs who completed three months of treatment (N.=32) and six months of treatment (N.=20) scored significantly lower on the Mayo compared to baseline. Patients on conventional treatment obtained significant drops from baseline on the HBI after one and three months of treatment (N.=30) and also at the six-month endpoint (N.=11). Both groups showed no improvement or worsening on the psychiatric rating scales. In this study, we found no evidence of psychiatric symptom worsening, as some literature would suggest. Our data suggest that the use of biological agents in IBD is safe.

Sections du résumé

BACKGROUND BACKGROUND
Biological agents were found to alter the psychopathological profile of a small subgroup of patients treated for a variety of conditions, including inflammatory bowel disease (IBD) and psychiatric disorders. The association between the administration of biological agents and psychopathology needs to be further investigated.
METHODS METHODS
In this naturalistic prospective cohort study, patients with IBD were assigned to two treatment groups, i.e., a biological agent (which also included tofacitinib) or conventional therapy. Clinician-administered scales were used to assess psychosomatic symptoms (Hamilton Depression Rating Scale [Ham-D], Hamilton Anxiety Rating Scale [Ham-A], Young Mania Rating Scale [YMRS], and Brief Psychiatric Rating Scale [BPRS]) and disease activity (Mayo Score and Harvey-Bradshaw Index [HBI]) at baseline, after one, three, and six months of treatment. Each group was assessed for the course of their scores during the observation period at each assessment point.
RESULTS RESULTS
Patients on biological drugs who completed three months of treatment (N.=32) and six months of treatment (N.=20) scored significantly lower on the Mayo compared to baseline. Patients on conventional treatment obtained significant drops from baseline on the HBI after one and three months of treatment (N.=30) and also at the six-month endpoint (N.=11). Both groups showed no improvement or worsening on the psychiatric rating scales.
CONCLUSIONS CONCLUSIONS
In this study, we found no evidence of psychiatric symptom worsening, as some literature would suggest. Our data suggest that the use of biological agents in IBD is safe.

Identifiants

pubmed: 39292181
pii: S2724-5985.24.03719-7
doi: 10.23736/S2724-5985.24.03719-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Antonio M D'Onofrio (AM)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy - antoniomdonofrio@gmail.com.

Lodovico M Balzoni (LM)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Gaspare F Ferrajoli (GF)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Federica DI Vincenzo (F)

School of Medicine, Unit of Gastroenterology and Liver Diseases, Department of Internal Medicine, IRCCS A. Gemelli University Polyclinic Foundation, Sacred Heart Catholic University, Rome, Italy.
Department of Medical and Surgical Sciences, CEMAD (Digestive Disease Center), IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Daniele Napolitano (D)

Department of Medical and Surgical Sciences, CEMAD (Digestive Disease Center), IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Elisa Schiavoni (E)

Department of Medical and Surgical Sciences, CEMAD (Digestive Disease Center), IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Georgios D Kotzalidis (GD)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Alessio Simonetti (A)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Marianna Mazza (M)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Ilenia Rosa (I)

Department of Neuroscience, Imaging and Clinical Sciences, G. D'Annunzio University, Chieti, Italy.

Mauro Pettorruso (M)

Department of Neuroscience, Imaging and Clinical Sciences, G. D'Annunzio University, Chieti, Italy.

Gabriele Sani (G)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Antonio Gasbarrini (A)

School of Medicine, Unit of Gastroenterology and Liver Diseases, Department of Internal Medicine, IRCCS A. Gemelli University Polyclinic Foundation, Sacred Heart Catholic University, Rome, Italy.
Department of Medical and Surgical Sciences, CEMAD (Digestive Disease Center), IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Franco Scaldaferri (F)

School of Medicine, Unit of Gastroenterology and Liver Diseases, Department of Internal Medicine, IRCCS A. Gemelli University Polyclinic Foundation, Sacred Heart Catholic University, Rome, Italy.
Department of Medical and Surgical Sciences, CEMAD (Digestive Disease Center), IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Giovanni Camardese (G)

Section of Psychiatry, Department of Neuroscience, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Classifications MeSH