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Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe - A multi-professional survey study.
Koido, Kati; Malmgren, Charlotta Ingvoldstad; Pojskic, Lejla; Almos, Peter Z; Bergen, Sarah E; Borg, Isabella; Bozina, Nada; Coviello, Domenico A; Degenhardt, Franziska; Ganoci, Lana; Jensen, Uffe B; Durand-Lennad, Louise; Laurent-Levinson, Claudine; McQuillin, Andrew; Navickas, Alvydas; Pace, Nikolai P; Paneque, Milena; Rietschel, Marcella; Grigoroiu-Serbanescu, Maria; Soller, Maria Johansson; Suvisaari, Jaana; Utkus, Algirdas; Van Assche, Evelien; Vissouze, Lily; Zuckerman, Shachar; Chaumette, Boris; Tammimies, Kristiina.
Afiliação
  • Koido K; Department of Physiology, Institute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.
  • Malmgren CI; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden; Center for Research and Bioethics, CRB, Uppsala University, Uppsala, Sweden.
  • Pojskic L; Laboratory for Human Genetics, University of Sarajevo - Institute for Genetic Engineering and Biotechnology, Sarajevo, Bosnia and Herzegovina.
  • Almos PZ; Department of Psychiatry, University of Szeged, Szeged, Hungary.
  • Bergen SE; Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
  • Borg I; Pathology Department, Faculty of Medicine and Surgery, University of Malta, Msida, Malta.
  • Bozina N; University of Zagreb School of Medicine, Department of Pharmacology, Zagreb, Croatia.
  • Coviello DA; Laboratory of Human Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Degenhardt F; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Ganoci L; University Hospital Centre Zagreb, Department of Laboratory Diagnostics, Division for Pharmacogenomics and Therapy Individualization, Zagreb, Croatia.
  • Jensen UB; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Durand-Lennad L; Université Paris Cité, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris, Paris, France.
  • Laurent-Levinson C; Faculté de Médecine-Sorbonne Université, Groupe de Recherche Clinique N°15 - Troubles Psychiatriques et Développement (PSYDEV) & Centre de Référence des Maladies Rares à Expression Psychiatrique, DMU ORYGINE Femmes-Mères-Enfants, Service de Psychiatrie de l'Enfant et de l'Adolescent, Assistance
  • McQuillin A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.
  • Navickas A; Psychiatric Clinic, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Pace NP; Centre for Molecular Medicine and Biobanking, University of Malta, Malta.
  • Paneque M; Center for Predictive and Preventive Genetics, Institute of Molecular and Cellular Biology, Institute for Research and Innovation in Health, University of Porto, Porto, Portugal.
  • Rietschel M; Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Germany.
  • Grigoroiu-Serbanescu M; Alexandru Obregia Clinical Psychiatric Hospital, Biometric Psychiatric Genetics Research Unit, Bucharest, Romania.
  • Soller MJ; Department of Clinical Genetics, Karolinska University Hospital, Stockholm and Karolinska Institutet, Stockholm, Sweden.
  • Suvisaari J; Finnish Institute for Health and Welfare, Department of Public Health and Welfare, Mental Health Team, Helsinki, Finland.
  • Utkus A; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Van Assche E; Department of Psychiatry, University of Münster, Münster, Germany.
  • Vissouze L; Université Paris Cité, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris, Paris, France.
  • Zuckerman S; Medical Genetic Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Chaumette B; Université Paris Cité, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris, GHU-Paris Psychiatrie et Neurosciences, Paris, France; Department of Psychiatry, McGill University, Montreal, Canada.
  • Tammimies K; Center of Neurodevelopmental Disorders (KIND), Centre for Psychiatry Research, Department of Women's and Children's Health, Karolinska Institute, Region Stockholm, Stockholm, Sweden; Astrid Lindgren Children's Hospital, Karolinska University Hospital, Region Stockholm, Stockholm, Sweden. Electronic
Eur J Med Genet ; 66(8): 104805, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37406854
ABSTRACT
Genetic research has identified a large number of genetic variants, both rare and common, underlying neurodevelopmental disorders (NDD) and major psychiatric disorders. Currently, these findings are being translated into clinical practice. However, there is a lack of knowledge and guidelines for psychiatric genetic testing (PsychGT) and genetic counseling (PsychGC). The European Union-funded COST action EnGagE (CA17130) network was started to investigate the current implementation status of PsychGT and PsychGC across 35 participating European countries. Here, we present the results of a pan-European online survey in which we gathered the opinions, knowledge, and practices of a self-selected sample of professionals involved/interested in the field. We received answers from 181 respondents. The three main occupational categories were genetic counselor (21.0%), clinical geneticist (24.9%), and researcher (25.4%). Of all 181 respondents, 106 provide GC for any psychiatric disorder or NDD, corresponding to 58.6% of the whole group ranging from 43.2% in Central Eastern Europe to 66.1% in Western Europe. Overall, 65.2% of the respondents reported that genetic testing is offered to individuals with NDD, and 26.5% indicated the same for individuals with major psychiatric disorders. Only 22.1% of the respondents indicated that they have guidelines for PsychGT. Pharmacogenetic testing actionable for psychiatric disorders was offered by 15%. Interestingly, when genetic tests are fully covered by national health insurance, more genetic testing is provided for individuals with NDD but not those with major psychiatric disorders. Our qualitative analyses of responses highlight the lack of guidelines and knowledge on utilizing and using genetic tests and education and training as the major obstacles to implementation. Indeed, the existence of psychiatric genetic training courses was confirmed by only 11.6% of respondents. The question on the relevance of up-to-date education and training in psychiatric genetics on everyday related practice was highly relevant. We provide evidence that PsychGC and PsychGT are already in use across European countries, but there is a lack of guidelines and education. Harmonization of practice and development of guidelines for genetic counseling, testing, and training professionals would improve equality and access to quality care for individuals with psychiatric disorders within Europe.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Aconselhamento Genético Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Aconselhamento Genético Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article