Marta Rapado-Castro

Dr. Marta Rapado-Castro

1. Ramón y Cajal Senior Research Fellow, Department of Child and Adolescent Psychiatry, Institute of Psychiatry and Mental Health, Hospital General Universitario Gregorio Marañón, School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, Madrid, Spain.
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Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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1 May 2019 in The Lancet Psychiatry
Verified
Journal Article
Open access
MFMarta Di Forti
Marta Di Forti
DQDiego Quattrone
Diego Quattrone
TFTom P Freeman
Tom P Freeman
GTGiada Tripoli
Giada Tripoli
CGCharlotte Gayer-Anderson
Charlotte Gayer-Anderson
EVElsje van der Ven
Elsje van der Ven
Cannabis use is associated with increased risk of later psychotic disorder but whether it affects incidence of the disorder remains unclear. We aimed to identify patterns of cannabis use with the strongest effect on odds of psychotic disorder across Europe and explore whether differences in such patterns contribute to variations in the incidence rates of psychotic disorder. We included patients aged 18-64 years who presented to psychiatric services in 11 sites across Europe and Brazil with first-episode psychosis and recruited controls representative of the local populations. We applied adjusted logistic regression models to the data to estimate which patterns of cannabis use carried the highest odds for psychotic disorder. Using Europe-wide and national data on the expected concentration of Δ9-tetrahydrocannabinol (THC) in the different types of cannabis available across the sites, we divided the types of cannabis used by participants into two categories: low potency (THC <10%) and high potency (THC ≥10%). Assuming causality, we calculated the population attributable fractions (PAFs) for the patterns of cannabis use associated with the highest odds of psychosis and the correlation between such patterns and the incidence rates for psychotic disorder across the study sites. Between May 1, 2010, and April 1, 2015, we obtained data from 901 patients with first-episode psychosis across 11 sites and 1237 population controls from those same sites. Daily cannabis use was associated with increased odds of psychotic disorder compared with never users (adjusted odds ratio [OR] 3·2, 95% CI 2·2-4·1), increasing to nearly five-times increased odds for daily use of high-potency types of cannabis (4·8, 2·5-6·3). The PAFs calculated indicated that if high-potency cannabis were no longer available, 12·2% (95% CI 3·0-16·1) of cases of first-episode psychosis could be prevented across the 11 sites, rising to 30·3% (15·2-40·0) in London and 50·3% (27·4-66·0) in Amsterdam. The adjusted incident rates for psychotic disorder were positively correlated with the prevalence in controls across the 11 sites of use of high-potency cannabis (r = 0·7; p=0·0286) and daily use (r = 0·8; p=0·0109). Differences in frequency of daily cannabis use and in use of high-potency cannabis contributed to the striking variation in the incidence of psychotic disorder across the 11 studied sites. Given the increasing availability of high-potency cannabis, this has important implications for public health. Medical Research Council, the European Community's Seventh Framework Program grant, São Paulo Research Foundation, National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) at South London and Maudsley NHS Foundation Trust and King's College London and the NIHR BRC at University College London, Wellcome Trust.

1 August 2013 in American Journal of Psychiatry
Verified
Journal Article
Closed access
CTCarla Torrent
Carla Torrent
CBCaterina del Mar Bonnin
Caterina del Mar Bonnin
AMAnabel Martinez-Aran
Anabel Martinez-Aran
JVJesús Valle
Jesús Valle
BABenedikt Amann
Benedikt Amann
Eduard VietaEduard Vieta
Eduard Vieta

1 August 2011 in European Neuropsychopharmacology
Verified
Journal Article
Closed access
DFDavid Fraguas
David Fraguas
CCChristoph U. Correll
Christoph U. Correll
JMJessica Merchán-Naranjo
Jessica Merchán-Naranjo
MRMarta Rapado-Castro
Marta Rapado-Castro
MPMara Parellada
Mara Parellada
CACelso Arango
Celso Arango

1 January 2012 in Archives of General Psychiatry
Verified
Journal Article
Open access
PDF file
CACelso Arango
Celso Arango
MRMarta Rapado-Castro
Marta Rapado-Castro
SRSantiago Reig
Santiago Reig
JCJosefina Castro-Fornieles
Josefina Castro-Fornieles
AGAna González-Pinto
Ana González-Pinto
DMDesco Menéndez Manuel
Desco Menéndez Manuel
Research from JAMA Psychiatry — Progressive Brain Changes in Children and Adolescents With First-Episode Psychosis

8 December 2005 in Bipolar Disorders
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Journal Article
Closed access
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Cesar Alejandro Soutullo-EsperonCesar Alejandro Soutullo-Esperon
Cesar Alejandro Soutullo-Esperon
KCKiki D Chang
Kiki D Chang
ADAzucena Díez‐Suárez
Azucena Díez‐Suárez
AFAna Figueroa‐Quintana
Ana Figueroa‐Quintana
IEInmaculada Escamilla‐Canales
Inmaculada Escamilla‐Canales
FOFelipe Ortuño
Felipe Ortuño

1 September 2016 in International Journal of Clinical and Health Psychology
Verified
Journal Article
Open access
MRMarina Romero
Marina Romero
JAJuan Manuel Aguilar
Juan Manuel Aguilar
ÁDÁngel Del-Rey-Mejías
Ángel Del-Rey-Mejías
FMFermín Mayoral
Fermín Mayoral
MRMarta Rapado-Castro
Marta Rapado-Castro
JLJosé Pablo Lara
José Pablo Lara
Background/Objective: The heterogeneous clinical presentations of individuals with Autism Spectrum Disorders (ASD) pose a significant challenge for sample characterization. Therefore the main goal of DSM-5 must be to identify subgroups of ASD, including comorbidity disorders and severity. The main goal of this study is to explore the psychiatric comorbidities and the severity of symptoms that could be relevant for the phenotype characterization in ASD and also to compare these results according to the different classification criteria between the DSM-IV-TR and the DSM-5. Method: A comparative study of severity and psychiatric comorbidities was carried out between a sample of participants that only met criteria for Pervasive Developmental Disorder (PDD) according to the DSM-IV-TR and a sample of participants that also met ASD criteria according to DSM-5 classification. The recruitment of children was via educational (N = 123). The psychiatric symptoms, comorbid disorders and severity of symptoms were assessed through The Nisonger Child Behavior Rating Form, clinical interview and The Inventory of Autism Spectrum Disorder, respectively. The psychiatric comorbidities considered were: anxiety, eating behavioural problems, self-aggressiveness, hetero-aggressiveness, self-harm, obsessive compulsive disorder and attention deficit and hyperactivity disorder. Results: Statistically significant differences between both groups were found regarding obsessive compulsive disorder, eating behavioural problems and severity. Conclusions: The results support the hypothesis that patients who meet the DSM-5 criteria have more severe symptoms, not only regarding the core autistic symptoms but also in relation with psychiatric comorbidities.