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Featured researches published by Mercè Madre.


Acta Psychiatrica Scandinavica | 2016

Brain structural changes in schizoaffective disorder compared to schizophrenia and bipolar disorder.

Benedikt Amann; Erick Jorge Canales-Rodríguez; Mercè Madre; Joaquim Radua; Gemma C. Monté; Silvia Alonso-Lana; Ramon Landin-Romero; Ana Moreno-Alcázar; C.M. Bonnin; Salvador Sarró; Jordi Ortiz-Gil; Jesus J. Gomar; Noemi Moro; Paloma Fernández-Corcuera; J.M. Goikolea; J. Blanch; Raymond Salvador; Eduard Vieta; Peter J. McKenna; Edith Pomarol-Clotet

Brain structural changes in schizoaffective disorder, and how far they resemble those seen in schizophrenia and bipolar disorder, have only been studied to a limited extent.


Psychological Medicine | 2013

Brain functional abnormality in schizo-affective disorder: an fMRI study.

Mercè Madre; Edith Pomarol-Clotet; Peter J. McKenna; Joaquim Radua; Jordi Ortiz-Gil; F. Panicali; J.M. Goikolea; Eduard Vieta; Salvador Sarró; Raymond Salvador; Benedikt Amann

BACKGROUND Schizo-affective disorder has not been studied to any significant extent using functional imaging. The aim of this study was to examine patterns of brain activation and deactivation in patients meeting strict diagnostic criteria for the disorder. METHOD Thirty-two patients meeting research diagnostic criteria (RDC) for schizo-affective disorder (16 schizomanic and 16 schizodepressive) and 32 matched healthy controls underwent functional magnetic resonance imaging (fMRI) during performance of the n-back task. Linear models were used to obtain maps of activations and deactivations in the groups. RESULTS Controls showed activation in a network of frontal and other areas and also deactivation in the medial frontal cortex, the precuneus and the parietal cortex. Schizo-affective patients activated significantly less in prefrontal, parietal and temporal regions than the controls, and also showed failure of deactivation in the medial frontal cortex. When task performance was controlled for, the reduced activation in the dorsolateral prefrontal cortex (DLPFC) and the failure of deactivation of the medial frontal cortex remained significant. CONCLUSIONS Schizo-affective disorder shows a similar pattern of reduced frontal activation to schizophrenia. The disorder is also characterized by failure of deactivation suggestive of default mode network dysfunction.


Acta Psychiatrica Scandinavica | 2016

Neuropsychological and neuroimaging underpinnings of schizoaffective disorder: a systematic review.

Mercè Madre; Erick Jorge Canales-Rodríguez; Jordi Ortiz-Gil; Andrea Murru; Carla Torrent; Elvira Bramon; V. Pérez; M. Orth; Paolo Brambilla; Eduard Vieta; Benedikt Amann

The neurobiological basis and nosological status of schizoaffective disorder remains elusive and controversial. This study provides a systematic review of neurocognitive and neuroimaging findings in the disorder.


Schizophrenia Research | 2014

Trait or state? A longitudinal neuropsychological evaluation and fMRI study in schizoaffective disorder

Mercè Madre; Joaquim Radua; Ramon Landin-Romero; Silvia Alonso-Lana; Raimond Salvador; Francesco Panicali; Edith Pomarol-Clotet; Benedikt Amann

Schizoaffective patients can have neurocognitive deficits and default mode network dysfunction while being acutely ill. It remains unclear to what extent these abnormalities persist when they go into clinical remission. Memory and executive function were tested in 22 acutely ill schizoaffective patients; they also underwent fMRI scanning during performance of the n-back working memory test. The same measures were obtained after they had been in remission for ≥ 2 months. Twenty-two matched healthy individuals were also examined. In clinical remission, schizomanic patients showed an improvement of memory but not of executive function, while schizodepressive patients did not change in either domain. All schizoaffective patients in clinical remission showed memory and executive impairment compared to the controls. On fMRI, acutely ill schizomanic patients had reversible frontal hypo-activation when compared to clinical remission, while activation patterns in ill and remitted schizodepressive patients were similar. The whole group of schizoaffective patients in clinical remission showed a failure of de-activation in the medial frontal gyrus compared to the healthy controls. There was evidence for memory improvement and state dependent changes in activation in schizomanic patients across relapse and remission. Medial frontal failure of de-activation in remitted schizoaffective patients, which probably reflects default mode network dysfunction, appears to be a state independent feature of the illness.


Australian and New Zealand Journal of Psychiatry | 2017

Surface-based brain morphometry and diffusion tensor imaging in schizoaffective disorder.

Ramon Landin-Romero; Erick Jorge Canales-Rodríguez; Fiona Kumfor; Ana Moreno-Alcázar; Mercè Madre; Teresa Maristany; Edith Pomarol-Clotet; Benedikt Amann

Background: The profile of grey matter abnormalities and related white-matter pathology in schizoaffective disorder has only been studied to a limited extent. The aim of this study was to identify grey- and white-matter abnormalities in patients with schizoaffective disorder using complementary structural imaging techniques. Methods: Forty-five patients meeting Diagnostic and Statistical Manual of Mental Disorders–Fourth Edition criteria and Research Diagnostic Criteria for schizoaffective disorder and 45 matched healthy controls underwent structural-T1 and diffusion magnetic resonance imaging to enable surface-based brain morphometry and diffusion tensor imaging analyses. Analyses were conducted to determine group differences in cortical volume, cortical thickness and surface area, as well as in fractional anisotropy and mean diffusivity. Results: At a threshold of p = 0.05 corrected, all measures revealed significant differences between patients and controls at the group level. Spatial overlap of abnormalities was observed across the various structural neuroimaging measures. In grey matter, patients with schizoaffective disorder showed abnormalities in the frontal and temporal lobes, striatum, fusiform, cuneus, precuneus, lingual and limbic regions. White-matter abnormalities were identified in tracts connecting these areas, including the corpus callosum, superior and inferior longitudinal fasciculi, anterior thalamic radiation, uncinate fasciculus and cingulum bundle. Conclusion: The spatial overlap of abnormalities across the different imaging techniques suggests widespread and consistent brain pathology in schizoaffective disorder. The abnormalities were mainly detected in areas that have commonly been reported to be abnormal in schizophrenia, and to some extent in bipolar disorder, which may explain the clinical and aetiological overlap in these disorders.


Journal of Affective Disorders | 2015

Transcultural adaption and validation of the Spanish version of the Bipolar Depression Rating Scale (BDRS-S)

Salvador Sarró; Mercè Madre; Paloma Fernández-Corcuera; Marc Valentí; J.M. Goikolea; Edith Pomarol-Clotet; Michael Berk; Benedikt Amann

BACKGROUND The Bipolar Depression Rating Scale (BDRS) arguably better captures symptoms in bipolar depression especially depressive mixed states than traditional unipolar depression rating scales. The psychometric properties of the Spanish adapted version, BDRS-S, are reported. METHODS The BDRS was translated into Spanish by two independent psychiatrists fluent in English and Spanish. After its back-translation into English, the BDRS-S was administered to 69 DSMI-IV bipolar I and II patients who were recruited from two Spanish psychiatric hospitals. The Hamilton Depression Rating Scale (HDRS), the Montgomery-Asberg Depression Rating Scale (MADRS) and the Young Mania Rating Scale (YMRS) were concurrently administered. 42 patients were reviewed via video by four psychiatrists blind to the psychopathological status of those patients. In order to assess the BDRS-S intra-rater or test-retest validity, 22 subjects were assessed by the same investigator performing two evaluations within five days. RESULTS The BDRS-S had a good internal consistency (Cronbach׳s α=0.870). We observed strong correlations between the BDRS-S and the HDRS (r=0.874) and MADRS (r=0.854) and also between the mixed symptom cluster score of the BDRS-S and the YMRS (r=0.803). Exploratory factor analysis revealed a three factor solution: psychological depressive symptoms cluster, somatic depressive symptoms cluster and mixed symptoms cluster. LIMITATIONS A relatively small sample size for a 20-item scale. CONCLUSIONS The BDRS-S provides solid psychometric performance and in particular captures depressive or mixed symptoms in Spanish bipolar patients.


NeuroImage | 2008

Abnormal P300 in people with high risk of developing psychosis

Elvira Bramon; Madiha Shaikh; Matthew R. Broome; Julia Lappin; Daniel Bergé; Fern Day; James Woolley; Paul Tabraham; Mercè Madre; Louise Johns; Oliver Howes; Lucia Valmaggia; Víctor Pérez; Pak Sham; Robin M. Murray; Philip McGuire


Trials | 2017

Eye movement desensitization and reprocessing therapy versus supportive therapy in affective relapse prevention in bipolar patients with a history of trauma: study protocol for a randomized controlled trial

Ana Moreno-Alcázar; Joaquim Radua; Ramon Landin-Romero; Laura Blanco; Mercè Madre; M. Reinares; Mercè Comes; Esther Jiménez; Jose Manuel Crespo; Eduard Vieta; Víctor Pérez; Patricia Novo; Marta Doñate; Romina Cortizo; Alicia Valiente-Gómez; Walter Lupo; Peter J. McKenna; Edith Pomarol-Clotet; Benedikt Amann


PsycTESTS Dataset | 2015

Bipolar Depression Rating Scale--Spanish Version

Salvador Sarró; Mercè Madre; Paloma Fernández-Corcuera; Marc Valentí; J.M. Goikolea; Edith Pomarol-Clotet; Michael Berk; Benedikt Amann


International Clinical Psychopharmacology | 2011

Brain dysfunction in schizomanic patients versus healthy controls: a fMRI study

Mercè Madre; Edith Pomarol-Clotet; Jordi Ortiz-Gil; Salvador Sarró; J.M. Goikolea; Raymond Salvador; Peter J. McKenna; Benedikt Amann

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Eduard Vieta

University of Barcelona

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Salvador Sarró

Autonomous University of Barcelona

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Ana Moreno-Alcázar

Autonomous University of Barcelona

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