WP1 Central infrastructure (Leader: CIMH / E Schwarz)
WP2 Diagnostic markers (Leader: RUNMC / B Franke)
WP3 Predictive markers (Leader: UNIBA / A Bertolini)
WP4 Pre-symptomatic and early diagnosis (Leader: KCL / G Schumann)
WP5 Clinical translation (Leader: BI / R Goebel)
WP6 Ethics (Leader: CIMH / M Rietschel)
WP7 Dissemination (Leader: CIMH / A Meyer-Lindenberg)
WP8 Project management (Leader: CIMH / A Meyer-Lindenberg)

 

WP1 Central infrastructure (Leader: CIMH / E Schwarz)

WP 1 aims at the creation of an extensive database of neuroimaging data linked to relevant biological and clinical markers. IMAGEMEND will assemble a database containing already available data on a total of 12667 subjects including 1493 schizophrenia patients, 1184 patients with bipolar disorder, 400 individuals affected by ADHD and 8554 healthy controls. For the large majority of cases and controls, neuroimaging, genetic and clinical data are already ascertained. In addition, data on 1036 relatives of the aforementioned diagnostic groups and longitudinal data on 1055 subjects will be available. IMAGEMEND project funding will primarily go towards expansion of this database to complement missing imaging, genetic and environmental risk data to allow extensive integrative analyses. Additionally, we will perform clinical and imaging follow-up measurements on a significant subset of patients for predictive and other longitudinal analyses. For each work package, based on the integrative analyses, we will deliver both optimal neuroimaging-based and optimal combined (i.e. adding genetic, clinical and environmental identifiers to the imaging data) classifiers and decision rules.

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WP2 Diagnostic markers (Leader: RUNMC / B Franke)

WP2 works on the identification of neuroimaging and multi-modal markers (combining imaging, genetics and environmental risk factors) to facilitate case-control and differential diagnosis between schizophrenia, bipolar disorder, attention-deficit hyperactivity disorder (ADHD) and healthy controls. The integration of genetic data is expected to meaningfully stratify patient populations and lead to classifiers with improved accuracy. Similarly, we anticipate that classifier performance will critically depend on the incorporation of environmental risk factors such as urbanicity and stressful life events. A second major aim of this WP is the identification of trans-diagnostic, neuroimaging and multi-modal disease markers, which index illness-associated biological processes beyond current categorical disease entities.

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WP3 Predictive markers (Leader: UNIBA / A Bertolini)

WP3 aims to identify neuroimaging and multi-modal markers linked to response, relapse and side-effect development in naturalistic, large-scale patient populations with follow-up data. Specifically, for 1855 subjects who are part of the IMAGEMEND database, neuroimaging and clinical follow-up data will be provided by project partners. IMAGEMEND funding will go primarily towards extending these follow-up data to allow extensive analysis of predictive markers and their longitudinal change.

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WP4 Pre-symptomatic and early diagnosis (Leader: KCL / G Schumann)

WP4 works on the translation of diagnostic and predictive marker panels to the pre-symptomatic and high-risk stage. This work package will investigate marker signatures associated with illness risk in large-scale population based samples. Specifically, for 4500 of such IMAGEMEND probands, symptom severity scores on anxiety, affective and cognitive function, ADHD symptoms or other measures of psychopathology are already available. We will also investigate multi-modal markers of remission and persistence of ADHD in adults.

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WP5 Clinical translation (Leader: BI / R Goebel)

WP5 will utilize IMAGEMEND results towards development of automated, clinical tests to aid in diagnosis and treatment selection for psychiatric disorders. Besides performance optimization, specific aims of this work-package are the evaluation of classifier utility regarding measurement stability, robustness, and cost-effectiveness, both for purely imaging-based and combined optimal markers. In addition, clinical real-time fMRI software will be developed to enable the direct imaging-based modification of disease relevant neural circuits in an integrated neurofeedback system. With this, IMAGEMEND will create new products that use, for the first time, clinical MRI scanners for the diagnosis and for the treatment of mental illness, providing a new treatment modality, in addition to the currently available pharmacotherapy and psychotherapy.

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WP6 Ethics (Leader: CIMH / M Rietschel)

WP6 will address ethical concerns associated with the development and application of novel predictive biomarkers for mental illness. Additionally, we will assess attitudes and ethical views of patients, relatives, health care professionals, and the general population towards diagnostic and predictive testing and ensure that all ethical implications are appropriately addressed throughout the IMAGMEND project.

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WP7 Dissemination (Leader: CIMH / A Meyer-Lindenberg)

WP7 will increase the visibility of IMAGEMEND by reaching out to the scientific community, industry, patient organisations and other interested or potential stakeholders. A communication plan will be implemented. IMAGEMEND findings will be disseminated to the public through high-impact, international research publications, conferences, articles in the laymen press as well as through development of commercially available software for clinical application of decision tools developed during IMAGEMEND.

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WP8 Project management (Leader: CIMH / A Meyer-Lindenberg)

Effective project management is a central element of successful research. This particularly applies to large research projects entailing a substantial amount of administrative work. The management WP makes sure that the project achieves its objectives and delivers its milestones and deliverables in time, within budget and with highest quality. It is furthermore concerned with communication, reporting, meeting organisation, financial management and intellectual property rights. The responsibility for project management lies primarily with the coordinator who is supported by concentris.
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Central Institute of Mental Health

Department of Psychiatry and Psychotherapy

J5
68159, Mannheim

Website

Project leader

Prof. Dr. Andreas Meyer-Lindenberg
Coordinator and Leader of WP1 Central infrastructure and WP7 Dissemination
Phone: +49 621 1703 2001
Fax: +49 621 1703 2005
E-mail

Project staff

Prof. Dr. Marcella Rietschel
Workpackage leader of WP6 Ethics
Phone: +49 621 1703 6051
E-mail
Emanuel Schwarz, Ph.D
Co-Coordinator and Co-Leader of WP1 Central infrastructure and WP7 Dissemination
Phone: +49 621 1703 6516
E-mail

Institute presentation

The Central Institute of Mental Health (CIMH) is one of Europe’s leading research institutions dedicated to mental health. Its wide-ranging research activities are based on a combination of extensive in- and outpatient programmes with full access to research dedicated, state-of the art magnetic resonance imaging facilities (MRI) of 1.5 and 3 Tesla as well as high-throughput facilities for genotyping and molecular biology. The department of psychiatry and psychotherapy and its 17 research groups focus on the characterization of risk mechanisms for psychiatric illnesses and their translation into novel therapeutic and diagnostic approaches, using structural and functional brain abnormalities and their genetic and environmental determinants as a main approach. CIMH’s Department of Genetic Epidemiology in Psychiatry focusses on identifying genetic and environmental causal factors for mental disorders, with a particular focus on affective, schizophrenia-spectrum, and addiction disorders. The department conducts detailed phenotype characterization of large, internationally collected samples of patients. Genotyping of the DNA of these patients and their relatives is performed in the Department’s fully equipped molecular genetics laboratory.

Prof. Dr. Meyer-Lindenberg is director of the Central Institute of Mental Health in Mannheim, chairman of its department of Psychiatry and Psychotherapy and chair at the University of Heidelberg. Meyer-Lindenberg has worked extensively on neural mechanisms of risk for psychiatric disorders, especially schizophrenia and affective disorders through an innovative approach which combines neuroimaging, genetics and behavioral characterizations to identify specific neural risk mechanisms which can be localized to specific functional networks and genes acting in the CNS. Among other work in the field of “imaging genetics”, his group has contributed first identification of a neural risk mechanism associated with a genome wide significant genetic risk variant related to schizophrenia. He has also characterized neural mechanisms for social risk factors for neuropsychiatric disorders and has developed several of his discoveries into potential biomarkers for antipsychotic medication.

Prof. Dr. Marcella Rietschel is Director of both the Department of Genetic Epidemiology in Psychiatry and the CIMH molecular genetics laboratory at Heidelberg University/Medical Faculty Mannheim. She is a Professor of Psychiatry and Psychotherapy and a medical geneticist, and is an expert in all aspects of formal and molecular psychiatric genetics. Her research focus is the search for genetic and environmental risk factors for psychiatric disorders, in particular affective disorders, schizophrenia, and alcohol dependence. A specific emphasis of her work is the refining of phenotype-genotype correlations across diagnostic categories through the application of advanced statistical techniques. Marcella Rietschel has established large collections of data from psychiatric patients and the general population, as well as a biomaterial bank for DNA, plasma, serum, and RNA samples. Her group is among the leading research teams in psychiatric genetics worldwide. Her other research interest is the study of the ethical, legal, and social aspects of psychiatric genetics.

Dr Emanuel Schwarz is a research scientist at the CIMH with significant experience in the discovery of diagnostic and predictive/prognostic biomarkers for psychiatric disorders. He coordinated the statistical analysis for numerous biomarker discovery projects for schizophrenia, affective and autism spectrum disorders. These investigations led to the development and clinical translation of VeriPsychTM, the first ever molecular test to aid in the diagnosis of schizophrenia.

Institute of Psychiatry, King’s College London

Social, Genetic and Developmental Psychiatry Centre

16 De Crespigny Park

London, SE5 8AF


Website

Project leader

Prof. Gunter Schumann
Leader of WP4 Pre-symptomatic and early diagnosis
Phone: +44 (0)207 848 5314
Fax: +44 (0)207 848 0940
E-mail

 

Project staff

Prof. Ilina Singh
Professor of Science, Ethics and Society
Phone: +44 (0)207 848 7074
Fax: n.a.
E-mail

Institute presentation

The Institute of Psychiatry (IoP) is a postgraduate medical school associated with the South London and Maudsley NHS Foundation Trust, and is a School of King's College London (KCL) of the University of London. The IOP is the largest academic community in Europe for Psychiatry, Clinical Psychology and Neuroscience and ranks within the top five psychiatric research institutions worldwide. As a partnership between the MRC (Medical Research Council) and the IoP, the Social, Genetic and Developmental Psychiatry Centre is a unique multi-disciplinary centre that studies social epidemiology, child and adult psychiatry, developmental psychopathology, development in the family, personality traits, cognitive abilities, statistical genetics, and molecular genetics. This unparalleled approach has inspired and nurtured collaborative research between the different departments within the Institute of Psychiatry and demonstrated its impressive multifaceted expertise.

For WP3 they will contribute three clinical samples comprising over 600 patients to aid in the identification of prognostic marker sets in patients with schizophrenia and bipolar disorder.

For WP4 they will analyse data from the IMAGEN project (Coordinator G. Schumann) where they have explored intermediate phenotypes of risk for adolescent mental illness based on cognitive, behavioural, clinical, genetic and neuroimaging data of over 2000 adolescents ssessed at age 14, 16 and 19 years (Schumann et al. 2010).

University of Bari "Aldo Moro"

Department of Basic Medical Science, Neuroscience and Sense Organs

Piazza Giulio Cesare, 11

70121, Bari


Website

Project leader

Prof. Alessandro Bertolino, MD, PhD
Phone: +39 080 5478572
Fax: +39 080 5593204
E-mail

Project staff

Dr. Ileana Andriola, MD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Dr. Giuseppe Blasi, MD, PhD
Phone: +39-080-5593629
Fax: +39-080-5593204
E-mail
Dr. Grazia Caforio, MD, PhD
Phone: +39-080-5593173
Fax: +39-080-5593204
E-mail
Dr. Annabella Di Giorgio, MD, PhD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Dr. Tiziana Quarto
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Leonardo Fazio, PhD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Barbara Gelao, PhD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Riccarda Lomuscio
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Rita Masellis
Phone: +39-080-5034710
Fax: +39-080-5593204
E-mail
Dr. Apostolos Papazacharias, MD, PhD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Giulio Pergola, PhD
Phone: +39-080-5593630
Fax: +39-080-5593204
E-mail
Dr. Antonio Rampino, MD, PhD
Phone: +39-080-5593630
Fax: +39-080-5593204
E-mail
Raffaella Romano, PhD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail
Paolo Taurisano, PhD
Phone: +39 080 5478572
Fax: +39-080-5593204
E-mail

Institute presentation

Prof. Bertolino’s lab is interested in characterizing the genetic mechanisms of susceptibility to schizophrenia, studying gene effects on brain information processing in patients, their siblings, and healthy volunteers. The lab pursues translational projects ranging from gene expression/regulation in cell systems and human brain tissue, to studies of brain function with neuroimaging in living subjects stratified by relevant genotype.

 

UNIBA Third Parties:

- University of Chieti "G. D'Annunzio", Cheti, Italy: Prof. Giancarlo Romani

- University of Udine, Udine, Italy: Dr. Paolo Brambilla, Eleonora Maggioni

Dr. Paolo Brambilla
Phone: n.a.
Fax: n.a.
E-mail
Eleonora Maggioni
Phone: n.a.
Fax: n.a.
E-mail

 

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