Early Intervention in Psychosis Obvious, Effective, Overdue
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
View and Metasynthesis (E30) Hamish Fulford, Linda Mcswiggan, Thilo Kroll, Stephen Macgillivray
JMIR Mental Health Internet interventions, technologies and digital innovations for mental health and behaviour change Volume 3 (2016), Issue 3 ISSN: 2368-7959 Editor in Chief: John Torous, MD Contents Original Papers Web-Based Intervention to Reduce Substance Abuse and Depressive Symptoms in Mexico: Development and Usability Test (e47) Marcela Tiburcio, Ma Lara, Araceli Aguilar Abrego, Morise Fernández, Nora Martínez Vélez, Alejandro Sánchez. 3 Exploring the Use of Information and Communication Technology by People With Mood Disorder: A Systematic Review and Metasynthesis (e30) Hamish Fulford, Linda McSwiggan, Thilo Kroll, Stephen MacGillivray. 19 Predicting Risk of Suicide Attempt Using History of Physical Illnesses From Electronic Medical Records (e19) Chandan Karmakar, Wei Luo, Truyen Tran, Michael Berk, Svetha Venkatesh. 34 Are Mental Health Effects of Internet Use Attributable to the Web-Based Content or Perceived Consequences of Usage? A Longitudinal Study of European Adolescents (e31) Sebastian Hökby, Gergö Hadlaczky, Joakim Westerlund, Danuta Wasserman, Judit Balazs, Arunas Germanavicius, Núria Machín, Gergely Meszaros, Marco Sarchiapone, Airi Värnik, Peeter Varnik, Michael Westerlund, Vladimir Carli. 52 mHealth for Schizophrenia: Patient Engagement With a Mobile Phone Intervention Following Hospital Discharge (e34) Dror Ben-Zeev, Emily Scherer, Jennifer Gottlieb, Armando Rotondi, Mary Brunette, Eric Achtyes, Kim Mueser, Susan Gingerich, Christopher Brenner, Mark Begale, David Mohr, Nina Schooler, Patricia Marcy, Delbert Robinson, John Kane. 66 Effectiveness of Internet-Based Interventions for the Prevention of Mental Disorders: A Systematic Review and Meta-Analysis (e38) Lasse Sander, Leonie Rausch, Harald Baumeister. 75 Cultural Adaptation of Minimally Guided Interventions for Common Mental Disorders: A Systematic Review and Meta-Analysis (e44) Melissa Harper Shehadeh, Eva Heim, Neerja Chowdhary, Andreas Maercker, Emiliano Albanese. -
The Kraepelinian Dichotomy – Going, Going . . . but Still Not Gone Nick Craddock and Michael J
The British Journal of Psychiatry (2010) 196, 92–95. doi: 10.1192/bjp.bp.109.073429 Reappraisal The Kraepelinian dichotomy – going, going . but still not gone Nick Craddock and Michael J. Owen Summary Recent genetic studies reinforce the view that current psychiatry will need to move from using traditional approaches to the diagnosis and classification of major descriptive diagnoses to clinical entities (categories and/or psychiatric illness are inadequate. These findings challenge dimensions) that relate more closely to the underlying the distinction between schizophrenia and bipolar disorder, workings of the brain. and suggest that more attention should be given to the relationship between the functional psychoses and neurodevelopmental disorders such as autism. We are Declaration of interest entering a transitional period of several years during which None. The Kraepelinian dichotomy – the broad division of major mood risk gene for schizophrenia,4 and CACNA1C,5 which was strongly and psychotic illness of adulthood into schizophrenia and ‘manic– implicated initially in GWAS of bipolar disorder.6 It is of interest depressive’ (bipolar) illness – has been enshrined in Western that there is evidence that variation at CACNA1C also influences psychiatry for over a century and continues to influence clinical risk of recurrent unipolar depression.5 More broadly, there is practice, research and public perceptions of mental illness. Nearly evidence for overlap in the identity of genes showing gene-wide 5 years ago, we published an editorial1 in which we summarised association signals in GWAS of schizophrenia and bipolar emerging evidence undermining the dichotomy, and argued that disorder.7 Perhaps most compellingly, there is strong evidence that continued adherence to this approach is hampering research and the aggregate polygenic contribution of many alleles of small effect clinical care. -
Wednesday, March 6, 2013
106th Annual Meeting of the American Psychopathological Association March 3-5, 2016 Crowne Plaza Times Square Manhattan Improving Psychiatric Research and Care through Differentiated Phenomenology Layout and Design by Daniela Reich-Erkelenz Ludwig-Maximilians-University, Munich 1 SPEAKERS Morton Beiser, CM, MD, FRCP Layla Kassem, PhD Ryerson University National Institute of Mental Health Joshua Breslau, PhD John Keilp, PhD RAND Corporation Columbia University Robert Brooner, PhD Matcheri Keshavan, MD Johns Hopkins University Harvard University Linda Brzustowicz, MD Katherine M. Keyes, PhD, MPH Rutgers University Columbia University Rita Charon, MD, PhD James R. Lupski, MD, PhD Columbia University Baylor College of Medicine Diana E. Clarke, PhD Francis J. McMahon, MD American Psychiatric Association National Institute of Mental Health Johns Hopkins Bloomberg School of Public Health Adey Nyamathi, PhD, ANP, FAAN C. Robert Cloninger, MD University of California, Los Angeles Washington University Dost Öngür, MD, PhD Francesc Colom, PhD McLean Hospital University of Barcelona, Catalonia Harvard University Bruce Cuthbert, PhD Josef Parnas, MD National Institute of Mental Health University of Copenhagen, Denmark Thomas Fuchs, MD, PhD Elise Robinson, ScD Heidelberg University Hospital, Germany Massachusetts General Hospital Hanga Galfalvy, PhD Ursula Staudinger, PhD Columbia University Columbia University Danielle Hairston, MD Sophia Vinogradov, MD Howard University University of California, San Francisco San Francisco VA Medical Center Stephan H. Heckers, MD Vanderbilt University Helen Wilson, PhD Stanford University John M. Kane, MD Hofstra Northwell School of Medicine 2 CHAIRS & DISCUSSANTS Paula J. Clayton, MD University of Minnesota Doreen M. Olvet, PhD University of New Mexico Stony Brook University Michael B. First, MD Maria A. Oquendo, MD Columbia University Columbia University Helen L. -
NINA R. SCHOOLER, Ph. D
1 Profiles December 10, 2915 Curriculum Vitae NINA R. SCHOOLER, Ph. D. ADDRESS: Home: 1731 34th Street NW Washington DC 20007 Office: Department of Psychiatry and Behavioral Sciences 450 Clarkson Avenue, MSC 1203 Brooklyn NY 11203-2098 TELEPHONE: Home: (202) 338-5591 Office: (718) 221 -6104 FAX (718) 270-3030 E:MAIL ADDRESS Office: [email protected] Cell 917 543 2740 DATE OF BIRTH & PLACE: July 26, 1934, New York, NY CITIZENSHIP: United States EDUCATION: 1951-1955 City College of NY B.S.S., Anthropology POST-GRADUATE TRAINING: 1956-1969 Columbia University Ph.D., Social Psychology PROFESSIONAL EMPLOYMENT AND HOSPITAL APPOINTMENTS: 1963 - 1967 Research Social Psychologist Clinical Studies Section Psychopharmacology Service Center National Institute of Mental Health Chevy Chase, Maryland 1968 Professional Services Contractor National Institute of Mental Health Chevy Chase, Maryland Nina R. Schooler, Ph.D. Page 2 1968 - 1980 Research Psychologist Psychopharmacology Research Branch National Institute of Mental Health Rockville, Maryland 1980 - 1984 Chief, Schizophrenic Disorders Section and Assistant Chief Pharmacologic and Somatic Treatments, Research Branch National Institute of Mental Health Rockville, Maryland Nina R. Schooler, Ph.D. Page 3 1985 Acting Chief Pharmacologic and Somatic Treatments Research Branch National Institute of Mental Health Rockville, Maryland 1985 - 1988 Assistant Chief Schizophrenia Research Branch National Institute of Mental Health Rockville, Maryland 1989 - 1997 Director of Research Special Studies Center -
Treatment of Bipolar Disorder with Antipsychotic Medication: Issues Shared with Schizophrenia
Allan H. Young Treatment of Bipolar Disorder With Antipsychotic Medication: Issues Shared With Schizophrenia Allan H. Young, M.B., Ch.B., M.Phil., Ph.D., F.R.C.Psych., F.R.C.P.(C) Atypical antipsychotics are increasingly used in bipolar disorder as antimanic, antidepressant, and maintenance treatments. Many of the clinical issues related to switching antipsychotics are similar between schizophrenia and bipolar disorder. These include similar motivations for switching due to limited efficacy and unacceptable adverse effects. Particular attention must be paid to the phase of treatment and coprescribed medications. (J Clin Psychiatry 2007;68[suppl 6]:24–25) True Apothecary Kraepelin sought to disentangle these 2 scourges on the Two diagnoses, both alike in dignity, basis of careful clinical description and observation of In fair Psychiatry, where we lay our scene, From ancient balms break to new treatments, natural history. Nevertheless, more than a century later, For psychoses truly patients’ lives demean. this diagnostic scheme is essentially still provisional. Re- cent research has reminded us of the shared etiopathogen- From forth the crises of these two foes esis of bipolar disorder and schizophrenia and has led to Many star-cross’d souls may take their life; 2 The adventured physician overthrows calls for an end to the “Kraepelinian dichotomy.” Al- Do with their wisdom bury their patients’ strife. though such calls may be premature, they do highlight The fearful passage of their delusions—mark’d above, how, on many levels, bipolar disorders and schizophrenia And the continuance of their parents’ sorrow, are inextricably linked. Which, but their children’s health, nought could remove, Is now the few pages’ traffic of our stage; ANTIPSYCHOTIC USE IN BIPOLAR DISORDER The which if you with patient eyes attend, What here shall miss, our toil shall strive to mend. -
Bipolar Ii Disorder and Borderline Personality
Psychiatria Danubina, 2012; Vol. 24, Suppl. 1, pp 197–201 Conference paper © Medicinska naklada - Zagreb, Croatia BIPOLAR II DISORDER AND BORDERLINE PERSONALITY DISORDER - CO-MORBIDITY OR SPECTRUM? Mark Agius1,2,3, Jean Lee2 , Jenny Gardner3,4 & David Wotherspoon 1Department of Psychiatry University of Cambridge, Cambridge, UK 2Clare College Cambridge, Cambridge, UK 3South Essex Partnership University Foundation Trust, UK 4Eastern Deanery, UK. SUMMARY We assess the number of patients who we have on the Database of a Community Mental Health Team in the UK who have Bipolar Disorder and Borderline Personality Disorder. We report how many of these have been seen as having both disorders. Hence we discuss the issue as to whether Borderline Personality disorder is to be placed within the bipolar spectrum. We note the difficulties regarding the use of phenomenology alone to decide this problem, and we note the similarities in genetics, neuroimaging observations and neurobiological mechanisms among the following conditions; Bipolar Disorder, Unipolar Depression, Post- traumatic Stress Disorder, and Borderline Personality Disorder. Ethiologies such as Trauma, Abuse, Childhood adversity and exposure to War appear to influence all these conditions via epigenetic mechanisms. Hence we argue that for a spectrum to be proposed, conditions in the spectrum need to be underpinned by similar or common Neuroimaging and neurobiological mechanisms.On this basis, it may be reasonable to include Borderline Personality Disorder within a broadly described bipolar -
The Kraepelinian Dichotomy in Terms of Suicidal Behaviour
Psychiatria Danubina, 2012; Vol. 24, Suppl. 1, pp 117–118 Conference paper © Medicinska naklada - Zagreb, Croatia THE KRAEPELINIAN DICHOTOMY IN TERMS OF SUICIDAL BEHAVIOUR Jamie King2,4, Mark Agius1,3,5 & Rashid Zaman1,5 1Department of Psychiatry University of Cambridge, Cambridge, UK 2School of Clinical Medicine University of Cambridge, Cambridge, UK 3Clare College Cambridge, Cambridge, UK 4Pembroke College Cambridge, Cambridge, UK 5South Essex Partnership University Foundation Trust, UK SUMMARY The Kraepelinian dichotomy sees schizophrenia and bipolar disorder as two distinctly separate diseases each with its own pathogenesis and disease process. This study looks at the difference between patients with schizophrenia and bipolar disorder in terms of suicidal behaviour. Both schizophrenia and bipolar disorder have been identified as significant risk factors for suicide, while bipolar and major depressive disorder appear to be the greatest diagnostic indicators. This study also aims to look at any differences in suicidal behaviour between the two major classes of bipolar disorder (bipolar I and bipolar II) to possibly determine how distinct these two conditions are in this respect. As expected, this study found that patients with a diagnosis of bipolar disorder were significantly more likely (OR=4.79) to have a history of suicidal behaviour than patients with a diagnosis of schizophrenia. Neither bipolar I nor bipolar II patients were significantly more likely to have a history of suicidal behaviour. However, this study yielded a weak association between bipolar II patients and suicidal behaviour (OR=1.83) compared to bipolar I patients, which may have been more significant under different circumstances such as a greater sample size. -
Family History of Schizophrenia and Bipolar Disorder As Risk Factors for Autism
ORIGINAL ARTICLE Family History of Schizophrenia and Bipolar Disorder as Risk Factors for Autism Patrick F. Sullivan, MD, FRANZCP; Cecilia Magnusson, MD, PhD; Abraham Reichenberg, PhD; Marcus Boman, BS; Christina Dalman, MD, PhD; Michael Davidson, MD; Eyal Fruchter, MD; Christina M. Hultman, PhD; Michael Lundberg, MPH; Niklas La˚ngstro¨m, MD, PhD; Mark Weiser, MD; Anna C. Svensson, PhD; Paul Lichtenstein, PhD Context: The clinical and etiologic relation between au- Results: The presence of schizophrenia in parents was as- tism spectrum disorders (ASDs) and schizophrenia is un- sociated with an increased risk for ASD in a Swedish na- clear. The degree to which these disorders share a basis tional cohort (odds ratio [OR], 2.9; 95% CI, 2.5-3.4) and in etiology has important implications for clinicians, re- a Stockholm County cohort (OR, 2.9; 95% CI, 2.0-4.1). searchers, and those affected by the disorders. Similarly, schizophrenia in a sibling was associated with an increased risk for ASD in a Swedish national cohort Objective: To determine whether a family history of (OR, 2.6; 95% CI, 2.0-3.2) and an Israeli conscription co- schizophrenia and/or bipolar disorder is a risk factor hort (OR, 12.1; 95% CI, 4.5-32.0). Bipolar disorder showed for ASD. a similar pattern of associations but of lesser magnitude. Design, Setting, and Participants: We conducted Conclusions: Findings from these 3 registers along with a case-control evaluation of histories of schizophrenia consistent findings from a similar study in Denmark sug- or bipolar disorder in first-degree relatives of probands gest that ASD, schizophrenia, and bipolar disorder share in 3 samples—population registers in Sweden, Stock- common etiologic factors. -
NCDEU 51St Annual Meeting a Meeting Sponsored by the American Society of Clinical Psychopharmacology (ASCP)
nCDEU 51st Annual meeting A meeting sponsored by the American Society of Clinical Psychopharmacology (ASCP) Anticipating the Future of Drug Development: New Targets, Integrative Biomarkers, and Beyond June 13-16, 2011 Boca Raton Resort & Club Boca Raton, Florida Steering Committee Chairs: William Z. Potter, M.D., Ph.D. and Nina R. Schooler, Ph.D. Program Committee Chairs: David J. Kupfer, M.D. and Carlos A. Zarate, M.D. www.nCdeumeeting.org Welcome to the 51st Meeting of NCDEU – the New NCDEU On behalf of the American Society of Clinical Psychopharmacology, we are pleased to welcome you to this year’s NCDEU meeting. The ASCP is proud to sponsor the meeting, now in its 51st year, which has played such a pivotal role in the development of modern-day psychopharmacology. The challenges and opportunities confronting this field have never been greater, and we are confident that the new iteration of NCDEU with increased partnership with all relevant federal agencies and the ongoing participation of researchers from academia, the pharmaceutical and biotechnology industries, as well as many other professionals engaged in various aspects of CNS research, will continue to stimulate and facilitate further progress. We are very appreciative to the members of the NCDEU Steering and Program Committees for their role in the success of the meeting. John M. Kane, M.D. President American Society of Clinical Psychopharmacology On behalf of the NCDEU Steering and Program Committees, we are delighted that you have chosen to attend this year’s meeting. Last year’s 50th Anniversary Meeting was a landmark event to celebrate our progress from a small gathering of investigators in a new field to a robust meeting of over 1,000 national and international researchers and staff from government, academia, industry and clinical practice. -
Neo-Kraepelinian Divergences from Kraepelin : What Are They and Why They Matter
Portland State University PDXScholar University Honors Theses University Honors College 2013 Neo-Kraepelinian Divergences from Kraepelin : What are They and Why They Matter Lindsay Hoeschen Portland State University Follow this and additional works at: https://pdxscholar.library.pdx.edu/honorstheses Let us know how access to this document benefits ou.y Recommended Citation Hoeschen, Lindsay, "Neo-Kraepelinian Divergences from Kraepelin : What are They and Why They Matter" (2013). University Honors Theses. Paper 104. https://doi.org/10.15760/honors.102 This Thesis is brought to you for free and open access. It has been accepted for inclusion in University Honors Theses by an authorized administrator of PDXScholar. Please contact us if we can make this document more accessible: [email protected]. Neo-Kraepelinian Divergences from Kraepelin; what are they and why they matter. by Lindsay Hoeschen An undergraduate honors thesis submitted in partial fulfillment of the requirements for the degree of Bachelor of Science in University Honors and Philosophy Thesis Adviser Tom Seppalainen Portland State University 2013 1 Introduction Throughout its development, psychiatry has struggled to legitimate itself as a scientific and medical discipline. Much of this struggle has been attributed to a lack of consensus regarding the nature of mental illness as well as a standard methodology for making diagnoses. In an attempt to eliminate this impediment to psychiatry's scientific advancement, the third edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM) was published in 1980 with significant methodological changes to the nature of classification and approach to clinical diagnoses. Similar to the characterization of modern psychiatry as being amidst a Kraepelinian revival, this highly influential text is often associated with and regarded as an adaptation of the psychiatric nosology of Emil Kraepelin (1856-1926). -
2019 Annual Report
BRAIN & BEHAVIOR RESEARCH FOUNDATION 2019 ANNUAL REPORT Awarding research grants to develop improved treatments, cures, and methods of prevention for mental illness. BBRF is the world’s largest private funder of mental health research grants, supporting transformative discoveries in order to develop improved treatments, cures, and methods of prevention for our loved ones. CONTENTS Mission 4 BBRF Events 28 Leadership Letter 6 The Research Partners Program 42 Important Advancements 8 Team Up for Research 50 BBRF Scientific Council 12 2019 Donor Listing 52 2019 Leading Research Achievements 14 Getting the Word Out 76 BBRF Grants 18 Financial Summary 78 2019 Grants by Illness 20 The Research We Fund We invest in innovative research because we believe that only by pursuing the boldest and most ambitious ideas will we find better treatments, cures, and methods of prevention for mental illness. We are at the Forefront of Critical Discoveries Since 1987, the Brain & Behavior Research Foundation has awarded more than $408 million in grants that have led to discoveries that change the way we think about recovery. BBRF-funded research has contributed to: • FDA approval of the first rapid-acting antidepressants (esketamine and brexanalone) to alleviate severe depression symptoms within hours. • Dietary supplements for pregnant women to potentially help prevent subsequent mental illness in the child. • Development of Transcranial Magnetic Stimulation (TMS) and continued improvement of TMS and other non-invasive brain stimulation treatments for treatment-resistant depression and obsessive compulsive disorder. • Computer-guided training for cognitive remediation in people with schizophrenia. MISSION The Brain & Behavior Research Foundation is committed to alleviating the suffering caused by mental illness by awarding grants that will lead to advances and breakthroughs in scientific research. -
Autism in Adults with Schizophrenia © Maria Unenge Hallerbäck 2012 [email protected]
Maria Unenge Hallerbäck Gillberg Neuropsychiatry Centre Institute of Neuroscience and Physiology Sahlgrenska Academy at University of Gothenburg Gothenburg 2012 Autism in adults with schizophrenia © Maria Unenge Hallerbäck 2012 [email protected] ISBN 978-91-628-8405-5 http://hdl.handle.net/2077/28249 Printed in Gothenburg, Sweden 2012 Ineko AB The story of autism and Asperger’s syndrome attests the truth of three wise sayings. There is nothing new under the sun. Nothing exists until it has a name. Nature never draws a line without smudging it. Lorna Wing, 2005 To Per-Olof, Sofia and Rickard Maria Unenge Hallerbäck Gillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology Sahlgrenska Academy at University of Gothenburg Background: Typical symptoms of schizophrenia usually appear in young adult life, but problems with social interaction, activity control, motor performance, and cognition have often been noted in childhood. This thesis explores similarities and differences regarding early development between individuals with clinical diagnoses of schizophrenia and Asperger syndrome (a clinical variant of autism spectrum disorder/ASD). Methods: A Swedish version of the “Reading the Mind in the Eyes Test”, was completed by 158 university students with a view to assessing the psychometric properties of this instrument before applying it in a clinical research setting. Fifty-eight of these students completed the test twice, three weeks apart. The Bland Altman test-retest reliability method was used. For the other three substudies 46 individuals (29 men, 17 women) with a clinical diagnosis of schizophrenic psychosis (SP) and 54 (26 men, 28 women) with a clinical diagnosis of Asperger syndrome (AS) were included.