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Schizophrenia Treatment The Next Ten Years

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Title: Schizophrenia Treatment The Next Ten Years


1
Schizophrenia Treatment The Next Ten Years
David C. Henderson, MD Director, MGH
Schizophrenia Clinical and Research
Program Director, MGH Chester M. Pierce Division
of Global Psychiatry Associate Professor of
Psychiatry, Harvard Medical School
2
No health without mental health WHO
  • WHO mental health budget approximately 1.8 of
    total budget and no line item for child mental
    health.

3
Mental health has become a major international
public health concern
  • "We believe that mental health is just as
    important as physical health, maybe even more
    so. Donna Shalala, former Secretary of the
    Department of Health and Human Services
  • "The challenge to humanity is to adopt new ways
    of thinking, new ways of acting, new ways of
    organizing itself in society in short, new ways
    of living. Our Creative Diversity, UNESCO

4
Consequences of stigma
  • BASAVARAJ
  • He suffers from chronic schizophrenia. He
    was chained for 15 years at his home in
    Bangalore till Vidyakar (below left) brought him
    to Udavum Karangal five years ago. Now in his
    forties, he is on medication and seems far
    happier

5
Contribution by different non-communicable
diseases to disability-adjusted life-years
worldwide in 2005
  • Prince et al, Lancet, 2007

6
Schizophrenia is Heritable
Disorder Approx. h2
Autism 90
Schizophrenia 80
Type II DM 80
Rheumatoid Arthritis 60
Alcohol Dependence 55
Asthma 48
Major Depressive Disorder 42
Breast Cancer 27
Smoller, Sheidley, Tsuang 2007 Psychiatric
Genetics Application in Clinical Practice
7
Schizophrenia Core Symptom Clusters
II. Negative symptoms
  • Blunted affect
  • Alogia
  • Avolition
  • Anhedonia

Social/occupational dysfunctionWork/interpersonal
relationshipsSelf-care
American Psychiatric Association. Diagnostic and
Statistical Manual of Mental Disorders. Fourth
ed. Text Revision. Washington DC American
Psychiatric Association. 2000.
8
Challenges Over the Next Decade
  • Despite the increasing number of psychotropic
    drugs available the mechanisms of action are
    predominantly the same as the original prototypes
    developed in the 1950s.
  • There have been few innovative new compounds
    developed despite an array of theoretically
    viable biologic targets.
  • Although different modes of brain stimulation
    beyond ECT have been invented (VNS, R-TMS, DBS,
    DCS), their effectiveness has yet to be
    established, and their availability is limited.
  • the psychosocial therapies that have been proven
    effective are not widely available and
    inconsistently reimbursed.
  • The health care financing system and lack of
    cohesion in public and private health care
    systems have not met the clinical need and left
    many patients partially or completely untreated.

9
  • Numerous studies have demonstrated the dramatic
    efficacy of antipsychotic drugs in suppressing
    psychotic symptoms and preventing their
    recurrence,
  • Their inability to alleviate the negative and
    cognitive symptoms of the illness are limited.
  • In addition, with the exception of clozapine in
    treatment-resistant patients, the effectiveness
    of the newer second-generation APDs is not
    significantly greater than the older
    first-generation medications.

10
  • Many psychosocial treatments with established
    efficacy have been developed but are not readily
    available or adequately reimbursed
  • Assertive community treatment,
  • Cognitive Behavioral Therapy
  • Supported employment and housing,
  • Psychoeducation,
  • Social-skills training,
  • Cognitive remediation

11
Strategies
  • Develop treatments based on precedented
    mechanisms of action and targets (for example,
    D-2, 5-HT2A receptors).
  • Refinements of existing therapeutic mechanisms
    and improvement in the benefit to risk ratios of
    medications
  • Pursue novel targets for which there is a
    theoretical rationale but no proof of the
    therapeutic concept (for example, drugs targeting
  • glutamate receptors,
  • muscarinic and
  • nicotinic cholinergic receptors,
  • intracellular signaling proteins like PDE and AKT.

12
Approach
  • Improve the quality of mental health care by the
    application of existing knowledge.
  • Changes in clinical practices, services provided,
    and reimbursement methods would make a huge
    difference in the quality of care and outcomes of
    patients.
  • ? Greater use of clozapine and long-acting
    injectables
  • Broader availability and reimbursement of
    psychosocial services, and better integration of
    substance abuse and primary care with mental
    health services.

13
  • As risk genes for schizophrenia are identified
    and their biology elucidated, their products will
    provide potential targets for new drug
    development
  • COMT, DISC-1, neuregulin, proline dehydrogenase,
    RGS proteins
  • Through these investigative strategies, new
    treatments will be developed that may eventually
    lead to fully effective treatments and ultimately
    a cure for schizophrenia.

14
Actions of Stress and AntidepressantTreatment on
Hippocampal Neurons
Hippocampus
CA1
sc
Dentate gyrus
Granule cell
CA3
mf pathway
Stress
Antidepressant treatment
Antidepressant treatment
Stress
? Glucocorticoid
? Glucocorticoid
? NE and 5-HT
? NE and 5-HT
? BDNF
? BDNF
Increased survival and growth
Atrophy or death
Increased neurogenesis
Decreased neurogenesis
Increased vulnerability as a result of
environmental and genetic factors
Derived from Duman RS et al. Biol Psychiatry.
19994618111191.
15
SAMe, Methylfolate and Omega-3 Fatty Acidsand
Inflammation
  • The anti-inflammatory effects of SAMe have been
    attributed to its ability to reduce the
    expression of the pro-inflammatory cytokine TNF-a
    and to increase the expression of the
    anti-inflammatory cytokine IL-10 (McClain et al,
    Alcohol 200227(3)185-92).
  • In the mouse macrophage cell line RAW264.7, SAMe
    has been shown to reduce TNF-a mRNA levels and
    protein secretion by affecting the binding of
    methylated histone 3 to the TNF-a promoter (Ara
    et al, Hepatology 200847(5)1655-66.).
  • Folic acid protects motor neurons against
    inflammation and apoptosis in SOD1 G93A
    transgenic mice (Zhang et al, Neuropharmacology.
    2008 Jun54(7)1112-9)
  • A significant reduction with Omega-3 fatty acids
    (fish oil) in plasma concentrations of
    inflammatory biomarkers, including TNF-a and
    IL-6, has been observed in numerous studies (Wang
    et al, Nutrition. 2012 Jun28(6)623-9 Moertl et
    al, Am Heart J 2011161(5)915-9 Zhao et al, J
    Int Med Res 200937(6)1831-41 Papageorgiou et
    al, Eur J Clin Nutr 201165(4)514-9 Tartibian
    et al, Clin J Sport Med 201121(2)131-7)

16
Amantadine and Inflammation
  • Treatment with amantadine (AMA), an
    N-methyl-D-aspartate (NMDA) receptor antagonist
    reduces the production of the pro-inflammatory
    cytokines, specifically interferon-gamma
    (IFN-gamma) and tumor necrosis factor-alpha
    (TNF-alpha).
  • In addition, amantadine treatment increased the
    production of the negative immunoregulator,
    interleukin-10 (IL-10).
  • Furthermore, the combined treatment of amantadine
    with the SSRI fluoxetine, but not imipramine, had
    a stronger immunomodulatory effect on cytokine
    production than amantadine alone.
  • Kubera et al, Pharmacol Rep. 2009
    Nov-Dec61(6)1105-12.

17
Riluzole Increases BDNF and Cell Proliferation
Katoh-Semba et al FASEB J. 2002
Aug16(10)1328-30.
18
Minocycline Effects on Inflammation and Neuronal
Plasticity
  • The second-generation tetracycline antibiotic
    drug minocycline has powerfully anti-inflammatory
    and neuroprotective effects (Maes et al., Metab
    Brain Dis 2009242753. Ponzini, Neurosci lett
    201250613640).
  • Minocycline inhibits mitochondrial
    permeability-transition mediated cytochrome c
    release from the mitochondria (Kim and Suh. Behav
    Brain Res 200919616879)
  • Minocylcine inhibits caspase-1 and -3
    expressions, and the suppression of microglial
    activation, involvement in some signal pathways,
    and metalloprotease activity inhibition (Kim and
    Suh. Behav Brain Res 200919616879)
  • Co-administration of minocycline synergized the
    antidepressant-like action of sub-threshold doses
    of desipramine (but not fluoxetine), mGluR1
    antagonist EMQMGM, mGluR5 antagonist MTEP, and
    NMDA receptor antagonist dizocilpine
    (Molina-Hernandez et al., Prog Neuropsychopharmaco
    l Biol Psychiatry 20083216606.)
  • Minocycline attenuated lipopolysaccharide
    (LPS)-induced expression of pro-inflammatory
    cytokines, and that this drug prevented
    LPSinduced development of depressive-like
    behaviors in mice (O'Gonnor et al., Mol
    Psychiatry 20091451122)

19
Cognitive Remediation
McGurk and Mueser, Am J Psychiatry, 2007
20
Cognitive Enhancement Therapy Prevents Brain
Volume Loss in Early-stage Schizophrenia
Eack, S. M. et al. Arch Gen Psychiatry
201067674-682
21
Integration of Mental Health in Primary Care
System
  • SMI has worst outcomes compared to general
    population in several chronic diseases such as
    obesity, diabetes and cardiovascular disease
  • Poorer outcomes even when utilizing primary
    health care system
  • Best Models
  • New approaches with changes in Health Care-
    Massachusetts leading the way

22
Family Psychoeducation Research
Effects of Family Intervention on 2-Year
Cumulative Relapse Rates in Schizophrenia (12
Studies)
100
75
59
Cumulative Relapse Rate ()
50
29
28
26
25
0
McFarlane WR et al. J Marital Fam Ther.
200329(2)223
23
Psychosocial Approaches to Specific Targets
  • Facial affect recognition can be enhanced with
    special training1
  • Cognitive training can improve working memory2
  • Attention can be improved with specialized
    training3
  • Cognitive Enhancement Therapy (CET) improved
    neurocognition and processing speed4

1. Wolwer W et al. Schizophr Res.
200580295-303 2. Bell MD et al. J Rehabil Res
Dev. 200542829-8383. Silverstein S et al.
Psychiatr Q. 19986995-105 4. Hogarty GE et
al. Psychiatr Serv. 2006571751-1757.
24
Prevention
  • Identify at risk individuals (such as children of
    individuals with schizophrenia)
  • Implement preventive strategies including the use
    of vitamins, agents that reduce inflammation and
    promote neurogenisis
  • Utilize existing psychosocial such as cognitive
    enhancement therapies that prevent brain volume
    loss

25
Conclusions
  • Compounds that increase brain energy metabolism
    may be useful augmentation strategies in TRD
  • Medications and nutraceuticals with
    antiinflammatory properties have shown promise in
    the treatment of MDD
  • Agents that increase neurogenesis and neuronal
    plasticity may be protective
  • New service delivery models need to be
    implemented to address both mental health and
    physical health
  • Prevention, Prevention, Prevention

26
Thank You!
  • You must be the change you want to see in the
    world.
  • Mahatma Gandhi
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