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Symptomatic Drugs Only

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Presentation on theme: "Symptomatic Drugs Only"— Presentation transcript:

1 Symptomatic Drugs Only
Alzheimer’s Disease Predictions 2-4 Million 16 Million Years Clinical Diagnosis 20 40 60 80 100 Symptomatic Drugs Only 2000 2030

2 Symptomatic Time Course
Alzheimer’s Disease Symptomatic Time Course Test Results Diagnosis of AD Nursing Home MCI (12-15%/yr) Diagnosis Autopsy Mild Moderate Severe 3-4 years/stage

3 Alzheimer’s Disease Rx
Speculative Timeline Years Gene? Amyloid deposition Cell damage Autopsy Clinical diagnosis LOD? 20 40 60 80 100 Test Results Inflammatory response

4 Major Theories in AD Causation:
Cholinergic Damage b-Amyloid Toxicity Tau Pathology Genetic Risk

5 Cholinergic Neuron in Aging
AChE CAT Choline uptake

6 Plaque Theory of Damage in AD
From Outside the Cell Plaque Soluble peptides Insoluble peptides Reactive peptides Neural cell Nucleus Chaperone proteins Beta amyloid peptides, secreted by brain cells, are normally soluble, and any excess is cleared away ... … but when they become insoluble, they collect in the space between cells, the fibrils herded together by chaperone proteins The large plaques that form damage brain cells and attract reactive cells, which cause further damage Sources: Dr. John Trojanowski and Dr. Virginia M.Y. Lee/University of Pennsylvania Medical Center

7 Tangle Theory of Damage in AD
From Outside the Cell Tangle Axon Microtubules Tau proteins Neuron Paired helical filament Dendrites Tau proteins, which normally stabilize microtubules in brain cells ... … undergo abnormal chemical changes and assemble into spirals called paired helical filaments ... … thus creating tangles that disrupt cell functions and lead to cell death Sources: Dr. John Trojanowski and Dr. Virginia M.Y. Lee/University of Pennsylvania Medical Center

8 Donepezil in Mild to Moderate Alzheimer’s Disease
2 1 -1 -2 -3 12 24 36 48 Endpoint Study Week MMSE, Least Squares Mean Change from Baseline Score Clinical Improvement Decline n = 135 n = 137 Donepezil Placebo 127 128 121 120 104 105 91 98 (135) (137) P = 0.053 P < 0.001 P = 0.019 P = 0.001 (Winblad B et al. Poster presented at: Therapeutics of Alzheimer’s Disease Conference; 2000; Stockholm)

9 Galantamine: Mean Change from Baseline in ADAS-Cog Scores
4 3 6 9 12 Months of Treatment Mean (± SEM) Change from Baseline in ADAS-Cog/11 Score Clinical Improvement Decline Placebo/galantamine 24 mg Galantamine 24 mg/galantamine 24 mg Open-Label Extension 2 1 -1 -2 -3 -4 -5 Double Blind P < 0.001 (Raskind MA et al. Neurology, 2000;54: )

10 Current View of Cholinergic Therapy
Proven benefits: – Effective in 6-month trials Emerging benefits: – Effective for at least 12 months – Slow loss of function – Improve or delay troublesome behaviors – Delay placement in long-term care facility (Tariot PN et al. Neurology. 2000;54: ; Raskind MA et al. Neurology. 2000;54: ; Knopman D et al. Neurology. 1996:47: ; McLendon BM et al. J Geriatr Psychiatry Neurol. 1999;12:39-48.)

11 Symptomatic Time Course
Alzheimer’s Disease Symptomatic Time Course Test Results Diagnosis of AD Nursing Home MCI (12-15%/yr) Diagnosis Autopsy Mild Moderate Severe 3-4 years/stage

12 Expanding Uses of AChEI’s
Placebo-controlled Open Studies Vascular dementia Lewy body dementia Adult attention deficit hyperactivity disorder Supranuclear palsy Down’s syndrome Mild cognitive impairment Multiple sclerosis Brain injury Brain tumors Post–CABG memory loss Schizophrenia, mania REM sleep disorder Parkinson’s Dementia Autism Post-ECT confusion Pre-Surgical Prophylaxis

13 Therapeutic Targets and Strategies Under Study
, -Secretase inhibitors Vaccine Anti-inflammatories Estrogen preparations Antioxidants Statins NMDA antagonists Cholinomimetics

14 Memantine in Mod-Severe AD
0.8 4 12 28 Weeks in Trial FAST Score Clinical Improvement Decline Memantine Placebo 0.6 0.4 0.2 -0.2 Change **p = 0.007 Reisberg et al., NEJM 384: , 2003

15 Percent Remaining Outside an Institution
Vitamin E Treatment Percent Remaining Outside an Institution ** 75 70 Non-NH (%) 65 60 55 Placebo Selegeline Vit E Combo (Sano et al. NEJM 336: , 1997)

16 (Le Bars et al. JAMA 278 (16): 1327-1332, 1997)
ADAS-Cog on GINKGO Weeks in Trial -10 26 52 Clinical Improvement Decline Ginkgo Placebo -8 -6 -4 -2 2.0 ADAS-Cog Change Score Only 1.4 Point Change! (Le Bars et al. JAMA 278 (16): , 1997)

17 Indomethacin Trial in AD
10 5 -5 -10 -15 % Change from BL ADAS MMSE BOSTON TOKEN NSAID (n = 14, mean D = +1.3%) ** Placebo (n = 14, mean D = -8.4%) (Rogers et al. Neurology 43: , 1993)

18 Putative Inflammatory Agents in AD
Interleukin-1 (IL-1) Interleukin-6 (IL-6) Senile plaques (SPs) Neurofibrillary tangles Tumor necrosis factor  (TNF ) NF-B Microglia Amyloid  COX-2

19 Cyclophosphamide Rx in AD: A Pilot Study
Mild-to-Moderate subjects with AD Ability to give Informed Consent themselves Willing to undergo 6 monthly infusions Placebo controlled vs. 2 doses of CYCLO 15 subjects in study to this point Larry Bauer, Coordinator

20 Vaccine Therapy for AD “History & Recent Developments”
AN 1792 (Elan Pharmaceuticals) - Vaccine that prevents plaque buildup in mice AN 1792 vaccine administered to humans causing meningitis-like reaction (2002) Alternative vaccine approaches possible

21 Normal Enzymatic Processing Alternative Enzymatic Processing
Amyloid Processing Structure of Precursor Molecule Normal Enzymatic Processing Alternative Enzymatic Processing Protease-Regulating Region Intact Beta-fragment Is released Beta-region is cut Amyloid Beta- Region Amino Terminal Carboxyl Membrane Terminal

22 Alzheimer’s Disease Diagnosis and Treatment: Speculative Timeline
Preventative Modifying Symptomatic Years Gene? Amyloid deposition Cell damage Autopsy Clinical diagnosis LOD? 20 40 60 80 100 Test Results Inflammatory response

23 Family “AT RISK” Study: Entry Criteria (Protocol 95-M-96)
First Degree Relative(s) with AD & Controls Over 50 Years of Age on Admission Cognitively Normal at Entry Baseline APO E Allele, Imaging & CSF Measures Interested in 8-year Follow-up Commitment Judy Bergeson, Coordinator

24 AD Survival Curves for ApoE Genotypes
1.0 0.5 0.0 Proportion Unaffected 20 30 40 50 60 70 80 90 100 110 Age (years) S182 Mutation APP APOE 4-4 3-4 3-3 2-3 (Roses Ann. Rev. Med. 47: , 1996)

25 Percentage of APO E4+ Subjects
Family “At Risk” Study Percentage of APO E4+ Subjects 20 % APO E+ 40 60 80 Controls At Risk Alzheimer 8% 45% 64%

26

27 Temporal Lobe FOLLOW-UP sMRI IMAGES IN “AT RISK” STUDY Sagital Orientation Amygdala Hippocampus

28 sMRI Hippocampal Volumes Speculative Changes Over Time
Observed 1.9 1.45 Volume 1. 5 1.55 1.6 1.65 1.7 1.75 1.8 1.85 AD Cutoff Baseline Year 1 Diagnosis 3 APO E4(–) APO E4(+) (Adapted from Cohen et al. Neurology 57 (12): , 2001)

29 Positron Emission Tomography in AD
CONTROL AD PATIENT

30 Plaque of b-Amyloid Protein in the Brain of an AD Patient

31 CSF b-amyloid1-42 in Older Controls and AD Subjects
1.200 200 400 600 800 1,000 Controls N=72 AD N=131 (Sunderland et al. JAMA 289: , 2003)

32 Results from Meta-Analysis of CSF b-amyloid1-42 Studies: EFFECT SIZE
0.0 –1.0 1.0 2.0 3.0 4.0 (Sunderland et al. JAMA 289: , 2003)

33 Neurofibrillary Tangles in AD

34 CSF tau Levels in Older Controls and AD Subjects
1,600 1,400 1,200 1,000 800 600 400 200 Controls N=72 AD N=131 pg/ml (Sunderland et al. JAMA 289: , 2003)

35 (Sunderland et al. JAMA 289: 2094-2103, 2003)
Effective Sizes of Results from Meta-analysis of CSF Tau Studies in the World Literature 0.0 –1.0 1.0 2.0 3.0 4.0 5.0 (Sunderland et al. JAMA 289: , 2003)

36 Scattergraph of CSF TAU and b-amyloid1-42 in AD and Controls
1,600 1,400 1,200 1,000 800 600 400 200 CSF TAU CSF b-amyloid 1-42 (Sunderland et al. JAMA 289: , 2003)

37 Symptomatic Time Course
Alzheimer’s Disease Symptomatic Time Course Autopsy MCI (12-15%/yr) Mild Moderate Severe Nursing Home Diagnosis of AD 3-4 years/stage Test Results ? Diagnosis

38 Symptomatic Drugs Only
Alzheimer’s Disease Predictions 2-4 Million 16 Million Years Clinical Diagnosis 20 40 60 80 100 2000 2030 Symptomatic Drugs Only

39 Alzheimer’s Disease Diagnosis and Treatment: Speculative Timeline
Inflammatory response Amyloid Cell Gene? deposition damage LOD? Autopsy Test Results Clinical diagnosis 20 40 60 80 100 Years Preventative Modifying Symptomatic

40 Alzheimer’s Disease Future Goals
2000 2-4 Million Clinical Diagnosis 20 40 60 80 100 Years 2030 Clinical Diagnosis 2-3 Million 20 40 60 80 100 Years ?Gene Therapy Secretase Inhib? Statins NSAIDs, HRT? & ? Vaccine? Symptomatic AChEIs Drugs + + +

41 Early Diagnosis & Treatment: The Race is on!
Research to find ways to predict and prevent Alzheimer's disease Research to find ways to treat the symptoms of Alzheimer's disease Early Diagnosis Effective Treatment Patient


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