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fMRI guided Microarray analysis

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Why fMRI and not postmortem? p.m. biased against earliest (and most discriminatory) stages ... fMRI imaging in-vivo, not post-mortem ... – PowerPoint PPT presentation

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Title: fMRI guided Microarray analysis


1
fMRI guided Microarray analysis
  • Imaging-Guided Microarray Isolating Molecular
    Profiles That Dissociate Alzheimers Disease from
    Normal Aging
  • A.C. Pereira, W. Wu S.A. Small
  • Ann NY Acad. Sci. 1097, Feb 2007
  • Combining Brain Imaging with Microarray
    Isolating Molecules Underlying the Physiologic
    Disorders of the Brain
  • A. Pierce S.A. Small
  • Neurochemical Research, Vol. 29, No. 6, June 2004

2
Crash course The CELL and microarrays in 3 slides
  • Cells internal processes and inter-cell
    communication based on proteins
  • Goal Figure out which proteins exist in a cell
    under some condition
  • Condition e.g. disease
  • Many times detect proteins differentially
    expressed e.g. disease vs. control
  • Basic staining a specific protein and follow it
    under a microscope
  • Next The CELL

3
From DNA to Protein
  • (Final) product Protein
  • Intermediate product mRNA
  • Idea measure mRNA to get protein measurements
  • Simultaneous measurements by hybridization

4
DNA Microarrays
  • mRNA concatenation of nucleotides
  • 4 types ATGC pegs/holes
  • Process
  • Crush cell
  • Wash all but mRNA
  • Glue lamps
  • Spill on chip
  • Shake well!

5
Sorry, 4 slides...
  • Chip design probes for genes
  • Light on --gt Protein exists
  • Light off --gt No protein at the moment

6
Problem setting
  • Given two sets of DNA microarrays
  • Disease
  • Control
  • Extract a set of differentially expressed genes
  • Feature selection for classification
  • Biological significant features for downstream
    research

7
Problem setting revisited
  • Given two sets of DNA microarrays
  • Disease
  • Control
  • fMRI measurements of the two populations
  • Extract a small set of differentially expressed
    pathogenic-behaving genes
  • Feature selection for classification
  • Biological significant features for downstream
    research

8
Nervous System Diseases
  • Multiple categorizations
  • Organic vs. Functional
  • Anatomic vs. Physiologic
  • Structural vs. Metabolic
  • Physiologic molecular pathway
  • Invisible to (non functional) imaging
  • Not evident under microscope, no histological
    markers
  • Anatomic loss/gain of tissue

9
A Needle in a Haystack
  • Target Find the one(?) molecule that
    malfunctions
  • Multiple molecular pathways within a neuron
  • Neuronal interconnection
  • Cascade/ripple throughout the system
  • Molecule -gt Neuron (population)
  • Neuron -gt Other neuron
  • Other neuron -gt Other molecules
  • Molecules might be in the same neuron population
    (feedback)
  • infeasible for standard statistical analysis

10
Aging and AD
  • Cognitive decrease (AD and aging)
  • Differential vulnerable vs. resistant
  • Memory Encoding
  • Hippocampus
  • Entorhinal Cortex
  • Dentate Gyrus
  • CA subfields
  • Subiculum
  • Common process
  • Synaptic Failure leads to
  • Cell loss / tangles / plaques
  • Function, not structure!

11
Hippocampus
  • AD
  • Aging
  • Known from postmortem,in-vitro, and fMRI
  • Interconn.
  • Asses all regions together

12
Microarray analysis
  • Differential expression analysis
  • Blind analysis
  • Thousands of parameters simultaneously
  • High false positives rate (multiple comparisons,
    recall FDR)
  • Poor signal-to-noise ratio
  • Usually produce a list of differentially
    expressed genes
  • list can be very long (up to hundreds)

13
Statistical Modeling
  • Temporal model
  • 2nd stage for fMRI
  • Double subtraction
  • With sickness - basal metabolic rate changes as
    well

14
Multiple Studies
  • Why fMRI and not postmortem?
  • p.m. biased against earliest (and most
    discriminatory) stages
  • Only fMRI can image the cell-sickness stage
  • EC found to be the primary source of dysfunction
    in AD
  • What about normal aging?
  • Age-related changes in the EC matched
    pathological decline
  • Age-related changes in the dentate gyrus (DG),
    and subiculum (SUB), matched normal aging

15
Spatio-Temporal Model
  • How a pathogenic molecule should behave?
  • Differentially expressed in the EC (vs. no
    differentially expression in the DG)
  • Differences between AD and controls should be age
    independent
  • once EC dysfunction begins it does not worsen
    across age groups or over time

16
Results
  • 5 Molecules matched the pattern
  • Much less than 100s!
  • Best molecule VPS35
  • Part of a complex that connects-to and transports
    substances within a cell
  • A-beta a known smoking gun for AD
  • Experiments validated
  • Low VPS35 --gt High A-beta
  • Required neuronal molecules in end-to-end
    transportation are not transported --gt brain
    dysfunction

17
Conclusion
  • Microarrays noisy, unfocused results
  • fMRI imaging in-vivo, not post-mortem
  • Create statistical model (criteria) using fMRI,
    for microarray differentiation
  • Lack of specific methods
  • Not a parametric model, like a thumb rule
  • Nice example for research advance
  • My personal research is on PD
  • Lots of imaging data
  • Any suggestions?
  • Thanks!
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