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MILD COGNITIVE IMPAIRMENT UNRESOLVED ISSUES

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FDA QUESTIONS 1 and 2. CAN MCI BE DEFINED IN A CLINICAL SETTING? ... Proposed Sequence of Biochemical Progression in the Posterior cingulate VOI. Control ... – PowerPoint PPT presentation

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Title: MILD COGNITIVE IMPAIRMENT UNRESOLVED ISSUES


1
MILD COGNITIVE IMPAIRMENTUNRESOLVED ISSUES
  • Ronald C. Petersen
  • Mayo Clinic
  • Rochester, MN

2
MILD COGNITIVE IMPAIRMENT
  • CONCEPTUAL OVERVIEW
  • CLINICAL CRITERIA
  • OUTCOME
  • PREDICTORS OF PROGRESSION
  • UNRESOLVED ISSUES

3
Cognitive Continuum
CP926864- 9
4
Function
Age
CP926864- 1
5
FDA QUESTIONS 1 and 2
  • CAN MCI BE DEFINED IN A CLINICAL SETTING?
  • ARE THERE VALID CRITERIA FOR THE DIAGNOSIS OF MCI?

6
MILD COGNITIVE IMPAIRMENTCRITERIA
  • Memory complaint
  • Normal general cognitive function
  • Normal activities of daily living
  • Memory impaired for age
  • Not demented

7
MMSE
Full Scale IQ
Logical Memory II
Visual Reproductions II
Controls MCI AD AD CDR 0 0.5 0.5 1
Controls MCI AD AD CDR 0 0.5 0.5 1
CP926864- 3
8
FDA QUESTION 4
  • WHAT OUTCOME MEASURES ARE APPROPRIATE TO USE IN
    CLINICAL DRUGS TRIALS OF MCI?

9
Mild Cognitive Impairment (MCI)
MCI AD 12/yr
Control AD 1-2/yr
Initial
12
24
36
48
Initial
12
24
36
48
exam
exam
Months
Months
Petersen RC et al Arch Neurol 56303-308, 1999
CP926864- 12
10
Mild Cognitive Impairment
Stable ()
Years
CP926864- 7
11
FDA QUESTION 5
  • SHOULD CLINICAL DRUG TRIALS IN MCI INCORPORATE
    ANY SPECIAL FEATURES IN THEIR DESIGN?

12
PREDICTORS OF CONVERSION
  • Clinical features
  • Memory performance
  • Apolipoprotein E
  • Neuroimaging

13
MCI Conversion to Dementia
APOE 4 noncarrier

APOE 4 carrier
Years
CP926864- 13
14
NEUROIMAGING
  • Structural MRI
  • Hippocampus
  • Entorhinal cortex
  • Functional Imaging
  • MRS
  • fMRI
  • PET/SPECT

15
Stable ()
Years
CP926864- 15
16
Proposed Sequence of Biochemical Progression in
the Posterior cingulate VOI
Control
MCI
AD
?? MI ? NAA
? MI
17
UNRESOLVED ISSUES
  • CLINICAL CRITERIA-RATING SCALES
  • REFERENCE GROUPS
  • SOURCE OF SUBJECTS
  • CLINICAL HETEROGENEITY
  • SEMANTIC ISSUES

18
Mild Cognitive ImpairmentCDR and GDS
CP926864- 5
19
CDR and GDS (means)
  • CDR (SOBox)
  • Norm 0.01
  • MCI 1.07
  • AD (.5) 2.71
  • GDS
  • Norm 1.12
  • MCI 2.69
  • AD (.5) 3.37

20
REFERENCE GROUPS
  • YOUNG NORMALS
  • CHANGE IN PERFORMANCE
  • AGE-APPROPRIATE NORMALS
  • CONTAMINATION

21
SOURCE OF SUBJECTS
  • REFERRAL CLINICS
  • ADVERTISING
  • GENERAL PRACTICE CLINICS

22
CLINICAL HETEROGENEITY
23
FDA QUESTION 3
  • CAN MCI BE DISTINGUISHED FROM ALZHEIMERS DISEASE
    AND OTHER FORMS OF DEMENTIA?

24
Mild cognitive impairment Amnestic
Mild cognitive impairment Multiple
domains slightly impaired
Mild cognitive impairment Single non- memory
domain
CP938653 - 24
25
SEMANTIC ISSUES
  • NORMAL AGING
  • THIS IS ALZHEIMERS DISEASE
  • IS THIS A CONTINUUM?
  • WILL NEUROPATHOLOGY ANSWER THE QUESTION?

26
MCI CONCLUSIONS
  • CLINICALLY RELEVANT CONCEPT
  • CURRENTLY NOT CODIFIED
  • RELIABLE CRITERIA EXIST
  • OUTCOME MEASURES KNOWN
  • NOT NORMAL
  • NOT DEMENTED
  • THERAPEUTIC TARGET

27
Cognitive Continuum
CP926864- 9
28
MAYO ALZHEIMERS DISEASE RESEARCH CENTER
  • ROCHESTER
  • Emre Kokmen
  • Brad Boeve
  • Eric Tangalos
  • Joe Parisi
  • Cliff Jack
  • Walter Rocca
  • Bob Ivnik
  • Glenn Smith
  • Steve Edland
  • Peter OBrien
  • JACKSONVILLE
  • Steve Younkin
  • John Hardy
  • Dennis Dickson
  • Neill Graff-Radford
  • Shu-Hui Yen
  • Todd Golde
  • Mike Hutton
  • John Lucas
  • Tanis Ferman
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