Correspondence: When an article is eligible for submission of
Correspondence, a link to the response form is available within the full-text
article. You must be a
current subscriber who has activated the online portion of your subscription
in order to send a Correspondence. Any reader can read published
Correspondence.
Correspondence to:
ARTICLES:
K. Pérès, V. Chrysostome, C. Fabrigoule, J. M. Orgogozo, J. F. Dartigues, and P. Barberger-Gateau
Restriction in complex activities of daily living in MCI: Impact on outcome
Neurology 2006; 67: 461-466
[Abstract][Full text][PDF]
Pérès et al conclude that inclusion of IADL restriction, particularly
for the four items known to be most sensitive to early dementia, improved
the prediction of dementia and the stability of this status (e.g. no
reversal back to normal) over a period of time as short as 2 years. [1] This
study is important because it helps define the MCI population most at risk
of progression to dementia usually Alzheimer’s disease (AD), and may
facilitate the evaluation of disease-modifying treatments.
These clinical observations can be supplemented by apolipoprotein E
(APOE å4) genotyping; results from the Cache County Study confirm the very
high risk of progression to AD in MCI subjects with at least one APOE å4
allele. [2] [11C]PIB scanning also appears promising in detecting
subjects with abnormal amyloid loading in asymptomatic individuals. [3]
It is possible to predict that persons with cognitive complaints found to have some abnormal neuropsychological tests but not clinically demented will be offered a combination of clinical and
biological predictors for progression to dementia. This strategy will make
sense if there are specific disease-modifying treatments such as the
amyloid-specific therapies under study (tramiprosate or Alzhemed, R-flurbiprofen or Flurizan, bapineuzumab or AAB-001).
This promising research must not detract from the daily reality of dealing with persons with memory complaints--most will not
have dementia. These patients should be made aware of their risk state and their
vascular risk factors treated appropriately. [4]
References:
1. Pérès K, Chrysostome V, Fabrigoule C, Orgogozo JM, Dartigues JF, Barberger-Gateau P.
Restriction in complex activities of daily living in MCI: Impact on outcome Neurology 2006; 67: 461-466.
2. Tschanz JT, Welsh-Bohmer KA, Lyketsos CG, et al. Conversion to dementia from mild cognitive disorder: the
Cache County Study. Neurology 2006;67: 229-234
3. Mintun MA, Larossa GN, Sheline YI, et
al. [11C] PIB in a nondemented population: potential antecedent marker of
Alzheimer disease. Neurology 2006;67: 446-452
4. Gauthier S, Reisberg B, Zaudig M, Petersen et al. Mild cognitive impairment. Lancet 2006;367: 1262-1270.
Disclosure: The author reports no conflicts of interest.
Reply from the Authors
31 October 2006
Karine Pérès, Inserm U593, the French Institute of Health and Medical Research, University Bordeaux 2 146 rue Léo Saignat 33076 Bordeaux Cedex France, Virginie Chrysostome, Colette Fabrigoule, Jean-Marc Orgogozo, Jean-François Dartigues, and Pascale Barberger-Gateau
Karine.Peres{at}isped.u-bordeaux2.fr Karine Pérès, et al.
We thank Dr. Hussain for his interest in our article. [1] In the PAQUID
study, restriction of complex activities in daily living seemed to capture
other information than those identified on the sole basis of
neuropsychological testing. This additional information could predict subsequent dementia in population-based studies.
Dr. Hussain
suggests that other factors could be added to the diagnostic criteria
of MCI, such as genetics [2] or imaging. [3] Better identification of
patients involved in the dementia process is essential,
especially at the stage of the evaluation of disease-modifying treatments.
If patients are not targeted at an early stage, evaluations of disease-modifying treatments will never be probative.
Restriction in complex ADL greatly improves the prediction of
subsequent dementia. we found that cognitively normal people restricted in IADL are more
likely to develop dementia than those with MCI but non-restricted in these
activities. Such an evaluation may identify difficulties experienced in daily
life but might be not captured in neuropsychological testing.
On
the other hand, people with low cognitive performance (maybe low
performers since ever) but functioning independently in daily life might not
be involved in the dementia process despite poor cognitive
performances on experimental testing. These latter would thus be
misclassified as MCI and wrongly considered at higher risk of dementia.
Functional assessment should put emphasis on change, decline, and
adaptation of activities because of incipient cognitive problems. The
concomitant or differential evolution of abilities in IADL and cognitive
functioning needs to be further investigated years before dementia. The
PAQUID cohort with its 17 years of hindsight provides the data required
for such analyses.
Dr. Hussain concludes that most of people with cognitive
complaints will not have dementia. He also concludes that patients
should be aware of their risk state. If no efficient
treatment will be available, the statement of over-risk of dementia at the MCI stage--with the consequences involved with such an announcement--should be approached more cautiously. However, we fully agree with
an optimal prevention of vascular risk factors. [4]
Disclosure: The authors report no conflicts of interest.