The Cognitive Abilities Screening Instrument (CASI) : A Practical Test For Cross-Cultural Epidemiological Studies of Dementia
The Cognitive Abilities Screening Instrument (CASI) : A Practical Test For Cross-Cultural Epidemiological Studies of Dementia
The Cognitive Abilities Screening Instrument (CASI) : A Practical Test For Cross-Cultural Epidemiological Studies of Dementia
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Third Place
1993 ZPA Research Awards in Psychogeriatrics
The Cognitive Abilities
Screening Instrument (CASI):
A Practical Test for Cross-Cultural
Epidemiological Studies of Dementia
Evelyn L. Teng, Kazuo Hasegawa, Akira Homma,
Yukimuchi Imai, Eric Larson, Amy Graves,
Keiko Sugimoto, Takenori Yamaguchi, Hideo Sasaki,
Darryl Chiu, and Lon R. White
From the University of Southern California School of Medicine, LQSAngeles, California, U.S.A. (E.
L. Teng, PhD); the St. Marianna University School of Medicine, Kawasaki, Japan (K. Hasegawa, MD;
A. Homma, MD, and Y. Imai, MD); the University of Washington School of Medicine, Seattle,
Washington, U.S.A. (E. Larson, M D and A. Graves, PhD); the NationalCardiovascular Center, Osaka.
Japan (K. Sugimoto, MA; and T. Yamaguchi, MD); the Radiation Effects Research Foundation,
Hiroshima, Japan (H. Sasaki,MD); and the Honolulu-Asia Aging Study, National Institute on Aging,
Honolulu, Hawaii, U.S.A. (D. Chiu, MS; and L. R. White, MD).
45
46 E. L Teng et al.
Neuropsychological assessment for dementia usually follows a two-step proce-
dure. A short screening test is given first, then a long test battery is administered to
those identifiedby the screening test as suspect cases. The reasons for using along test
battery includethe following:(a) Ingeneral,alongertest is more reliable than ashorter
one; (b) a test with a wider score range can better monitor disease progression and
treatment effects; and (c) abattery of tests with arangeof scores for separatecognitive
domains can provide profiles of performance that may help distin-guish different
forms of dementia. The use of neuropsychologicaltest batteriesis a common practice
at major universities and research centers in a number of countries.
On the other hand, smaller clinics often do not have qualified personnel to
administer the tests and interpret the results. It is difficult for various research
centers to agree on a comprehensive set of common tests to facilitate data
comparison. For cognitively impaired patients or individuals with little or no
schooling, lengthy cognitive testing can be very stressful.
The Cognitive Abilities Screening Instrument (CASI) is a short, practical test
that has been designed to serve multiple functions. It can be used (a) as a screening
instrument for dementia, (b) to monitor disease progression, and (c) to provide a
profile of impairment among various cognitive domains.
Results
CASIadministruiiontime. Based on the pooled data from all four sites,the mean,
SD, and range of the loth to 90th percentile of testing time in minutes were
respectively 18.2,8.6,and 10 to 30 for dementiapatients, and 13.7,6.3,and 8 to 20
for control subjects.
Performance on the CASI by control subjects in relation to age and education.
In general, at each study site, performance increased with education and decreased
with advancing age at each education level, as shown in Table 2. Table 2 also shows
that at comparable education and age ranges, the average level of performance
differed among the four sites. This is at least partly attributableto the differences in
subject recruitment. The group with the highest general level of performance
(Seattle) were volunteers in a long-term research project and had an unusually large
proportion of older subjects with more than high-school education (Kukull et al.,
1992);many of them had been tested at return annual visits and might have benefited
from the practiceeffects from similartests. Participants with the lowest general level
of performance (Osaka) were actually patients who had had minor strokes; they
might have sustained some subtle lasting cognitive impairment even though they
appeared to be well recovered according to clinical interview and observation.
Item andysis. To compare the relative sensitivity of the various CASI items in
distinguishing dementia patients from controls among the four sites, for each site a
“relative prevalence ratio for dementia” (RP) was calculated for each item in the
following manner: First, based on the pooled data from both patients and controls
from all four sites, the median score was used to dichotomize subjects into “pass”
versus “fail” categories. The RP for eachitem was calculated separately for each site,
defined as the rate of dementia among those who failed the item divided by the rate
of dementia among those who passed the item. The higher the RP, the better the item
distinguisheddementia patients from controls. The results are presented in Table 3.
The absolute values of the RPs differed among the sites, and this again is at least
partly accounted for by the differences in subject recruitment. However, when the
Education in years
< 12 = 12 > 12
Site Age (yr.) Mean ( N ) Mean ( N) Mean ( N )
c 70 - ( 0) 97.0( 2) 97.1 ( 6)
Seattle 70 - 79 90.9 ( 6) 92.7( 9) 95.5 (27)
>= 80 87.5 ( 2) 88.7 (13) 91.9 (21)
< 70 90.3 ( 4) 93.0( 2) 95.0 ( 2)
Tokyo 70 - 79 85.2 (14) 79.0 ( 1) 94.8 (10)
>= 80 84.0 ( 4) - ( 0) 92.0( 1)
items were evenly divided into three groups of relatively high, medium, and low
discriminative power for each site, a remarkably consistent pattern among all four
sites emerged: In general, items that assess short-term memory, temporal orienta-
tion, and list-generating fluency were most sensitivein distinguishingpatients from
controls, whereas items that assess attention, language abilities, and long-term
memory of vital personal information were least sensitive.
The use of selected CASI &emto screenfor dementia To examine how well a
small subset of judiciously selected CASI items can be used instead of the whole
CASI to screen for dementia, for each subject the scores from the four items of
repeatingthree words, temporal orientation,generating animal names, and (thefirst)
recall of three words were combined and designated as the score of CASI-Short.For
each site, the sensitivity (the proportion of patients performing at or below the cutoff
score) and specificity (the proportion of controls performing above the cutoff score)
at an “optimal” cutoff point were determined for CASI, CASI-Short, HDSS-CE,
MMSE-CE, and the 3MS-CE, where “-CE indicates that the score was estimated
from a subset of the CASI items. The optimal cutoff point was defined as the score
closest to the point where the sensitivity curve crossed the specificity curve. The
results are presented in Table 4 and show that all five measures were fairly
comparable in their sensitivity and specificity for dementia.
The use of CASI total score for monitoring within-individual change. How
useful a test can be for monitoring diseaseprogression depends in part on the range
of its difficulty level and its sensitivityin detecting differences within this range. In
general, the larger the ranges of the obtained as well as the possible scores, and the
larger the SD of the score distribution, the better a test can fulfill this function. In this
regard, the CASI was comparable to the 3MS-CE but clearly better than the CASI-
Short, the HDSS-CE, and the MMSE-CE, as shown in Table 5. Other studies have
shown that the 3MS Test has less floor and ceiling effects than the MMSE (Teng et
50 E. L Teng et al.
Table 3. The Relative Prevalence Ratio for Dementia of the Various CASI Items
~ ~
. al., 1990), and it is also more sensitive than the MMSE in detecting deteriorationin
dementia patients (Teng & Chui, 1987). Table 5 also shows that although CASI-
Short consists of only four items, its scorerange and SD compared favorablyto those
of the HDSS-CE and the MMSE-CE. Data reported elsewherebased on 57 dementia
patients and 88 normal controls show that the CASI-estimated MMSE score is very
close to the conventionally obtained MMSE score: The two types of scores had a
mean differenceof 0.1 point and acorrelationcoefficientof .92 (Graves et al., 1993).
The use of CASldomain scores to provide profiles of cognitive impairment.
The utility of CASI domain scores is illustrated with the findingson two patients
from the Seattle site. Both patients had the identical CASI total score of 58.
Their domain scores, expressed in units of SD from the mean of the scores of the
control group from the same site, provide the additional information of the
relative impairments among the various cognitive domains, and highlight the
differences as well as the similarities between the two patients, as shown in
Tlte Cognitive Abilities Screening Instrument 51
Table 4. Cut-Off Score (C.S.), Sensitivity, and Specificity of the CASI, CASI-Short,
HDSS-CE, MMSE-CE, and 3MS-CE
Los Angeles Osaka Seattle Tokyo
Test C.S. Sens. Spec. C.S. Sens. Spec. C.S. Sens. Spec. C.S. Sens. Spec.
Figure 1. To reduce crowding in the graph, the domain scores for language, in
which neither patient showed any impairment, were omitted.
Discussion
The pilot testing of the CASI E-1.0 and CASI J-1.0 was conducted mainly with
convenience samples of subjects without population-based sampling. No strict
52 E. L Teng et al.
matching on age and education was attempted either among the four sites or
between dementia patients and control subjects. In addition, examiners used only
instructions in the manual as aguide in administration and scoring, and no attempt
was made to check how well the instructions were understood and followed.
Nevertheless, the results show that CASI characteristics did not vary significantly
among the four sites despite differences in language, subject characteristics, and
testing personnel and settings. At all four sites, performance on the CASI by the
control subjects increased with education and decreased with aging within each
education range. The most sensitive and the least sensitive items for distinguish-
ing dementiapatients from the controls were quite consistent across the sites; the
CASI-Short score, based on the summed score from four selected items of the
CASI, showed comparable sensitivity and specificity as the CASI total score and
the estimated HDSS, MMSE, and 3MS scores. The CASI total score yielded a
larger score range than the estimated HDSS and MMSE. The CASI domain scores
could be used to provide profiles of cognitive impairment.
The influence of aging and education on test performance has been a robust finding
in practically all studies that sample subjects with sufficient variation in these
variables. The effects of education include not only the learning of specific knowledge
and skill, but also improved general efficiency in information processing and manage-
ment. It is unrealistic to expect that the influenceof education can be fully eliminated
in dementia screening tests. On the other hand, cognitive skills are not equally
important for individuals of different occupations, cultures, and life roles. Many
individuals may never have had the opportunity or the need to develop their cognitive
skills in some of the areas deemed elemental and important by academicians who
design dementia screening tests. In assessing dementia, care should be taken to
consider the “ecological validity”of the test for the studypopulation; test items, cutoff
points, and even cognitive domains may need to be adjusted accordingly. The
grouping of items into various cognitive domains and the inclusion of a version code
to distinguish different versions of the CASI adapted for different study populations
ATTENTION
CONCENTRAT.
0RIENTATION
MEMORY
DRAWING
ANIMALS
ABS.-JUDG.
I I 1
-8 -6 -4 -2 0
2 = (X - M) I SD
Figure 1. Profiles of cognitive impairment of two patients with the identical
CASI total score of 58.
The CognitiveAbilities Screening Instrument 53
have been designed in part to facilitateand encourage local modifications of the CASI
items to suit the particular backgrounds of the subjects.
Item analysis of the CASI showed that practically all items distinguished
dementia patients from the controls, but some items performed much better than
others (Table 3). Items with low RPs should not be considered useless. These are
typically items performed relatively well by patients with mild-to-moderate
dementia. Some of these items assess attention and serve to help distinguish
dementia from delirium. Other items serve to monitor the progression of dementia
into its more severe stages.
Data shown in Table 4, including the cutoff points, sensitivities, and specifici-
ties, are presented mainly to provide comparisons among the five measures of
CASI, CASI-Short, HDSS-CE, MMSE-CE, and 3MS-CE. These values are
influenced by the composition of the particular groups of patients and controls.
It should be emphasized that no effort was made to closely match the patients and
the controls on age and education except that age was closely matched at the
Seattle site (Kukull et al., 1992); although most of the dementia patients were
estimated to be in the mild-to-moderatedementiarange, no standardized indepen-
dent measure of severity was obtained for all patients.
The most interesting finding from Table 4 is that the four-item CASI-Short was
comparable to the other measures in its sensitivity and specificity for detecting
dementia. Since the four items of repeating three words, temporal orientation,
generating animal names, and recalling three words do not involve reading,
writing, drawing, or arithmetic, the CASI-Short should be particularly suitable
for individuals with little or no formal education.
REFERENCES
American Psychiatric Association. (1987). Diagnostic and statistical manual of mental
disorders (3rd &.-rev.). Washington, DC:Author.
Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975). “Mini-Mental State”: A practical
method for grading the cognitivestateof patients for the clinician. Journalof Psychiatric
Research, 12, 189-198.
Graves, A. B., Larson, E. B., Kukull, W. A,, White, L.R., & Teng, E. L. (1993). Screening for
dementia in the communityin cross-nationalstudies:Comparison between the Cognitive
Abilities ScreeningInstrumentand the Mini-MentalStateExamination.In B. Corain, K.
Iqbal, M. Nicolini, B. Winblad, H. Wisniewski, & P. Zatta (Eds.),Alzheimer’sdisease:
Advances in clinical and basic research (pp. 113-119). New York: John Wiley & Sons.
Hasegawa,K. (1983). The clinical assessmentof dementia in the aged: A dementia screening
scale for psychogeriatric patients. In M. Bergener, U. Lehr, E. Lang, & R. Schmitz-
Scherzer (Eds.), Aging in the eighties and beyond (pp. 207-218).New York: Springer.
Kukull, W. A., Hinds, T. R., Schellenberg, G. D., van Belle, G., & Larson, E. B. (1992).
Increased platelet membrane fluidity as a diagnostic marker for Alzheimer’s disease: A
test in population-based cases and controls. Annals of NeuroZogy, 42, 607-614.
Pauker, J. D. (1988). Constructingoverlappingcell tables to maximize theclinicalusefulness
of normative test data: Rationale and an example from neuropsychology. Journal of
Clinical Psychology, 44, 930-933.
Teng, E. L., & Chui, H. C. (1987). The Modified Mini-Mental State (3MS) examination.
Journal of Clinical Psychiatry,48,3 14-318.
Teng, E. L., Chui, H. C., & Gong, A. (1990). Comparisons between the Mini-Mental State
Exam (MMSE) and its modified version -the 3MS test. In K. Hasegawa & A. Homma
(Eds.),Psychogeriatrics:Biomedicalandsocialadvances(pp. 189-192).Tokyo: Excerpta
Medica.
White, L. R. (1992). The Ni-Won-Sea dementia project: Description and progress report. In
H. Orimo, Y. Fukuchi, K. Kuramoto, & M. Zriki (Eds.),New horizons in aging science
(pp. 324-325). Tokyo: University of Tokyo Press.
Acknowledgment. This paper was presented at the Sixth Congress of the Interna-
tional Psychogeriatric Association, Berlin, Germany, September 5-10,1993.
Offprints and other requesfi. Requests for offprints should be directed to Evelyn L.
Teng, PhD, Department of Neurology (GNH 5641), University of Southern Califor-
nia School of Medicine, 2025 Zonal Avenue, Los Angeles, CA 90033, U S A .
To request a copy of the manual and other related material for CASI E- 1 .O, write to:
CASI Materials,d o L. White, EDB Program,National Institute on Aging, Gateway
Building, Room 3C309, National Institute of Health, Bethesda, MD 20892, U.S.A.
The Cognitive Abilities Screening Instrument 55
APPENDIX: Record form and scoring sheet for the CASI E-1.1.
The Difference Between CASI E-1.0 and CASI E-1.1
CASI E-1.1 is identical to CASI E-1.0 except that the raw scores for all items (except
3-step Command) that enter into the domains of Short-term Memory and Language
have been modified in version E-1.1 such that these two domain scores can be obtained
in the same manner as is the case for all the other domains, i.e., by the direct summing
of the raw scores of the constituent items. (In CASI E-1.0, the raw scores are always
integers, but some raw scores are first divided by 2 or 3 before being summed for the
domain scores for Language and Short-termMemory.) Although versions E- 1.O and E-
l. l have different raw scoreson some items, the two versions will always yield identical
domain and total scores. Version E-1.0 is more suitable for large research programs
where item scores are entered into a computerand the domain scoresare calculated with
computer programs. Version E-1.1 is more suitable for the hand calculation of the
domain scores without the use of a computer.
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SCORING SHEET for CASI E - 1 . 1 Domain Scores, T o t a l Score, and MMSE-CE
CODE SCORE ATT CCT ORT LTM STM LAN VC FLU A&J MMSE-CE
BPL 0 0
BYR 0 0 MMSE-CE = C A S I e x c e p t :
BDAY ( j 0
AGE ( 1 0 ? N: I f CASI = N
MNT ( 1 0 MMSE-CE = 1
SUN ( I 0 E l s e MMSE-CE = 0
(VRS#)
RGSl ( ) ( ) ................................................... (
(RGS2)
DBA ( 1 0 (
DBB ( 0 (
DBC ( 1 0 (
RClA ( ) ........................ ( ) .................... ? 1.5 (
RClB ( 0 ? 1.5 (
RClC ( ) 0 ? 1.5 (
SUB3A( ) 0
SUB3B( ) 0
SUB3C( ) 0
YR ( ) ............( ) ................................ ? 4 0
MO ( 1 0 ? Z 0
DATE ( ) 0 ? 3 0
DAY ( ( ) ....................................... 0
SSN ( 1 0 0
SPA ( 1 0 0
SPB ( ) 0 0
ANML ( .......................................... 0
SIM ( 1 0
JDMT ( ) 0
RPTA ( ( 1
RPTB ( ) ( ) .............................................. ? 3 0
READ 0 ? 1.5 ( )
WRITE 0 ? 2.5 ( )
DRAW ) ( ) ? 8, 9, or 10 ( )
CMD 0 0
RCZA ) . . ...................... 0
RCZB 1 0
RCZC ( 1 0
BODY ( ) .............................. 0
OBJA ( ) ( ) ....... OBJA 1 0.3 = ( )
OBJB ( ) 0
(RPNM)
RCOBJ( ) 0
-=-+__
t __ t t -t ___ t --.-+-
t
MMSE-CE
~