COLOURED PROGRESSIVE MATRICES: ERROR TYPE IN DEMENTIA AND MEMORY DYSFUNCTION. D. Salmaso, G. Villaggio, S. Copelli, P. Caffarra

Similar documents
Goodness of Pattern and Pattern Uncertainty 1

LOTCA Assessment review. Georgina Wrack. University of the Sunshine Coast

Math Released Item Grade 3. Find the Area and Identify Equal Areas 1749-M23082

University of Groningen. Visual hallucinations in Parkinson's disease Meppelink, Anne Marthe

We are IntechOpen, the world s leading publisher of Open Access books Built by scientists, for scientists. International authors and editors

M P---- Ph.D. Clinical Psychologist / Neuropsychologist

Pharmacologyonline 3: (2010)

Overview of Experimentation

CPAG Summary Report for Clinical Panel Hyperbaric Oxygen Therapy for Carbon Monoxide Poisoning

Convergence Principles: Information in the Answer

Discriminant Analysis with Categorical Data

CHAPTER 5 NEUROPSYCHOLOGICAL PROFILE OF ALZHEIMER S DISEASE

CHAPTER VI RESEARCH METHODOLOGY

NEUROPSYCHOLOGICAL ASSESSMENT S A R A H R A S K I N, P H D, A B P P S A R A H B U L L A R D, P H D, A B P P

Understanding Users. - cognitive processes. Unit 3

SOCIABLE DELIVERABLE D7.2a Interim Assessment of the SOCIABLE Platform and Services

Visual Processing (contd.) Pattern recognition. Proximity the tendency to group pieces that are close together into one object.

Concurrent validity of WAIS-III short forms in a geriatric sample with suspected dementia: Verbal, performance and full scale IQ scores

Using contextual analysis to investigate the nature of spatial memory

MindmetriQ. Technical Fact Sheet. v1.0 MindmetriQ

Selection and Combination of Markers for Prediction

26:010:557 / 26:620:557 Social Science Research Methods

SAMPLE PSYCHOEDUCATIONAL REPORT. Atlanta Pediatric Psychology Associates 3580 Habersham at Northlake Tucker, Georgia (770)

Abstract Reasoning Test 1

Use a diagnostic neuropsychology HOW TO DO IT PRACTICAL NEUROLOGY

Storage and processing working memory functions in Alzheimer-type dementia

Are people with Intellectual disabilities getting more or less intelligent II: US data. Simon Whitaker

! Introduction:! ! Prosodic abilities!! Prosody and Autism! !! Developmental profile of prosodic abilities for Portuguese speakers!

Test Assessment Description Ref. Global Deterioration Rating Scale Dementia severity Rating scale of dementia stages (2) (4) delayed recognition

AGED SPECIFIC ASSESSMENT TOOLS. Anna Ciotta Senior Clinical Neuropsychologist Peninsula Mental Health Services

NO LOWER COGNITIVE FUNCTIONING IN OLDER ADULTS WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER

The significance of sensory motor functions as indicators of brain dysfunction in children

CHAPTER - 6 STATISTICAL ANALYSIS. This chapter discusses inferential statistics, which use sample data to

Stroke Drivers Screening Assessment European Version 2012

CRITICALLY APPRAISED PAPER (CAP)

Cognitive Screening in Risk Assessment. Geoffrey Tremont, Ph.D. Rhode Island Hospital & Alpert Medical School of Brown University.

Selection and estimation in exploratory subgroup analyses a proposal

fmri and Voxel-based Morphometry in Detection of Early Stages of Alzheimer's Disease

Thesis for doctoral degree (Ph.D.) 2007 Predictors of cognitive decline in memory clinic patients. Christin Andersson. Christin Andersson

ADMS Sampling Technique and Survey Studies

Assessing cognitive function after stroke. Glyn Humphreys

Department of Psychology, Florida State University, Tallahassee, FL, USA

Effects of Adult Age on Structural and Operational Capacities in Working Memory

Capacity and Older Adults. Kenneth I. Shulman

Cognitive disorders. Dr S. Mashaphu Department of Psychiatry

Kingston Caregiver Stress Scale

Test Code : RZI/RZII (Short Answer type) Junior Research Fellowship in Psychology

Knowledge of Living and Nonliving Things in Dementia of the Alzheimer s Type

Experimental design. Alexa Morcom Edinburgh SPM course Thanks to Rik Henson, Thomas Wolbers, Jody Culham, and the SPM authors for slides

Cognitive recovery after severe head injury 2. Wechsler Adult Intelligence Scale during post-traumatic amnesia

Mechanisms of generalization perceptual learning

Experimental Design I

This PDF is available for free download from a site hosted by Medknow Publications

CONTEXTUAL ASSOCIATIONS AND MEMORY FOR SERIAL POSITION 1

MS&E 226: Small Data

PLS 506 Mark T. Imperial, Ph.D. Lecture Notes: Reliability & Validity

innate mechanism of proportionality adaptation stage activation or recognition stage innate biological metrics acquired social metrics

Reveal Relationships in Categorical Data

The Role of Feedback in Categorisation

cloglog link function to transform the (population) hazard probability into a continuous

Effect of Visuo-Spatial Working Memory on Distance Estimation in Map Learning

Process of a neuropsychological assessment

The Assessment in Advanced Dementia (PAINAD) Tool developer: Warden V., Hurley, A.C., Volicer, L. Country of origin: USA

21/05/2018. Today s webinar will answer. Presented by: Valorie O Keefe Consultant Psychologist

VALIDITY OF QUANTITATIVE RESEARCH

Experimental Design. Thomas Wolbers Space and Aging Laboratory Centre for Cognitive and Neural Systems

Alternative Explanations for Changes in Similarity Judgments and MDS Structure

Analysis of Environmental Data Conceptual Foundations: En viro n m e n tal Data

The Role of Action in Object Categorization

Mantel-Haenszel Procedures for Detecting Differential Item Functioning

***This is a self-archiving copy and does not fully replicate the published version*** Auditory Temporal Processes in the Elderly

Information Gathering Obtaining history is the most critical first step Patient-provided history may not be reliable Need info from relatives, friends

The reality.1. Project IT89, Ravens Advanced Progressive Matrices Correlation: r = -.52, N = 76, 99% normal bivariate confidence ellipse

COUNSELING FOUNDATIONS INSTRUCTOR DR. JOAN VERMILLION

UDS version 3 Summary of major changes to UDS form packets

Mini Mental State Examination and the Addenbrooke s Cognitive Examination: Effect of education and norms for a multicultural population

C-1: Variables which are measured on a continuous scale are described in terms of three key characteristics central tendency, variability, and shape.

Technical Specifications

UNDERSTANDING INDIVIDUAL DIFFERNCES: THE CASE OF INTELLIGNCE

Supplementary Online Content

Cognitive Neuroscience Section 8

Rapidly-administered short forms of the Wechsler Adult Intelligence Scale 3rd edition

Elderly Mental Health and Substance Abuse. Case 1. Dr. John McCahill, MRCPsych, FRCPC Alberta Hospital Edmonton September 11, 2008 Case Studies

3-86 Psychological Tests and Evaluation Procedures ^ General Ability Measures

Cognitive Design Principles and the Successful Performer: A Study on Spatial Ability

Selective bias in temporal bisection task by number exposition

Interpreting change on the WAIS-III/WMS-III in clinical samples

A feature-integration account of sequential effects in the Simon task

National MFT Exam Study System

Assessing Functional Neural Connectivity as an Indicator of Cognitive Performance *

Table 1: Summary of measures of cognitive fatigability operationalised in existing research.

UN Handbook Ch. 7 'Managing sources of non-sampling error': recommendations on response rates

ADHD in children and adolescents: examination of the association of neurological subtle signs with working memory problems

COGNITIVE FACTORS IN EPILEPSY BY MARGARET DAVIES-EYSENCK

9698 PSYCHOLOGY. Mark schemes should be read in conjunction with the question paper and the Principal Examiner Report for Teachers.

Personality and Individual Differences

(Received 30 March 1990)

Table 7.2B: Summary of Select Screening Tools for Assessment of Vascular Cognitive Impairment in Stroke Patients

The Short NART: Cross-validation, relationship to IQ and some practical considerations

VALIDITY STUDIES WITH A TEST OF HIGH-LEVEL REASONING

Transcription:

COLOURED PROGRESSIVE MATRICES: ERROR TYPE IN DEMENTIA AND MEMORY DYSFUNCTION. D. Salmaso, G. Villaggio, S. Copelli, P. Caffarra CNR-Istituto di Psicologia, Roma and Istituto di Neurologia, Universita' di Parma. Genetic Counseling, 1997, 8(2), 181-182. 1

ABSTRACT The importance of the cognitive assessment in determining an early diagnosis for neurological diseases, is widely emphasized. Nevertheless, not much has been made for the development of adequate tools of investigation. These tools must be easy to administer and with a high sensitivity and specificity for different disorders. This work describes the results obtained with Raven's Coloured Progressive Matrices (CPM), a test designed to assess the intellectual processes of children, mentally defective individuals and elderly people. The test was administered to 92 subjects (mean age= 66.2, sd= 11.3) belonging to 3 different groups: 31 demented patients, 34 dismnesic patients e 27 normal subjects. All subjects underwent a comprehensive neuropsychological examination that included, among other tests, the Mini Mental State Examination (MMSE). CPM scores resulted to be different across groups: demented patients had (CPM=12.3) lower scores than dismnesic (CPM=22.3) and normal (CPM=27.4) subjects. The same findings were obtained with MMSE scores. Considering, for demented patients, as cut-off scores CPM<20 and MMSE<26 we obtained 90% of sensitivity. When dismnesic patients are considered, the MMSE categorizes as inferior 53% of the patients, while the CPM identifies as much only the 35%. When CPM errors are analysed, instead of the correct responses, the best diagnostic utility of this test results evident. A factorial analysis conducted on the different types of error reveals 2 factors: a factor choice and a factor orientation. On the first type of error, dismnesic patients perform like normal subjects, while on the second type of error demented and dismnesic present an equal number of errors. This result is very important to diagnostic goals, since the first type of error might be more closely related to a diffused degeneration, while the second type might be caused by alterations of specific cerebral structures. 2

AIMS The purpose of this work is to examine correct responses and errors made on the Raven Coloured Progressive Matrices in subjects with different degrees of cognitive impairment. INTRODUCTION The importance of the cognitive assessment in determining an early diagnosis for neurological diseases is widely emphasized. Nevertheless, not much has been made for the development of adequate instruments of investigation. These tools must be easy to administer and should have high sensitivity and specificity for different disorders. This work focuses on the usefulness of Raven's Coloured Progressive Matrices (CPM; Raven, 1947)), a test designed to assess the intellectual processes of children, mentally defective individuals and elderly people. The CPM test is a popular measure of intellectual ability as responses require neither verbalization nor skilled manipulation ability. In addition, verbal instruction is kept to a minimum. For all these reasons CPM is widely used in clinical practice. 3

FIGURE 1 4

TEST DESCRIPTION The test consists of 36 coloured tables, grouped into three sets (A, Ab, B) of 12 items each. Each table (see one example in figure 1) contains a drawing with one part removed and six different inserts, one of which contains the correct pattern. The subject's responses have no time limit. Each set involves different principles of matrix transformations, and within each set the items become increasingly more difficult. Set A consists of problems in the form of a continuous pattern. Tables in the Ab and B series are made up of 4 parts, 3 of which are given and one is to be selected from the response alternatives. Through the Ab and B sets, there is a gradual shift from four parts which form a coherent whole (gestalt) to problems in which each part is a symbol in an analogy test and there is no discrete perceptual gestalt per se. 5

Raven (1947) differentiated 4 classes of incorrect responses (see Table I). TABLE I: CATEGORIZATION OF INCORRECT RESPONSES (FROM RAVEN, 1947). DIFFERENCE A - Responses without any figure. B - Responses in which the figure shown is irrelevant. INADEQUATE INDIVIDUATION C - Responses contaminated by irrelevancies. D - Responses contaminated by distortions. E - Responses which are the whole or half the pattern to be completed. REPETITION OF ONE PART F - Left and above the space to be filled. G - Above the space to be filled. H - To the left of the space to be filled. INCOMPLETE I - Wrongly oriented J - Incomplete 6

SUBJECTS The study was carried out on 92 subjects (49 males, 43 females; mean age=66.2; mean schooling=7.6) belonging to three different groups: 31 demented patients, 34 dismnesic patients and 27 normal subjects. All subjects underwent a comprehensive neuropsychological examination that included, among other tests, the Mini Mental State Examination (MMSE). Table II summarizes some demographic data. TABLE II: DEMOGRAPHIC DATA N AGE SCHOOL MMSE NORMALS 27 Mean 60.9 10.4 28.0 sd 11.5 4.7 1.9 DISMNESICS 34 Mean 66.4 7.7 24.8 sd 12.4 4.3 4.0 DEMENTED 31 Mean 70.3 5.4 16.8 sd 7.7 3.1 6.4 7

RESULTS AND DISCUSSION Internal consistency (0.87) and validity (the correlation CPMxMMSE, 0.78) were both acceptable: 9 out of the 36 items, obtained percentage of correct responses greater than 80%. To study the influence of visual spatial defects on correct responses, an analysis has been conducted on location preferences. This analysis indicated a prevalence of responses located in the upper row and positions 1 and 2. These effects were equivalent in normals and dismnesics, while demented manifested only the upper/lower effect. For better understanding the diagnostic power of the CPM, the results have been analyzed according to different views. The means for the CPM, for subtests (A, Ab, B) and for the three sets (1,2,3) identified by Villardita (1985), are listed in Table III. All means were statistically different except those marked with an "=" sign. TABLE III: MEANS OF CPM AND SUBTEST SCORES FOR EACH GROUP NORMALS DISMNESICS DEMENTED CPM 27.4 22.3 12.3 sd 4.7 6.4 5.7 Set A 10.4 9.2 6.1 Set Ab 9.6 7.2 3.3 Set B 7.4 = 6.0 3.0 Set 1 10.9 = 10.3 7.2 Set 2 15.0 10.7 4.5 Set 3 1.6 = 1.3 = 1.0 8

As for CPM scores, intergroup scores resulted to be significantly different (F(2,89)=54, p<.000): demented scored lower than dismnesic and normals scored higher than dismnesics. Only 55% of the variance in CPM is accounted for by diagnostic category and hence the total score alone would not be a good predictor of deterioration of intelligence. The MMSE scores (see Table II) revealed the same difference among groups. The analysis of each subset of the CPM confirmed the assumption that set A is easier than set Ab and B. Demented scored always lower than dismnesics and normals. As illustrated in Table III for set B dismnesics did not differ from normals. This result seems to be more easily explained by a decrease of performance in normals more than by a differential effect of set B on dismnesic patients. As known, the age of subjects is supposed to be more relevant as task complexity increases. Subset distinction as indicated by Villardita provided no better explanations on the nature of group differences. Actually, Set 3 was unusable and Set 1 did not differentiate between normals and dismnesics. Only Set 2, in which the principle of symmetry is, presumably, required, revealed intergroup differences. In conclusion, it seems to us that the total score is enough to differentiate our patients. Considering as cut-off scores CPM<20 we obtained 90% of sensitivity, for demented, and 65% and 93% of specificity for dismnesics and normals. Taking into consideration that dismnesics were not deteriorated, these estimates provide an acceptable categorization of the population. 9

As typical of other cognitive diagnostic contexts, the analysis of the correct responses could provide only moderate information, especially whenever an early detection of cognitive impairment is necessary. On the other hand, error analysis provides better diagnostic information. Incorrect responses given by each subject in each table were classified according to the scheme reported in Table 1. A-type errors resulted to be only 0.7% of the total errors; for this reason they were excluded from the analysis. A principal component analysis revealed 2 factors accounting for 51% of the total variance. The first factor (E-1, CHOICE) incorporates B, C, E and J error, while the second (E-2, ORIENTATION) contains F, H, I, G errors. When single errors are pooled according to the previous 2 factors we obtained the following results (Table IV). Statistical analysis indicates that dismnesics perform like normal subjects as to the first group of errors, while they are equivalent to demented as to the second group. TABLE IV: ERROR MEANS FOR CHOICE (E1) AND ORIENTATION (E2) NORMALS DISMNESICS DEMENTED E1 1.7 = 2.8 8.5 sd 2.1 2.4 5.0 E2 6.6 10.5 = 11.1 sd 3.7 4.5 5.2 10

CONCLUSIONS The analysis of the correct responses to the CPM provides the obvious confirmation that the 3 groups differ. By contrast, the analysis of the errors made by the subject in each table highlights 2 separate components of the process of their analysis; such components turn out to be distinctly altered in subjects with different degrees of cognitive impairment. This last result seems to be very relevant to the construction of increasingly more sensitive diagnostic tests. In fact, the first type of error might be more closely related to a diffused degeneration, while the second type might be caused by alterations of specific cerebral structures. 11