TY - JOUR
T1 - CAMCOG as a screening tool for diagnosis of mild cognitive impairment and dementia in a Brazilian clinical sample of moderate to high education
AU - Nunes, Paula V.
AU - Diniz, Breno S.
AU - Radanovic, Marcia
AU - Abreu, Izabella D.
AU - Borelli, Danilo T.
AU - Yassuda, Monica S.
AU - Forlenza, Orestes V.
PY - 2008/12/1
Y1 - 2008/12/1
N2 - Background: The CAMCOG is a brief neuropsychological battery designed to assess global cognitive function and ascertain the impairments that are required for the diagnosis of dementia. To date, the cut-off scores for mild cognitive impairment (MCI) have not been determined. Given the need for an earlier diagnosis of mild dementia, new cut-off values are also necessary, taking into account cultural and educational effects. Methods: One hundred and fifty-seven older adults (mean age: 69.6±7.4 years) with 8 or more years of formal education (mean years of schooling 14.2±3.8) attending a memory clinic at the Institute of Psychiatry University of Sao Paulo were included. Subjects were divided into three groups according to their cognitive status, established through clinical and neuropsychological assessment: normal controls, n=62; MCI, n=65; and mild or moderate dementia, n=30. ROC curve analyses were performed for dementia vs controls, MCI vs controls and MCI vs dementia. Results: The cut-off values were: 92/93 for dementia vs controls (AUC=0.99: sensitivity: 100%, specificity: 95%); 95/96 for MCI vs controls (AUC=0.83, sensitivity: 64%, specificity: 88%), and 85/86 for MCI vs dementia (AUC=0.91, sensitivity: 81%, specificity: 88%). The total CAMCOG score was more accurate than its subtests Mini-mental State Examination, Verbal Fluency Test and Clock Drawing Test when used separately. Conclusions: The CAMCOG discriminated controls and MCI from demented patients, but was less accurate to discriminate MCI from controls. The best cut-off value to differentiate controls and demented was higher than suggested in the original publication, probably because only cases of mild to moderate dementia were included. This is important given the need for a diagnostic at earlier stages of Alzheimer's disease.
AB - Background: The CAMCOG is a brief neuropsychological battery designed to assess global cognitive function and ascertain the impairments that are required for the diagnosis of dementia. To date, the cut-off scores for mild cognitive impairment (MCI) have not been determined. Given the need for an earlier diagnosis of mild dementia, new cut-off values are also necessary, taking into account cultural and educational effects. Methods: One hundred and fifty-seven older adults (mean age: 69.6±7.4 years) with 8 or more years of formal education (mean years of schooling 14.2±3.8) attending a memory clinic at the Institute of Psychiatry University of Sao Paulo were included. Subjects were divided into three groups according to their cognitive status, established through clinical and neuropsychological assessment: normal controls, n=62; MCI, n=65; and mild or moderate dementia, n=30. ROC curve analyses were performed for dementia vs controls, MCI vs controls and MCI vs dementia. Results: The cut-off values were: 92/93 for dementia vs controls (AUC=0.99: sensitivity: 100%, specificity: 95%); 95/96 for MCI vs controls (AUC=0.83, sensitivity: 64%, specificity: 88%), and 85/86 for MCI vs dementia (AUC=0.91, sensitivity: 81%, specificity: 88%). The total CAMCOG score was more accurate than its subtests Mini-mental State Examination, Verbal Fluency Test and Clock Drawing Test when used separately. Conclusions: The CAMCOG discriminated controls and MCI from demented patients, but was less accurate to discriminate MCI from controls. The best cut-off value to differentiate controls and demented was higher than suggested in the original publication, probably because only cases of mild to moderate dementia were included. This is important given the need for a diagnostic at earlier stages of Alzheimer's disease.
KW - Alzheimer's disease
KW - Clock Drawing Test
KW - Mild cognitive impairment
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U2 - 10.1002/gps.2038
DO - 10.1002/gps.2038
M3 - Article
C2 - 18464287
AN - SCOPUS:54049085880
SN - 0885-6230
VL - 23
SP - 1127
EP - 1133
JO - International Journal of Geriatric Psychiatry
JF - International Journal of Geriatric Psychiatry
IS - 11
ER -