Cognitive function in systemic lupus erythematosus: results of a 5-year prospective study
Cognitive function in systemic lupus erythematosus: results of a 5-year prospective study
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DOI:
10.1002/art.1780400825
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发表时间:
1997-08-01
影响因子:
--
通讯作者:
Fisk, JD
中科院分区:
文献类型:
--
作者:
Hanly, JG;Cassell, K;Fisk, JD
Neuropsychological assessment techniques have heightened the awareness of abnormalities in cognitive function in systemic lupus erythematosus (SLE). Cross-sectional studies (1-6) have defined the characteristics of cognitive dysfunction and its prevalence, which has varied from 21% to 66% due to differences in study populations, the particular neuropsychological tests used, and the definition of cognitive impairment. Most studies have identified subclinical cognitive dysfunction in a substantial proportion of patients (1-4). It is important to know whether these abnormalities in cognitive function progress over time to more profound cognitive dysfunction or whether they signal the eventual emergence of other clinically overt manifestations of neuropsychiatric SLE (NPSLE). To address this question, we describe the results of a 5-year evaluation of cognitive function and clinically overt NPSLE in an unselected group of female SLE patients. In 1989-1990, 70 consecutive SLE patients underwent neuropsychological assessment (2). After a 12-month interval, 59 patients had a repeat assessment (7), and 60 months from the time of the initial assessment, 53 patients were reevaluated. Clinically overt neuropsychiatric events attributed to SLE were recorded, as was the corticosteroid dosage. Neuropsychological evaluation was based on 3 standardized tests of cognitive function: the Wechsler Adult Intelligence Scale-Revised (WAIS-R)(8), the Wechsler Memory Scale-Revised (WMS-R)(9), and the California Verbal Learning Test (CVLT)(10). This test battery is focused primarily on verbal learning. Decision rules for cognitive impairment have been described previously (2). To determine the functional significance of cognitive impairment, 2 validated, self-administered quality-of-life questionnaires were used at the final assessment, ie, the Medical Outcomes Survey Short Form-36 (SF-36)(11) and the Sickness Impact Profile (SIP)(12). A comparison of the proportion of patients in different subgroups was performed by chi-square analysis. Mean scores for the SF-36 and SIP were compared by t test. Changes in neuropsychological test performance over the 5-year period of study were examined by 2-way repeated-measures analysis of variance (ANOVA). Time was the within-subjects factor, and a separate analysis was conducted for each of the following between-subjects factors: clinically overt NPSLE at any time in the disease course, presence or absence of corticosteroid treatment at the time of each assessment (with those patients who alternated between taking and not taking corticosteroids forming a third group), and presence of cognitive impairment at the initial assessment (as determined by the previously described decision rules)(2). Separate analyses were conducted for each of the following response variables: information, similarities, picture completion, block design, and digit symbol subtests of the WAS-R; digit span forward, digit span backward, visual memory span forward, and visual memory span backward of the WMS-R; and list A trials 1-5, list A trial 1, List A trial 5, long-delay free recall, and discriminability (ie, recognition memory) of the CVLT. At the initial assessment, 15 of the 70 SLE patients (21%) demonstrated cognitive impairment. At the second assessment, after a mean of 12.8 months (range 11-17 months), 8 of 59 patients (14%) were impaired. Of the 19 patients who were cognitively impaired at either of the first 2 assessments, all but 4 were available for evaluation at the final assessment, which was completed a mean of 64.1 months (range 52-71 months) after the initial assessment. At the final assessment, 7 of 53 patients (13%) were impaired …