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PO.1.14 Evaluation of cognitive impairment in SLE – a comparison of two assessment tools
  1. E Fazekas1,
  2. G Bodor1,
  3. S Burcsár1,
  4. R Hemelein1,
  5. J Kálmán2,
  6. B Rafael3 and
  7. L Kovács1
  1. 1University of Szeged, Department of Rheumatology and Immunology ~ Szeged ~ Hungary
  2. 2University of Szeged, Department of Psychiatry ~ Szeged ~ Hungary
  3. 3University of Szeged, Department of Psychology ~ Szeged ~ Hungary


Background, aims Cognitive impairment is estimated to occur in 10–30% of systemic lupus erythematosus (SLE) patients. Its screening and early recognition is not well established in routine clinical care. Assessment tools for common types of dementia are insufficient to detect early signs of cognitive dysfunction, furthermore, few tests have been studied specifically in SLE patients to screen and follow cognitive functions.

The aim of this study was to evaluate the efficacy of Quick mild cognitive impairment screen (Qmci) and the Montreal Cognitive Assessment (MoCA) to find a brief screening tool for the everyday practice. Furthermore, our aim was to analyse which cognitive functions are mostly affected in SLE patients compared to healthy controls to detect mild cognitive impairment early, before it progresses to dementia.

Methods We enrolled consecutive SLE patients aged < 65 years who met the Systemic Lupus International Collaborating Clinics (SLICC) 2012 classification criteria. Disease activity was measured by SLEDAI-2K. We evaluated the patients’ cognitive function with the MoCA and Qmci tests. We recorded the patients’ demographic, clinical, immunoserological parameters and data about education, social and health habits. We also used this study to validate the Hungarian translation of the Qmci test in SLE patients.

Results Eighty-seven patients (mean age: 44.97/range: 20–64/), of whom 75 were women (86.2%) and 12 were men (13.8%) were studied. 32 patients (36.8%) had < 12 years of education, 32 patients had grammar school or college educational level (36.8%) and 23 had university degree. Regarding MoCA, the participants’ test score was in the range between 17 and 30 points (maximum score in the MoCA test is 30), with mean score of 26.28 (SD = 3.08), which is considered as normal cognition with the 24 cut-off score of the MoCa test. Patients scored a mean of 3.64 point (SD = 1.32) from the maximal 5 points on the delayed recall scale. The Qmci scores were in the range between 49 and 94 points (mean: 80.68/SD = 10.10/), which is classified as normal cognition using the 62 cut-off score (potential maximum for Qmci is 100). Highest deviations from the maximum were observed in the delayed recall domain (13,79, SD = 5.58) and the verbal fluency task (mean 11.78, SD = 2.96 out of the maximal 20 points). With MoCA we detected 16 patients (18,4%) with cognitive impairment, whereas Qmci classified 4 participants (4,6%) with this.

Conclusions Cognitive impairment is present in a considerable proportion of SLE patients under 65 years of age, but the rate is dependent on the tool used. MoCA was a more sensitive test in this cohort, it therefore seems more useful for screening. Although Qmci has a less stringent numerical range to detect mild cognitive impairment, furthermore, it is a quick instrument, it classified less patients with cognitive impairment in our cohort. Analysis of subsets of cognitive function in the tests could help to better delineate the character of cognitive impairment developing in SLE. Further research is required in larger clinical and healthy sample to examine the diagnostic and follow-up value of the tests.

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