ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 0859

Evaluation of the Montreal Cognitive Assessment as a Screening Tool for Cognitive Dysfunction in Systemic Lupus Erythematosus

Sudha Raghunath1, Yifat Glikmann-Johnston1, Eric Morand2, Julie Stout1 and Alberta Hoi3, 1Monash University, Melbourne, Australia, 2School of Clinical Sciences at Monash Health, Monash University Faculty of Medicine, Nursing and Health Sciences, Monash Medical Centre Clayton, Melbourne, Australia, 3Department of Rheumatology, Monash Health & Department of Medicine, School of Clinical Sciences, Monash University, Melbourne, Australia

Meeting: ACR Convergence 2021

Keywords: Cognitive dysfunction, Systemic lupus erythematosus (SLE)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Sunday, November 7, 2021

Title: SLE – Diagnosis, Manifestations, & Outcomes Poster II: Manifestations (0855–0896)

Session Type: Poster Session B

Session Time: 8:30AM-10:30AM

Background/Purpose: Cognitive dysfunction (CD) affects approximately 40% of SLE patients (1), impacting on employment, daily function, and quality of life (2)(3). Diagnostic neuropsychological testing is time-consuming and requires specialised staff, limiting access and resulting in under-detection in routine practice. Therefore, effective screening of SLE patients in the clinical setting is essential in selecting patients for formal cognitive testing. The Montreal Cognitive Assessment (MoCA) is a brief screening tool, initially designed to screen for mild cognitive impairment (MCI) or dementia, which preliminary studies suggest may have utility in SLE. This study aimed to comprehensively evaluate the MoCA as a screening tool for CD in SLE.

Methods: We tested SLE patients (n=95) and demographically matched healthy control (HC) participants (n=48) using the MoCA and the one-hour neuropsychiatric test battery recommended by the ACR for use in SLE (4). CD in SLE patients was defined using standard deviations from the HC group mean. We compared three CD definitions, all based on thresholds from the 2007 ACR response criteria for neurocognitive impairment in SLE clinical trials (5). We used regression analyses to determine associations between MoCA and cognitive test scores, and assessed sensitivity, specificity, positive predictive value and negative predictive value of various MoCA cut-offs for predicting CD. We then determined the diagnostic accuracy of MoCA cut-off thresholds using receiver operator curves.

Results: The SLE and HC groups were well matched with no significant differences in age, gender, ethnicity, premorbid IQ or education level. The median age was 45 (range 22-64), 60% were Caucasian and the rest predominantly Asian, and all had good English proficiency. The prevalence of CD in the SLE group varied from 19% to 49% depending on the definition used; the median MoCA score was 26 (range 19-30). On multivariate analysis, MoCA score correlated significantly with nine of the ten cognitive endpoints studied (all p < 0.001; Table 1). Receiver operator curve analysis suggested that the MoCA cut-off of < 27 yielded the highest diagnostic accuracy across the three cognitive impairment definitions (AUC 0.76-0.78; Figure 1). The MoCA cut-off of < 28 had sensitivity of 83-94% with specificity of 46-58%, depending on the impairment definition used (Table 2).

Conclusion: The MoCA correlates strongly with gold-standard cognitive test results in SLE and is sufficiently sensitive for use in screening. We recommend the MoCA cut-off of < 28 as the threshold with the optimal sensitivity for screening for CD in SLE to ensure potential cases are detected. This threshold is higher than the MoCA cut-off used for MCI and dementia. This brief, freely available and practical tool for screening SLE patients for CD should be considered for inclusion in SLE management guidelines.

References: 1) Al Rayes et al. Semin Arthritis Rheum 2018. 2) Arntsen et al. Joint report by Lupus Research Alliance, Lupus Foundation of America & Lupus and Allied Diseases Association 2018. 3) Appenzeller et al. Arthritis Rheum 2009. 4) Liang et al. Arthritis Rheum 1999. 5) Mikdashi et al. Lupus 2007.

Table 1: Multivariate Analysis of the Montreal Cognitive Assessment (MoCA), Age and Cognitive Test Results in SLE. CI = Confidence Interval, *p value <0.05 **p value <0.005. Premorbid IQ was highly collinear with MoCA score and therefore was not included in the multivariate model.
1) Impairment defined by number of cognitive domains either 1.5 or 2 SD below healthy control group mean. 2) Specific cognitive tests used for each domain are as follows: Visual Memory – Rey Ostrrieth Complex Figure Test Recall Score, Verbal Memory -California Verbal Learning Test trials 1-5, Verbal Fluency – Controlled Oral Word Association Test FAS Sum, Working Memory – Letter Number Sequencing score, Processing Speed – Coding score, Complex Attention – Trail making test B time inverse, Psychomotor speed – finger tap test dominant hand score. Test scores were expressed as Z-scores in comparison to healthy control group data.

Table 2: Sensitivity, Specificity, Positive Predictive Value and Negative Predictive Value of Montreal Cognitive Assessment (MoCA) for detection of Cognitive Impairment in SLE.
1) Defined by number of cognitive domains either 1.5 or 2 SD below healthy control group mean.
Acronyms: HC – Healthy Control, PPV – Positive Predictive Value, NPV – Negative Predictive Value.

Figure 1: Receiver Operating Curves (ROC) for different Montreal Cognitive Assessment (MoCA) cut-offs by Cognitive Dysfunction (CD) Definition.
Area under the curve interpretation: 0.7-0.9 = moderate accuracy, 0.5-0.7 = low accuracy, ≤0.5 = equal to chance.


Disclosures: S. Raghunath, None; Y. Glikmann-Johnston, None; E. Morand, Amgen, 2, AbbVie, 2, Biogen, 2, Bristol Myers Squibb, 2, 5, AstraZeneca, 2, 5, 6, Genentech, 2, Servier, 2, Capella Biosciences, 2, Eli Lilly, 5, 6, EMD Serono, 5, 6, Janssen, 2, 5, UCB, 2, GlaxoSmithKline, 2, 5; J. Stout, Zindametrix, Pty Ltd, 4; A. Hoi, AstraZeneca, 2, 5, Janssen, 6, Abbvie, 6.

To cite this abstract in AMA style:

Raghunath S, Glikmann-Johnston Y, Morand E, Stout J, Hoi A. Evaluation of the Montreal Cognitive Assessment as a Screening Tool for Cognitive Dysfunction in Systemic Lupus Erythematosus [abstract]. Arthritis Rheumatol. 2021; 73 (suppl 9). https://acrabstracts.org/abstract/evaluation-of-the-montreal-cognitive-assessment-as-a-screening-tool-for-cognitive-dysfunction-in-systemic-lupus-erythematosus/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2021

ACR Meeting Abstracts - https://acrabstracts.org/abstract/evaluation-of-the-montreal-cognitive-assessment-as-a-screening-tool-for-cognitive-dysfunction-in-systemic-lupus-erythematosus/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology