PMID- 38011484 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231129 IS - 2717-011X (Electronic) IS - 2717-011X (Linking) VI - 21 IP - 2 DP - 2022 Apr 4 TI - The association between body mass index, demographic and clinical characteristics with cognitive performance in patients with neuromyelitis optica spectrum disorder. PG - 74-82 LID - 10.18502/cjn.v21i2.10490 [doi] AB - Background: Cognitive dysfunction is one of the problems that patients with neuromyelitis optica spectrum disorder (NMOSD) suffer from. We aimed to assess the association between demographic and clinical features as well as body mass index (BMI) and cognitive function in patients with NMOSD. Methods: A cross-sectional study was performed on 41 patients with definite diagnosis of NMOSD. Serum status of neuromyelitis optica immunoglobulin G (NMO-IgG) was determined using enzyme-linked immunosorbent assay (ELISA) method. Cognitive function was assessed by Minimal Assessment of Cognitive Function in Multiple Sclerosis (MACFIMS) battery which is validated for Persian people before and North American Adult Reading Test (NAART). Results: The mean score of NAART test was higher in participants with normal weight compared with overweight patients (40.47 +/- 3.51 vs. 36.00 +/- 5.74, P = 0.02). Current age was negatively correlated with Delis-Kaplan Executive Function System (D-KEFS)-Sorting (P = 0.05, r = -0.30). The correlation of duration of disease and cognitive performance was not significant (P > 0.05). Higher physical disability based on Expanded Disability Status Scale (EDSS) was correlated with lower results in Brief Visuospatial Memory Test-Revised (BVMT-R) (P < 0.01, r = -0.50), California Verbal Learning Test-second edition (CVLT-II)-Delayed Recall (P = 0.02, r = -0.35), and Symbol Digit Modalities Test (SDMT) (P = 0.03, r = -0.33) subtests of MACFIMS. Annual relapse rate was indirectly correlated with CVLT-II (P = 0.03, r = -0.34) and CVLT-II-Delayed Recall (P = 0.01, r = -0.38). Male participants obtained better scores in Paced Auditory Serial Addition Test (PASAT) subtest (P = 0.05). NMO-IgG seropositive patients had poorer performance in terms of CVLT-II-Delayed Recall, Controlled Oral Word Association Test (COWAT), and D-KEFS-Descriptive (P < 0.05). Participants with bachelor and master education degrees showed significantly better results compared to those with high school degree (P < 0.05). Conclusion: Investigating the clinical and demographic factors affecting cognitive impairment can increase the awareness of health care providers for early diagnosis of cognitive impairment in patients with NMOSD and increase the quality of health services. CI - Copyright (c) 2022 Iranian Neurological Association, and Tehran University of Medical Sciences Published by Tehran University of Medical Sciences. FAU - Rezaeimanesh, Nasim AU - Rezaeimanesh N AD - Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran. FAU - Saeedi, Roghayyeh AU - Saeedi R AD - Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran. FAU - Sahraian, Mohammad Ali AU - Sahraian MA AD - Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran. FAU - Ghadiri, Fereshteh AU - Ghadiri F AD - Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran. FAU - Naser Moghadasi, Abdorreza AU - Naser Moghadasi A AD - Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran. LA - eng PT - Journal Article PL - Iran TA - Curr J Neurol JT - Current journal of neurology JID - 101769679 PMC - PMC9860205 OTO - NOTNLM OT - Neuromyelitis Optica; Cognition; Body Mass Index; Demography EDAT- 2022/04/04 00:00 MHDA- 2022/04/04 00:01 PMCR- 2022/04/04 CRDT- 2023/11/27 15:00 PHST- 2021/11/25 00:00 [received] PHST- 2022/02/02 00:00 [accepted] PHST- 2022/04/04 00:01 [medline] PHST- 2022/04/04 00:00 [pubmed] PHST- 2023/11/27 15:00 [entrez] PHST- 2022/04/04 00:00 [pmc-release] AID - CJN-21-74 [pii] AID - 10.18502/cjn.v21i2.10490 [doi] PST - ppublish SO - Curr J Neurol. 2022 Apr 4;21(2):74-82. doi: 10.18502/cjn.v21i2.10490.