Skip to main content
. 2023 Mar 28;38:103390. doi: 10.1016/j.nicl.2023.103390

Table 2.

NPSLE manifestations among the 64 patients in the SLE cohort, presented as number of patients (percentage of SLE patients), according to three NPSLE attribution models (SLICC A, SLICC B and NPACR).


SLICC A
SLICC B
NPACR
Patients with NPSLE manifestations 13 (20 %) 19 (30 %) 38 (59 %)
CNS Cognitive dysfunction 0 (0 %) 4 (6 %) 23 (36 %)
Headache N/A N/A 20 (31 %)
Depression 0 (0 %) 0 (0 %) 9 (14 %)
Anxiety N/A N/A 9 (14 %)
Cerebrovascular disease 1 (2 %) 4 (6 %) 4 (6 %)
Acute confusion 1 (2 %) 2 (3 %) 3 (5 %)
Demyelinating disease 2 (3 %) 2 (3 %) 2 (3 %)
Epilepsy 1 (2 %) 1 (2 %) 1 (2 %)
Psychosis 1 (2 %) 1 (2 %) 1 (2 %)
Aseptic meningitis 1 (2 %) 1 (2 %) 1 (2 %)
Chorea 0 (0 %) 1 (2 %) 1 (2 %)
Myelopathy 0 (0 %) 1 (2 %) 1 (2 %)



PNS Autonomic neuropathy 7 (11 %) 8 (13 %) 10 (16 %)
Cranial neuropathy 5 (8 %) 5 (8 %) 5 (8 %)
Mononeuropathy 1 (2 %) 2 (3 %) 2 (3 %)
Polyneuropathy 1 (2 %) 1 (2 %) 2 (3 %)
Plexopathy 0 (0 %) 0 (0 %) 0 (0 %)
Guillain-Barré 0 (0 %) 0 (0 %) 0 (0 %)
Myasthenia Gravis 0 (0 %) 0 (0 %) 0 (0 %)

A single patient might present with multiple manifestations, and the patients in SLICC A are by definition also included in SLICC B.

NPSLE = Neuropsychiatric systemic lupus erythematosus, SLICC = Systemic Lupus International Collaborating Clinics, NPACR = American College of Rheumatology case definitions for NPSLE, CNS = Central nervous system, PNS = Peripheral nervous system, N/A = Not applicable.