Clinical Features and Therapeutic Effects of Anti-leucine-rich Glioma Inactivated 1 Encephalitis: A Systematic Review
Overview
Affiliations
Clinical presentations and treatment programs about anti-leucine-rich glioma inactivated 1 (LGI1) encephalitis still remain incompletely understood. This study analyzed the clinical features and therapeutic effects of anti-LGI1 encephalitis. PubMed, EMBASE, and the Cochrane Library were searched to identify published English and Chinese articles until April 2021. Data were extracted, analyzed, and recorded in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. A total of 80 publications detailing 485 subjects matched our inclusion criteria. Short-term memory loss (75.22%), faciobrachial dystonic seizures (FBDS) (52.53%), other seizures excluding FBDS (68.48%), psychiatric symptoms (57.67%), and sleep disturbances (34.30%) were the most frequently described symptoms in anti-LGI1 encephalitis. Hyponatremia (54.90%) was the most common hematologic examination change. The risk of incidence rate of malignant tumors was higher than in healthy people. The positive rate of anti-LGI1 in serum (99.79%) was higher than CSF (77.38%). Steroids (93.02%), IVIG (87.50%), and combined use (96.67%) all had a high remission rate in the initial visit. A total of 35 of 215 cases relapsed, of which 6/35 (17.14%) did not use first-line treatment, and 21 (60.00%) did not maintain long-term treatment. Plasma exchange (PE) could be combined in severe patients, immunosuppressant could be used for refractory patients or for recurrence and using an anti-epileptic drug to control seizures may benefit cognition. Short-term memory loss, FBDS, psychiatric symptoms, and hyponatremia were key features in identifying anti-LGI1 encephalitis. Serum and CSF antibody tests should be considered in diagnosis criteria. Steroids with IVIG should be recommended, PE was combined for use in severe patients, immunosuppressant therapy might improve outcomes if recurrence or progression occurred, and control seizures might benefit cognition. The useful ways to reduce relapse rate were early identification, clear diagnosis, rapid treatment, and maintaining long-term treatment. The follow-up advice was suggested according to the research of paraneoplastic syndrome, and concern about tumors was vital as well.
Rare mixed dementia: A case report.
Chen X, Xia W, Ma J, Chen J, Hu J, Shi X World J Radiol. 2025; 17(1):102579.
PMID: 39876884 PMC: 11755906. DOI: 10.4329/wjr.v17.i1.102579.
Acute Hyperhidrosis: A Clue to Underlying Autonomic Dysfunction and a Rare Neurological Disorder.
Peh R, Yip C, Liew Z Cureus. 2025; 16(12):e76387.
PMID: 39867015 PMC: 11762238. DOI: 10.7759/cureus.76387.
Decoding Dystonia in Autoimmune Disorders: A Scoping Review.
Dutta D, Yadav R Tremor Other Hyperkinet Mov (N Y). 2024; 14:60.
PMID: 39651491 PMC: 11623079. DOI: 10.5334/tohm.915.
Guo X, Shi H, Sun Y, Xing Y, Guo X, Shen Z J Inflamm Res. 2024; 17:7881-7891.
PMID: 39494201 PMC: 11531283. DOI: 10.2147/JIR.S485190.
Meng H, Chen X, Chen S Curr Neurol Neurosci Rep. 2024; 24(12):645-663.
PMID: 39297918 DOI: 10.1007/s11910-024-01377-4.