Abstract:Objective To study the difference in intestinal flora between children with focal epilepsy and healthy children and the change in intestinal flora after treatment in children with epilepsy. Methods A total of 10 children with newly diagnosed focal epilepsy were recruited as the case group and were all treated with oxcarbazepine alone. Their clinical data were recorded. Fecal specimens before treatment and after 3 months of treatment were collected. Fourteen aged-matched healthy children were recruited as the control group. Total bacterial DNA was extracted from the fecal specimens for 16S rDNA sequencing and bioinformatics analysis. Results After 3 months of carbamazepine treatment, the seizure frequency was reduced by >50% in the case group. At the phylum level, the abundance of Actinobacteria in the case group before treatment was significantly higher than that in the control group (P<0.05), and it was reduced after treatment (P<0.05). At the genus level, the abundances of Escherichia/Shigella, Streptococcus, Collinsella, and Megamonas in the case group before treatment were significantly higher than those in the control group (P<0.05), and the abundances of these bacteria decreased significantly after treatment (P<0.05). Conclusions There is a significant difference in intestinal flora between children with focal epilepsy and healthy children. Oxcarbazepine can significantly improve the symptoms and intestinal flora in children with epilepsy.
$author.xingMing_EN,$author.xingMing_EN,$author.xingMing_EN et al. Change in intestinal flora after treatment in children with focal epilepsy[J]. CJCP, 2022, 24(3): 290-296.
Chen XQ, Zhang WN, Yang ZX, et al. Efficacy of levetiracetam in electrical status epilepticus during sleep of children: a multicenter experience[J]. Pediatr Neurol, 2014, 50(3): 243-249. PMID: 24316167. DOI: 10.1016/j.pediatrneurol.2013.10.015.
Zhang YJ, Zhou SZ, Zhou YF, et al. Altered gut microbiome composition in children with refractory epilepsy after ketogenic diet[J]. Epilepsy Res, 2018, 145: 163-168. PMID: 30007242. DOI: 10.1016/j.eplepsyres.2018.06.015.
Huang NN, Hua DY, Zhan GF, et al. Role of Actinobacteria and Coriobacteriia in the antidepressant effects of ketamine in an inflammation model of depression[J]. Pharmacol Biochem Behav, 2019, 176: 93-100. PMID: 30528936. DOI: 10.1016/j.pbb.2018.12.001.
Mao LY, Ding J, Peng WF, et al. Interictal interleukin-17A levels are elevated and correlate with seizure severity of epilepsy patients[J]. Epilepsia, 2013, 54(9): e142-e145. PMID: 23944193. DOI: 10.1111/epi.12337.
Cattaneo A, Cattane N, Galluzzi S, et al. Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly[J]. Neurobiol Aging, 2017, 49: 60-68. PMID: 27776263. DOI: 10.1016/j.neurobiolaging.2016.08.019.
Jiang WW, Wu N, Wang XM, et al. Dysbiosis gut microbiota associated with inflammation and impaired mucosal immune function in intestine of humans with non-alcoholic fatty liver disease[J]. Sci Rep, 2015, 5: 8096. PMID: 25644696. PMCID: PMC4314632. DOI: 10.1038/srep08096.
Joseph J, Depp C, Shih PAB, et al. Modified Mediterranean diet for enrichment of short chain fatty acids: potential adjunctive therapeutic to target immune and metabolic dysfunction in schizophrenia?[J]. Front Neurosci, 2017, 11: 155. PMID: 28396623. PMCID: PMC5366345. DOI: 10.3389/fnins.2017.00155.
Erny D, Hrabě de Angelis AL, Jaitin D, et al. Host microbiota constantly control maturation and function of microglia in the CNS[J]. Nat Neurosci, 2015, 18(7): 965-977. PMID: 26030851. PMCID: PMC5528863. DOI: 10.1038/nn.4030.