Prenatal, perinatal and neonatal birth risk factors of children with epileptic encephalopathies
DOI:
https://doi.org/10.15574/PP.2023.96.64Keywords:
children, epileptic encephalopathies, prenatal period, perinatal period, hypoxic-ischemic encephalopathy, fetal distressAbstract
The negative impact of perinatal factors on the brain can play a significant role in the etiopathogenesis of epileptic seizures in young children and the development of epileptic encephalopathies (EE).
Purpose - to study the characteristics of the course of the prenatal and neonatal periods in young children with EE for the further formation of risk groups of children who need active monitoring.
Materials and methods. An analysis of prenatal and neonatal features of anamnesis of 157 children with EE and their mothers was carried out. The children were divided into 3 groups: the Group I - children with EE who had the debut of epileptic seizures before the age of 1 year (n=75); the Group II - children with EE who had the debut of epileptic seizures after the age of 1 year (n=44); the Group III - children with epileptiform and developmental encephalopathies (EDE) (n=38).
Results. The course of pregnancy in mothers of children with EDE is characterized by a high frequency of early gestosis, the threat of abortion in the second half of pregnancy and polyhydramnios (28.9%, 31.6%, 23.7%, respectively). Some (31.6%) of children with EDE were born prematurely, 21.1% by emergency caesarean section. Childbirth in mothers of children with EDE was characterised by a pathological course (44.7%), weakness of labor activity and prolonged dehydration (36.8% and 28.9%, respectively), and the birth of a child with distress (21.1%). The course of the neonatal period in children with EDE was characterized by a higher frequency of hypoxic-ischemic encephalopathy (23.7%) than in children with other forms of EE. In children of the Group I, syndromes of motor disorders (20.0%) and muscle hypotonia (17.3%) were more often observed.
Conclusions. Aggravating factors of obstetric-gynecological and somatic anamnesis in women, and the course of prenatal and neonatal periods of life, which can act as a basis for the formation of EE and EDE in children, have been established. Among them are preeclampsia, placental pathology, changes in the amount of amniotic fluid during pregnancy, pathological childbirth, central nervous system depression syndrome and convulsive syndrome in infants. The obtained data will contribute to the formation of high-risk groups of children who need active monitoring.
The research was carried out in accordance with the principles of the Helsinki Declaration. The study protocol was approved by the Local Ethics Committee of the participating institution. The informed consent of the patient was obtained for conducting the studies.
No conflict of interests was declared by the authors.
References
Bartolini E. (2021). Inherited Developmental and Epileptic Encephalopathies. Neurology international. 13(4): 555-568. https://doi.org/10.3390/neurolint13040055; PMid:34842787 PMCid:PMC8628919
Berg AT, Berkovic SF, Brodie MJ, Buchhalter J, Cross JH, van Emde Boas W et al. (2010). Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009. Epilepsia. 51(4): 676-685. https://doi.org/10.1111/j.1528-1167.2010.02522.x; PMid:20196795
Chang YT, Hong SY, Lin WD, Lin CH, Lin SS, Tsai FJ, Chou IC. (2023). Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics. Children (Basel, Switzerland). 10(3): 556. https://doi.org/10.3390/children10030556; PMid:36980114 PMCid:PMC10047509
Davis AS, Hintz SR, Van Meurs KP, Li L, Das A, Stoll BJ et al. (2010). Seizures in extremely low birth weight infants are associated with adverse outcome. The Journal of pediatrics. 157(5): 720-725.e52. https://doi.org/10.1016/j.jpeds.2010.04.065; PMid:20542294 PMCid:PMC2939969
Dubov T, Toledano-Alhadef H, Bokstein F, Constantini S, Ben-Shachar S. (2016). The effect of parental age on the presence of de novo mutations - Lessons from neurofibromatosis type I. Molecular genetics & genomic medicine. 4(4): 480-486. https://doi.org/10.1002/mgg3.222; PMid:27468422 PMCid:PMC4947867
Fukao T, Sano F, Nemoto A, Naito A, Yanagisawa T, Imai K et al. (2023). Factors associated with the development of epilepsy in very low birth weight infants. Pediatrics and neonatology. 64(6): 637-643. https://doi.org/10.1016/j.pedneo.2022.12.019; PMid:37117074
Glass HC, Hong KJ, Rogers EE, Jeremy RJ, Bonifacio SL, Sullivan JE et al. (2011). Risk factors for epilepsy in children with neonatal encephalopathy. Pediatric research. 70(5): 535-540. https://doi.org/10.1203/PDR.0b013e31822f24c7; PMid:21796017 PMCid:PMC3189270
Hryhorova IA, Sokolova LI. (2020). Nevrolohiia. Nats. pidruch. dlia studentiv med. zakl. vyshch. osvity. Za red. I.A. Hryhorovoi, L.I. Sokolovoi. 3-ye vyd. pererobl. ta dopov. Kyiv: Medytsyna: 639.
Martyniuk VIu, Moiseienko RO, Panasiuk LO ta in. (2013). Perynatalni urazhennia nervovoi systemy u ditei: klinika, diahnostyka, rannia medyko-sotsialna reabilitatsiia. Zbirnyk naukovykh prats spivrobitnykiv NMAPO im. P. L. Shupyka. 22(3): 217-223.
Martyniuk V.Iu. ta in. (2001). Klasyfikatsiia urazhen nervovoi systemy u ditei ta pidlitkiv. Za red. Martyniuka V.Iu. K.: Feniks: 192.
Mohiuddin M, Kooy RF, Pearson CE. (2022). De novo mutations, genetic mosaicism and human disease. Frontiers in genetics. 13: 983668. https://doi.org/10.3389/fgene.2022.983668; PMid:36226191 PMCid:PMC9550265
Myers CT, Mefford HC. (2016). Genetic investigations of the epileptic encephalopathies: Recent advances. Progress in brain research. 226: 35-60. https://doi.org/10.1016/bs.pbr.2016.04.006; PMid:27323938
Perfilov OV, Vasylenko MA, Kyrylova LH ta in. (2001). Hipoksychno-ishemichni urazhennia holovnoho mozku u novonarodzhenykh i ditei pershoho roku zhyttia ta metody yikh likuvannia. Sotsialna pediatriia. Rozdil «Medyko-sotsialni aspekty reabilitatsii ditei z orhanichnymy urazhenniamy nervovoi systemy». Kyiv: 161-163.
Pisani F, Facini C, Bianchi E, Giussani G, Piccolo B, Beghi E. (2018). Incidence of neonatal seizures, perinatal risk factors for epilepsy and mortality after neonatal seizures in the province of Parma, Italy. Epilepsia. 59(9): 1764-1773. https://doi.org/10.1111/epi.14537; PMid:30132843
Singhal NS, Sullivan JE. (2014). Continuous Spike-Wave during Slow Wave Sleep and Related Conditions. ISRN neurology: 619079. https://doi.org/10.1155/2014/619079; PMid:24634784 PMCid:PMC3929187
Stafstrom CE, Kossoff EM. (2016). Epileptic Encephalopathy in Infants and Children. Epilepsy currents. 16(4): 273-279. https://doi.org/10.5698/1535-7511-16.4.273; PMid:27582673 PMCid:PMC4988066
Stenshorne I, Syvertsen M, Ramm-Pettersen A, Henning S, Weatherup E, Bjørnstad A et al. (2022). Monogenic developmental and epileptic encephalopathies of infancy and childhood, a population cohort from Norway. Frontiers in pediatrics. 10: 965282. https://doi.org/10.3389/fped.2022.965282; PMid:35979408 PMCid:PMC9376386
Thakran S, Guin D, Singh P, Singh P, Kukal S, Rawat C et al. (2020). Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment. International journal of molecular sciences. 21(20): 7784. https://doi.org/10.3390/ijms21207784; PMid:33096746 PMCid:PMC7589654
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