Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants

Abstract Objective To summarize the clinical features of collagen type IV alpha 1/2 chain (COL4A)1/2‐related epilepsy and the seizure outcomes of patients undergoing epilepsy surgery. Methods We retrospectively analyzed the clinical, electroencephalography, and neuroimaging data; genetic characteris...

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Main Authors: Jie Shi, Jiuluan Lin, Jianjun Bai, Haixiang Wang, Bingqing Zhang, Qian Feng, Zhaohui Sun, Yiou Liu, Jing He, Xiancheng Song, Siyu Wang, Xiaoyan Liu, Wenjing Zhou
Format: Article
Language:English
Published: Wiley 2025-06-01
Series:Epilepsia Open
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Online Access:https://doi.org/10.1002/epi4.70014
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author Jie Shi
Jiuluan Lin
Jianjun Bai
Haixiang Wang
Bingqing Zhang
Qian Feng
Zhaohui Sun
Yiou Liu
Jing He
Xiancheng Song
Siyu Wang
Xiaoyan Liu
Wenjing Zhou
author_facet Jie Shi
Jiuluan Lin
Jianjun Bai
Haixiang Wang
Bingqing Zhang
Qian Feng
Zhaohui Sun
Yiou Liu
Jing He
Xiancheng Song
Siyu Wang
Xiaoyan Liu
Wenjing Zhou
author_sort Jie Shi
collection DOAJ
description Abstract Objective To summarize the clinical features of collagen type IV alpha 1/2 chain (COL4A)1/2‐related epilepsy and the seizure outcomes of patients undergoing epilepsy surgery. Methods We retrospectively analyzed the clinical, electroencephalography, and neuroimaging data; genetic characteristics; surgical details; and prognosis of 8 patients (4 boys) treated for COL4A1/2‐related epilepsy at Tsinghua University Yuquan Hospital. Results Two of the probands had COL4A1 variants and six had COL4A2 variants. Four of the variants were de novo. Prenatal abnormalities consisted of intrauterine growth retardation and ventriculomegaly. Three patients had a low birth weight, and one had perinatal retinal hemorrhage. The median age of seizure onset was 8 months, with 75% (6/8) experiencing epilepsy before age 1. Status epilepticus occurred in 38% (3/8) of patients. All patients experienced focal seizures, and 50% (4/8) had focal epileptic spasms. Hemiparesis was observed in 88% (7/8) of patients, and all 8 had developmental delays. The median number of anti‐seizure drugs was 5, and all patients had drug‐resistant epilepsy. Seven patients had seizures localized to one of the posterior quadrants, consistent with the magnetic resonance imaging features of blurring of the gray‐white matter junction and positron emission tomography features of metabolic abnormalities. Other neuroimaging features included bilateral mild white matter abnormalities; unilateral porencephaly near the basal ganglia; ventriculomegaly; focal cerebral calcification; contralateral schizencephaly; and contralateral cortical thickening and cerebellar abnormalities. Six patients underwent unilateral posterior quadrant disconnection, five (83%) of whom had no recurrence for at least 11 months and experienced developmental improvement. No surgical complications were reported. Pathological examination revealed malformations of cortical development in all six surgical cases (five with focal cortical dysplasia [FCD] type Ia and one with FCD type II). Significance The results of this case series suggest that early surgical intervention in patients with COL4A1/2‐related epilepsy with well‐defined epileptogenic zones may improve seizure control and developmental outcomes. Plain Language Summary In this case series of eight patients, epilepsy related to variants in the collagen type IV alpha 1/2 chain genes was characterized by drug‐resistant localized seizures with an early onset, one‐sided muscle weakness, and developmental delay. Neuroimaging revealed various brain abnormalities. Structural abnormalities outside the seizure‐onset zone did not appear to affect surgical prognosis. Early surgical intervention in patients with well‐defined seizure‐onset zones improved seizure control and developmental outcomes.
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spelling doaj-art-df64ec14b387417dac535b81797b09fa2025-08-20T02:05:59ZengWileyEpilepsia Open2470-92392025-06-0110372573510.1002/epi4.70014Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variantsJie Shi0Jiuluan Lin1Jianjun Bai2Haixiang Wang3Bingqing Zhang4Qian Feng5Zhaohui Sun6Yiou Liu7Jing He8Xiancheng Song9Siyu Wang10Xiaoyan Liu11Wenjing Zhou12Department of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaDepartment of Neurosurgery, Epilepsy Center Tsinghua University Yuquan Hospital Beijing ChinaAbstract Objective To summarize the clinical features of collagen type IV alpha 1/2 chain (COL4A)1/2‐related epilepsy and the seizure outcomes of patients undergoing epilepsy surgery. Methods We retrospectively analyzed the clinical, electroencephalography, and neuroimaging data; genetic characteristics; surgical details; and prognosis of 8 patients (4 boys) treated for COL4A1/2‐related epilepsy at Tsinghua University Yuquan Hospital. Results Two of the probands had COL4A1 variants and six had COL4A2 variants. Four of the variants were de novo. Prenatal abnormalities consisted of intrauterine growth retardation and ventriculomegaly. Three patients had a low birth weight, and one had perinatal retinal hemorrhage. The median age of seizure onset was 8 months, with 75% (6/8) experiencing epilepsy before age 1. Status epilepticus occurred in 38% (3/8) of patients. All patients experienced focal seizures, and 50% (4/8) had focal epileptic spasms. Hemiparesis was observed in 88% (7/8) of patients, and all 8 had developmental delays. The median number of anti‐seizure drugs was 5, and all patients had drug‐resistant epilepsy. Seven patients had seizures localized to one of the posterior quadrants, consistent with the magnetic resonance imaging features of blurring of the gray‐white matter junction and positron emission tomography features of metabolic abnormalities. Other neuroimaging features included bilateral mild white matter abnormalities; unilateral porencephaly near the basal ganglia; ventriculomegaly; focal cerebral calcification; contralateral schizencephaly; and contralateral cortical thickening and cerebellar abnormalities. Six patients underwent unilateral posterior quadrant disconnection, five (83%) of whom had no recurrence for at least 11 months and experienced developmental improvement. No surgical complications were reported. Pathological examination revealed malformations of cortical development in all six surgical cases (five with focal cortical dysplasia [FCD] type Ia and one with FCD type II). Significance The results of this case series suggest that early surgical intervention in patients with COL4A1/2‐related epilepsy with well‐defined epileptogenic zones may improve seizure control and developmental outcomes. Plain Language Summary In this case series of eight patients, epilepsy related to variants in the collagen type IV alpha 1/2 chain genes was characterized by drug‐resistant localized seizures with an early onset, one‐sided muscle weakness, and developmental delay. Neuroimaging revealed various brain abnormalities. Structural abnormalities outside the seizure‐onset zone did not appear to affect surgical prognosis. Early surgical intervention in patients with well‐defined seizure‐onset zones improved seizure control and developmental outcomes.https://doi.org/10.1002/epi4.70014COL4A1COL4A2epilepsyepilepsy surgeryseizure outcomes
spellingShingle Jie Shi
Jiuluan Lin
Jianjun Bai
Haixiang Wang
Bingqing Zhang
Qian Feng
Zhaohui Sun
Yiou Liu
Jing He
Xiancheng Song
Siyu Wang
Xiaoyan Liu
Wenjing Zhou
Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants
Epilepsia Open
COL4A1
COL4A2
epilepsy
epilepsy surgery
seizure outcomes
title Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants
title_full Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants
title_fullStr Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants
title_full_unstemmed Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants
title_short Phenotype and surgical management of drug‐resistant epilepsy in patients with COL4A1 and COL4A2 variants
title_sort phenotype and surgical management of drug resistant epilepsy in patients with col4a1 and col4a2 variants
topic COL4A1
COL4A2
epilepsy
epilepsy surgery
seizure outcomes
url https://doi.org/10.1002/epi4.70014
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