Evidence map›Paper›PMID 42149211›Full record

ArticleNeuroradiology2026

Neuroimaging spectrum of GATOR1-related epilepsy (GATORopathies).

Revanth Rb, Aditya Ajith, Abhishek Nayak, Ashalatha Radhakrishnan, Bejoy Thomas, Chandrasekharan Kesavadas

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Article in Neuroradiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Revanth RbDepartment of Imaging and Interventional Radiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Trivandrum, India. revanthrbhat@gmail.com.
Aditya AjithDepartment of Imaging and Interventional Radiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Trivandrum, India.
Abhishek NayakDepartment of Imaging and Interventional Radiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Trivandrum, India.
Ashalatha RadhakrishnanDepartment of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India.
Bejoy ThomasDepartment of Imaging and Interventional Radiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Trivandrum, India.
Chandrasekharan KesavadasDepartment of Imaging and Interventional Radiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Trivandrum, India. chandkesav@gmail.com.

Funding

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6 · The paper itself

Abstract

backgroundThe mTOR pathway is important for neurodevelopment. The GATOR1 complex, composed of DEPDC5, NPRL2, and NPRL3, functions as a negative regulator of mTORC1 activity and pathogenic variants in the genes which comprise this complex cause focal epilepsy and malformation of cortical development, all named as GATORopathies. While focal cortical dysplasia is commonly reported, the full spectrum of associated neuroimaging findings remains incompletely defined.

objectiveTo characterize the neuroimaging features associated with GATOR1 complex mutations and to explore potential associations between imaging phenotypes and specific genotypes.

methodsMRI studies were retrospectively reviewed from January 2019 to December 2025 in patients with genetically confirmed GATOR1 mutations. Clinical, radiological, and genetic data were analyzed to identify imaging patterns and genotype-phenotype correlations.

resultsTwenty patients (median age : 6 years; range 1-25 years) were included. DEPDC5 mutations were most frequent (n = 12), followed by NPRL3 (n = 5) and NPRL2 (n = 3). MRI abnormalities were identified in 16 patients (80%). Focal cortical malformations were the most common finding (n = 8), followed by diffuse cortical malformations (n = 5) and generalized neuroparenchymal atrophy (n = 3); four patients had MRI-negative studies. Imaging findings varied considerably across genotypes. DEPDC5 and NPRL2 mutations showed a broad and heterogeneous radiological spectrum, whereas NPRL3 mutations showed a tendency toward cortical malformations, though the small subgroup size limits interpretation. Seizure onset spanned from infancy to adulthood; however, patients with diffuse cortical abnormalities or generalized neuroparenchymal atrophy tended to present earlier and experienced a greater seizure burden.

conclusionGATOR1-related epilepsy demonstrates substantial variability in neuroimaging and electroclinical features, extending beyond focal cortical malformations to include diffuse cortical malformations, generalized neuroparenchymal atrophy, and MRI-negative presentations. These findings highlight the value of integrated genetic, imaging, and electroclinical assessment in routine clinical practice.

Indexed as

EpilepsyFocal Cortical DysplasiaGTPase-Activating ProteinsMagnetic Resonance ImagingMalformations of Cortical DevelopmentNeuroimagingRepressor ProteinsAdolescentAdultChildChild, PreschoolFemaleHumansInfantMaleMutationDEPDC5 protein, humanGTPase-Activating ProteinsNPRL2 protein, humanNPRL3 protein, humanRepressor ProteinsTumor Suppressor ProteinsDEPDC5Focal cortical dysplasiaGATOR1 complexMagnetic resonance imagingMalformations of cortical developmentPediatric epilepsy

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