# Predicting progression from SeLECTS with SWAS to EE-SWAS: risk factor identification and model development

**Authors:** Qiao Hu, Yuanyuan Luo, Yu Deng, Lingling Xie, Jiannan Ma, Siqi Hong, Ping Yuan, Li Jiang

PMC · DOI: 10.3389/fnhum.2025.1641421 · 2026-01-15

## TL;DR

This study identifies risk factors and develops a predictive model to determine which patients with SeLECTS are likely to progress to EE-SWAS, helping clinicians intervene early.

## Contribution

The study introduces a validated predictive model for early risk stratification in SeLECTS patients progressing to EE-SWAS.

## Key findings

- Prolonged spike-and-wave clusters and high-amplitude spikes predict EE-SWAS progression.
- Younger age at first seizure is an independent predictor of progression.
- The nomogram model achieved high accuracy with a C-index of 0.932 in derivation and 0.934 in validation.

## Abstract

This study sought to identify early risk factors and develop a predictive model for progression from self-limited epilepsy with centrotemporal spikes (SeLECTS) accompanied by spike-and-wave activation in sleep (SWAS) to epileptic encephalopathy with SWAS (EE-SWAS), aiming to facilitate early clinical intervention.

From a pediatric cohort with spike-and-wave index >50%, we analyzed 77 SeLECTS patients (33 progressed to EE-SWAS, 36 remained stable over ≥2 years of follow-up). Baseline clinical and EEG features were comprehensively evaluated. Multivariate logistic regression identified independent predictors of cognitive regression, which were incorporated into a nomogram-based predictive model. Model performance was assessed using the C-index in both derivation and external validation cohorts.

Prolonged spike-and-wave clusters, high-amplitude spikes with secondary generalization, and younger age at first seizure emerged as independent predictors of EE-SWAS progression. The nomogram model demonstrated high discriminative ability, with a C-index of 0.932 in the derivation cohort and 0.934 in external validation.

This study provides the first validated tool for early risk stratification in SWAS-associated SeLECTS, enabling clinicians to anticipate EE-SWAS progression and optimize therapeutic strategies. The model’s robustness supports its potential utility in clinical decision-making to mitigate cognitive decline.

## Linked entities

- **Diseases:** EE-SWAS (MONDO:0800501)

## Full-text entities

- **Diseases:** self-limited epilepsy (MESH:C536711), seizure (MESH:D012640), cognitive decline (MESH:D003072), epileptic encephalopathy (MESH:D001927)
- **Chemicals:** EE (MESH:D004997)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12852369/full.md

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Source: https://tomesphere.com/paper/PMC12852369