Disease areas:
  • brain
Last updated:
Author(s):
Tianmi Yang, Dejiang Pang, Jingxuan Huang, Yi Xiao, Chunyu Li, Qianqian Wei, Ruwei Ou, Yangfan Cheng, Junyu Lin, Ningning Che, Jiajia Fu, Qirui Jiang, Shichan Wang, Jiyong Liu, Sirui Zhang, Huifang Shang
Publish date:
4 April 2025
Journal:
Translational Psychiatry
PubMed ID:
40185700

Abstract

Amyotrophic lateral sclerosis-frontotemporal spectrum disorder (ALS-FTSD) is a fatal neurodegenerative condition, and identifying its modifiable risk factors is a critical public health issue. This large-scale prospective cohort study investigated the role of sleep-related factors in ALS-FTSD risk using data from 396,918 UK Biobank participants. Eight sleep-related exposures were assessed, and Cox proportional hazards regression was employed to evaluate their associations with ALS-FTSD incidence. Subgroup and sensitivity analyses were conducted to validate the robustness of our findings. At baseline, participants had a mean age of 56.31 ± 8.12 years, with 47.5% being male. In the fully adjusted Cox model, organic sleep disorders (G47) (HR: 1.81, 95% CI: 1.21, 2.72, P = 0.004), hypersomnia (G47.1) (HR: 36.53, 95% CI: 9.04, 147.55, P < 0.001), and extreme short sleep (<5 h per day) (HR: 2.09, 95% CI: 1.09, 3.99, P = 0.046) were significantly associated with increased ALS-FTSD risk. In conclusions, these findings revealed the relationship between sleep and the risk of ALS-FTSD, identifying new modifiable risk factors and potential preventive possibilities for ALS-FTSD. Further research is warranted to elucidate the mechanistic links between sleep disturbances and ALS-FTSD pathogenesis.

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Institution:
West China Hospital of Sichuan University, China

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