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Dysfunction in Automatic Processing of Emotional Facial Expressions in Patients with Obstructive Sleep Apnea Syndrome: An Event-Related Potential Study

  • Lv, Renjun1, 1, 1, 1, 2
  • Nie, Shanjing1, 1, 1, 1
  • Liu, Zhenhua1
  • Guo, Yunliang1, 1, 1, 1
  • Zhang, Yue3
  • Xu, Song1, 1, 1, 1
  • Hou, Xunyao1, 1, 1, 1
  • Chen, Jian1, 1, 1, 1
  • Ma, Yingjuan4
  • Fan, Zhongyu1, 1, 1, 1, 2
  • Liu, Xueping1, 1, 1, 1
  • 1 Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, 250021, Shandong
  • 2 Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, 250021, Shandong
  • 3 Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, Shandong
  • 4 Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250021
Published Article
Nature and Science of Sleep
Publication Date
Sep 15, 2020
DOI: 10.2147/NSS.S267775
PMID: 32982522
PMCID: PMC7501974
PubMed Central


Aim Obstructive sleep apnea syndrome (OSAS) is a prevalent chronic disease characterized by sleep fragmentation and intermittent hypoxemia. Several studies suggested that electrophysiological changes and neurocognitive abnormalities occurred in OSAS patients. In this study, we compared automatic processing of emotional facial expressions schematic in OSAS patients and matched healthy controls via assessing expression-related mismatch negativity (EMMN). Methods Twenty-two OSAS patients (mean age 44.59 years) and twenty-one healthy controls (mean age 42.71 years) were enrolled in this study. All participants underwent Montreal Cognitive Assessment (MoCA) scale test and polysomnographic recording. An expression-related oddball paradigm was used to elicit EMMN and the electroencephalogram was recorded and analyzed. Furthermore, Pearson’s correlations were calculated to discuss the correlation between neuropsychological test scores, clinical variables and electrophysiological data. Results Compared with healthy controls, OSAS sufferers demonstrated significantly reduced EMMN mean amplitudes within corresponding time intervals, regardless of happy or sad conditions. Meanwhile, we observed that amplitude of sad EMMN was larger (more negative) than happy EMNN in healthy controls, while not in patients. Moderate correlations were found between MoCA test scores, sleep parameters and EMMN amplitudes. Conclusion Our findings suggested pre-attentive dysfunction of processing emotional facial expressions in patients with OSAS, without the existence of negative bias effect. Moreover, correlation analysis showed that clinical characteristics of OSAS patients could affect EMMN amplitudes. Further studies on the advantages of EMMN as clinical and electrophysiological indicators of OSAS are warranted.

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