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Published on: September 22, 2020
Associations between REM-related respiratory disturbances, metabolic biomarkers, and memory impairment in pediatric
Kai Zhang1, Dandi Ma1, Ruobing Song1
1Clinical Department of National Clinical Research Center for Respiratory Diseases, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Insights
Children with sleep-disordered breathing (SDB) experience REM sleep disruption and metabolic issues, impacting declarative memory. Early detection and metabolic interventions are crucial for preventing cognitive deficits in pediatric SDB.
Area of Science:
- Pediatric Sleep Medicine
- Neuroendocrinology
- Cognitive Neuroscience
Background:
- Sleep-disordered breathing (SDB) is increasingly linked to cognitive impairment in children, but underlying mechanisms are not fully understood.
- This study investigates the relationship between SDB severity, sleep patterns, metabolic markers, and declarative memory in children.
Purpose of the Study:
- To explore the associations among SDB severity, sleep architecture, metabolic biomarkers, and declarative memory in children.
- To elucidate the role of REM sleep disturbances and metabolic dysregulation in cognitive deficits associated with pediatric SDB.
Main Methods:
- 117 children with snoring underwent polysomnography (PSG) and a paired-associate learning test for declarative memory.
- Serum levels of leptin, adiponectin, soluble leptin receptor, leptin/adiponectin (L/A) ratio, and free leptin index (FLI) were measured.
- REM-specific respiratory disturbance indices were analyzed in relation to cognitive performance and metabolic biomarkers.
Main Results:
- REM-related respiratory disturbance indices were negatively correlated with immediate and delayed recognition accuracy.
- Higher leptin and FLI levels were associated with poorer memory performance, while adiponectin was lower in severe SDB.
- The L/A ratio and FLI correlated positively with REM disturbances and negatively with cognitive function.
Conclusions:
- Pediatric SDB is associated with REM sleep disruption and metabolic dysregulation, leading to impaired declarative memory.
- Leptin resistance, potentially mediated by hippocampal dysfunction, may underlie these cognitive deficits.
- Early detection and metabolic interventions targeting REM-specific SDB are essential for preventing cognitive impairment.
Background:
Sleep-disordered breathing (SDB) in children is increasingly associated with cognitive impairment, though the mechanisms remain unclear. This study explored associations among SDB severity, sleep architecture, metabolic biomarkers, and declarative memory.
Methods:
A total of 117 children who presented with snoring were enrolled in the study. All participants underwent overnight polysomnography. Declarative memory was assessed using a modified paired-associate learning test. Fasting venous blood samples were collected to measure serum levels of leptin, adiponectin, and soluble leptin receptor. The leptin/adiponectin (L/A) ratio and free leptin index (FLI) were also calculated.
Results:
REM-related respiratory disturbance indices (OAHIREM, AHIREM, ODIREM) were significantly negatively correlated with immediate and delayed recognition accuracy (p < 0.05). Higher levels of leptin and FLI were significantly associated with poorer memory performance (p < 0.05), whereas adiponectin levels were lower in children with severe SDB and negatively correlated with multiple respiratory parameters. The L/A ratio and FLI were positively correlated with REM-specific respiratory disturbances and negatively associated with cognitive performance.
Conclusion:
Children with SDB show REM sleep disruption and metabolic dysregulation linked to impaired declarative memory. Leptin resistance may mediate these effects via hippocampal dysfunction. Findings underscore the importance of early detection and metabolic targeting to prevent cognitive deficits in pediatric SDB.
Impact:
REM-predominant sleep-disordered breathing is associated with poorer declarative memory performance in children. Higher leptin/free leptin index (FLI) is linked to worse memory outcomes in this pediatric cohort. We highlight sleep-stage specificity by evaluating REM-related PSG indices (including REM/NREM ratios), beyond global AHI/OAHI measures. We integrate PSG phenotyping with metabolic biomarkers (leptin, FLI, adiponectin) to better characterize neurocognitive risk. Our findings support improved risk stratification and motivate longitudinal and interventional studies targeting REM-related SDB and metabolic dysfunction to protect cognition.
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