KMID : 1151920230050040190
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Chronobiology in Medicine 2023 Volume.5 No. 4 p.190 ~ p.193
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The Impact of Melatonin on Inflammatory Status and Quality of Life
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Chae Bo-Ram
Park Young-Min Lee So-Jin Lee Jin-Seong Kang Seung-Gul Na Kyoung-Sae Kim Eui-Joong Yoon Ho-Kyoung
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Abstract
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Objective: This study aimed to assess whether the use of melatonin as an initial insomnia treatment can enhance inflammatory status and quality of life (QoL). We also explored a potential correlation between these improvements and sleep pattern ameliorations and whether baseline status correlated to differences in sleep quality, inflammatory status, and QoL.
Methods: We enrolled 67 subjects from 6 different hospitals who met Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) insomnia criteria. The patients took 2 mg per day of prolonged-release melatonin (PRM) for 8 weeks. We administered the Pittsburgh Sleep Quality Index (PSQI) to assess sleep quality and the WHO-5 Well-Being Index to assess QoL at baseline, week 4, and week 8. We measured tumor necrosis factor-alpha (TNF-¥á) levels to determine inflammatory status at baseline and week 8.
Results: The mean global PSQI score declined significantly from 13.97 to 10.39 (p<0.001) after 8 weeks of PRM treatment. The mean WHO-5 Well-Being Index score improved significantly from 7.30 to 11.0 (p<0.001) over the study period. The mean TNF-¥á nonsignificantly declined from 0.62 to 0.60 (p=0.28). The PSQI improvement over 8 weeks was correlated to the baseline PSQI score (r=0.40, p=0.001). The decrease in TNF-¥á over 8 weeks was correlated to the baseline TNF-¥á level (r=0.43, p<0.001).
Conclusion: This study reported measurable improvement in sleep quality and QoL after 8 weeks of PRM. Although the decrease in TNF-¥á level over 8 weeks was not significant, it showed correlation to the baseline TNF-¥á level. PRM can prevent excessive inflammation and may be beneficial in chronic inflammation involving TNF-¥á.
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KEYWORD
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Melatonin, Insomnia, Inflammation, Quality of life, Tumor necrosis factor-alpha
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