Jing Li, Pei-Pei Liu, Yan Wang, Chong-Yang Ren, Mei Zhang
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Logistic regression modeling was used to analyze the correlation between different insomnia subtypes, YKL-40 level, and telomere length.</p><p><strong>Results: </strong>People with telomere lengths in the lowest tertile were more likely to have trouble falling asleep (odds ratio (OR) 2.13, 95% confidence interval (CI) 1.22-3.63; <i>p</i> = 0.03) and had a higher frequency of mixed symptoms (OR 1.49, 95% CI 1.30-2.81; <i>p</i> = 0.04). People in the highest tertile of YKL-40 level had an increased chance of waking up early (OR 2.98, 95% CI 1.54-5.33; <i>p</i> = 0.01) and more mixed symptoms (OR 1.47, 95% CI 1.22-2.79; <i>p</i> = 0.02). Furthermore, using receiver operating characteristic curve analysis, the area under the curve of YKL-40 level and telomere length was 0.806 and 0.746, respectively.</p><p><strong>Conclusions: </strong>Telomere length in patients with difficulty initiating sleep and mixed symptoms was significantly shortened and the level of YKL-40 in people who have early morning awakening and mixed symptoms was significantly increased. Our findings provide the first evidence that leukocyte telomere length and YKL-40 level are individually linked to mixed symptoms.</p>","PeriodicalId":16160,"journal":{"name":"Journal of integrative neuroscience","volume":"23 9","pages":"180"},"PeriodicalIF":2.5000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lectin YKL-40 Level and Telomere Length are Indicators of Insomnia Disorder.\",\"authors\":\"Jing Li, Pei-Pei Liu, Yan Wang, Chong-Yang Ren, Mei Zhang\",\"doi\":\"10.31083/j.jin2309180\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To explore the relationship between YKL-40 level, telomere length, and different subtypes of insomnia disorder.</p><p><strong>Methods: </strong>A total of 145 individuals suffering from insomnia were enrolled and divided into four groups according to the insomniac subtypes: difficulty initiating sleep, early morning awakening, difficulty maintaining sleep, and mixed symptoms. Eighty healthy controls were also collected at the same time. Peripheral leukocyte genomic DNA was extracted, relative telomere lengths were measured using the real-time quantitative polymerase chain reaction method, and YKL-40 levels were determined using enzyme-linked immunoassay. Logistic regression modeling was used to analyze the correlation between different insomnia subtypes, YKL-40 level, and telomere length.</p><p><strong>Results: </strong>People with telomere lengths in the lowest tertile were more likely to have trouble falling asleep (odds ratio (OR) 2.13, 95% confidence interval (CI) 1.22-3.63; <i>p</i> = 0.03) and had a higher frequency of mixed symptoms (OR 1.49, 95% CI 1.30-2.81; <i>p</i> = 0.04). People in the highest tertile of YKL-40 level had an increased chance of waking up early (OR 2.98, 95% CI 1.54-5.33; <i>p</i> = 0.01) and more mixed symptoms (OR 1.47, 95% CI 1.22-2.79; <i>p</i> = 0.02). 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引用次数: 0
摘要
目的:探讨YKL-40水平、端粒长度与不同亚型失眠症之间的关系:探讨YKL-40水平、端粒长度与失眠症不同亚型之间的关系:方法:共收集了145名失眠症患者,并根据失眠症亚型分为四组:入睡困难、早醒、维持睡眠困难和混合症状。同时还收集了 80 名健康对照者。研究人员提取了外周白细胞基因组 DNA,使用实时定量聚合酶链式反应法测定了端粒的相对长度,并使用酶联免疫测定法测定了 YKL-40 的水平。采用逻辑回归模型分析了不同失眠亚型、YKL-40水平和端粒长度之间的相关性:结果:端粒长度处于最低三分位数的人更容易出现入睡困难(几率比(OR)2.13,95% 置信区间(CI)1.22-3.63;P = 0.03),而且出现混合症状的频率更高(OR 1.49,95% CI 1.30-2.81;P = 0.04)。YKL-40水平最高三分位数的人早醒的几率更高(OR 2.98,95% CI 1.54-5.33;p = 0.01),混合症状更多(OR 1.47,95% CI 1.22-2.79;p = 0.02)。此外,通过接收器操作特征曲线分析,YKL-40水平和端粒长度的曲线下面积分别为0.806和0.746:结论:入睡困难和混合症状患者的端粒长度明显缩短,而早醒和混合症状患者的YKL-40水平明显升高。我们的研究结果首次证明了白细胞端粒长度和YKL-40水平与混合症状有个别联系。
Lectin YKL-40 Level and Telomere Length are Indicators of Insomnia Disorder.
Objective: To explore the relationship between YKL-40 level, telomere length, and different subtypes of insomnia disorder.
Methods: A total of 145 individuals suffering from insomnia were enrolled and divided into four groups according to the insomniac subtypes: difficulty initiating sleep, early morning awakening, difficulty maintaining sleep, and mixed symptoms. Eighty healthy controls were also collected at the same time. Peripheral leukocyte genomic DNA was extracted, relative telomere lengths were measured using the real-time quantitative polymerase chain reaction method, and YKL-40 levels were determined using enzyme-linked immunoassay. Logistic regression modeling was used to analyze the correlation between different insomnia subtypes, YKL-40 level, and telomere length.
Results: People with telomere lengths in the lowest tertile were more likely to have trouble falling asleep (odds ratio (OR) 2.13, 95% confidence interval (CI) 1.22-3.63; p = 0.03) and had a higher frequency of mixed symptoms (OR 1.49, 95% CI 1.30-2.81; p = 0.04). People in the highest tertile of YKL-40 level had an increased chance of waking up early (OR 2.98, 95% CI 1.54-5.33; p = 0.01) and more mixed symptoms (OR 1.47, 95% CI 1.22-2.79; p = 0.02). Furthermore, using receiver operating characteristic curve analysis, the area under the curve of YKL-40 level and telomere length was 0.806 and 0.746, respectively.
Conclusions: Telomere length in patients with difficulty initiating sleep and mixed symptoms was significantly shortened and the level of YKL-40 in people who have early morning awakening and mixed symptoms was significantly increased. Our findings provide the first evidence that leukocyte telomere length and YKL-40 level are individually linked to mixed symptoms.
期刊介绍:
JIN is an international peer-reviewed, open access journal. JIN publishes leading-edge research at the interface of theoretical and experimental neuroscience, focusing across hierarchical levels of brain organization to better understand how diverse functions are integrated. We encourage submissions from scientists of all specialties that relate to brain functioning.