A Risk Correlative Model for Sleep Disorders in Chinese Older Adults Based on Blood Micronutrient Levels: A Matched Case-Control Study
The physical abilities of older adults decline with age, making them more susceptible to micronutrient deficiency, which may affect their sleep quality. This study aimed to construct a risk correlative model for sleep disorders in Chinese older adults based on blood micronutrient levels. In this mat...
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Veröffentlicht in: | Nutrients 2024-09, Vol.16 (19), p.3306 |
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Zusammenfassung: | The physical abilities of older adults decline with age, making them more susceptible to micronutrient deficiency, which may affect their sleep quality.
This study aimed to construct a risk correlative model for sleep disorders in Chinese older adults based on blood micronutrient levels.
In this matched case-control study, we recruited 124 participants with sleep disorders and 124 matched controls from the Tianjin Elderly Nutrition and Cognition cohort in China. Micronutrient levels in whole blood were measured using the dried blood spot technique. We compared the differences in micronutrient levels between the two groups and also constructed a receiver operating characteristic (ROC) model and nomogram for sleep disorders.
In comparison to the control group, the sleep disorders group showed lower levels of blood vitamin A, vitamin E (VE), folate, magnesium, copper, iron, and selenium (Se) in the univariate analysis (
< 0.05). The ROC curve analysis indicated that the combination of VE + folate + Se may have an excellent diagnostic effect on sleep disorders, with an area under the curve of 0.964. This VE + folate + Se was integrated into a nomogram model to demonstrate their relationship with sleep disorders. The consistency index of the model was 0.88, suggesting that the model assessed sleep disorders well.
The sleep disorders risk correlative model constructed by the levels of VE, folate, and Se in whole blood might show good performance in assessing the risk of sleep disorders in older adults. |
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ISSN: | 2072-6643 2072-6643 |
DOI: | 10.3390/nu16193306 |