Adolescent sleep patterns, genetic predisposition, and risk of multiple sclerosis

被引:1
|
作者
Johansson, Eva [1 ]
Olsson, Tomas [1 ,2 ]
Strid, Pernilla [1 ]
Kockum, Ingrid [1 ]
Alfredsson, Lars [1 ,3 ,4 ]
Hedstrom, Anna Karin [1 ,2 ]
机构
[1] Karolinska Inst, Dept Clin Neurosci, Visionsgatan 18 L8, S-17176 Stockholm, Sweden
[2] Karolinska Univ Hosp, Dept Neurol, Stockholm, Sweden
[3] Inst Environm Med, Karolinska Inst, Stockholm, Sweden
[4] Ctr Occupat & Environm Med, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
multiple sclerosis; sleep duration; sleep quality; human leukocyte antigen; SOCIAL MEDIA USE; SHIFT WORK; QUALITY;
D O I
10.1093/sleep/zsae156
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives Shift work, insufficient sleep, and poor sleep quality at young age have been associated with increased risk of multiple sclerosis (MS). This study aimed to investigate the potential interaction between aspects of inadequate sleep (short sleep, phase shift, and poor sleep quality) during adolescence and HLA-DRB1*15:01 in relation to MS risk. Methods We used a Swedish population-based case-control study (1253 cases and 1766 controls). Participants with different sleep patterns during adolescence and HLA-DRB1*15:01 status were compared regarding MS risk by calculating odds ratios with 95% confidence intervals (CI) using logistic regression models. Additive interaction between aspects of inadequate sleep and HLA-DRB1*15:01 status was assessed by calculating the attributable proportion due to interaction (AP) with 95% CI. Results Short sleep duration (<7 hours/night) during adolescence acted synergistically with HLA-DRB1*15:01, increasing the risk of MS (AP 0.38, 95% CI: 0.01 to 0.75, p = .04). Similarly, subjective low sleep quality during adolescence interacted with HLA-DRB1*15:01 regarding risk of MS (AP 0.30, 95% CI: 0.06 to 0.56, p = .03), whereas phase shift did not significantly influence the risk of the disease, irrespective of HLA-DRB1*15:01 status. Conclusions Our findings underscore the importance of addressing inadequate sleep during adolescence, particularly in the context of the HLA-DRB1*15:01 allele, as it appears to amplify the risk of subsequently developing MS.
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页数:6
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