Comorbidity and medication in REM sleep behavior disorder: a multicenter case-control study
Language English Country United States Media print-electronic
Document type Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't
Grant support
CIHR - Canada
UL1 RR024992
NCRR NIH HHS - United States
UL1 TR000448
NCATS NIH HHS - United States
KL2 RR024994
NCRR NIH HHS - United States
KL2 TR000450
NCATS NIH HHS - United States
PubMed
24553425
PubMed Central
PMC3962997
DOI
10.1212/wnl.0000000000000247
PII: WNL.0000000000000247
Knihovny.cz E-resources
- MeSH
- Administration, Inhalation MeSH
- Depression drug therapy epidemiology MeSH
- Glucocorticoids therapeutic use MeSH
- Myocardial Ischemia epidemiology MeSH
- Cohort Studies MeSH
- Comorbidity MeSH
- Smoking epidemiology MeSH
- Middle Aged MeSH
- Humans MeSH
- REM Sleep Behavior Disorder drug therapy epidemiology MeSH
- Surveys and Questionnaires MeSH
- Risk Factors MeSH
- Selective Serotonin Reuptake Inhibitors therapeutic use MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Glucocorticoids MeSH
- Serotonin Uptake Inhibitors MeSH
OBJECTIVE: This controlled study investigated associations between comorbidity and medication in patients with polysomnographically confirmed idiopathic REM sleep behavior disorder (iRBD), using a large multicenter clinic-based cohort. METHODS: Data of a self-administered questionnaire on comorbidity and medication use of 318 patients with iRBD and 318 matched controls were analyzed. Comparisons between cases and controls were made using logistic regression analysis. RESULTS: Patients with iRBD were more likely to report depression (odds ratio [OR] 2.0, 95% confidence interval [CI] 1.3-2.9) and concomitant antidepressant use (OR 2.2, 95% CI 1.4-3.6). Subanalysis of antidepressant agents revealed that the increased use of antidepressants in iRBD was due to selective serotoninergic reuptake inhibitors (OR 3.6, 95% CI 1.8-7.0) and not due to other antidepressant classes. Patients with iRBD reported more lifetime antidepressant use than comorbid depression (antidepressant use: OR 1.9, 95% CI 1.1-3.3; depression: OR 1.6, 95% CI 1.0-2.5). Patients with iRBD reported more ischemic heart disease (OR 1.9, 95% CI 1.1-3.1). This association did not change substantially when adjusting for cardiovascular risk factors (OR 2.3, 95% CI 1.3-3.9). The use of inhaled glucocorticoids was higher in patients with iRBD compared to controls (OR 5.3, 95% CI 1.8-15.8), likely reflecting the higher smoking rate in iRBD (smoking: OR 15.3, 95% CI 2.0-118.8; nonsmoking: OR 2.4, 95% CI 0.4-13.2) and consequent pulmonary disease. CONCLUSIONS: This large study confirms the association between comorbid depression and antidepressant use in iRBD. In addition, there was an unexpected association of iRBD with ischemic heart disease that was not explained by cardiovascular risk factors.
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