系统性红斑狼疮患者睡眠呼吸障碍与中度至重度抑郁之间的关系:TRUMP2-SLE 研究

Yuichi Ishikawa, Nao Oguro, Takanori Ichikawa, Dai Kishida, Natsuki Sakurai, Chiharu Hidekawa, Kenta Shidahara, Keigo Hayashi, Yoshia Miyawaki, Yasuhiro Shimojima, Ryusuke Yoshimi, Ken-ei Sada, Nobuyuki Yajima, Noriaki Kurita
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摘要

目的:抑郁症是系统性红斑狼疮(SLE)患者最常见的情绪障碍,会影响患者的生活质量和服药依从性。虽然睡眠呼吸障碍(SDB)是导致普通人群抑郁的一个因素,但其在系统性红斑狼疮患者中的发病率及其对抑郁的影响尚不清楚。我们采用临床流行病学的方法,对系统性红斑狼疮患者的多中心队列进行了研究:这是一项横断面研究,对象是在五所大学医院就诊的 414 名日本成人系统性红斑狼疮患者。主要暴露因素是高危 SDB,通过柏林问卷进行评估。主要结果是中度至重度抑郁,使用患者健康问卷-9进行评估。采用稳健误差方差拟合泊松回归模型,以估算调整后患病率(aPRs):平均年龄为 47.5 岁,平均体重指数(BMI)为 22.1 kg/m2。高危 SDB 患病率为 15.2%(95% 置信区间 [95% CI] 11.9%-19.0%)。中度或重度抑郁症患病率为 19.1%(95% 置信区间为 15.4%-23.2%)。高风险 SDB 与中度至重度抑郁的可能性增加有关(aPR 2.62,95% CI 1.62-4.24)。所有 1、2 和 3 阳性 SDB 风险类别均与中度至重度抑郁相关,且呈剂量依赖性。结论在系统性红斑狼疮患者中,SDB很常见,高危SDB与中度至重度抑郁密切相关。出现 SDB 的体征和症状时,应同时评估是否伴有抑郁症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between sleep-disordered breathing and moderate to severe depression in systemic lupus erythematosus: the TRUMP2-SLE study
Objective: Depression is the most frequent mood disorder that impairs quality of life and medication adherence in patients with systemic lupus erythematosus (SLE). Although sleep-disordered breathing (SDB) is a contributor to depression in the general population, its prevalence in SLE patients and its impact on depression are not clear. We employed a clinical epidemiologic approach to examine them in a multicenter cohort of SLE patients. Methods: This was a cross-sectional study of 414 Japanese adults with SLE at five university hospitals. The main exposure was high-risk SDB, assessed with the Berlin Questionnaire. The main outcome was moderate to severe depression assessed using the Patient Health Questionnaire-9. Poisson regression models were fitted with a robust error variance to estimate adjusted prevalence ratios (aPRs). Results: The mean age was 47.5 years and the mean body mass index (BMI) was 22.1 kg/m2. The prevalence of high-risk SDB was 15.2% (95% confidence interval [95% CI] 11.9%-19.0%). The prevalence of moderate or severe depression was 19.1% (95% CI 15.4%-23.2%). High-risk SDB was associated with a greater likelihood of moderate to severe depression (aPR 2.62, 95% CI 1.62-4.24). All the 1-, 2-, and 3-positive risk categories for SDB were associated with moderate to severe depression, in a dose-dependent manner. Conclusion: Among patients with SLE, SDB is common, and high-risk SDB is strongly associated with moderate to severe depression. The signs and symptoms of SDB should prompt a simultaneous evaluation for concomitant depression.
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