Serafin Marco, Vaninetti Martina, Mohamed Ismahan, Strambi Luigi Ferini, Caprioglio Alberto
Department of Biomedical Sciences for Health, University of Milan, Via Mangiagalli 31, Milan, 20133, Italy.
Department of Biomedical Surgical and Dental Sciences, University of Milan, Milan, Italy.
Sleep Breath. 2024 Dec 9;29(1):53. doi: 10.1007/s11325-024-03167-1.
The aim of the present systematic review was to corroborate existing evidence on how serum25(OH)D levels affect obstructive sleep apnea syndrome (OSAS) severity in the absence of comorbidities.
From inception to May 2024, PubMed, Scopus, and Embase electronic databases were systematically screened to identify randomized controlled trials (RCTs), quasi-RCTs, prospective, and retrospective studies. A strict search protocol was applied following the application of PROSPERO, under the registration number CRD42023468744. The formulated question based on PICO process was: "how do serum25(OH)D levels affect the severity of OSAS or result in enhanced sleep function?". Collected results were finally reviewed for meta-analysis and quality assessment according to the ROBINS-I tool.
Data from 24 studies were pooled and divided into 15 case-control studies and 9 cross-sectional studies. All studies involved a total of 2640 OSAS subjects and 933 healthy subjects. All studies underwent qualitative analysis whereas only 20 were collected for meta-analysis. Mild OSAS showed 25(OH)D levels non-statistically significant (P = 0.12) than the healthy patients whereas moderate OSAS (P = 0.004) and severe OSAS (P < 0.001) differed significantly from control groups. Meta-regression suggested that OSAS severity correlated inversely to the deficiency of 25(OH)D serum levels. Qualitative assessment and Egger's test revealed an elevated risk of bias but low presence of publication bias, respectively.
Serum levels of 25(OH)D were observed to be inversely proportional to OSAS severity in patients without coexisting morbidities. 25(OH)D levels in mild OSAS patients were not significantly different from non-OSAS patients, suggesting vitamin supplementation to improve potential sleep disorders.
本系统评价的目的是确证现有证据,以了解在无合并症的情况下血清25(OH)D水平如何影响阻塞性睡眠呼吸暂停综合征(OSAS)的严重程度。
从开始到2024年5月,对PubMed、Scopus和Embase电子数据库进行系统筛选,以识别随机对照试验(RCT)、半随机对照试验、前瞻性和回顾性研究。在注册号为CRD42023468744的PROSPERO应用之后,采用了严格的检索方案。基于PICO流程提出的问题是:“血清25(OH)D水平如何影响OSAS的严重程度或导致睡眠功能增强?”。最终根据ROBINS-I工具对收集到的结果进行综述,以进行荟萃分析和质量评估。
汇总了24项研究的数据,分为15项病例对照研究和9项横断面研究。所有研究共涉及2640名OSAS受试者和933名健康受试者。所有研究都进行了定性分析,而仅收集了20项进行荟萃分析。轻度OSAS患者的25(OH)D水平与健康患者相比无统计学意义(P = 0.12),而中度OSAS(P = 0.004)和重度OSAS(P < 0.001)与对照组有显著差异。荟萃回归表明,OSAS严重程度与血清25(OH)D水平缺乏呈负相关。定性评估和Egger检验分别显示偏倚风险升高但发表偏倚较低。
在无合并症的患者中,观察到血清25(OH)D水平与OSAS严重程度呈反比。轻度OSAS患者的25(OH)D水平与非OSAS患者无显著差异,提示补充维生素可能改善潜在的睡眠障碍。