Chronicity and comorbidities: Is estimated longer duration of obstructive sleep apnoea linked to higher cardiometabolic risk?

IF 1.5 Q4 RESPIRATORY SYSTEM
Lung India Pub Date : 2026-07-01 Epub Date: 2026-06-24 DOI:10.4103/lungindia.lungindia_888_25
Krishnapriya S Kumar, Kritarth Rawat, Lokesh Kumar Saini, Barun Kumar, Kalyani Sridharan, Ravi Gupta, Saikat Banerjee, Mayank Mishra, Ruchi Dua, Prakhar Sharma, Girish Sindhwani
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Abstract

Background and objectives: Obstructive sleep apnea (OSA) is associated with an increased risk of cardiometabolic disorders. Still, the role of OSA duration in the development and severity of these conditions remains unclear. This study aimed to evaluate the association between estimated OSA duration and cardio-metabolic comorbidities.

Materials and methods: In this cross-sectional study, 279 adults (≥35 years; body mass index ≥20 kg/m 2 ) with moderate-severe OSA diagnosed by level-1 polysomnography were included. Diagnosis of cardiometabolic disorders was based on examination, medical records, and laboratory investigations. Duration of OSA was estimated using the OSA-Onset algorithm, and comorbidity prevalence was compared across tertiles of estimated duration.

Results: In this cross-sectional exploratory analysis, the median estimated OSA duration was 18.7 years, and the median estimated age of onset was 32.3 years. Systemic hypertension was the most prevalent comorbidity (79.6%) and showed a higher prevalence across tertiles of estimated OSA duration (68.8%, 83.9%, and 86%, respectively; P = 0.007). In multivariable models, estimated OSA duration was statistically associated with hypertension (odds ratio [OR] 1.039, 95% confidence interval [CI] 1.012-1.068; P = 0.005). Sensitivity analysis excluding participants with implausible negative onset estimates yielded similar results (OR 1.036, 95% CI 1.006-1.066; P = 0.017). No statistically significant associations were observed for other cardiometabolic conditions. Given multiple comparisons and correlated outcomes, findings should be interpreted as exploratory.

Conclusion: In this cross-sectional exploratory study, longer algorithm-estimated OSA duration was statistically associated with hypertension but not with other cardiometabolic comorbidities. These findings are hypothesis-generating and require confirmation in longitudinal studies.

慢性和合并症:阻塞性睡眠呼吸暂停持续时间较长是否与较高的心脏代谢风险相关?
背景和目的:阻塞性睡眠呼吸暂停(OSA)与心脏代谢障碍的风险增加有关。然而,阻塞性睡眠呼吸暂停持续时间在这些疾病的发展和严重程度中的作用仍不清楚。本研究旨在评估估计的OSA持续时间与心脏代谢合并症之间的关系。材料和方法:本横断面研究纳入279例经1级多导睡眠图诊断为中重度OSA的成人(≥35岁,体重指数≥20 kg/ m2)。心脏代谢紊乱的诊断是基于检查、医疗记录和实验室调查。使用OSA发病算法估计OSA的持续时间,并比较估计持续时间内各分位数的合并症患病率。结果:在横断面探索性分析中,估计OSA病程中位数为18.7年,估计发病年龄中位数为32.3岁。全身性高血压是最常见的合并症(79.6%),并且在估计的OSA持续时间中显示更高的患病率(分别为68.8%,83.9%和86%;P = 0.007)。在多变量模型中,估计的OSA持续时间与高血压有统计学相关性(优势比[OR] 1.039, 95%可信区间[CI] 1.012-1.068; P = 0.005)。敏感度分析排除了难以置信的阴性发病估计的参与者,得到了类似的结果(OR 1.036, 95% CI 1.006-1.066; P = 0.017)。其他心脏代谢疾病未观察到统计学上显著的关联。鉴于多重比较和相关结果,研究结果应被解释为探索性的。结论:在这项横断面探索性研究中,较长的算法估计的OSA持续时间与高血压相关,但与其他心脏代谢合并症无关。这些发现是假设产生的,需要在纵向研究中证实。
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来源期刊
Lung India
Lung India RESPIRATORY SYSTEM-
CiteScore
2.30
自引率
12.50%
发文量
114
审稿时长
37 weeks
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