2 型糖尿病和阻塞性睡眠呼吸暂停对心血管、肝脏、糖尿病相关和癌症结果的累积影响。

IF 5.4 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
David R Riley, Alex Henney, Matthew Anson, Gema Hernadez, Sizheng S Zhao, Uazman Alam, John P H Wilding, Sonya Craig, Daniel J Cuthbertson
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引用次数: 0

摘要

目的:阻塞性睡眠呼吸暂停(OSA)与 2 型糖尿病(T2D)之间存在双向关系。我们旨在研究同时患有阻塞性睡眠呼吸暂停(OSA)和 2 型糖尿病(T2D)对患者预后的累积影响:我们利用全球联合研究网络 TriNetX(n = 1.28 亿),采用时间到事件分析法进行了两项回顾性队列研究。分析 1 比较了 OSA 和 T2D 与单纯 OSA;分析 2 比较了 T2D 和 OSA 与单纯 T2D。使用贪婪近邻(calliper 0.1)进行倾向评分匹配,对重要的协变量对队列进行平衡(1:1)。主要结果为1-5年内的心血管、肝脏、糖尿病相关(微血管)和癌症事件:分析 1(n = 179 688):结果:分析 1(n = 179 688):T2D/OSA 协同诊断显著增加全因死亡风险(危险比 [HR] 1.52;置信区间 [CI]:1.48, 1.57)、痴呆风险(HR 1.19;CI:1.12, 1.26)、肝脏风险(HR 2.20;CI:1.77, 2.73)、胰腺癌(HR 1.62;CI:1.35,1.93)、结肠癌、肾癌和子宫内膜癌;所有与心血管、微血管和肝脏相关的结果与 OSA 诊断后 1-5 5 年间单纯 OSA 相比。分析 2(n = 240 094):与单纯的 T2D 相比,合并诊断 OSA/T2D 会显著增加外周(HR 1.39;CI:1.36, 1.43)和自主神经(HR 1.63;CI:1.51, 1.75)病变、视网膜病变(HR 1.13;CI:1.09, 1.18)、慢性肾脏病(HR 1.21;CI:1.18, 1.23)、所有心血管和肝脏疾病、全因死亡率和几种肥胖相关癌症的风险:结论:T2D 明显增加了 OSA 患者心血管、恶性肿瘤和肝脏相关疾病的风险。伴有 T2D 的 OSA 会显著增加心血管疾病、恶性肿瘤、死亡和多种微血管并发症(视网膜病变、慢性肾脏病、外周/自主神经病变)的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The cumulative impact of type 2 diabetes and obstructive sleep apnoea on cardiovascular, liver, diabetes-related and cancer outcomes.

Aim: A bidirectional relationship exists between obstructive sleep apnoea (OSA) and type 2 diabetes (T2D). We aimed to examine the cumulative impact of having both OSA and T2D on patient outcomes, relative to having either condition alone.

Materials and methods: Using TriNetX, a global federated research network (n = 128 million), we undertook two retrospective cohort studies, using time-to-event analysis. Analysis 1 compared OSA with T2D versus OSA alone; analysis 2 compared T2D with OSA versus T2D alone. Propensity score matching using greedy nearest neighbour (calliper 0.1) balanced the cohorts (1:1) for significant covariates. Primary outcomes were cardiovascular, liver, diabetes-related (microvascular) and cancer events over 1-5 years.

Results: Analysis 1 (n = 179 688): A codiagnosis of T2D/OSA significantly increased risk of all-cause mortality (hazard ratio [HR] 1.52; confidence interval [CI]: 1.48, 1.57), dementia (HR 1.19; CI: 1.12, 1.26), liver (HR 2.20; CI: 1.77, 2.73), pancreatic (HR 1.62; CI: 1.35, 1.93), colon, renal and endometrial cancers; all cardiovascular, microvascular and liver related outcomes versus OSA alone over 1-5 5 years following OSA diagnosis. Analysis 2 (n = 240 094): A codiagnosis of OSA/T2D significantly increased the risk of peripheral (HR 1.39; CI: 1.36, 1.43) and autonomic (HR 1.63; CI: 1.51, 1.75) neuropathy; retinopathy (HR 1.13; CI: 1.09, 1.18), CKD (HR 1.21; CI: 1.18, 1.23); all cardiovascular and liver outcomes; all-cause mortality and several obesity related cancers versus T2D alone.

Conclusions: T2D significantly potentiates risk of cardiovascular, malignancy and liver-related outcomes in individuals with OSA. OSA, in individuals with T2D, significantly potentiates risk of cardiovascular disease, malignancy, death and several microvascular complications (retinopathy, CKD, peripheral/autonomic neuropathy).

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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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