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内源性库欣综合征对全因和病因特异性死亡率的影响。

The Effect of Endogenous Cushing Syndrome on All-cause and Cause-specific Mortality.

机构信息

School of Medicine, University of Leeds, Leeds LS2 9NL, UK.

Division of Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hatyai, Songkhla 90110, Thailand.

出版信息

J Clin Endocrinol Metab. 2022 Jul 14;107(8):2377-2388. doi: 10.1210/clinem/dgac265.

Abstract

OBJECTIVE

We aimed to perform a systematic review and meta-analysis of all-cause and cause-specific mortality of patients with benign endogenous Cushing syndrome (CS).

METHODS

The protocol was registered in PROSPERO (CRD42017067530). PubMed, EMBASE, CINHAL, Web of Science, and Cochrane Central searches were undertaken from inception to January 2021. Outcomes were the standardized mortality ratio (SMR), proportion, and cause of deaths. The I2 test, subgroup analysis, and meta-regression were used to assess heterogeneity across studies.

RESULTS

SMR was reported in 14 articles including 3691 patients (13 Cushing disease [CD] and 7 adrenal CS [ACS] cohorts). Overall SMR was 3.0 (95% CI, 2.3-3.9; I2 = 80.5%) for all CS, 2.8 (95% CI, 2.1-3.7; I2 = 81.2%) for CD and 3.3 (95% CI, 0.5-6.6; I2 = 77.9%) for ACS. Proportion of deaths, reported in 87 articles including 19 181 CS patients (53 CD, 24 ACS, and 20 combined CS cohorts), was 0.05 (95% CI, 0.03-0.06) for all CS subtypes with meta-regression analysis revealing no differences between CS subtypes (P = .052). The proportion of deaths was 0.1 (10%) in articles published before 2000 and 0.03 (3%) in 2000 until the last search for CS (P < .001), CD (P < .001), and ACS (P = .01). The causes of death were atherosclerotic diseases and thromboembolism (43.4%), infection (12.7%), malignancy (10.6%), active disease (3.5%), adrenal insufficiency (3.0%), and suicide (2.2%). Despite improved outcomes in recent years, increased mortality from CS persists. The causes of death highlight the need to prevent and manage comorbidities in addition to treating hypercortisolism.

摘要

目的

本研究旨在对良性内源性库欣综合征(CS)患者的全因和特定病因死亡率进行系统评价和荟萃分析。

方法

本研究方案已在 PROSPERO(CRD42017067530)注册。从建库到 2021 年 1 月,对 PubMed、EMBASE、CINHAL、Web of Science 和 Cochrane Central 进行了检索。结局指标为标准化死亡率(SMR)、比例和死亡原因。采用 I2 检验、亚组分析和 meta 回归来评估研究间的异质性。

结果

14 篇文章报告了 SMR,共纳入 3691 例患者(13 例库欣病[CD]和 7 例肾上腺 CS[ACS]队列)。整体 SMR 为 3.0(95%CI,2.3-3.9;I2=80.5%),CS 为 2.8(95%CI,2.1-3.7;I2=81.2%),CD 为 2.8(95%CI,2.1-3.7;I2=81.2%),ACS 为 3.3(95%CI,0.5-6.6;I2=77.9%)。87 篇文章报告了死亡率比例,共纳入 19181 例 CS 患者(53 例 CD、24 例 ACS 和 20 例混合 CS 队列),所有 CS 亚型的死亡率比例为 0.05(95%CI,0.03-0.06),meta 回归分析显示 CS 亚型之间无差异(P=0.052)。2000 年前发表的文章中死亡率比例为 0.1(10%),2000 年至最后一次 CS 检索期间发表的文章中死亡率比例为 0.03(3%)(P<0.001),CD(P<0.001)和 ACS(P=0.01)也是如此。死亡原因是动脉粥样硬化疾病和血栓栓塞(43.4%)、感染(12.7%)、恶性肿瘤(10.6%)、疾病活动(3.5%)、肾上腺皮质功能不全(3.0%)和自杀(2.2%)。尽管近年来预后有所改善,但 CS 的死亡率仍持续升高。死亡原因强调了除治疗皮质醇增多症外,还需要预防和管理合并症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a950/9282270/631e737c7ae5/dgac265f0001.jpg

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