Modeling of Disease Progression of Type 2 Diabetes Using Real-World Data: Quantifying Competing Risks of Morbidity and Mortality.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Hanna Kunina, Stefan Franzén, Maria C Kjellsson
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Abstract

Type 2 diabetes (T2D) is a progressive metabolic disorder that could be an underlying cause of long-term complications that increase mortality. The assessment of the probability of such events could be essential for mortality risk management. This work aimed to establish a framework for risk predictions of macrovascular complications (MVC) and diabetic kidney disease (DKD) in patients with T2D, using real-world data from the Swedish National Diabetes Registry (NDR), in the presence of mortality as a competing risk. The study consisted of 41,517 patients with T2D registered in NDR between 2005 and 2013. At inclusion, patients were newly diagnosed (T2D < 1 year) and had no prior evidence of DKD or MVC. Using three-quarters of the data, a five-state multistate model was established to describe competing events of MVC, DKD, a combination thereof, and the terminal state, death. Two hypotheses were investigated: (1) the risk of MVC and DKD are mutually independent, and (2) mortality is independent of morbidities. At the end of the study, the majority of individuals remained in uncomplicated T2D; however, the probability of transition to complications and death increased over time. The mortality hazard depended on the presence of morbidities and was quantified as a life expectancy decreased by 5.0, 9.7, and 12.2 years for MVC, DKD, and the combined morbidity, respectively, compared to uncomplicated T2D. An established framework with a five-state model incorporating competing events was shown to be a useful tool for comorbidities risk assessment in newly diagnosed patients with T2D.

使用真实世界数据的2型糖尿病疾病进展建模:量化发病和死亡的竞争风险。
2型糖尿病(T2D)是一种进行性代谢紊乱,可能是增加死亡率的长期并发症的潜在原因。评估此类事件发生的概率对于死亡率风险管理至关重要。本研究旨在建立t2dm患者大血管并发症(MVC)和糖尿病肾病(DKD)的风险预测框架,使用来自瑞典国家糖尿病登记处(NDR)的真实世界数据,将死亡率作为竞争风险。该研究包括2005年至2013年间在NDR登记的41,517例T2D患者。纳入时,患者为新诊断的T2D
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来源期刊
CiteScore
5.00
自引率
11.40%
发文量
146
审稿时长
8 weeks
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