Impact of Cardio-Renal-Metabolic Comorbidities on Cardiovascular Outcomes and Mortality in Type 2 Diabetes Mellitus

被引:41
作者
Cherney, David Z., I [1 ,2 ]
Repetto, Enrico [3 ]
Wheeler, David C. [4 ,9 ,10 ]
Arnold, Suzanne, V [5 ,6 ]
MacLachlan, Sharon [7 ]
Hunt, Philip R. [3 ]
Chen, Hungta [3 ]
Vora, Jiten [8 ]
Kosiborod, Mikhail [5 ,6 ,9 ,10 ]
机构
[1] Univ Toronto, Univ Hlth Network, Div Nephrol, 585 Univ Ave,8N-845, Toronto, ON M5G 2N2, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] AstraZeneca, Global Med Affairs, Cardiovasc Renal & Metab, Gaithersburg, MD USA
[4] UCL, Dept Renal Med, London, England
[5] St Lukes Mid Amer Heart Inst, Kansas City, MO USA
[6] Univ Missouri, Kansas City, MO 64110 USA
[7] Evidera, Dept Real World Evidence, London, England
[8] Univ Liverpool, Dept Diabet & Endocrinol, Liverpool, Merseyside, England
[9] George Inst Global Hlth, Sydney, NSW, Australia
[10] Univ New South Wales, Sydney, NSW, Australia
关键词
Type; 2; diabetes; Diabetic kidney disease; Cardiovascular disease; Heart failure; Cardio-renal-metabolic comorbidities; CHRONIC KIDNEY-DISEASE; GLOMERULAR-FILTRATION-RATE; ALL-CAUSE MORTALITY; RISK; DEATH; HEART;
D O I
10.1159/000504558
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: We evaluated the incremental contribution of chronic kidney disease (CKD) to the risk of major adverse cardiovascular (CV) events (MACE), heart failure (HF), and all-cause mortality (ACM) in type 2 diabetes mellitus (T2DM) patients and its importance relative to the presence of other cardio-renal-metabolic (CaReMe) comorbidities. Methods: Patients (>= 40 years) were identified at the time of T2DM diagnosis from US (Humedica/Optum) and UK (Clinical Practice Research Datalink) databases. Patients were monitored post-diagnosis for modified MACE (myocardial infarction, stroke, ACM), HF, and ACM. Adjusted hazard ratios were obtained using Cox proportional-hazards regression to evaluate the relative risk of modified MACE, HF, and ACM due to CKD. Patients were stratified by the presence or absence of atherosclerotic CV disease (ASCVD) and age. Results: Between 2011 and 2015, of 227,224 patients identified with incident T2DM, 40,063 (17.64%) had CKD. Regardless of prior ASCVD, CKD was associated with higher risk of modified MACE, HF, and ACM; this excess hazard was more pronounced in older patients with prior ASCVD. In time-to-event analyses in the overall cohort, patients with T2DM + CKD or T2DM + CKD + hypertension + hyperlipidemia had increased risks for modified MACE, HF, and ACM versus patients with T2DM and no CaReMe comorbidities. Patients with CKD had higher risks for and shorter times to modified MACE, HF, and ACM than those without CKD. Conclusion: In T2DM patients, CKD presence was associated with higher risk of modified MACE, HF, and ACM. This may have risk-stratification implications for T2DM patients based on background CKD and highlights the potential importance of novel renoprotective strategies.
引用
收藏
页码:74 / 82
页数:9
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