De novo major cardiovascular events in kidney transplant recipients: a comparative matched cohort study

Author:

Kim Ji Eun12,Park Jina3,Park Sehoon4,Yu Mi-yeon5,Baek Seon Ha6,Park Sang Hyun7,Han Kyungdo8,Kim Yong Chul19,Kim Dong Ki1910,Oh Kook-Hwan19,Joo Kwon Wook1910,Kim Yon Su14910,Lee Hajeong19

Affiliation:

1. Department of Internal Medicine, Seoul National University Hospital , Seoul , Republic of Korea

2. Department of Internal Medicine, Korea University Guro Hospital , Seoul , Republic of Korea

3. Biomedical Research Institute, Seoul National University Hospital , Seoul , Republic of Korea

4. Department of Biomedical Sciences, Seoul National University College of Medicine , Seoul , Republic of Korea

5. Department of Internal Medicine, Hanyang University Guri Hospital , Guri , Republic of Korea

6. Department of Internal Medicine, Hallym University Dongtan Sacred Heart Hospital , Hwaseong , Republic of Korea

7. Department of Biostatistics, College of Medicine, Catholic University of Korea , Seoul , Republic of Korea

8. Department of Statistics and Actuarial Science, Soongsil University , Seoul , Republic of Korea

9. Department of Internal Medicine, Seoul National University College of Medicine , Seoul , Republic of Korea

10. Kidney Research Institute, Seoul National University , Seoul , Republic of Korea

Abstract

ABSTRACT Background Although cardiovascular disease is known to be one of the leading causes of death after kidney transplantation (KT), evidence on the risk difference of de novo major adverse cardiovascular events (MACEs) in kidney transplant recipients (KTRs) compared with that in dialysis patients or the general population (GP) remains rare. Methods We identified KTRs using the nationwide health insurance database in South Korea and then 1:1 matched them with the dialysis and GP controls without a pre-existing MACE. The primary endpoint was defined as de novo MACEs consisting of myocardial infarction, coronary revascularization and ischemic stroke. The secondary endpoints were all-cause mortality and death-censored graft failure (DCGF) in KTRs. Results We included 4156 individuals in each of the three groups and followed them up for 4.7 years. De novo MACEs occurred in 3.7, 21.7 and 2.5 individuals per 1000 person-years in the KTRs, dialysis controls and GP controls, respectively. KTRs showed a lower MACE risk {adjusted hazard ratio (aHR) 0.16 [95% confidence interval (CI) 0.12–0.20], P < .001} than dialysis controls, whereas a similar MACE risk to GP controls [aHR 0.81 (95% CI 0.52–1.27), P = .365]. In addition, KTRs showed a similar MACE risk compared with the GP group, regardless of age, sex and the presence of comorbidities, including hypertension, diabetes and dyslipidemia. Among KTRs, de novo MACEs were associated with an increased risk of all-cause mortality, but not with DCGF. Conclusions De novo MACEs in KTRs were much lower than that in dialysis patients and had a similar risk to the GP, but once it occurred it caused elevated mortality risk in KTRs.

Funder

Ministry of Health and Welfare

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference34 articles.

1. Cardiovascular disease in the kidney transplant recipient: epidemiology, diagnosis and management strategies;Rangaswami;Nephrol Dial Transplant,2019

2. Kidney transplantation halts cardiovascular disease progression in patients with end-stage renal disease;Meier-Kriesche;Am J Transplant,2004

3. Epidemiology of cardiovascular disease in chronic renal disease;Foley;J Am Soc Nephrol,1998

4. Clinical epidemiology of cardiovascular disease in chronic renal disease;Foley;Am J Kidney Dis,1998

5. Premature cardiovascular disease in chronic renal failure;Baigent;Lancet,2000

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