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Review
. 2023 Apr 14;132(8):902-914.
doi: 10.1161/CIRCRESAHA.122.321748. Epub 2023 Apr 13.

The Cardio-Kidney Patient: Epidemiology, Clinical Characteristics and Therapy

Affiliations
Review

The Cardio-Kidney Patient: Epidemiology, Clinical Characteristics and Therapy

Katharina Schuett et al. Circ Res. .

Abstract

Patients with chronic kidney disease (CKD) are at high risk to develop cardiovascular disease with its manifestations coronary artery disease, heart failure, arrhythmias, and sudden cardiac death. In addition, the presence of CKD has a major impact on the prognosis of patients with cardiovascular disease, leading to an increased morbidity and mortality if both comorbidities are present. Therapeutic options including medical therapy and interventional treatment are often limited in patients with advanced CKD, and in most cardiovascular outcome trials, patients with advanced CKD have been excluded. Thus, in many patients, treatment strategies for cardiovascular disease need to be extrapolated from trials conducted in patients without CKD. The current article summarizes the epidemiology, clinical presentation, and treatment options for the most prevalent manifestations of cardiovascular disease in CKD and discusses the currently available treatment options to reduce morbidity and mortality in this high-risk population.

Keywords: cardiovascular diseases; coronary artery disease; heart failure; prognosis; renal insufficiency, chronic.

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Conflict of interest statement

K. Schuett has received personal fees from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Lilly, Merck Sharp and Dohme, Novo Nordisk, Novartis, and OmniaMed and served as a consultant for Amgen, AstraZeneca, Bayer, and Boehringer Ingelheim. N. Marx has received support for clinical trial leadership from Boehringer Ingelheim and Novo Nordisk; served as a consultant to Boehringer Ingelheim, Merck, Novo Nordisk, AstraZeneca, and Bristol Myers Squibb; received grant support from Boehringer Ingelheim, Merck, and Novo Nordisk; and served as a speaker for Boehringer Ingelheim, Merck, Novo Nordisk, Lilly, BMS, and AstraZeneca. M. Lehrke received grants and personal fees from Boehringer Ingelheim, MSD, and Novo Nordisk and personal fees from Amgen, Sanofi, AstraZeneca, Bayer, Lilly, Daiichi Sankyo, Novarits, Amylin, MSD, Novo Nordisk, and Abiomed.

Figures

Figure 1.
Figure 1.
Simplified scheme depicting the interaction of cardiovascular disease and chronic kidney disease. RAAS indicates renin-angiotensin-aldosterone; and SNS, sympathetic nerve system.
Figure 2.
Figure 2.
Reduction of cardiorenal risk in patients with chronic kidney disease (CKD). ACE indicates angiotensin-converting enzyme; ARB, angiotensin-II receptor blocker; CV, cardiovascular; Hba1c, glycated hemoglobin; HHF, hospitalization for heart failure; HR, hazard ratio; LDL, low-density lipoprotein; OR, odds ratio; SGLT2, sodium-glucose cotransporter 2; and T2D, type 2 diabetes mellitus. 1Fatal or nonfatal myocardial infarction, stroke, and heart failure; cardiovascular death. 2Doubling of serum creatinine level, 50% decline in eGFR, or end-stage kidney disease (ESKD). 3All SGLT2 inhibitor CVOTs (cardiovascular outcome trials). 4Only SGLT2 inhibitor trials in patients with CKD. 5Sustained decrease in eGFR (estimated glomerular filtration rate) (≥50%) from randomization, a sustained low eGFR, end-stage kidney disease, or death from kidney failure. 6Kidney failure (ESKD or an eGFR <15 mL/min per 1.73 m2), sustained ≥57% decrease in eGFR from baseline, or renal death. 7ESKD or an eGFR <15 mL/min per 1.73 m2.

References

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