Key result
A doubling of serum-free kynurenine levels was associated with an 18% increased hazard of cardiovascular events (HR 1.18; 95% CI 1.02-1.33) in patients with chronic kidney disease.
Why the study?
Kynurenine is increased in CKD and has deleterious cardiovascular effects in experimental studies, but its association with cardiovascular events and mortality in CKD patients was unclear.
Are higher serum kynurenine levels associated with increased cardiovascular events and mortality in patients with chronic kidney disease?
Cohort
Are higher serum kynurenine levels associated with increased cardiovascular events and mortality in patients with chronic kidney disease?
Higher serum-free kynurenine levels are independently associated with an increased risk of fatal and nonfatal cardiovascular events, particularly non-atheromatous events, in patients with chronic kidney disease.
Background: Kynurenine is a protein-bound uremic toxin. Its circulating levels are increased in chronic kidney disease (CKD). Experimental studies showed that it exerted deleterious cardiovascular effects. We sought to evaluate an association between serum kynurenine levels and adverse fatal or nonfatal cardiovascular events and all-cause mortality in CKD patients. Methods: The CKD-REIN study is a prospective cohort of people with CKD having an estimated glomerular filtration rate (eGFR) <60 ml/min/1.73 m². Baseline frozen samples of total and free fractions of kynurenine and tryptophan were measured using a validated liquid chromatography tandem mass spectrometry technique. Cause-specific Cox models were used to estimate hazard ratios (HRs) for each outcome. Results: ), 52% had a history of cardiovascular disease. A doubling of serum-free kynurenine levels was associated with an 18% increased hazard of cardiovascular events [466 events, HR (95%CI):1.18(1.02,1.33)], independently of eGFR, serum-free tryptophan level or other uremic toxins, cardioprotective drugs, and traditional cardiovascular risk factors. Serum-free kynurenine was significantly associated with non-atheromatous cardiovascular events [HR(95%CI):1.26(1.03,1.50)], but not with atheromatous cardiovascular events [HR(95%CI):1.15(0.89,1.50)]. The association of serum-free kynurenine with cardiovascular mortality was also independently significant [87 events; adjusted HR(95%CI):1.64(1.10,2.40)]. However, the association of serum-free kynurenine with all-cause mortality was no more significant after adjustment on serum-free tryptophan [311 events, HR(95%CI):1.12(0.90, 1.40)]. Conclusions: Our findings imply that serum-free kynurenine, independently of other cardiovascular risk factors (including eGFR), is associated with fatal or nonfatal cardiovascular outcomes, particularly non-atheromatous cardiovascular events; in patients with CKD. Strategies to reduce serum kynurenine levels should be evaluated in further studies.
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Chamieh et al. (2023) conducted a cohort in chronic kidney disease (CKD). Serum-free kynurenine levels was evaluated on cardiovascular events (HR 1.18, 95% CI 1.02, 1.33). A doubling of serum-free kynurenine levels was associated with an 18% increased hazard of cardiovascular events (HR 1.18; 95% CI 1.02-1.33) in patients with chronic kidney disease.
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