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The effect of a diet reduction in advanced glycation end products on metabolic markers in patients with chronic coronary artery disease and type 2 diabetes

K. L. Kuwabara, N. Faria, R. Freitas, E. A. F. S. Torres, C. Strunz, R. Maranhao, L. Cesar, A. Mansur

European Heart Journal, 2025

36 participants

Abstract

Chronic coronary artery disease (CAD) remains the leading cause of death worldwide. Its complex pathophysiology is influenced by multiple risk factors, with diabetes being one of the most significant. In recent years, advanced glycation end products (AGE) have gained attention as key markers of diabetes-related cardiovascular complications. Carboxymethyl-lysine (CML), a major product of oxidative modification of glycated proteins, is widely recognized as a biomarker of oxidative stress and long-term protein damage in aging, atherosclerosis, and diabetes. However, much contradictory information regarding the low-AGE diet and its precise clinical implications remains incompletely understood.

To evaluate the impact of a low-AGE diet on plasma CML concentration and glucose and lipid profiles in patients with chronic coronary artery disease (CAD) and type 2 diabetes.

A randomized controlled trial was conducted in patients with type 2 diabetes (glucose level ≥126 mg/dL) and chronic coronary artery disease (CAD) over 15 days. Participants were randomly assigned to either a control group following their usual diet or an intervention group adhering to a low-AGE diet. Carboxymethyl-lysine (CML), triglycerides, total cholesterol, HDL-C, LDL-C, glucose, and insulin plasma concentration were measured at baseline and after 15 days of dietary intervention.

36 participants were included, of which 17 were allocated to the low-AGE diet group. The mean age was 60±3 years. At 15 days of…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 36 participants or records.

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