Key result
Early renal dysfunction in adolescent T1D is linked to ~8% lower HDL-mediated nitric oxide bioavailability.
Why the study?
Adolescents with Type 1 diabetes often have elevated HDL, but its vasoprotective properties and relationship to endothelial function had not been assessed.
Does elevated HDL-c and systemic inflammation associate with endothelial dysfunction in adolescents with Type 1 diabetes?
Cross-Sectional (n=100)
No
Does elevated HDL-c and systemic inflammation associate with endothelial dysfunction in adolescents with Type 1 diabetes?
Elevated HDL-c in adolescents with Type 1 diabetes may be detrimental to endothelial function when accompanied by early renal dysfunction and chronic inflammation.
May signal endothelial risk despite high HDL-c in T1D adolescents with renal dysfunction; hypothesis-generating and requires prospective validation.
AIMS: High-density lipoprotein (HDL) function may be altered in patients with chronic disease, transforming the particle from a beneficial vasoprotective molecule to a noxious pro-inflammatory equivalent. Adolescents with Type 1 diabetes often have elevated HDL, but its vasoprotective properties and relationship to endothelial function have not been assessed. METHODS AND RESULTS: Seventy adolescents with Type 1 diabetes (age 10-17 years) and 30 age-matched healthy controls supplied urine samples for the measurement of early renal dysfunction (albumin:creatinine ratio; ACR), blood samples for the assessment of cardiovascular risk factors (lipid profiles, HDL functionality, glycaemic control, and inflammatory risk score), and had their conduit artery endothelial function tested using flow-mediated dilation (FMD). HDL-c levels (1.69 ± 0.41 vs. 1.44 ± 0.29mmol/L; P < 0.001), and glycated haemoglobin (HbA1c) (8.4 ± 1.2 vs. 5.4 ± 0.2%; P < 0.001) were increased in all patients compared with controls. However, increased inflammation and HDL dysfunction were evident only in patients who also had evidence of early renal dysfunction (mean ± standard deviation for high-ACR vs. low-ACR and healthy controls: inflammatory risk score 11.3 ± 2.5 vs. 9.5 ± 2.4 and 9.2 ± 2.4, P < 0.01; HDL-mediated nitric-oxide bioavailability 38.0 ± 8.9 vs. 33.3 ± 7.3 and 25.0 ± 7.7%, P < 0.001; HDL-mediated superoxide production 3.71 ± 3.57 vs. 2.11 ± 3.49 and 1.91 ± 2.47nmol O2 per 250 000 cells, P < 0.05). Endothelial function (FMD) was impaired only in those who had both a high inflammatory risk score and high levels of HDL-c (P < 0.05). CONCLUSION: Increased levels of HDL-c commonly observed in individuals with Type 1 diabetes may be detrimental to endothelial function when accompanied by renal dysfunction and chronic inflammation.
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Chiesa et al. (2019) conducted a cross-sectional in Type 1 diabetes (n=100). Early renal dysfunction (high albumin:creatinine ratio) vs. Low albumin:creatinine ratio was evaluated on HDL-mediated endothelial nitric oxide (NO) bioavailability (% change from buffer-treated cells) (MD -8, 95% CI -12 to -4, p=<0.001). Adolescents with Type 1 diabetes and early renal dysfunction had significantly reduced HDL-mediated nitric oxide bioavailability (mean difference -8%) compared to those without renal dysfunction.
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