4.3 Article

Triglyceride content of lipoprotein subclasses and kidney hemodynamic function and injury in adolescents with type 1 diabetes

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Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jdiacomp.2022.108384

Keywords

Triglycerides; Lipoprotein subclasses; Intraglomerular hemodynamic function; Youth; Type 1 diabetes

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This study found that elevated triglycerides in youth with type 1 diabetes (T1D) are associated with kidney disease development and progression, and the distribution of triglycerides across lipoprotein subclasses can predict kidney dysfunction in adults. Little is known about these relationships in youth.
Aims: Elevated triglycerides (TG) are associated with development and progression of kidney disease, and TG distributions across lipoprotein subclasses predict kidney dysfunction in adults with type 1 diabetes (T1D). Little is known regarding these relationships in youth. Methods: In this single center study conducted from October 2018-2019, lipid constituents from lipoprotein subclasses were quantified by targeted nuclear magnetic resonance spectroscopy. Glomerular filtration rate (GFR), renal plasma flow (RPF), afferent arteriolar resistance (RA), efferent arteriolar resistance (RE), intra-glomerular pressure (PGLO), urine albumin-to-creatinine ratio (UACR), and chitinase-3-like protein 1 (YKL-40), a marker of kidney tubule injury, were assessed. Cross-sectional relationships were assessed by correlation and multivariable linear regression (adjusted for age, sex, HbA1c) models. Results: Fifty youth with T1D (age 16 +/- 3 years, 50 % female, HbA1c 8.7 +/- 1.3 %, T1D duration 5.7 +/- 2.6 years) were included. Very-low-density lipoprotein (VLDL)-TG concentrations correlated and associated with intra-glomerular hemodynamic function markers including GFR, PGLO, UACR, as did small low-density lipoprotein (LDL)-TG and small high-density lipoprotein (HDL)-TG. YKL-40 correlated with all lipoprotein subclasses. Conclusion: TG within lipoprotein subclasses, particularly VLDL, associated with PGLO, GFR, albuminuria, and YKL-40. Lipid perturbations may serve as novel targets to mitigate early kidney disease.

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