Familial lecithin:cholesterol acyltransferase (LCAT) deficiency (FLD) is an ultra-rare autosomal recessive disease characterized by very low high-density lipoprotein cholesterol (HDL-C) levels, corneal opacity, anemia, and progressive renal disease. The rate and severity of renal disease are variable across FLD patients and the biomarkers and risk factors for disease progression are poorly understood. Here we report a 30 year-long comparative analysis of the clinical and laboratory biomarkers in an FLD patient with accelerated renal decline, who underwent two kidney and one liver transplantations. Results show that elevated triglyceride and non-HDL-C levels may promote the formation of LpX and accelerate renal function decline, whereas markers of anemia may be early predictors. Conversely, corneal opacity progresses at a steady rate and does not correlate with lipid, hematologic, or renal biomarkers. Our study suggests that monitoring of markers of anemia may aid the early detection and timely management of kidney disease with conservative therapies. Furthermore, it suggests that controlling hypercholesterolemia and hypertriglyceridemia may help improve renal disease prognosis.
Keywords: Anemia; Biomarkers; Case study; Corneal opacity; Estimated glomerular filtration rate (eGFR); Familial lcat deficiency (FLD); Hemoglobin; Hypercholesterolemia; Hypertriglyceridemia; Hypoalphalipoproteinemia; Lecithin:cholesterol acyltransferase (LCAT); Lipoprotein x (LPX); Longitudinal study; Red blood cells count.
Copyright © 2024. Published by Elsevier Inc.