@article{0434997b195e447692ad682f3ac8c3b5,
title = "Lovastatin therapy in receptor-negative homozygous familial hypercholesterolemia: Lack of effect on low-density lipoprotein concentrations or turnover",
abstract = "To determine whether at least part of the fall in low density lipoprotein (LDL) levels during lovastatin therapy might be the result of a reduced secretion of lipoproteins by the liver, three children 6 to 9 years of age with receptor-negative homozygous familial hypercholesterolemia underwent treatment with lovastatin. These patients have no capacity to synthesize LDL receptors. During lovastatin therapy, at a dose of 2 mg/kg/day, there was no decrease in LDL-cholesterol levels, nor was the turnover rate of LDL affected by the drug. The only significant change was a 74% drop in very low-density lipoprotein during treatment. We conclude that lovastatin is not effective in treatment of receptor-negative homozygous familial hypercholesterolemia. The most likely mechanism of action for this drug is to increase LDL receptor activity.",
author = "Ricardo Uauy and Vega, {Gloria L} and Grundy, {Scott M} and Bilheimer, {David M.}",
note = "Funding Information: Patients with familial hypercholesterolemia have abnormalities in the gene encoding for cell-surface receptors for low-density lipoproteins. 1 Genes inherited from each parent are physiologically active, and when one gene is abnormal, the result is heterozygous FH, with half the Usual number of LDL receptors and LDL-cholesterol concentrations approximately twice normal. About one in 500 person has heterozygous FH. Two categories of homozygous FH have been identified: receptor2defective homozygous FH, with small quantities of residual LDL-receptor activity, because one or both abnormal genes Supported by Grants GCRC M01-RR00633, R37-HL29252, and R01-HD22380 from the National Institutes of Health. Submitted for publication Jan. 20, 1988; accepted March 11, 1988. Reprint requests: Scott M. Grundy, MD, PhD, Center for Human Nutrition, Y3.206, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines B!vd., Dallas, TX 75235-9052.",
year = "1988",
month = aug,
doi = "10.1016/S0022-3476(88)80289-0",
language = "English (US)",
volume = "113",
pages = "387--392",
journal = "Journal of Pediatrics",
issn = "0022-3476",
publisher = "Mosby Inc.",
number = "2",
}