Marked high density lipoprotein deficiency due to apolipoprotein A-I Tomioka (codon 138 deletion)
2009; Elsevier BV; Volume: 207; Issue: 1 Linguagem: Inglês
10.1016/j.atherosclerosis.2009.04.018
ISSN1879-1484
AutoresMasamichi Wada, Tatsuya Iso, Bela F. Asztalos, Noriaki Takama, Tadashi Nakajima, Yukihiro Seta, Katsumi Kaneko, Yasuhiro Taniguchi, Hideo Kobayashi, Katsuyuki Nakajima, Ernst J. Schaefer, Masahiko Kurabayashi,
Tópico(s)Peroxisome Proliferator-Activated Receptors
ResumoWe report a novel apolipoprotein A-I (apoA-I) mutation identified in a 64-year-old patient with marked plasma high density lipoprotein (HDL) cholesterol (4 mg/dl) and apoA-I (5mg/dl) deficiency, prior myocardial infarction, and moderate corneal opacities. Coronary angiography revealed extensive atherosclerosis in all three major vessels. Genomic DNA sequencing of the proband revealed a homozygous novel deletion of two successive adenine residues in codon 138 in the apoA-I gene, resulting in a frameshift mutation at amino acid residues 138-178, which we have designated as apoA-I Tomioka. His elder brother was also homozygous for apoA-I Tomioka with marked HDL cholesterol and apoA-I deficiency, but had no clinical evidence of coronary heart disease. Other family members including three siblings and two sons were heterozygous for the mutation, and had approximately 50% of normal plasma HDL cholesterol, and apoA-I. Analysis of apoA-I-containing HDL particles by two-dimensional gel electrophoresis revealed undetectable apoA-I HDL particles in the homozygotes, while in heterozygotes, the mean concentrations of apoA-I in large alpha-1 and very small prebeta-1 HDL subpopulations were significantly decreased at about 35% of normal. Thus, apoA-I Tomioka, a novel deletion mutation in codon 138 of the apoA-I gene, is the causative defect in this case of HDL deficiency.
Referência(s)