Journal
TRANSLATIONAL RESEARCH
Volume 149, Issue 4, Pages 205-210Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.trsl.2006.11.007
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- NHLBI NIH HHS [HL-61369] Funding Source: Medline
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The ATP-binding cassette transporter-1 (ABCA1) mediates cholesterol efflux and genotypic variation in ABCA1 and may impact reverse cholesterol transport and influence cardiovascular disease (CVD) risk. However, although mutations in ABCA1 have generally been identified with low HDL-C, few have undertaken a comparative evaluation between high and low high-density lipoprotein-cholesterol (HDL-C). Therefore, to evaluate for potential gain-of-function polymorphisms/mutations in ABCA1, 56 consecutive subjects were screened presenting with high (60 -99 mg/dL (1.6-2.6 mmol/L)) or very high HDL-C (> 100 mg/dL (2.6 mmol/L)) and were compared with subjects with average or low HDL-C (n = 68). Carrier frequencies of common ABCA I polymorphisms, R219K, V771M, V8251,1883M, E1172D, and R1587K were also assessed. All 50 exons and exon-intron boundaries of ABCA1 were screened using single-stranded conformation polymorphism (SSCP). DNA samples with SSCP-shifts or differing band patterns were sequenced. For the 6 common polymorphisms, genotyping was determined by polymerase chain reaction (PCR)-restriction fragment length polymorphism. Overall, 5 novel nonsynonymous mutations were identified, all of which were associated with low HDL-C. Of the 6 common ABCA I polymorphisms, very high HDL-C was associated with a higher genotype frequency for R219K (P-trend = 0.04) and higher genotype and allelic frequency for El 172D (P-trend = 0.0004, P-trend = 0.0002, respectively) compared with lower HDL-C. These data reaffirm that rare mutations in ABCA I are associated with low HDL-C. However, at least I ABCA I polymorphism (eg, E I 172D) may contribute to the high HDL-C phenotype.
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