PMID: 24385509

Westerterp M, Bochem AE, Yvan-Charvet L, Murphy AJ, Wang N, Tall AR
ATP-binding cassette transporters, atherosclerosis, and inflammation.
Circ Res. 2014 Jan 3;114(1):157-70. doi: 10.1161/CIRCRESAHA.114.300738., [PubMed]
Sentences
No. Mutations Sentence Comment
59 ABCA1 p.Ile883Met
X
ABCA1 p.Ile883Met 24385509:59:282
status: NEW
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ABCA1 p.Asn1800His
X
ABCA1 p.Asn1800His 24385509:59:511
status: NEW
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ABCA1 p.Asn1800His
X
ABCA1 p.Asn1800His 24385509:59:930
status: NEW
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ABCA1 p.Lys776Asn
X
ABCA1 p.Lys776Asn 24385509:59:136
status: NEW
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ABCA1 p.Val825Ile
X
ABCA1 p.Val825Ile 24385509:59:275
status: NEW
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ABCA1 p.Val771Met
X
ABCA1 p.Val771Met 24385509:59:269
status: NEW
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ABCA1 p.Glu1172Asp
X
ABCA1 p.Glu1172Asp 24385509:59:289
status: NEW
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ABCA1 p.Gly1216Val
X
ABCA1 p.Gly1216Val 24385509:59:503
status: NEW
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ABCA1 p.Gly1216Val
X
ABCA1 p.Gly1216Val 24385509:59:907
status: NEW
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ABCA1 p.Arg2144*
X
ABCA1 p.Arg2144* 24385509:59:519
status: NEW
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ABCA1 p.Arg2144*
X
ABCA1 p.Arg2144* 24385509:59:941
status: NEW
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ABCA1 p.Pro1065Ser
X
ABCA1 p.Pro1065Ser 24385509:59:495
status: NEW
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ABCA1 p.Pro1065Ser
X
ABCA1 p.Pro1065Ser 24385509:59:896
status: NEW
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In a Mendelian randomization approach in a prospective cohort comprising ࣈ9000 individuals, heterozygosity for the ABCA1 mutation K776N led to a 2-to-3 times higher risk of ischemic heart disease.105 Furthermore, 5 single-nucleotide polymorphisms (SNPs) inABCA1 (V771M,V825I, I883M, E1172D, R1587K) were shown to predict risk of ischemic heart disease in a cohort of 9259 individuals.106 However, the same group reported more recently that heterozygosity for 4 loss-of-function mutations (P1065S, G1216V, N1800H, R2144X) was not associated with a higher risk of ischemic heart disease in 3 prospective cohorts comprising 56ߙ886 individuals.107 It must be noted, however, that only small decreases in HDL, of ࣈ28% as opposed to ࣈ50% in previously reported ABCA1 heterozygotes, were observed.94,101-103,107 Also, the residual cholesterol efflux was substantial (74%-79% for P1065S and G1216V and 48%-49% for N1800H and R2144X for homozygous mutations compared with controls),107 whereas in patients with TD there was only 20% to 30% residual cholesterol efflux.108 In addition, LDL levels were reduced by ࣈ25%, probably offsetting the effects of reduced HDL on CVD.107 Thus, the conflicting results in these studies could be related to inclusion of relatively mild ABCA1 mutations as well as offsetting effects of reduced LDL cholesterol levels.109 In a meta-analysis of genome-wide association studies, SNPs near the ABCA1 gene have been associated with HDL and total cholesterol levels,110,111 but not with cardiovascular risk.112 Although these studies have the benefit of huge statistical power, some caution is merited in the interpretation of findings. Login to comment