This article is available online at http://www.jlr.org cated at the intestinal brush border membrane. In fact, cholesterol and plant sterols are taken up by the enterocyte through the Niemann-Pick C1 Like 1 (NPC1L1) transporter ( 1 ). The ATP-binding cassette (ABC) transporters G5 and G8 actively effl ux plant sterols and, to lesser extent cholesterol, back into the intestinal lumen. In addition, ABCG5 and ABCG8 are located at the canalicular membranes of hepatocytes, where they facilitate effl ux of cholesterol and plant sterols into bile ( 2 ).The ABCG5 and ABCG8 genes are located in a headto-head confi guration on chromosome 2p21 ( 3 ). Mutations in either of these genes can cause sitosterolemia, a rare autosomal, recessively inherited disorder, characterized by xanthomas, arthralgia, anemia, and premature atherosclerosis ( 3 ). The underlying mechanism involves increased intestinal absorption of plant sterols and concomitantly decreased biliary secretion of sterols due to the absence of a functional ABCG5/G8 transporter protein ( 4 ). In addition to rare sequence changes causing sitosterolemia, several more common sequence variants in ABCG5/G8 were identifi ed in both healthy and hypercholesterolaemic individuals. These single nucleotide polymorphisms (SNP) were found to be associated with plasma cholesterol and noncholesterol sterol levels ( 5-8 ), as well as with the response to various cholesterol-lowering strategies, including diet interventions ( 7, 9 ), consumption of plant sterols or stanols ( 10, 11 ), and treatment with statins ( 12 ).Abstract Genetic variation at the ABCG5/G8 locus has been associated with markers of cholesterol homeostasis. As data originate from small-scale studies, we performed a meta-analysis to study these associations in a large dataset. We fi rst investigated associations between fi ve common ABCG5/G8 polymorphisms (p.Q604E, p.D19H, p.Y54C, p. T400K, and p.A632V) and plasma sterol levels in 245 hypercholesterolaemic individuals. No signifi cant associations were found. Subsequently, our data were pooled into a meta-analysis that comprised 3,364 subjects from 16 studies Intestinal cholesterol absorption is an active and selective process, mediated by several transporter proteins lo-