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Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis




TekijätScholz Markus, Horn Katrin, Pott Janne, Gross Arnd, Kleber Marcus E., Delgado Graciela E., Mishra Pashupati Prasad, Kirsten Holger, Gieger Christian, Müller-Nurasyid Martina, Tönjes Anke, Kovacs Peter, Lehtimäki Terho, Raitakari Olli, Kähönen Mika, Gylling Helena, Baber Ronny, Isermann Berend, Stumvoll Michael, Loeffler Markus, März Winfried, Meitinger Thomas, Peters Annette, Thiery Joachim, Teupser Daniel, Ceglarek Uta

KustantajaNature Portfolio

Julkaisuvuosi2022

JournalNature Communications

Tietokannassa oleva lehden nimiNATURE COMMUNICATIONS

Lehden akronyymiNAT COMMUN

Artikkelin numero 143

Vuosikerta13

Sivujen määrä12

eISSN2041-1723

DOIhttps://doi.org/10.1038/s41467-021-27706-6

Verkko-osoitehttps://doi.org/10.1038/s41467-021-27706-6

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/176965077


Tiivistelmä
Phytosterol serum concentrations are under tight genetic control. The relationship between phytosterols and coronary artery disease (CAD) is controversially discussed. We perform a genome-wide meta-analysis of 32 phytosterol traits reflecting resorption, cholesterol synthesis and esterification in six studies with up to 9758 subjects and detect ten independent genomewide significant SNPs at seven genomic loci. We confirm previously established associations at ABCG5/8 and ABO and demonstrate an extended locus heterogeneity at ABCG5/8 with different functional mechanisms. New loci comprise HMGCR, NPC1L1, PNLIPRP2, SCARB1 and APOE. Based on these results, we perform Mendelian Randomization analyses (MR) revealing a risk-increasing causal relationship of sitosterol serum concentrations and CAD, which is partly mediated by cholesterol. Here we report that phytosterols are polygenic traits. MR add evidence of both, direct and indirect causal effects of sitosterol on CAD.

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Last updated on 2024-26-11 at 23:53