Monogenic and Polygenic Contributions to QTc Prolongation in the Population
Valerie N. Morrill,
Seung Hoan Choi,
Amelia W. Hall,
Jennifer L. Halford,
Christopher M Haggerty,
Stephanie L Harris,
Dan E. Arking,
Emelia J Benjamin,
Brandon K Fornwalt,
Susan R. Heckbert,
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium,
Henry J Lin,
Ruth JF Loos,
Kenneth M Rice,
Thomas W Blackwell,
Braxton D Mitchell,
Bruce M Psaty,
Wendy S. Post,
Heidi L Rehm,
Elsayed Z. Soliman,
Patrick T Ellinor,
Steven A. Lubitz
Posted 21 Jun 2021
medRxiv DOI: 10.1101/2021.06.18.21258578
Posted 21 Jun 2021
Background: Rare sequence variation in genes underlying the long QT syndrome (LQTS) and common polygenic variation influence QT interval duration. It is unclear how rare and common variation contribute to QT interval duration in the general population. Objectives: Investigate monogenic and polygenic contributions to QT interval duration and the role of polygenic variation in modulating phenotypic expression of rare monogenic variation. Methods: We performed a genome wide association study (GWAS) of QTc duration in 44,979 United Kingdom Biobank (UKBB) participants and created a polygenic risk score (PRS). The PRS was validated in 39,800 independent UKBB participants. Among 26,976 participants with whole genome sequencing and ECG data in the TransOmics for Precision Medicine (TOPMed) program, we identified 160 carriers of putative pathogenic rare variants in 10 LQTS genes. We examined QTc associations with the PRS and with LQTS rare variants in TOPMed. Results: Twenty independent loci (4 novel) were identified by GWAS. The PRS comprising 565 common variants was significantly associated with QTc duration in TOPMed (p=1.1x10-64). Carriers of LQTS rare variants had longer QTc intervals than non-carriers (deltaQTc=10.9 ms [7.4-14.4] for all LQTS genes; deltaQTc=26.5 ms [20.7-32.3] for KCNQ1, KCNH2 and SCN5A). 16.7% of individuals with QTc>480 ms carried either a rare variant in a LQTS gene or had a PRS in the top decile (3.4% monogenic, 13.6% top decile of PRS). We observed a greater effect of rare variants on the QTc among individuals with a higher polygenic risk (lowest PRS tertile:deltaQTccarrier/non-carrier=4.8 ms [-1.2-10.7];highest PRS tertile:deltaQTccarrier/non-carrier=18.9 ms [12.8-25.1];p-interaction=0.001). Conclusions: QTc duration is influenced by both rare variants in established LQTS genes and polygenic risk. The phenotypic expression of monogenic variation is modulated by polygenic variation. Nevertheless, over 80% of individuals with prolonged QTc do not carry a rare monogenic variant or polygenic risk equivalent.
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