Low frequency variants associated with leukocyte telomere length in the Singapore Chinese population

Author:

Chang XulingORCID,Gurung Resham L.,Wang Ling,Jin Aizhen,Li ZhengORCID,Wang Renwei,Beckman Kenneth B.ORCID,Adams-Haduch Jennifer,Meah Wee Yang,Sim Kar SengORCID,Lim Weng KhongORCID,Davila Sonia,Tan PatrickORCID,Teo Jing Xian,Yeo Khung KeongORCID,M. Yiamunaa,Liu Sylvia,Lim Su ChiORCID,Liu JianjunORCID,van Dam Rob M.,Friedlander Yechiel,Koh Woon-Puay,Yuan Jian-MinORCID,Khor Chiea ChuenORCID,Heng Chew-KiatORCID,Dorajoo RajkumarORCID

Abstract

AbstractThe role of low frequency variants associated with telomere length homeostasis in chronic diseases and mortalities is relatively understudied in the East-Asian population. Here we evaluated low frequency variants, including 1,915,154 Asian specific variants, for leukocyte telomere length (LTL) associations among 25,533 Singapore Chinese samples. Three East Asian specific variants in/near POT1, TERF1 and STN1 genes are associated with LTL (Meta-analysis P 2.49×10−14–6.94×10−10). Rs79314063, a missense variant (p.Asp410His) at POT1, shows effect 5.3 fold higher and independent of a previous common index SNP. TERF1 (rs79617270) and STN1 (rs139620151) are linked to LTL-associated common index SNPs at these loci. Rs79617270 is associated with cancer mortality [HR95%CI = 1.544 (1.173, 2.032), PAdj = 0.018] and 4.76% of the association between the rs79617270 and colon cancer is mediated through LTL. Overall, genetically determined LTL is particularly associated with lung adenocarcinoma [HR95%CI = 1.123 (1.051, 1.201), Padj = 0.007]. Ethnicity-specific low frequency variants may affect LTL homeostasis and associate with certain cancers.

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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