Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies

被引:0
作者
Rajkumar Dorajoo
Xuling Chang
Resham Lal Gurung
Zheng Li
Ling Wang
Renwei Wang
Kenneth B. Beckman
Jennifer Adams-Haduch
Yiamunaa M
Sylvia Liu
Wee Yang Meah
Kar Seng Sim
Su Chi Lim
Yechiel Friedlander
Jianjun Liu
Rob M. van Dam
Jian-Min Yuan
Woon-Puay Koh
Chiea Chuen Khor
Chew-Kiat Heng
机构
[1] Agency for Science,Genome Institute of Singapore
[2] Technology and Research,Department of Paediatrics, Yong Loo Lin School of Medicine
[3] National University of Singapore,Khoo Teck Puat – National University Children’s Medical Institute
[4] National University Health System,Clinical Research Unit
[5] Khoo Teck Puat Hospital,Division of Cancer Control and Population Sciences, UPMC Hillman Cancer Center
[6] University of Pittsburgh,University of Minnesota Genomics Center
[7] University of Minnesota,Diabetes Centre
[8] Khoo Teck Puat Hospital,Saw Swee Hock School of Public Health
[9] National University of Singapore,School of Public Health and Community Medicine
[10] Hebrew University of Jerusalem,Department of Medicine, Yong Loo Lin School of Medicine
[11] National University of Singapore,Department of Epidemiology, Graduate School of Public Health
[12] University of Pittsburgh,Health Systems and Services Research
[13] Duke-NUS Medical School Singapore,Singapore Eye Research Institute
[14] Singapore National Eye Centre,undefined
来源
Nature Communications | / 10卷
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摘要
Genetic factors underlying leukocyte telomere length (LTL) may provide insights into telomere homeostasis, with direct links to disease susceptibility. Genetic evaluation of 23,096 Singaporean Chinese samples identifies 10 genome-wide loci (P < 5 × 10−8). Several of these contain candidate genes (TINF2, PARP1, TERF1, ATM and POT1) with potential roles in telomere biology and DNA repair mechanisms. Meta-analyses with additional 37,505 European individuals reveals six more genome-wide loci, including associations at MPHOSPH6, NKX2-3 and TYMS. We demonstrate that longer LTL associates with protection against respiratory disease mortality [HR = 0.854(0.804–0.906), P = 1.88 × 10−7] in the Singaporean Chinese samples. We further show that the LTL reducing SNP rs7253490 associates with respiratory infections (P = 7.44 × 10−4) although this effect may not be strongly mediated through LTL. Our data expands on the genetic basis of LTL and may indicate on a potential role of LTL in immune competence.
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