Associations between Longer Leukocyte Telomere Length and Increased Lung Cancer Risk among Never Smokers in Urban China

Author:

Wong Jason Y.Y.1ORCID,Shu Xiao-Ou2ORCID,Hu Wei3ORCID,Blechter Batel3ORCID,Shi Jianxin3ORCID,Wang Kevin3ORCID,Cawthon Richard4ORCID,Cai Qiuyin2ORCID,Yang Gong2ORCID,Rahman Mohammad L.3ORCID,Ji Bu-tian3ORCID,Gao Yutang5ORCID,Zheng Wei2ORCID,Rothman Nathaniel3ORCID,Lan Qing3ORCID

Affiliation:

1. 1Epidemiology and Community Health Branch, National Heart Lung and Blood Institute, Bethesda, Maryland.

2. 2Division of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee.

3. 3Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.

4. 4Department of Human Genetics, University of Utah, Salt Lake City, Utah.

5. 5Department of Epidemiology, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

Abstract

Abstract Background: The complex relationship between measured leukocyte telomere length (LTL), genetically predicted LTL (gTL), and carcinogenesis is exemplified by lung cancer. We previously reported associations between longer pre-diagnostic LTL, gTL, and increased lung cancer risk among European and East Asian populations. However, we had limited statistical power to examine the associations among never smokers by gender and histology. Methods: To investigate further, we conducted nested case–control analyses on an expanded sample of never smokers from the prospective Shanghai Women's Health Studies (798 cases and 792 controls) and Shanghai Men's Health Studies (161 cases and 162 controls). We broke the case–control matching and used multivariable unconditional logistic regression models to estimate the ORs and 95% confidence intervals (CI) of incident lung cancer and adenocarcinoma (LUAD), in relation to LTL measured using quantitative PCR and gTL determined using a polygenic score. In addition, we conducted Mendelian randomization (MR) using MR-PRESSO. Results: We found striking dose–response relationships between longer LTL and gTL, and increased lung cancer risk among never-smoking women (P trendLTL = 4×10−6; P trendgTL = 3×10−4). Similarly, among never-smoking men, longer measured LTL was associated with over triple the risk compared with those with the shortest (OR, 3.48; 95% CI, 1.85–6.57). The overall results were similar for LUAD among women and men. MR analyses supported causal associations with LUAD among women (OR1 SD gTL, 1.19; 95% CI, 1.03–1.37; P = 0.03). Conclusions: Longer pre-diagnostic LTL is associated with increased lung cancer risk among never smokers. Impact: Our findings firmly support the role of longer telomeres in lung carcinogenesis.

Funder

National Cancer Institute

State Key Project Specialized for Infectious Diseases, China

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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