Heritable Traits and Lung Cancer Risk: A Two-Sample Mendelian Randomization Study

Author:

Pettit Rowland W.1ORCID,Byun Jinyoung12ORCID,Han Younghun12ORCID,Ostrom Quinn T.3ORCID,Coarfa Cristian4ORCID,Bondy Melissa L.5ORCID,Amos Christopher I.124ORCID

Affiliation:

1. 1Institute for Clinical and Translational Research, Baylor College of Medicine, Houston, Texas.

2. 2Section of Epidemiology and Population Sciences, Department of Medicine, Baylor College of Medicine, Houston, Texas.

3. 3Duke Cancer Institute, Duke University Medical Center, Durham, North Carolina.

4. 4Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.

5. 5Department of Epidemiology and Population Health, School of Medicine, Stanford University, Stanford, California.

Abstract

Abstract Introduction: Lung cancer is a complex polygenic disorder. Analysis with Mendelian randomization (MR) allows for genetically predicted risks to be estimated between exposures and outcomes. Methods: We analyzed 345 heritable traits from the United Kingdom Biobank and estimated their associated effects on lung cancer outcomes using two sample MR. In addition to estimating effects with overall lung cancer, adenocarcinoma, small cell lung cancer, and squamous cell lung cancers, we performed conditional effect modeling with multivariate MR (MVMR) and the traits of alcohol use, smoking initiation, average pre-tax income, and educational attainment. Results: Univariate MR provided evidence for increased age at first sexual intercourse (OR, 0.55; P = 6.15 × 10−13), educational attainment (OR, 0.24; P = 1.07 × 10−19), average household income (OR, 0.58; P = 7.85 × 10−05), and alcohol usually taken with meals (OR, 0.19; P = 1.06 × 10−06) associating with decreased odds of overall lung cancer development. In contrast, a lack of additional educational attainment (OR, 8.00; P = 3.48 × 10−12), body mass index (OR, 1.28; P = 9.00 × 10−08), pack years smoking as a proportion of life span (OR, 9.93; P = 7.96 × 10−12), and weekly beer intake (OR, 3.48; P = 4.08 × 10−07) were associated with an increased risk of overall lung cancer development. Conclusions: Many heritable traits associated with an increased or inverse risk of lung cancer development. Effects vary based on histologic subtype and conditional third trait exposures. Impact: We identified several heritable traits and presented their genetically predictable impact on lung cancer development, providing valuable insights for consideration.

Funder

National Institute of Environmental Health Sciences

Division of Cancer Epidemiology and Genetics, National Cancer Institute

Cancer Prevention Research Institute of Texas

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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