MRSL: a causal network pruning algorithm based on GWAS summary data

Author:

Hou Lei1,Geng Zhi2,Yuan Zhongshang3456,Shi Xu7,Wang Chuan89,Chen Feng10,Li Hongkai3456ORCID,Xue Fuzhong345689ORCID

Affiliation:

1. Beijing International Center for Mathematical Research, Peking University , Beijing , People’s Republic of China , 100871

2. School of Mathematics and Statistics, Beijing Technology and Business University , Beijing , People’s Republic of China , 100048

3. Department of Epidemiology and Health Statistics , School of Public Health, Cheeloo College of Medicine, , Jinan , People’s Republic of China , 250000

4. Shandong University , School of Public Health, Cheeloo College of Medicine, , Jinan , People’s Republic of China , 250000

5. Institute for Medical Dataology , Cheeloo College of Medicine, , Jinan , People’s Republic of China , 250000

6. Shandong University , Cheeloo College of Medicine, , Jinan , People’s Republic of China , 250000

7. Department of Biostatistics, University of Michigan , Ann Arbor , USA

8. Qilu Hospital , Cheeloo College of Medicine, , Jinan , People's Republic of China , 250000

9. Shandong University , Cheeloo College of Medicine, , Jinan , People's Republic of China , 250000

10. School of Public Health, Nanjing Medical University , Nanjing , China , 211166

Abstract

Abstract Causal discovery is a powerful tool to disclose underlying structures by analyzing purely observational data. Genetic variants can provide useful complementary information for structure learning. Recently, Mendelian randomization (MR) studies have provided abundant marginal causal relationships of traits. Here, we propose a causal network pruning algorithm MRSL (MR-based structure learning algorithm) based on these marginal causal relationships. MRSL combines the graph theory with multivariable MR to learn the conditional causal structure using only genome-wide association analyses (GWAS) summary statistics. Specifically, MRSL utilizes topological sorting to improve the precision of structure learning. It proposes MR-separation instead of d-separation and three candidates of sufficient separating set for MR-separation. The results of simulations revealed that MRSL had up to 2-fold higher F1 score and 100 times faster computing time than other eight competitive methods. Furthermore, we applied MRSL to 26 biomarkers and 44 International Classification of Diseases 10 (ICD10)-defined diseases using GWAS summary data from UK Biobank. The results cover most of the expected causal links that have biological interpretations and several new links supported by clinical case reports or previous observational literatures.

Funder

National Key Research and Development Program of China

State Key Program of National Natural Science of China

Key R&D Program of Shandong Province

National Natural Science Foundation of China

National Natural Science Foundation of China General Project

Beijing Natural Science Foundation

Publisher

Oxford University Press (OUP)

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