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| Association between leukocyte telomere length and cataracts: a bidirectional Mendelian randomization study |
| CHEN Rong1, Mokoumani2, KE Xiaohong3, WANG Chuhuai1
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1. Department of Rehabilitation Medicine, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510030, China;
2. The People's Hospital of Leshan Shizhong District, Leshan, Sichuan 614000, China;
3. Sun Yat-sen University, Guangzhou, Guangdong 510030, China |
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Abstract Objective To examine the association between leukocyte telomere length and cataract using bidirectional Mendelian randomization (MR) approach, so as to provide the basis for early diagnosis and prevention of cataracts. Methods Leukocyte telomere length data were collected through a meta analysis of genome-wide association studies (GWAS), including 78 952 participants, and the GWAS data of cataract were collected through the UK Biobank, including 8 890 cases and 454 120 controls. A bidirectional MR analysis was performed using the inverse-variance weighted (IVW) method, and single nucleotide polymorphisms (SNPs) which were associated with leukocyte telomere length were selected as instrumental variables. The heterogeneity was assessed using the Cochran's Q test, the horizontal pleiotropy was assessed using the MR-Egger regression and the outlier was verified with the leave-one-out and MR-PRESSO test. Results Forward MR analysis results showed that shortened leukocyte telomere length had an increased risk of cataract (OR=0.991, 95%CI: 0.990-0.997). Reverse MR analysis results showed no statistically significant association between leukocyte telomere length and cataract (P>0.05). Cochran's Q test detected no heterogeneity, and neither the MR-Egger regression nor the MR-PRESSO test revealed horizontal pleiotropy of instrumental variables (both P>0.05). Leave-one-out analysis showed robustness of the MR analysis results. Conclusion Shorter leukocyte telomere length might be associated with increased risk of cataract.
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Received: 23 February 2024
Revised: 16 May 2024
Published: 19 July 2024
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