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DOI: 10.1055/s-0044-1791679
Reply to “Commentary: ‘No Genetic Causality between Tobacco Smoking and Venous Thromboembolism: A Two-Sample Mendelian Randomization Study’ ”
We recently received comments on our findings[1] from Liu et al for which we are grateful, and we appreciate their careful scholarship and thoughtfulness. We would like to respond to the comments of Liu et al as follows:
First, Liu et al argue that a major issue in our study is the failure to account for sample overlap. However, as pointed out by Liu et al, the bias due to sample overlap is mainly due to false-positive errors, whereas our findings are not significant. However, we also replaced venous thromboembolism (VTE) data from different data sources ([Table 1])[2] for validation in this response, and the results showed that our conclusions were stable ([Table 2]).
Phenotypic name |
No. of cases |
No. of controls |
Sample size |
Ancestry |
Sex |
Consortium (cohort)/author |
Public release year |
Study reference or description URL |
---|---|---|---|---|---|---|---|---|
Age of initiation of regular smoking |
NA |
NA |
728,826 |
Mixed (84.35%European) |
Both sexes |
GSCAN/Gretchen R. B. Saunders et al[3] |
2022 |
Nature. 2022 Dec;612(7941):720–724. doi: 10.1038/s41586-022-05477-4. |
Ever smoked regularly |
NA |
NA |
3,383,199 |
Mixed (79.11%European) |
Both sexes |
GSCAN/Gretchen R. B. Saunders et al[3] |
2022 |
Nature. 2022 Dec;612(7941):720–724. doi: 10.1038/s41586-022-05477-4. |
Cigarettes per day |
NA |
NA |
784,353 |
Mixed (79.03%European) |
Both sexes |
GSCAN/Gretchen R. B. Saunders et al[3] |
2022 |
Nature. 2022 Dec;612(7941):720–724. doi: 10.1038/s41586-022-05477-4. |
Smoking cessation |
NA |
NA |
1,400,535 |
Mixed (82.26%European) |
Both sexes |
GSCAN/Gretchen R. B. Saunders et al[3] |
2022 |
Nature. 2022 Dec;612(7941):720–724. doi: 10.1038/s41586-022-05477-4. |
Venous thromboembolism |
21,021 |
391,160 |
412,181 |
European |
Both sexes |
FinnGen.R10/Mitja I. Kurki et al[2] |
2023 |
|
Deep venous thrombosis |
6,501 |
357,111 |
363,612 |
European |
Both sexes |
FinnGen.R10/Mitja I. Kurki et al[2] |
2023 |
|
Pulmonary embolism |
10,046 |
401,128 |
411,174 |
European |
Both sexes |
FinnGen.R10/Mitja I. Kurki et al[2] |
2023 |
Abbreviation: MR, Mendelian randomization.
Second, Liu et al identified a second major issue in this study is the choice of data, including the use of outdated datasets and an incomplete consideration of the exposure phenotype. In response to their point about outdated datasets, we employed the Round 10 VTE GWAS (genome-wide association study) summary statistics released in 2023 by FinnGen in our current response, and it is clear that the results ([Table 2]) are also consistent with our previous findings.
Incomplete consideration of smoking phenotypes, which we must recognize as correct, does not affect our results. Please note that we also included this time four smoking phenotypes ([Table 1])[3] published by the GWAS and Sequencing Consortium of Alcohol and Nicotine use (GSCAN) in 2022, and the results showed that the association of all six smoking phenotypes with VTE was not statistically significant ([Table 2]). As for their subtypes, we note that the inverse variance-weighted (IVW) method suggests possible age of initiation of regular smoking–DVT (deep vein thrombosis), ever smoked regularly–DVT, and ever smoked regularly–PE (pulmonary embolism) associations ([Table 2]), but we must point out that the age of initiation of regular smoking–DVT association suffers from too small several instrumental variables and large differences in the estimates of the five methods. As for the ever smoked regularly–DVT and ever smoked regularly–PE associations, none of the methods were significant except for the IVW method. Moreover, considering that the associations of all six smoking phenotypes with VTE were not statistically significant, the significant results in their subtypes should be treated with caution.
In addition, and also due to the third question posed to us by Liu et al, the instrumental variables addressed in our current response did not undergo the exclusion of single nucleotide polymorphisms (SNPs) associated with confounders to control for horizontal pleiotropy as described in our previous studies.[1] For the conflicting association results in VTE and its subtypes, it is likely that bias due to SNPs associated with confounders was attributed.
Publikationsverlauf
Eingereicht: 30. Juli 2024
Angenommen: 15. September 2024
Artikel online veröffentlicht:
03. Oktober 2024
© 2024. Thieme. All rights reserved.
Georg Thieme Verlag KG
Stuttgart · New York
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References
- 1 Du HC, Zheng YF, Shen MQ, Deng BY. No genetic causality between tobacco smoking and venous thromboembolism: a two-sample Mendelian randomization study. Thromb Haemost 2024; 124 (08) 795-802
- 2 Kurki MI, Karjalainen J, Palta P. et al; FinnGen. FinnGen provides genetic insights from a well-phenotyped isolated population. Nature 2023; 613 (7944) 508-518
- 3 Saunders GRB, Wang X, Chen F. et al; 23andMe Research Team, Biobank Japan Project. Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature 2022; 612 (7941) 720-724