From paradox to biology: shared genetic architecture underlies the inverse association between smoking and Sjögren’s disease
Clicks: 2
ID: 322300
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Steady Performance
0.3
/100
2 views
0 readers
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #164 of 202 articles by views in Lara D. Veeken
Most read
Least read
Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 202 in total.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
Abstract Objectives Smoking has been consistently associated with a paradoxically lower risk of Sjögren’s disease (SjD). We used genetic approaches to investigate whether this association reflects a causal effect of smoking or shared genetic architecture, and to identify shared loci that may help explain this paradox and inform disease biology. Methods We applied an integrated cross-trait genetic framework using genome-wide association data for smoking initiation and SjD. Conventional Mendelian randomisation (MR) was used as an initial test of association, followed by genome-wide causal modelling (CAUSE and latent causal variable analysis) to distinguish directional causality from shared genetic architecture. Shared loci were identified using cross-trait pleiotropy analysis, refined through colocalisation, and further explored using proteome-informed mediation analyses. Results Conventional MR showed an inverse association between genetic liability to smoking initiation and SjD risk (OR 0.53, 95% CI 0.34-0.84). However, genome-wide modelling did not support a causal effect and instead suggested the association was driven by shared genetic influences. Cross-trait pleiotropy analysis identified 1,536 variants across 11 loci, with colocalisation supporting shared causal variants at five regions (3q13.32, 2q22.3, 8p21.2, 14q24.3 and 5q34). These loci implicated pathways related to neuroimmune signalling, epithelial organisation and interferon regulation. Proteome-informed analyses identified no circulating proteins that robustly mediated the smoking-SjD relationship. Conclusions The inverse smoking-SjD association likely reflects shared genetic liability rather than a protective causal effect. These findings highlight biological pathways relevant to SjD pathogenesis and emphasise the importance of cautious interpretation of MR estimates when traits share genetic architecture.
| Reference Key |
openalex_W7170243573
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Stefanie van der Merwe, Benjamin Zuckerman, Weijie Liu, Wenjie Cheng, Sizheng Steven Zhao |
| Journal | Lara D. Veeken |
| Year | 2026 |
| DOI |
10.1093/rheumatology/keag385
|
| URL | |
| Keywords | Keywords not found |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.