| Title: | Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms |
| Journal: | Genetic Epidemiology |
| Published: | 24 Jul 2020 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/32710482/ |
| DOI: | https://doi.org/10.1002/gepi.22343 |
| URL: | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/gepi.22343 |
Publication 4801
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Abstract
It has been hypothesised that nonsyndromic cleft lip/palate (nsCL/P) and cancer may share aetiological risk factors. Population studies have found inconsistent evidence for increased incidence of cancer in nsCL/P cases, but several genes (e.g., CDH1, AXIN2) have been implicated in the aetiologies of both phenotypes. We aimed to evaluate shared genetic aetiology between nsCL/P and oral cavity/oropharyngeal cancers (OC/OPC), which affect similar anatomical regions. Using a primary sample of 5,048 OC/OPC cases and 5,450 controls of European ancestry and a replication sample of 750 cases and 336,319 controls from UK Biobank, we estimate genetic overlap using nsCL/P polygenic risk scores (PRS) with Mendelian randomization analyses performed to evaluate potential causal mechanisms. In the primary sample, we found strong evidence for an association between a nsCL/P PRS and increased odds of OC/OPC (per standard deviation increase in score, odds ratio [OR]: 1.09; 95% confidence interval [CI]: 1.04, 1.13; p = .000053). Although confidence intervals overlapped with the primary estimate, we did not find confirmatory evidence of an association between the PRS and OC/OPC in UK Biobank (OR 1.02; 95% CI: 0.95, 1.10; p = .55). Mendelian randomization analyses provided evidence that major nsCL/P risk variants are unlikely to influence OC/OPC. Our findings suggest possible shared genetic influences on nsCL/P and OC/OPC.</p>
11 Authors
- Laurence J. Howe
- Gibran Hemani
- Corina Lesseur
- Valérie Gaborieau
- Kerstin U. Ludwig
- Elisabeth Mangold
- Paul Brennan
- Andy R. Ness
- Beate St Pourcain
- George Davey Smith
- Sarah J. Lewis
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