MH_I_P: Mental Health Sciences I. Posters
Introduction
Perseverative negative thinking, such as rumination on past stress, predicts future depression, which makes it a promising candidate in prevention. Or recent study (Eszlari et al, submitted for publication) revealed circadian clock gene ARNTL in the background of rumination, if controlling for depression.
Aims
Our present aim was to explore the role of ARNTL variants in depression, and the potential mediating role of rumination in these associations.
Methods
Our sample consisted of 72,395 participants of the UK Biobank database. Rumination was measured by the question "Do you worry too long after an embarrassing experience?", and depression was assessed by lifetime depression based on interview, and by depressive symptoms of the past two weeks. Regression models were run in Plink v1.9, with each of 256 ARNTL variants as predictor, for each of the two depression phenotypes as outcome, to search for significant variants that had also been significant for rumination in similar models. In case of such a shared variant, mediating role of rumination was tested in its association with depression, in Mplus v7.4.
Results
No variant survived Bonferroni correction for lifetime depression. However, rs3816360 survived correction for both current depression and rumination. Hypothesising direct and indirect effects within the same model, rs3816360 significantly affected current depression, both directly and as mediated by rumination.
Conclusion
Rs3816360 within ARNTL has a high regulatory potential, and has been implicated in rapid cycling of bipolar and schizoaffective patients. Our results extend its relevance to perseverative negative thinking and depression, pointing to the potential of circadian clock gene ARNTL as a promising drug target in multimorbid conditions.
Funding
ÚNKP-20-4-II-SE-9 New National Excellence Program of The Ministry for Innovation and Technology from the source of the National Research, Development and Innovation Fund; 2017-1.2.1-NKP-2017-00002; 2019-2.1.7-ERA-NET-2020-00005 under the frame of ERAPERMED.
Semmelweis University, Doctoral School of Mental Health Sciences