Periodic Reporting for period 1 - UNRAVEL-CAUSALITY (Mental illness, substance use, and cardiovascular disease: Unravelling causal relationships)
Período documentado: 2023-04-01 hasta 2025-09-30
In this ambitious project, I will bring together innovative epidemiological and genetic approaches to unravel the relationships of mental illness with substance (mis)use and cardiovascular disease. My aims are to: 1) assess bidirectional relationships between mental illness and its comorbidities by conducting longitudinal analyses in (multi-ancestry) prospective cohort studies, 2) distinguish bidirectional relationships from shared genetic liability by jointly modelling the complete genetic architecture of mental illness and its comorbidities (genomic structural equation modelling), 3) establish causality by using only highly significant genetic variants as instruments for one variable and testing causal effects on another (Mendelian randomization), 4) fully unravel the nature of relationships between mental illness and its comorbidities by ‘triangulating’ evidence from aims 1 to 3, and 5) assess how informing medical doctors about the outcomes of aim 4 influences their clinical decisions in a randomized online experiment. This interdisciplinary project sets the stage for more effective prevention and treatment of mental illness, across ancestry groups.
So far, I have (co-)published 5 papers on mental illness and cardiovascular disease. First, an important overview article, which I was invited to write for the prestigious European Heart Journal and in which I set out the main aims, methods, and considerations for the ERC project. Next, I published an empirical study on the link between schizophrenia and cardiological (specifically arhythmic) traits as first author, an empirical paper on the link between PTSD and a range of cardiovascular traits, and I was involved as a co-author in a major collaborative effort to investigate the link between major depressive disorder and cardiovascular disease. In all three of these empirical papers, I triangulated multiple advanced genetic methodologies to elucidate underlying mechanisms, including genomic SEM (gSEM) and Mendelian randomization (MR). Besides these empirical papers, I also senior-authored an important systematic review study in the specialized journal Heart Rhythm.
So far, I have (co-)published 5 papers on mental illness and substance use. First, a review on the causal nature of the link between alcohol use and mental health problems and how Mendelian randomization can help obtain reliable evidence. Second, a very extensive review of the role that gray matter volume changes might have in the (causal) effects of smoking on depression, summarizing neuro-imaging studies. Third, a review I worked on with fellow leading researchers in the field of substance use genetics, wherein we provide an overview of recent developments in genetic research on substance use. In addition, I was invited to write a commentary on a new study that looked at the link between smoking and obesity. Finally, one of the key empirical papers planned for this project was recently accepted for publication at Psychological Medicine. This paper describes extensive advanced genetic analyses to assess (gSEM and multivariable MR) whether subcortical brain volume measures mediate the effects of smoking on developing serious mental illness.
Finally, published an important guide on evidence triangulation in psychiatric epidemiology.
• By triangulating genetic advanced methods, I was able to convincingly show that PTSD shows robust causal effects on developing serious mental illness, and this is considerably mediated by smoking, alcohol use, and inflammation markers.3 Particularly innovative in this study, was the use of MR in combination with gSEM, which has never before been done applied to a complex causal question like this one.
• There are distinct biological pathways that connect the rare disorder of schizophrenia with the even rarer disorder of Brugada syndrome (an arrhythmic trait).2 The link between these two disorders is of great clinical interest (because it hugely increases the risk of sudden cardiac death), but because of the very low prevalence research so far had not been able to disentangle their connections. With my study, I was able to circumvent these issues holding back other research, by linking large GWAS databases together allowing a range of sophisticated follow-up analyses.
• Besides applying triangulation in empirical studies, a major break-through/moving beyond the state of the art, is my work on improving triangulation as a research approach and developing more systematic frameworks and ways to do so.10 Due to my work with the ERC project, I am now in a leading position in pushing triangulation forward, being involved in continuing discussions and collaborations with experts from around the world around these topics. I have a particularly unique position, as I connect different disciplines (psychology, psychiatry, epidemiology, genetics) and methods (quantitative, qualitative, different datasets, population studies, clinical studies).