Key result
Carrying a hiPSI TTNtv is linked to ~442% higher DCM risk across diverse populations.
Why the study?
The effect of TTNtvs on dilated cardiomyopathy risk was historically studied primarily in European-ancestry populations, leaving questions about their effect in diverse populations.
Does carrying a high percentage spliced in (hiPSI) titin truncating variant (TTNtv) increase the risk of dilated cardiomyopathy across diverse populations?
Cohort (n=43,731)
No
Does carrying a high percentage spliced in (hiPSI) titin truncating variant (TTNtv) increase the risk of dilated cardiomyopathy across diverse populations?
Answers are grounded in this paper and cite their sources.
High percentage spliced in titin truncating variants increase the risk of dilated cardiomyopathy independent of genetic background, suggesting genetic similarity to reference populations should not restrict screening for genetic causes of DCM.
Importance The effect of high percentage spliced in (hiPSI) TTN truncating variants (TTNtvs) on risk of dilated cardiomyopathy (DCM) has historically been studied among population subgroups defined by genetic similarity to European reference populations. This has raised questions about the effect of TTNtvs in diverse populations, especially among individuals genetically similar to African reference populations. Objective To determine the effect of TTNtvs on risk of DCM in diverse population as measured by genetic distance (GD) in principal component (PC) space. Design Cohort study Setting Penn Medicine Biobank (PMBB) is a large, diverse biobank. Participants Participants were recruited from across the Penn Medicine healthcare system and volunteered to have their electronic health records linked to biospecimen data including DNA which has undergone whole exome sequencing. Main Outcomes and Measures Risk of DCM among individuals carrying a hiPSI TTNtv. Results Carrying a hiPSI TTNtv was associated with DCM among PMBB participants across a range of GD deciles from the 1000G European centroid; the effect estimates ranged from odds ratio (OR) = 3.29 (95% confidence interval [CI] 1.26 to 8.56) to OR = 9.39 (95% CI 3.82 to 23.13). When individuals were assigned to population subgroups based on genetic similarity to the 1000G reference populations, hiPSI TTNtvs conferred significant risk of DCM among those genetically similar to the 1000G European reference population (OR = 7.55, 95% CI 4.99 to 11.42, P <0.001) and individuals genetically similar to the 1000G African reference population (OR 3.50, 95% CI 1.48 to 8.24, P =0.004). Conclusions and Relevance TTNtvs are associated with increased risk of DCM among a diverse cohort. There is no significant difference in effect of TTNtvs on DCM risk across deciles of GD from the 1000G European centroid, suggesting genetic background should not be considered when screening individuals for titin-related DCM. Key Points Question Do high percentage spliced in (hiPSI) titin truncating variants (TTNtvs) confer similar levels of risk for dilated cardiomyopathy (DCM) across diverse populations? Findings In a cohort study that comprised 43,731 individuals of diverse genetic background with electronic health records linked to whole exome sequencing data, hiPSI TTNtvs conferred increased risk of DCM across all individuals irrespective of genetic background as measured by genetic distance from the 1000 Genomes Project European centroid. Meaning The findings of this study suggest that TTNtvs increase risk of DCM among individuals independent of genetic background and that genetic similarity to a reference population should not play a role in screening for genetic causes of dilated cardiomyopathy.
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DePaolo et al. (2024) conducted a cohort in Dilated Cardiomyopathy (DCM) (n=43,731). High percentage spliced in (hiPSI) titin truncating variants (TTNtvs) vs. Non-carriers of hiPSI TTNtvs was evaluated on Risk of dilated cardiomyopathy (DCM) (OR 5.42, 95% CI 4.01 to 7.32, p=<0.001). Carrying a high percentage spliced in titin truncating variant (hiPSI TTNtv) was associated with a significantly increased risk of dilated cardiomyopathy (OR 5.42) across diverse populations.
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