Body Complexion and Circulating Lipids in the Risk of TDP-43 Related Disorders

Noelia Esteban-García; Luis C Fernández-Beltrán; Juan Miguel Godoy-Corchuelo; Jose L Ayala; Jordi A Matias-Guiu; Silvia Corrochano

doi:10.3389/fnagi.2022.838141

Body Complexion and Circulating Lipids in the Risk of TDP-43 Related Disorders

Front Aging Neurosci. 2022 Mar 25:14:838141. doi: 10.3389/fnagi.2022.838141. eCollection 2022.

Authors

Noelia Esteban-García¹, Luis C Fernández-Beltrán¹, Juan Miguel Godoy-Corchuelo¹, Jose L Ayala², Jordi A Matias-Guiu¹, Silvia Corrochano¹

Affiliations

¹ Neurological Disorders Group, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
² Department of Computer Architecture and Automation, Universidad Complutense de Madrid, Madrid, Spain.

Abstract

Objective: Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two distinct degenerative disorders with overlapping genetics, clinical manifestations, and pathology, including the presence of TDP-43 aggregates in nearly 50% of patients with FTD and 98% of all patients with ALS. Here, we evaluate whether different genetically predicted body lipid metabolic traits are causally associated with the risk of FTD with TDP-43 aggregates, compare it to their causal role in the risk of ALS, and identify genetic variants shared between these two TDP43 related disorders in relation to lipid metabolic traits.

Methods: We conducted two-sample Mendelian randomization analyses (2SMR) to evaluate the causal association of 9 body complexion and 9 circulating lipids traits with the risk of FTD with TDP-43 aggregates and the risk of ALS. The inverse-variance weighted method was the primary analysis, followed by secondary sensitive analyses. We then looked for common genetic variants between FTD and ALS in relation to lipid metabolic traits.

Results: Genetically increased trunk-predicted mass, fat-free mass, and higher circulating triglycerides levels were suggestively associated with a higher risk of FTD with TDP-43 aggregates. Circulating lipids, mainly LDL cholesterol, were causally associated with a higher risk of ALS. We identified two genetic variants, EIF4ENIF1 and HNRNPK, in relation to body complexion and circulating lipids shared between FTD with TDP-43 aggregates and ALS.

Conclusion: This work provides evidence that body complexion and circulating lipids traits impact differentially on the risk of FTD and ALS, suggesting new and specific interventional approaches in the control of body lipid metabolism for FTD and ALS, and identified HNRNPK as a potential link between circulating lipids levels and these disorders.

Keywords: Mendelian randomization; TDP-43 related disorders; amyotrophic lateral sclerosis; frontotemporal dementia; lipid metabolism.