» Articles » PMID: 35371017

Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study

Overview
Journal Front Immunol
Date 2022 Apr 4
PMID 35371017
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Observational studies suggested that multiple sclerosis (MS) is associated with cardiovascular diseases (CVDs). However, the causal association has not been fully elucidated. Thus, we aim to assess the causality of the associations of MS with risk of CVDs.

Methods: A two-sample Mendelian randomization (MR) study was performed to explore the causality. Genetic instruments were identified for MS from a genome-wide association study (GWAS) involving 115,803 individuals. Summary-level data for CVDs were obtained from different GWAS meta-analysis studies. MR analysis was conducted mainly using the inverse-variance weighted (IVW) method. Sensitivity analyses were further performed to ensure the robustness of the results.

Results: This MR study found suggestive evidence that genetic liability to MS was associated with an increased risk of coronary artery disease (CAD) [odds ratio (OR), 1.02; 95% confidence interval (CI), 1.00-1.04; = 0.03], myocardial infarction (MI) (OR, 1.03; 95% CI, 1.00-1.06; = 0.01), heart failure (HF) (OR, 1.02; 95% CI, 1.00-1.04; = 0.02), all-cause stroke (AS) (OR, 1.02; 95% CI, 1.00-1.05; = 0.02), and any ischemic stroke (AIS) (OR, 1.02; 95% CI, 1.00-1.05; = 0.04). The null-association was observed between MS and the other CVDs. Further analyses found little evidence of pleiotropy.

Conclusions: We provided suggestive genetic evidence for the causal associations of MS with increased risk of CAD, MI, HF, AS, and AIS, which highlighted the significance of active monitoring and prevention of cardiovascular risk to combat cardiovascular comorbidities in MS patients.

Citing Articles

Genetic Insights Into the Role of Cathepsins in Alzheimer's Disease, Parkinson's Disease, and Amyotrophic Lateral Sclerosis: Evidence From Mendelian Randomization Study.

Jiang Y, Fan W, Li Y, Xue H Brain Behav. 2024; 15(1):e70207.

PMID: 39740768 PMC: 11688054. DOI: 10.1002/brb3.70207.


Development of Human Monoclonal Antibodies With Broad Reactivity for Rabies Postexposure Prophylaxis.

Wu M, Peng X, Xu W, Zhang H, Fang L, Liu X J Med Virol. 2024; 96(11):e70068.

PMID: 39601104 PMC: 11600393. DOI: 10.1002/jmv.70068.


Autoimmune diseases and cardiovascular risk: Mendelian randomization analysis for the impact of 19 autoimmune diseases on 14 cardiovascular conditions.

Bao Y, Gu L, Chen J, Wang H, Wang Z, Wang H J Transl Autoimmun. 2024; 9:100259.

PMID: 39554254 PMC: 11565429. DOI: 10.1016/j.jtauto.2024.100259.


Investigating the Interplay between Cardiovascular and Neurodegenerative Disease.

Cousineau J, Dawe A, Alpaugh M Biology (Basel). 2024; 13(10).

PMID: 39452073 PMC: 11505144. DOI: 10.3390/biology13100764.


Current understanding of cardiovascular autonomic dysfunction in multiple sclerosis.

Zahoor I, Pan G, Cerghet M, Elbayoumi T, Mao-Draayer Y, Giri S Heliyon. 2024; 10(15):e35753.

PMID: 39170118 PMC: 11337049. DOI: 10.1016/j.heliyon.2024.e35753.


References
1.
Roth G, Forouzanfar M, Moran A, Barber R, Nguyen G, Feigin V . Demographic and epidemiologic drivers of global cardiovascular mortality. N Engl J Med. 2015; 372(14):1333-41. PMC: 4482354. DOI: 10.1056/NEJMoa1406656. View

2.
Lennon R, Claussen K, Kuersteiner K . State of the Heart: An Overview of the Disease Burden of Cardiovascular Disease from an Epidemiologic Perspective. Prim Care. 2018; 45(1):1-15. DOI: 10.1016/j.pop.2017.11.001. View

3.
Burgess S, Bowden J, Fall T, Ingelsson E, Thompson S . Sensitivity Analyses for Robust Causal Inference from Mendelian Randomization Analyses with Multiple Genetic Variants. Epidemiology. 2016; 28(1):30-42. PMC: 5133381. DOI: 10.1097/EDE.0000000000000559. View

4.
Tavallaei M, Tavallaei A, Ebrahimi N, Ghoshouni H, Afshari-Safavi A, Badihian S . The prevalence of Myocardial Infarction among Multiple Sclerosis Patients: a Systematic Review and Meta-analysis. Mult Scler Relat Disord. 2021; 56:103292. DOI: 10.1016/j.msard.2021.103292. View

5.
Shah S, Henry A, Roselli C, Lin H, Sveinbjornsson G, Fatemifar G . Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nat Commun. 2020; 11(1):163. PMC: 6952380. DOI: 10.1038/s41467-019-13690-5. View