Key result
GLIS1 variant linked to ~23% higher risk of mitral valve prolapse.
Why the study?
The triggering mechanisms underlying nonsyndromic mitral valve prolapse, a common degenerative valvular heart disease, are mostly unknown.
Case-Control (n=12,082)
Yes
Odds Ratio: 1.23
p-value: p=1.2×10-7
Identifies GLIS1 as a susceptibility gene for nonsyndromic mitral valve prolapse, highlighting the role of disrupted endothelial to mesenchymal transition in its pathogenesis.
GLIS1 variation may increase mitral valve prolapse susceptibility; animal models leave open human replication and clinical relevance.
Nonsyndromic Mitral valve prolapse (MVP) is a common degenerative valvular heart disease with severe health consequences, including arrhythmia, heart failure and sudden death. MVP is characterized by excess extracellular matrix secretion and cellular disorganization which leads to bulky valves that are unable to co-apt properly during ventricular systole. However, the triggering mechanisms of this process are mostly unknown. Using pathway enrichment tools applied to GWAS we show that genes at risk loci are involved in biological functions relevant to cell adhesion and migration during cardiac development and in response to shear stress. Through genetic, in silico and in vivo experiments we demonstrates the presence of several genes involved in gene regulation, including GLIS1 , a transcription factor that regulates Hedgehog signaling. Our findings define genetic, molecular and cellular mechanisms underlying non-syndromic MVP and implicate disrupted endothelial to mesenchymal transition and cell migration as a potential common cause to this disease.
No takes yet. Share an insight, caveat, or question.
Yu et al. (2018) conducted a case-control in Mitral Valve Prolapse (n=12,082). GLIS1 locus variant rs1879734 vs. Reference allele was evaluated on Association with Mitral Valve Prolapse (OR 1.23, p=1.2×10-7). Genetic variation at the GLIS1 locus (rs1879734) is significantly associated with susceptibility to mitral valve prolapse (OR 1.23, P=1.2x10^-7), supported by functional validation in zebrafish and mouse models.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: