» Articles » PMID: 25367286

Alteration of Gene Expression Profiling Including GPR174 and GNG2 is Associated with Vasovagal Syncope

Overview
Journal Pediatr Cardiol
Date 2014 Nov 5
PMID 25367286
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Vasovagal syncope (VVS) causes accidental harm for susceptible patients. However, pathophysiology of this disorder remains largely unknown. In an effort to understanding of molecular mechanism for VVS, genome-wide gene expression profiling analyses were performed on VVS patients at syncope state. A total of 66 Type 1 VVS child patients and the same number healthy controls were enrolled in this study. Peripheral blood RNAs were isolated from all subjects, of which 10 RNA samples were randomly selected from each groups for gene expression profile analysis using Gene ST 1.0 arrays (Affymetrix). The results revealed that 103 genes were differently expressed between the patients and controls. Significantly, two G-proteins related genes, GPR174 and GNG2 that have not been related to VVS were among the differently expressed genes. The microarray results were confirmed by qRT-PCR in all the tested individuals. Ingenuity pathway analysis and gene ontology annotation study showed that the differently expressed genes are associated with stress response and apoptosis, suggesting that the alteration of some gene expression including G-proteins related genes is associated with VVS. This study provides new insight into the molecular mechanism of VVS and would be helpful to further identify new molecular biomarkers for the disease.

Citing Articles

Guidelines for the diagnosis and treatment of neurally mediated syncope in children and adolescents (revised 2024).

Wang C, Liao Y, Wang S, Tian H, Huang M, Dong X World J Pediatr. 2024; 20(10):983-1002.

PMID: 39110332 PMC: 11502568. DOI: 10.1007/s12519-024-00819-w.


Genetic Analysis of Cardiac Syncope-Related Genes in Korean Patients with Recurrent Neurally Mediated Syncope.

Lee S, Park J, Ki C, Park S, On Y, Park K J Cardiovasc Dev Dis. 2022; 9(8).

PMID: 36005429 PMC: 9409957. DOI: 10.3390/jcdd9080265.


Characterizing Neonatal Heart Maturation, Regeneration, and Scar Resolution Using Spatial Transcriptomics.

Misra A, Baker C, Pritchett E, Burgos Villar K, Ashton J, Small E J Cardiovasc Dev Dis. 2022; 9(1).

PMID: 35050211 PMC: 8779463. DOI: 10.3390/jcdd9010001.


Association of Oxidative Stress with Neurological Disorders.

Hassan W, Noreen H, Rehman S, Kamal M, da Rocha J Curr Neuropharmacol. 2021; 20(6):1046-1072.

PMID: 34781871 PMC: 9886831. DOI: 10.2174/1570159X19666211111141246.


Towards Understanding the Genetic Nature of Vasovagal Syncope.

Matveeva N, Titov B, Bazyleva E, Pevzner A, Favorova O Int J Mol Sci. 2021; 22(19).

PMID: 34638656 PMC: 8508958. DOI: 10.3390/ijms221910316.


References
1.
Serletis A, Rose S, Sheldon A, Sheldon R . Vasovagal syncope in medical students and their first-degree relatives. Eur Heart J. 2006; 27(16):1965-70. DOI: 10.1093/eurheartj/ehl147. View

2.
Lelonek M, Pietrucha T, Matyjaszczyk M, Goch J . A novel approach to syncopal patients: association analysis of polymorphisms in G-protein genes and tilt outcome. Europace. 2008; 11(1):89-93. DOI: 10.1093/europace/eun277. View

3.
Schwindinger W, Robishaw J . Heterotrimeric G-protein betagamma-dimers in growth and differentiation. Oncogene. 2001; 20(13):1653-60. DOI: 10.1038/sj.onc.1204181. View

4.
Dascal N . Signalling via the G protein-activated K+ channels. Cell Signal. 1998; 9(8):551-73. DOI: 10.1016/s0898-6568(97)00095-8. View

5.
Newton J, Kenny R, Lawson J, Frearson R, Donaldson P . Prevalence of family history in vasovagal syncope and haemodynamic response to head up tilt in first degree relatives: preliminary data for the Newcastle cohort. Clin Auton Res. 2003; 13(1):22-6. DOI: 10.1007/s10286-003-0077-7. View