Association between PDE4D gene and ischemic stroke: recent advancements

No Thumbnail Available

Date

2016

Journal Title

Journal ISSN

Volume Title

Publisher

Taylor and Francis Ltd

Abstract

Stroke is a severe complication and a leading cause of death worldwide and genetic studies among different ethnicities has provided the basis for involvement of phosphodiesterase 4D (PDE4D) gene in cerebrovascular diseases. Recent advancements have evaluated the role of this gene in stroke and these studies have provided a stronger support for the involvement of this gene in stroke development and few studies also suggest that it may influence outcome. Furthermore, case-control studies and meta-analysis studies have provided strong evidence for certain variants in PDE4D to predispose to stroke only among certain ethnicities. Thus, this review focuses on recent progress made in PDE4D gene research involving genetic, molecular and pharmacological aspect. A strong conclusion has emerged that clearly indicates a pivotal role played by this gene in ischemic stroke globally. Studies have also noticeably highlighted that PDE4D gene/pathway can be a suitable drug target for managing stroke; however, a more comprehensive research is still required to understand the molecular and cellular intricacies this gene plays in stroke development, progression and its outcome. ? 2015 Taylor and Francis.

Description

Keywords

phosphodiesterase 4D; phosphodiesterase IV; platelet derived growth factor; small interfering RNA; unclassified drug; PDE4D protein, human; phosphodiesterase IV; arterial wall thickness; blood brain barrier; blood vessel permeability; brain ischemia; cardioembolic stroke; cell proliferation; ethnic difference; female; gene; gene frequency; genetic association; genetic epidemiology; genetic predisposition; genetic variability; genotype; haplotype; human; immunoreactivity; ligand binding; magnetic

Citation

Das, S., Roy, S., & Munshi, A. (2016). Association between PDE4D gene and ischemic stroke: recent advancements. International Journal of Neuroscience, 126(7), 577-583. doi: 10.3109/00207454.2015.1051621

Endorsement

Review

Supplemented By

Referenced By