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Intracerebral Hemorrhage Genetics. | LitMetric

Intracerebral Hemorrhage Genetics.

Genes (Basel)

Center of Neurology, Faculty of Medicine, Vilnius University, LT-03101 Vilnius, Lithuania.

Published: July 2022

AI Article Synopsis

  • Intracerebral hemorrhage (ICH) is a severe type of stroke affecting about 15% of stroke patients, with a high mortality rate.
  • Despite its prevalence, treatment options for ICH are limited, highlighting the need for effective prevention and management strategies.
  • Recent studies emphasize the role of genetic factors in ICH, identifying both monogenic disorders and polygenic risk factors like hypertension and small vessel disease, which may influence future treatment approaches.

Article Abstract

Intracerebral hemorrhage (ICH) is a devastating type of stroke, frequently resulting in unfavorable functional outcomes. Up to 15% of stroke patients experience ICH and approximately half of those have a lethal outcome within a year. Considering the huge burden of ICH, timely prevention and optimized treatment strategies are particularly relevant. Nevertheless, ICH management options are quite limited, despite thorough research. More and more trials highlight the importance of the genetic component in the pathogenesis of ICH. Apart from distinct monogenic disorders of familial character, mostly occurring in younger subjects, there are numerous polygenic risk factors, such as hypertension, neurovascular inflammation, disorders of lipid metabolism and coagulation cascade, and small vessel disease. In this paper we describe gene-related ICH types and underlying mechanisms. We also briefly discuss the emerging treatment options and possible clinical relevance of the genetic findings in ICH management. Although existing data seems of more theoretical and scientific value so far, a growing body of evidence, combined with rapidly evolving experimental research, will probably serve clinicians in the future.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322856PMC
http://dx.doi.org/10.3390/genes13071250DOI Listing

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