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A Roadmap for Developing Plasma Diagnostic and Prognostic Biomarkers of Cerebral Cavernous Angioma With Symptomatic Hemorrhage (CASH).

AbstractBACKGROUND:
Cerebral cavernous angioma (CA) is a capillary microangiopathy predisposing more than a million Americans to premature risk of brain hemorrhage. CA with recent symptomatic hemorrhage (SH), most likely to re-bleed with serious clinical sequelae, is the primary focus of therapeutic development. Signaling aberrations in CA include proliferative dysangiogenesis, blood-brain barrier hyperpermeability, inflammatory/immune processes, and anticoagulant vascular domain. Plasma levels of molecules reflecting these mechanisms and measures of vascular permeability and iron deposition on magnetic resonance imaging are biomarkers that have been correlated with CA hemorrhage.
OBJECTIVE:
To optimize these biomarkers to accurately diagnose cavernous angioma with symptomatic hemorrhage (CASH), prognosticate the risk of future SH, and monitor cases after a bleed and in response to therapy.
METHODS:
Additional candidate biomarkers, emerging from ongoing mechanistic and differential transcriptome studies, would further enhance the sensitivity and specificity of diagnosis and prediction of CASH. Integrative combinations of levels of plasma proteins and characteristic micro-ribonucleic acids may further strengthen biomarker associations. We will deploy advanced statistical and machine learning approaches for the integration of novel candidate biomarkers, rejecting noncorrelated candidates, and determining the best clustering and weighing of combined biomarker contributions.
EXPECTED OUTCOMES:
With the expertise of leading CA researchers, this project anticipates the development of future blood tests for the diagnosis and prediction of CASH to clinically advance towards precision medicine.
DISCUSSION:
The project tests a novel integrational approach of biomarker development in a mechanistically defined cerebrovascular disease with a relevant context of use, with an approach applicable to other neurological diseases with similar pathobiologic features.
AuthorsRomuald Girard, Yan Li, Agnieszka Stadnik, Robert Shenkar, Nicholas Hobson, Sharbel Romanos, Abhinav Srinath, Thomas Moore, Rhonda Lightle, Abdallah Shkoukani, Amy Akers, Timothy Carroll, Gregory A Christoforidis, James I Koenig, Cornelia Lee, Kristina Piedad, Steven M Greenberg, Helen Kim, Kelly D Flemming, Yuan Ji, Issam A Awad
JournalNeurosurgery (Neurosurgery) Vol. 88 Issue 3 Pg. 686-697 (02 16 2021) ISSN: 1524-4040 [Electronic] United States
PMID33469662 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Copyright© Congress of Neurological Surgeons 2021.
Chemical References
  • Biomarkers
  • Inflammation Mediators
Topics
  • Biomarkers (blood)
  • Brain Neoplasms (blood, diagnostic imaging)
  • Capillary Permeability (physiology)
  • Cerebral Hemorrhage (blood, diagnostic imaging)
  • Female
  • Hemangioma, Cavernous (blood, diagnostic imaging)
  • Hemangioma, Cavernous, Central Nervous System (blood, diagnostic imaging)
  • Humans
  • Inflammation Mediators (blood)
  • Longitudinal Studies
  • Machine Learning
  • Magnetic Resonance Imaging (methods)
  • Male
  • Prognosis
  • Transcriptome (physiology)

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