Related Experiment Video
Updated: Aug 8, 2026

A Murine Model of Subarachnoid Hemorrhage
Published on: November 21, 2013
High rate of microbleed formation following primary intracerebral hemorrhage
Jason Mackey1, Jeffrey J Wing2, Gina Norato3
1Department of Neurology, Indiana University, Indianapolis, IN, USA.
Background:
We sought to investigate the frequency of microbleed development following intracerebral hemorrhage in a predominantly African-American population and to identify predictors of new microbleed formation.
Aims And/Or Hypothesis:
To investigate the frequency and predictors of new microbleeds following intracerebral hemorrhage.
Methods:
The DECIPHER study was a prospective, longitudinal, magnetic resonance-based cohort study designed to evaluate racial/ethnic differences in risk factors for microbleeds and to evaluate the prognostic impact of microbleeds in this intracerebral hemorrhage population. We evaluated new microbleed formation in two time periods: from baseline to 30 days and from 30 days to year 1.
Results:
Of 200 subjects enrolled in DECIPHER, 84 had magnetic resonance imaging at all required time points to meet criteria for this analysis. In the baseline to day 30 analysis, 11 (13·1%) had new microbleeds, compared with 25 (29·8%) in the day 30 to year 1 analysis. Logistic regression analysis demonstrated that baseline number of microbleeds [odds ratio 1·05 (95% confidence interval 1·01, 1·08), P = 0·01] was associated with new microbleed formation at 30 days. A logistic regression model predicting new microbleed at one-year included baseline number of microbleeds [odds ratio 1·05 (1·00, 1·11), P = 0·046], baseline age [odds ratio 1·05 (1·00, 1·10), P = 0·04], and white matter disease score [odds ratio 1·18 (0·96, 1·45). P = 0·115]. Overall, 28 of 84 (33·3%) intracerebral hemorrhage subjects formed new microbleeds at some point in the first year post-intracerebral hemorrhage.
Conclusions:
We found that one-third of intracerebral hemorrhage subjects in this cohort surviving one-year developed new microbleeds, which suggests a dynamic and rapidly progressive vasculopathy. Future studies are needed to examine the impact of new microbleed formation on patient outcomes.
Insights
One-third of intracerebral hemorrhage survivors developed new microbleeds within a year, indicating a progressive vasculopathy. The baseline number of microbleeds and age predicted new microbleed formation.
Area of Science:
- Neurology
- Radiology
- Vascular Medicine
Background:
- Intracerebral hemorrhage (ICH) survivors are at risk for developing new microbleeds.
- Understanding the frequency and predictors of new microbleeds is crucial for patient management.
- Previous studies have not sufficiently focused on microbleed development in diverse populations.
Purpose of the Study:
- To determine the incidence of new microbleed formation after ICH.
- To identify clinical and imaging predictors of new microbleed development.
- To investigate these factors in a predominantly African-American cohort.
Main Methods:
- Prospective, longitudinal, magnetic resonance imaging (MRI)-based cohort study (DECIPHER).
- Evaluation of new microbleed formation at two time points: baseline to 30 days and 30 days to 1 year.
- Logistic regression analysis to identify predictors of new microbleed formation.
Main Results:
- Of 84 eligible subjects, 13.1% developed new microbleeds by 30 days and 29.8% by 1 year.
- The baseline number of microbleeds predicted new microbleed formation at 30 days (OR 1.05, P=0.01).
- Predictors for new microbleeds at 1 year included baseline microbleed count (OR 1.05, P=0.046), age (OR 1.05, P=0.04), and white matter disease score (OR 1.18, P=0.115).
Conclusions:
- Approximately one-third of ICH survivors in this cohort developed new microbleeds within the first year.
- This suggests a dynamic and progressive underlying vasculopathy following ICH.
- Further research is warranted to explore the clinical impact of new microbleed formation on patient outcomes.
Related Concept Videos
Ischemic Stroke ll: Pathophysiology
Hemorrhagic Stroke l: Introduction
Hemorrhagic Stroke ll: Pathophysiology
Cerebral Edema ll: Pathophysiology

