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Graph Lasso-Based Test for Evaluating Functional Brain Connectivity in Sickle Cell Disease
Julie Coloigner1, Ronald Phlypo2, Thomas D Coates3
11 CIBORG, Division of Radiology, Children's Hospital Los Angeles , Los Angeles, California.
Insights
Sickle cell disease (SCD) patients show altered brain connectivity, even without visible MRI damage. Anemia and silent strokes correlate with reduced similarity to healthy brain connectivity patterns.
Area of Science:
- Neurology
- Neuroimaging
- Vascular Biology
Background:
- Sickle cell disease (SCD) is a vascular disorder linked to ischemia-reperfusion injury, anemia, vasculopathy, and strokes.
- Cerebral injuries in SCD can cause neurological dysfunction, impacting patient development.
- Cognitive impairment in SCD may occur without apparent brain abnormalities on conventional MRI, suggesting diffuse injury.
Purpose of the Study:
- To investigate if alterations in cerebral connectivity serve as a sensitive biomarker for SCD severity.
- To compare brain connectivity patterns in SCD patients to a healthy reference model.
Main Methods:
- Functional MRI (fMRI) was used to analyze brain connectivity in individual SCD patients.
- A graphical lasso model and Fréchet mean were employed to establish a healthy brain connectivity descriptor.
- An individual similarity index was calculated to compare each SCD patient's connectivity matrix to the healthy model.
Main Results:
- The healthy connectivity model was not suitable for 4 out of 27 SCD patients.
- Anemia and white matter hyperintensities (WMH) were significant predictors of lower similarity to the healthy connectivity model (p=0.02 and p=0.03, respectively).
- Patients with lower hemoglobin levels or WMH exhibited the least similarity to the reference connectivity.
Conclusions:
- Cerebral connectivity alterations may represent a sensitive biomarker for SCD severity.
- Anemia and WMH are associated with significant deviations from healthy brain connectivity patterns in SCD.
- Further research is needed to clarify if these connectivity changes are pathological or compensatory.
Abstract:
Sickle cell disease (SCD) is a vascular disorder that is often associated with recurrent ischemia-reperfusion injury, anemia, vasculopathy, and strokes. These cerebral injuries are associated with neurological dysfunction, limiting the full developing potential of the patient. However, recent large studies of SCD have demonstrated that cognitive impairment occurs even in the absence of brain abnormalities on conventional magnetic resonance imaging (MRI). These observations support an emerging consensus that brain injury in SCD is diffuse and that conventional neuroimaging often underestimates the extent of injury. In this article, we postulated that alterations in the cerebral connectivity may constitute a sensitive biomarker of SCD severity. Using functional MRI, a connectivity study analyzing the SCD patients individually was performed. First, a robust learning scheme based on graphical lasso model and Fréchet mean was used for estimating a consistent descriptor of healthy brain connectivity. Then, we tested a statistical method that provides an individual index of similarity between this healthy connectivity model and each SCD patient's connectivity matrix. Our results demonstrated that the reference connectivity model was not appropriate to model connectivity for only 4 out of 27 patients. After controlling for the gender, two separate predictors of this individual similarity index were the anemia (p = 0.02) and white matter hyperintensities (WMH) (silent stroke) (p = 0.03), so that patients with low hemoglobin level or with WMH have the least similarity to the reference connectivity model. Further studies are required to determine whether the resting-state connectivity changes reflect pathological changes or compensatory responses to chronic anemia.
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