
What is Dementia?
Dementia is not a single disease, but a term used to describe a wide range of conditions, including Alzheimer’s disease. Dementia is caused by abnormal brain changes that affect cognitive abilities and can impact one’s feelings, behavior and relationships.
Alzheimer’s disease is the most common cause of dementia, a disease that robs millions of people each year of critical thinking capabilities required for a healthy and happy lifestyle. The impact of Alzheimer’s is staggering.1
- 6th leading cause of death in the United States.
- More than 5 million Americans are living with the disease.
- 1 in 3 seniors dies with Alzheimer’s or another form of dementia.
- Alzheimer’s kills more people than breast cancer and prostate cancer COMBINED.
Early diagnosis of the cause of cognitive impairment can help a patient begin treatment or therapy that can provide a longer period of healthier mental function.
10 Early Signs and Symptoms of Alzheimer’s Disease1
One of the most common signs of Alzheimer’s disease, especially in the early stage, is forgetting recently learned information. Others include forgetting important dates or events, asking the same question over and over again, or increasingly needing to rely on memory aids (e.g., reminder notes or electronic devices) or family members for things the person used to handle on their own.
What’s a typical age-related change? Sometimes forgetting names or appointments, but remembering them later.
Advanced Imaging Solutions
Alzheimer’s disease is caused by shrinkage (atrophy) in a region of the brain called the hippocampus, which helps regulate emotions, manages long-term memory, and also plays a vital role in a person’s spatial navigation abilities. One specialized technique that uses Magnetic Resonance Imaging (MRI) is called 3-D volumetric quantitative analysis. At HALO Diagnostics, we use Icobrain DM from Icometrix to quantify clinically relevant brain structures in individual patients with neurological disorders, such dementia, and and Icobrain MS for multiple sclerosis plaque quantification as well as for other white matter diseases. We provide physicians with a report that provides a detailed volumetric report.

Icobrain DM - Evaluate Relevant Brain Structures in Dementia Patients
Sample Report Page 1: Lobular and hippocampal volume loss

MRI dates = dates of the MRI scans on which the report is based. When only one MRI exam is available, a baseline report is created which reports volumes but no volume changes.
Status of semi automated quality control (Approved / Approved with remarks / rejected) and remarks on the quality of the original images and the segmentation.
Color-coded segmentation of substructures
- Frontal cortex (green)
- Parietal cortex (blue)
- Temporal cortex (red)
- Hippocampi (orange)
This segmentation is also available in DICOM format.
Brain volumes are corrected for head size. The normal range and normative percentiles serve as a reference based on healthy controls. Annualized volume change describes the percentage of brain volume change per year compared to the previous scan. The normal annualized volume change represents the average expected annual volume change for a healthy age- and gender-matched person.
Population graphs show the age- and gender-matched average and normal ranges for each substructure. The current (black) and previous (white) time points are marked with an ‘x’. The error bars are computed from the pooled results of several test-retest experiments. They represent the interval in which the differences between test- and retest results can be found with 90% confidence.
Volume signature compares the normative percentile of the substructures and its change between the current (full black line) and previous (dashed white line) time point.
Flair white matter hyperintensities are reported when a FLAIR sequence is included. Volume change = total difference in volume compared to the previous scan.
The icobrain software version and its approval for clinical practice.
Sample Report Page 2: Global Brain Volume Loss

MRI dates = dates of the MRI scans on which the report is based. When only one MRI exam is available, a baseline report is created which reports volumes but no volume changes.
Lateral ventricles (green) segmentation are depicted in three planes. This segmentation is also available in DICOM format.
Whole brain and lateral ventricles volume are corrected for head size. The normal range and normative percentiles serve as a reference based on healthy controls. Annualized volume change describes the percentage of brain volume change per year compared to the previous scan. The normal annualized volume change represents the average expected annual volume change for a healthy age- and gender-matched person.
Flair white matter hyperintensities are reported when a FLAIR sequence is included. Volume change = total difference in volume compared to the previous scan.
The graph shows the age- and gender-matched average and normal range for the whole brain and lateral ventricles volume (left) and the ratio of the lateral ventricles over the whole brain percentage (right) of healthy people. The time point is marked with an ‘x’. The error bars are computed from the pooled results of several test-retest experiments. They represent the interval in which the differences between test- and retest results can be found with 90% confidence.
The icobrain software version and its approval for clinical practice
Functional Imaging in Dementia
Another technique for pinpointing the cause of a cognitive dysfunction is functional imaging. This approach uses Positron Emission Tomography (PET) and Computed Tomography (CT) in combination to observe the brain’s function. Functional imaging is used by physicians to determine how well specific brain regions are using sugar or oxygen, which can help reveal the site and cause of memory or problem-solving ability deficits. PET/CT imaging also allows the physician to see what’s happening inside the brain at a molecular level, so they can identify or rule out cellular or chemical changes that indicate a specific disease.
Individuals at Risk for Dementia Show Reduced Glucose Metabolism
Mild cognitive impairment (MCI) is an intermediate stage between normal cognitive decline and dementia. Radiopharmaceuticals like Fluorodeoxyglucose (18F) or fluorodeoxyglucose F 18 (FDG-18) are used, along with positron emission tomography (PET), to better understand the progression of MCI into dementia, including Alzheimer's disease (AD). This approach can provide information about neuronal activity in the brain by measuring glucose metabolic rate; the progression of dementia is accompanied by a continued decrease in the uptake or metabolism of glucose.
Studies have also shown that FDG-PET has the potential to differentiate patients with AD and patients with other causes of dementia. This has been an important advancement in the evaluation of patients with MCI and a critical tool in quickly detecting progression into various forms of dementia.
Normal FDG-18
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Alzheimer’s Disease
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What is Beta Amyloid and What Role Does it Play in Dementia?
Although the cause of Alzheimer’s disease has not been fully established, evidence suggests that the amyloid-β or beta amyloid (Aβ) protein plays an important role. Accumulation of this protein or peptide in the form of amyloid plaques is a hallmark of dementia caused by Alzheimer’s. Aβ deposits are thought to occur before cognitive symptoms in Alzheimer’s disease and are therefore a potential marker of the disease. Amyloid imaging agents, like Amyvid™ (Eli Lilly), bind to Aβ deposits and allow physicians to see amyloid plaque in the brain when paired with PET-CT imaging.
Amyloid Negative
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Amyloid Positive
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What is a Tau Tangle?
TAUVID™ from Eli Lilly was approved by the FDA for positron emission tomography (PET) imaging of the brain to estimate the density and distribution of aggregated tau neurofibrillary tangles (NFT). NFTs are aggregates or clusters of a protein called tau - a widely accepted primary marker of Alzheimer's disease that can become "tangled". The tau protein in the brains of people with AD are abnormally shaped and cannot serve their normal function of assisting in the transport of nutrients and other important substances from one part of a nerve cell to another.
Available January 2021
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Neuroscience Biomarker Longitudinal Observational Study (NBLOS),
“Community and Care Givers at the Front Line" Webinar
Evidence-based dementia care management remains poorly integrated across the nation as well within most healthcare systems. Dr. Chris Hancock of HALO Diagnostics discusses encouraging developments in coordinated care for dementia patients through the National Institute on Aging IMPACT Collaboratory. Specifically he addresses the growing support for embedded pragmatic clinical trials for PLWD and their caregivers coupled to a national neuroscience biomarker longitudinal observational study (NBLOS). Watch the full presentation below!
Additional Educational Resources

- https://impactcollaboratory.org/impact-resources/
- https://impactcollaboratory.org/upcoming-events/