Rowan Researchers Develop
Blood Test
that Detects Early Alzheimer’s Disease
Rowan
University , June 8, 2016 -- A research team, led by Dr. Robert
Nagele from Rowan University School of Osteopathic Medicine and Durin
Technologies, Inc., has announced the development of a blood test that
leverages the body’s immune response system to detect an early stage of
Alzheimer’s disease – referred to as the mild cognitive impairment (MCI) stage
– with unparalleled accuracy. In a “proof of concept” study involving 236 subjects,
the test demonstrated an overall accuracy, sensitivity and specificity rate of
100 percent in identifying subjects whose MCI was actually caused by an early
stage of Alzheimer’s disease.
that Detects Early Alzheimer’s Disease
“About 60 percent of all MCI
patients have MCI caused by an early stage of Alzheimer’s disease. The
remaining 40 percent of cases are caused by other factors, including vascular
issues, drug side-effects and depression. To provide proper care, physicians
need to know which cases of MCI are due to early Alzheimer’s and which are
not,” said Cassandra DeMarshall, the study’s lead author, and a PhD candidate
at the Rowan University Graduate School of Biomedical Sciences. “Our results
show that it is possible to use a small number of blood-borne autoantibodies to
accurately diagnose early-stage Alzheimer’s. These findings could eventually
lead to the development of a simple, inexpensive and relatively noninvasive way
to diagnose this devastating disease in its earliest stages.”
“It is now generally believed
that Alzheimer’s-related changes begin in the brain at least a decade before
the emergence of telltale symptoms,” Nagele explained. “To the best of our
knowledge, this is the first blood test using autoantibody biomarkers that can
accurately detect Alzheimer’s at an early point in the course of the disease
when treatments are more likely to be beneficial – that is, before too much
brain devastation has occurred.” Nagele is the study’s corresponding author and
the director of the Biomarker
Discovery Center
at Rowan’s New Jersey Institute for Successful Aging. He is also the co-founder
and chief scientific officer of Durin Technologies, Inc.
The researchers presented their
results in an article published in Alzheimer’s & Dementia: Diagnosis,
Assessment & Disease Monitoring that also reported the test’s ability
to accurately “stage the disease,” meaning it can distinguish early-stage
Alzheimer’s at MCI from later, more advanced stages. The test was also
disease-specific. It readily distinguished early Alzheimer’s at the MCI stage
from other diseases including Parkinson’s disease, multiple sclerosis, and
early stage breast cancer.
For the study, the Rowan University
researchers analyzed blood samples from 236 subjects, including 50 MCI subjects
with low levels of amyloid-beta 42 peptide in their cerebrospinal fluid. The
latter is a reliable indicator of ongoing Alzheimer’s pathology in the brain
and predicts a likely rapid progression to Alzheimer’s.
Employing human protein
microarrays, each containing 9,486 unique human proteins that are used as bait
to attract blood-borne autoantibodies, the researchers identified the top 50
autoantibody biomarkers capable of detecting ongoing early-stage Alzheimer’s
pathology in patients with MCI. In multiple tests, the 50 biomarkers were 100
percent accurate in distinguishing patients with MCI due to Alzheimer’s from
healthy age- and gender-matched controls. Further testing of the selected MCI
biomarker panel demonstrated similar high overall accuracy rates in
differentiating patients with early Alzheimer’s at the MCI stage from those
with more advance, mild-moderate Alzheimer’s (98.7 percent), early-stage
Parkinson’s disease (98.0 percent), multiple sclerosis (100 percent) and breast
cancer (100 percent).
In their report, the
researchers acknowledge that the utility of their MCI biomarker panel as a
blood test for early detection of Alzheimer’s disease will hinge on a
successful larger replication study using an independent patient cohort.
However, they also point out that, because this blood-based diagnostic strategy
is dependent on the presence of Alzheimer’s pathology which can be underway
many years before symptoms emerge, this approach could open the door to even
earlier pre-symptomatic detection of Alzheimer’s disease.
According to the authors, early
diagnosis of Alzheimer’s disease and the ability to stage the disease through a
simple blood test would offer many potential benefits. Patients could possibly
delay disease progression through lifestyle adjustments, begin treatment sooner
and plan future medical care. Clinicians would have a way to measure the
effectiveness of therapeutic intervention and clinical trials could enroll
patients who were truly at the earliest stage of their disease.
This research was supported, in
part, by the Osteopathic Heritage Foundation and the Michael J. Fox Foundation.
The researchers reported that neither organization had a role in the study
design, data collection and analysis, decision to publish or preparation of the
article.
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