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Quest Diagnostics DGX recently launched its new laboratory blood test, AD-Detect Abeta, which combines 42/40 and p-tau217 Evaluation. It is designed to help physicians confirm amyloid brain pathology due to Alzheimer's disease (AD) in patients with mild cognitive impairment or dementia.
The latest launch expands the company’s AD-Detect suite of advanced diagnostics.
DGX Stock’s Likely Trend Following the News
After the announcement, DGX’s shares edged 2.7% to close the session at $164.04 on Wednesday.
On a promising note, Quest Diagnostics’ AD-Detect suite of advanced diagnostics has grown to include a range of validated blood-based biomarkers, giving providers options for personalized testing for patients.
Further, the company plans to expand the portfolio with new biomarkers to help providers better assess Alzheimer's and other forms of dementia. We expect the market sentiment toward DGX stock to remain positive surrounding the latest launch of new test panels for AD.
Quest Diagnostics has a market capitalization of $18.21 billion at present. Going by the Zacks Consensus Estimate, the company’s 2025 earnings are expected to grow 8.5% on a 9.1% improvement in revenues.
About DGX’s New AD-Detect Blood Test
The AD-Detect Abeta combines results of blood levels of amyloid beta (AB) 42/40 with blood levels of p-tau217. The test results are then used to produce the AD-Detect Likelihood Score, a composite interpretation created through a proprietary algorithm validated utilizing a well-characterized cohort from the Florida Alzheimer's Disease Research Center.
Significance of DGX’s New AD-Detect Blood Test
In AD, a protein called amyloid forms plaques in the brain, triggering changes in another protein, tau, and causing it to twist into tangles. These plaques and tangles disrupt brain cell function while also causing abnormal levels of both proteins to circulate in the bloodstream. While amyloid PET imaging and cerebral spinal fluid testing are established methods for aiding the diagnosis of AD, they are significantly more expensive, invasive and specialist-dependent than blood-based tests.
At the American Academy of Neurology's annual meeting, Quest Diagnostics' researchers presented favorable data demonstrating that the new blood test assesses AD pathology with greater than 90% sensitivity and accuracy due to the addition of ApoE, a genetic risk marker.
The blood test fulfills acceptable performance criteria set forth by the CEOi. It gives providers greater confidence in moving patients (with a high likelihood score for AD) on the path to treatment. It could also potentially prevent the use of PET and lumbar puncture in patients whose blood values strongly indicate that they do not have AD.