EPISODE · Jul 26, 2022 · 12 MIN
FDA-approved test expands options for Alzheimer's disease: Joshua Bornhorst, Ph.D.
from Answers from the Lab · host Mayo Clinic Laboratories
(00:32) Can you please tell our listeners a little about yourself and your background?(01:00) Mayo Clinic Laboratories already offers one test for Alzheimer's disease, right?(01:32) Could you tell our listeners about the new FDA-approved test that Mayo Clinic Laboratories will launch soon?(02:43) The test results will report the ratio of the amyloid isoforms, not the individual test components, right?(03:26) Does the new test require a certain tube?(04:15) Can you provide a little more detail on the commercially available tube that will be required?(04:36) Which patient population would benefit most from this test?(05:30) Can you compare and contrast the existing Alzheimer's disease test and the new amyloid ratio evaluation?(08:58) Is Mayo Clinic's ADEVL the only test that measures the tau component?(09:51) When would one of these tests be more appropriate than the other?(10:52) Can you help our listeners understand what a "laboratory developed" test means?(11:43) From a physician's standpoint, how might this new test improve patient care?
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What this episode covers
Joshua Bornhorst, Ph.D., explains the differences between the new, FDA-approved Alzheimer's disease (AD) test and Mayo Clinic Laboratories' existing AD evaluation. The laboratory will offer both tests, to give physicians flexibility and options for optimal patient care.
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FDA-approved test expands options for Alzheimer's disease: Joshua Bornhorst, Ph.D.
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