Case Study | September 28, 2023
Discovery of a Biomarker of Biological Processes for Rare Disease
There are more than a thousand genes that affect the mitochondria, and many that may be altered within the biochemical pathways of mitochondrial disease. In this study, Sapient analyzed samples from over 100 individuals from a rare disease population with sequence-verified mitochondrial disease and found there are specific small molecules that are altered in these patients. In fact, a set of chemically-related biomarkers were found which represent a new biochemical pathway not yet described before in humans.
Watch the video to learn how Sapient validated a key biomarker in independent datasets of patients with mitochondrial disease to confirm its diagnostic value as a readout of mitochondrial dysfunction. You will also see how this rare disease biomarker maps onto common human diseases.
