Pharmacogenetic Testing: Does it Improve Therapy in Patients With MDD?
Testing for genetic variants may allow clinicians to predict how patients with major depressive disorder metabolize antidepressants.
Testing for genetic variants may allow clinicians to predict how patients with major depressive disorder metabolize antidepressants.
23andMe, a consumer genetics company, has licensed its first drug compound to Almirall, a global pharmaceutical company.
The researchers wrote that “genetic counseling must be further explored to find an optimal balance of clinical quality with increased access and financial sustainability.”
Results of an epidemiologic analysis indicated that approximately 12,800 individuals in the United States may have biallelic mutations in key proteins along the MC4R pathway.
Risks related to DTC testing include lack of understanding of the test by the consumer, incorrect test results, and erroneous interpretation of the results.
Researchers from the American Society of Breast Surgeons outlined recommendations for genetic testing that medical professionals can use for assessing hereditary risk for breast cancer.
A strategy using initial evaluation with whole-exome sequencing or epilepsy panel, and then, if these are negative, chromosomal microarray, is supported for patients with epilepsy of unknown etiology, according to study results.
Genetic testing for cancer, cardiovascular, and neurodegenerative diseases presents a low psychological burden in patients and should be considered.
While more than 100 variants in the MUTYH gene have been linked with MUTYH-associated polyposis, the MUTYH-Associated Polyposis Genetic Health Risk report identifies the 2 most common genetic variants in people of Northern European ancestry.
Approximately 5.5 million Americans have Alzheimer disease or dementia.