NAVARRA, Spain, Sept. 11 (UPI) -- A Spanish researcher has proposed a genetic diagnostic method for multiple myeloma that permits earlier detection of the bone marrow cancer.
The dissertation by Borja Saez of the University of Navarra is oriented toward the study of the genetic basis of the cancer, and the posterior development of cytogenetic diagnostic strategies for the detection of alterations with prognostic value.
Saez statistically analyzed cytogenetic changes in a group of multiple myeloma patients to determine associations between specific chromosomal changes and thus the description of a new classification of the disease.
In addition, the technique of hybridization in situ with fluorescence allowed him to identify new recurrent genetic changes that are involved in the appearance of this pathology.
Multiple myeloma is a disease which primarily affects people older than 60 years. According to Saez, the new method of diagnosis will enable detection of genetic alterations rapidly during the early stages of the disease, permitting its early diagnosis.
