Page 77 - Annual Report 2018
P. 77

4. THE VALLECAS PROJECT



















          ropsychological profile is completed by getting in-  genetic and biochemical markers. Samples are ob-
          formation related to other cognitive domains such   tained according to the protocol "Collection and
          as language, visuospatial ability and visuoconstruc-  Processing of Human Blood Samples in the Vallecas
          tion. All these data allow identifying the strengths  Project" and processed to obtain the various frac-
          and weaknesses in the cognitive profile and cha-    tions indicated in the protocol, which are stored at -
          racterizing, if necessary, the type of cognitive im-  80°C. On one hand, DNA is extracted from blood
          pairment that an individual presents. Table XXX     cells to determine, by PCR and sequencing techni-
          below lists the different tests that make up the neu-  ques, genetic markers associated with the various
          ropsychological battery of the Vallecas Project, as  polymorphisms in the following genes: APOE, CR1,
          well as the visit number in which they have been ap-  BIN1, CLU, PICALM, ABCA7, SORL1, PRNP, GRM8, and
          plied to all study participants.                    BACE1. These genes are studied using DNA obtained
                                                              from the extraction of samples from the first visit.
          4.3.6. Determination of biomarkers
                                                              Also, in the context of the project funded by the MI-
          It is currently widely accepted that the molecular  NECO (Projects RETOS) entitled "miRNA and lipid me-
          changes associated with AD, including the forma-    tabolism markers as potential links between vascular
          tion of amyloid plaques and neurofibrillary tangles  dysfunction and Alzheimer's pathophysiology", and
          begin many years before the appearance of clini-    whose main researchers are Drs. Miguel Medina and
          cal symptoms. In recent years, the need to define   Miguel Calero, in collaboration with the group of Dr.
          and develop new early biomarkers of AD that allow   Tobias Engel (Royal College of Surgeons, Dublin, Ire-
          us to assess the risk and early diagnosis of the disease  land) plasma-derived microRNAs are being analy-
          has become clear. Thus, blood samples will be co-   zed as potential biomarkers, as well as molecules
          llected within the Vallecas Project for the study of  related to vascular dysfunction, lipid metabolism




































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