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Foroud, Tatiana

0000-0002-5549-2212

Mayo Clinic

Indiana University Indianapolis

Citations 118

Feasibility and Safety of Multicenter Tissue and Biofluid Sampling for α -Synuclein in Parkinson’s Disease: The Systemic Synuclein Sampling Study (S4)
Chahine, Lana M. , Beach, Thomas G. , Seedorff, Nicholas , Caspell‐Garcia, Chelsea , Coffey, Christopher S. , Brumm, Michael C. , Linder, Carly, Mosovsky, Sherri, Riss, Holly, Ecklund, Dixie , Seibyl, John , Jennings, Danna , Arnedo, Vanessa , Riley, Lindsey , Dave, Kuldip D. , Mollenhauer, Brit , study, on behalf of the Systemic sSynuclein Sampling, Adler, Charles H. , Serrano, Geidy E. , Foroud, Tatiana , study, on behalf of the Systemic sSynuclein Sampling

Journal of Parkinson’s Disease | September 21, 2018 | Volume: 8 | Issue: 4 | Pages: 517-527

10.3233/jpd-181434 Get It

Background: α-synuclein is a lead Parkinson’s disease (PD) biomarker. There are conflicting reports regarding accuracy of α-synuclein in different tissues and biofluids as a PD biomarker, and the within-subject anatomical distribution of α-synuclein is not well described. The Systemic Synuclein Sampling Study (S4) aims to address these gaps in knowledge. The S4 is a multicenter, cross-sectional, observational study evaluating α-synuclein in multiple tissues and biofluids in PD and healthy controls (HC). Objective: To describe the baseline characteristics of the S4 cohort and safety and feasibility of this study. Methods: Participants underwent motor and non-motor clinical assessments, dopamine transporter SPECT, biofluid collection (cerebrospinal fluid, saliva, and blood), and tissue biopsies (skin, sigmoid colon, and submandibular gland). Biopsy adequacy was determined based on presence of adequate target tissue. Tissue sections were stained with the 5C12 monoclonal antibody against unmodified α-synuclein. All specimens were acquired and processed in a standardized manner. Adverse events were systematically recorded. Results: The final cohort consists of 82 participants (61 PD, 21 HC). In 68 subjects (83%), all types of specimens were obtained but only 50 (61%) of subjects had all specimens both collected and evaluable for α-synuclein. Mild adverse events were common, especially for submandibular gland biopsy, but only 1 severe adverse event occurred. Conclusion: Multicenter tissue and biofluid sampling for α-synuclein is feasible and generally safe. S4 will inform understanding of the concurrent distribution of α-synuclein pathology and biomarkers in biofluids and peripheral nervous system in PD.
Heritability of Different Forms of Memory in the Late Onset Alzheimer's Disease Family Study
Barral, Sandra , Lee, Joseph H. , Bird, Thomas D., Mayeux, Richard , Bennett, David A. , Wilson, Robert S. , Bennett, David A. , Wilson, Robert S., Leurgans, Sue E. , Foroud, Tatiana , Sweet, Robert A. , Graff, Caroline

Journal of Alzheimer's Disease | May 16, 2018 | Volume: 23 | Issue: 2 | Pages: 249-255

10.3233/jad-2010-101515 Get It