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People with Disabilities - SD Awareness

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    FDA Grand Rounds

    Paul Willie D...#1
    Paul Willie D...#1


    Posts : 20
    Join date : 2017-10-19
    Location : Here and There and Everywhere but Nowhere

    FDA Grand Rounds Empty FDA Grand Rounds

    Post by Paul Willie D...#1 Mon Dec 11, 2017 12:54 pm

    The FDA Grand Rounds is webcast every other month to highlight cutting-edge research underway across the Agency and its impact on protecting and advancing public health. Each session features an FDA scientist presenting on a key public health challenge and how FDA is applying science to its regulatory activities. The 45-minute presentation is followed by questions from the audience. #FDAGrandRounds.

    Thursday, Jan. 11, 2018
    12:00 p.m. - 1:00 p.m.

    Presented by

    Sherry Ferguson, PhD
    Research Psychologist
    Division of Neurotoxicology
    FDA’s National Center for Toxicological Research (NCTR)

    Vijayalakshmi Varma, PhD
    Research Biologist, NCTR
    Webcast Lecture

    Ethnicity- and Gender-related Differences in Alzheimer’s Disease
    About the Presentation

    Minorities and women are particularly vulnerable to Alzheimer’s disease (AD). Women have a higher incidence of AD at later ages; among people who are 71 years of age or older, 16% of women have AD compared with only 11% of men. Better understanding of sex differences involved in the cause and progression of AD could contribute to better drugs and other types of interventions to slow the disease progression.

    Relative to Caucasians, "the threat [of AD] is even more substantial in the African-American and Hispanic communities,” noted former Alzheimer’s Association President and CEO Harry Johns. This is partially related to the higher incidence of dementia and AD as well as increased severity of symptoms in African Americans. More research into African Americans and other minority populations with AD is crucial to the goals of precision medicine. Studies show the advantage of using different approaches to understanding what is likely to be a complex picture of AD-related ethnicity differences.

    This presentation will discuss research into protein levels in post-mortem African American and Caucasian brain tissue from both genders to explore ethnicity- and gender-related differences. The selected proteins include those thought to be critically involved in AD. Those proteins were examined in samples of the middle temporal gyrus that were matched for age at death since this region is critically involved in language processing and generation and has been shown to be significantly affected by AD.
    About the Presenters

    Research psychologist Sherry Ferguson, PhD, has conducted neurotoxicological research since joining FDA’s National Center for Toxicological Research (NCTR) in 1990. Dr. Ferguson earned a PhD in Physiological Psychology from the University of Wisconsin at Madison. She is on the editorial board of several scientific journals and is a past president of the Developmental Neurotoxicology Society (formerly, the Neurobehavioral Teratology Society). She holds adjunct status at the University of Arkansas for Medical Sciences and the University of Arkansas at Little Rock.

    Vijayalakshmi Varma, PhD, joined NCTR’s Division of Systems Biology in 2009 as a research biologist . She earned a PhD in Biochemistry and Cell Biology from Manipal Academy of Higher Education, Manipal University, India. For over 13 years, she has conducted research into metabolic syndrome and its co-morbidities, including obesity, insulin resistance, and obesity-induced inflammation, in clinical translational studies and in disease modeling, using in vitro cell culture and in vivo rodent systems. She leads research efforts to explore the impact of obesity on drug-induced toxicities.
    Requirements to Receive Credit for Each Lecture/Session

    Participants must create an account to attest their attendance and complete the final activity evaluation via the CE Portal (www.ceportal.fda.gov). The training point of contact will email the evaluation to participants within 24 hours after each session. Final activity evaluations must be completed within two weeks after the activity - no exceptions.

    Register and Resource: https://www.fda.gov/ScienceResearch/AboutScienceResearchatFDA/ucm486711.htm

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