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Statement of Marilyn Albert, Ph.D. Director, Division of Cognitive Neuroscience Department of Neurology, Johns Hopkins University School of Medicine Co-Director, Johns Hopkins Alzheimer’s Disease Research Center Baltimore, Md. Presented to the Aging Subcommittee, Senate Health, Education, Labor and Pensions Committee Good morning Madame Chair and Senator Burr. My name is Marilyn Albert, and I am Director of the Division of Cognitive Neuroscience in the Department of Neurology at Johns Hopkins University School of Medicine and Co-Director of the Johns Hopkins Alzheimer’s Disease Research Center. I am also a member of the national board of the Alzheimer’s Association and former chair of the Association’s Medical and Scientific Advisory Council. I speak to you today as a scientist and as someone who has worked with hundreds of people with Alzheimer's disease and their families for over 20 years. Reducing the risk of Alzheimer’s disease Our challenge now is to continue the research and to educate the public and health care practitioners to act on this information. We have a lot of work to do. A recent national survey by the Alzheimer’s Association found that most Americans are not aware of the progress being made against Alzheimer’s and that only14 percent are taking any action to reduce their risk for Alzheimer’s disease. We’ve begun to make some progress in this area. Just last year, the Alzheimer’s Association’s Maintain Your Brain workshops educated 26,000 people in communities across the nation. The average age of participants was 61 and many were baby boomers, the target audience for the program. Nearly half came to the workshops with no prior family or other experience with Alzheimer’s disease, which means there is interest in brain health in the general population. We don’t know whether participation in the Maintain Your Brain workshops have lead to changes in lifestyle or improvements in brain healthy behavior, but the first step in behavior change is knowledge and 90 percent said they learned something new and could apply this new knowledge. In addition, with support from the CDC, the Alzheimer’s Association is now testing a program on brain health in two communities – Southern California and the Greater Atlanta area – targeted to African-American baby boomers. Given the higher rates among African-Americans of cardiovascular disease, diabetes, obesity and high blood pressure, all of which are risks for Alzheimer’s, a program targeted to this population could have enormous benefit for public health. At this time next year, this exciting demonstration project will be reporting initial results. The CDC is also working with organizations, such as the AARP, the American Society on Aging and National Council on the Aging to educate professionals and the public about cognitive health. Some programs are targeted to school age populations in the hopes of starting at the youngest age to address brain healthy behavior. Reducing the Impact of Alzheimer’s Disease These NIH-funded studies have shown that relatively simple interventions, such as caregiver education, can reduce the behavioral and psychological symptoms in people with the disease that create the greatest challenges for family caregivers and our health and long term care systems. They can reduce depression, stress, burden and unmet needs in caregivers. They can improve quality of life for both the person with the disease and the caregiver. And they can delay nursing home placement, in one study by more than a year and a half. Through the Alzheimer Demonstration Grant Program at the Administration on Aging, states are matching modest federal grants and are developing practical ways to incorporate evidence-based programs to help patients and caregivers into their health and long term care systems. For example, North Carolina developed a guide for families and a companion manual for nurses to improve hospital care for people with dementia. Georgia developed a mobile day care program to bring these important services to rural areas that did not have the resources to support a full program on their own. Maryland extended caregiver outreach services into rural and underserved minority communities. California developed a model to mobilize community resources to support Alzheimer families in underserved areas, starting first in a Latino community in Los Angeles and then adapting the program for African-American and Asian communities. Translating research to practice That is why your proposed Alzheimer’s Breakthrough Act is so important, Senator Mikulski. It would provide the authority and resources to deliver on the exciting promise of the Alzheimer’s Association/CDC Brain Health Initiative, the Maintain Your Brain, and the community demonstrations with African-American baby boomers. And it would extend the opportunity to develop innovative Alzheimer programs under AoA’s Demonstration Grant Program to all 50 states. And, perhaps most important, it will lay the groundwork to increase funding at NIH to pursue the many promising avenues in Alzheimer research. We have a strong foundation and the scientific community is well on its way to the answers needed to change a diagnosis of Alzheimer’s disease from a death sentence to one of hope for generations to come. With your continued support and leadership, we can create a world without Alzheimer’s.
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