[Congressional Record Volume 170, Number 124 (Tuesday, July 30, 2024)]
[Senate]
[Pages S5567-S5568]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
Alzheimer's Disease
Ms. COLLINS. Mr. President, I rise today to support passage of two
bipartisan bills aimed at continuing the significant progress we are
making in treating and, one day, preventing and curing Alzheimer's
disease.
These bills--S. 133, the National Alzheimer Project Act, or NAPA, as
it is referred to, Reauthorization Act, and S. 134, the Alzheimer
Accountability and Investment Act would help coordinate the tools of
the Federal Government toward reaching these important goals.
And I would note, on the floor is the cochair of the Alzheimer's task
force in the Senate, Senator Markey, along with the other two
cosponsors we are fortunate to have, Senators Warner and Capito.
When I first joined the Senate in 1997, there really wasn't much of a
focus on Alzheimer's in Washington. It was often called senility and
was thought of not as a disease but just as part of growing old.
To increase public awareness of Alzheimer's disease, to advance
research, and to bring the disease to the forefront of the
Congressional agenda, I founded the Congressional Task Force on
Alzheimer's in 1999 here in the Senate.
A true milestone in focusing our efforts was the passage of the
Bipartisan National Alzheimer's Project Act that I coauthored with
then-Senator Evan Bayh in 2011.
Before we passed that legislation, which became known as NAPA, there
was no coordinated strategic plan to focus our efforts to defeat this
devastating disease and ensure that our resources were maximized and
leveraged.
[[Page S5568]]
NAPA tackled this problem by convening a panel of experts to create a
coordinated strategic plan to prevent and effectively treat Alzheimer's
disease by the year 2025, an ambitious goal, to be sure.
The expert council updates its plan annually. While the 2025 goal
regrettably will not be met, it was still important to set an ambitious
objective in order to spur research and to instill hope.
And, indeed, since then, researchers have made great strides in
understanding this complex disease. To put our progress in context, 20
years ago we knew of only four genes that were associated with
Alzheimer's disease. Now, researchers have identified more than 70
associated genetic areas, opening multiple new avenues for potential
prevention and treatment.
There is another point that helps put this into perspective. In the
early 2000s, the only sure way to know whether a person had Alzheimer's
was through an autopsy.
Since then, the National Institutes of Health Research has led to the
development of imaging techniques, biomarker tests, and data-driven
approaches to enable more precise and earlier diagnoses.
And, most recently, decades of NIH research have paved the way for
disease-modifying therapies targeting amyloid plaques' role in certain
dementias.
After directing this decade of progress, the National Alzheimer's
Project Act law is scheduled to expire soon. We must reauthorize the
law to ensure that research investments remain coordinated to maximize
their impact.
Toward that end, I introduced the NAPA Reauthorization Act with
Senator Warner, which would extend NAPA through 2035 and modernize the
legislation to reflect the strides that have been made to better
understand the disease, such as including a new focus on promoting
healthy aging, reducing risk factors, and supporting family caregivers.
The NAPA Reauthorization Act will allow the important work of the
expert panel to continue through 2035. Among its provisions, the bill
would reauthorize and expand the Advisory Council that assists annually
in the development and evaluation of the National Plan. It will also
ensure that underserved populations, including individuals with Down
syndrome who are at greatly increased risk for Alzheimer's as they age,
are included in this important work.
I have also introduced the Alzheimer's Accountability and Investment
Act with my colleague from Massachusetts who has been such a leader in
this area. It would continue through the year 2035 a requirement that
the NIH submit an annual budget directly to Congress, estimating the
funding necessary to fully implement NAPA's research goals.
Only two other areas of biomedical research--cancer and HIV/AIDS--
have been the subject of special budget development aimed at speeding
discovery. This ``bypass budget'' helps us understand what additional
funding is required to find better treatments, a means of prevention,
and ultimately a cure.
As cochair along with Senators Warner, Capito, and Markey of the
Congressional Task Force on Alzheimer's, I am committed to this effort
both on a personal level as well as professionally as a Senator
concerned about the impact on our families and our healthcare budgets.
On a personal level, I know just how devastating this disease is. I
just recently lost my brother-in-law to the disease. My father,
grandfather, and two of my uncles also succumbed to Alzheimer's. It is
truly a heartbreaking disease. It is heartbreaking when you talk to a
loved one and receive only a confused look in reply.
Alzheimer's disease is also one of the greatest health challenges of
our time. It is currently ranked as the seventh leading cause of death
in the United States, and nearly 7 million Americans are living with
the disease. It is also one of the most expensive diseases for society,
costing an estimated $360 billion last year alone.
Reauthorization of NAPA and the Alzheimer's Accountability and
Investment Act would ensure our country is maintaining momentum in our
fight against Alzheimer's, just as our investments in research are
beginning to translate into promising new treatments.
Both laws have no mandatory spending effects, according to the
Congressional Budget Office. Both bills are cosponsored by nearly half
the Members of this Senate. Both bills have wide-ranging support from
national stakeholders, including the Alzheimer's Association, Us
Against Alzheimer's, the National Down Syndrome Society, and the
National Down Syndrome Congress. And both bills were reported out of
the Senate HELP Committee with broad bipartisan support last summer.
In order to change the trajectory of this disease that otherwise is
projected to claim the minds of 13.8 million seniors and nearly surpass
$1 trillion in annual costs by 2050, Congress has a responsibility to
pursue effective public policy.
Ultimately, I think we are going to discover that this is a
multifactorial disease, and that is why all of the research that is
going on is so critical to finding effective treatments, a means of
prevention, and, one day, a cure. And that is the purpose of these two
bills.
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