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2022 Annual Report

This is the 2022 Annual Report for Van Andel Institute.

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Department of<br />

Neurodegenerative<br />

Science<br />

Worldwide, between 7 million and 10 million people<br />

have Parkinson’s disease, a progressive neurological<br />

condition marked by tremor, rigidity and the gradual<br />

loss of voluntary movement, along with a host of other<br />

symptoms, such as loss of sense of smell, cognitive<br />

issues, constipation, trouble sleeping and pain.<br />

Additionally, more than 30 million people have Alzheimer’s<br />

disease and related dementias.<br />

Currently, there are no cures and no effective ways<br />

to slow or stop disease progression in Parkinson’s<br />

and Alzheimer’s. Our scientists aim to change that<br />

by investigating the complex factors that give rise to<br />

neurodegenerative and psychiatric disorders, from<br />

genetics and epigenetics to aging, inflammation, and the<br />

structure of the brain itself — even the role of the gut and<br />

the immune system.<br />

With the exception of a small number of people whose<br />

Parkinson’s is directly linked to family genetic inheritance,<br />

most cases are sporadic, meaning they have no known<br />

cause. A growing body of evidence suggests that genetic<br />

and epigenetic predisposition coupled with environmental<br />

factors, such as exposure to certain inflammatory<br />

agents, may trigger the disease, which progresses for<br />

years or even decades before the onset of its signature<br />

movement-related symptoms.<br />

As the global population ages, the number of people<br />

with Parkinson’s or Alzheimer’s is expected to<br />

significantly increase in the coming years, underscoring<br />

the importance and urgency of developing improved<br />

treatment strategies. By leveraging discoveries made<br />

in VAI’s labs and collaborating with researchers around<br />

the world, our scientists are working to translate<br />

breakthroughs into life-changing new treatments.<br />

Darren Moore, Ph.D.<br />

Chair and Professor<br />

Dr. Darren Moore seeks new<br />

diagnostic and treatment<br />

approaches for Parkinson’s<br />

by investigating the inherited<br />

form of the disease, which<br />

comprises 5% to 10% of cases. He aims to translate the<br />

understanding of these genetic mutations into better<br />

treatments and new diagnostic tools for Parkinson’s,<br />

both inherited and non-inherited. Discoveries from<br />

Dr. Moore’s lab routinely elucidate the faulty molecular<br />

interactions that transform healthy, functioning neurons<br />

into diseased ones.<br />

José Brás, Ph.D.<br />

Associate Professor<br />

Dr. José Brás investigates how<br />

variations in our genes impact<br />

the onset and progression of<br />

neurodegenerative diseases such<br />

as Parkinson’s, Alzheimer’s and<br />

dementia with Lewy bodies. Using<br />

cutting-edge technologies and bioinformatic approaches,<br />

he has identified new genetic mutations that impact<br />

disease risk.<br />

Lena Brundin, M.D., Ph.D.<br />

Professor<br />

As a psychiatrist and a scientist,<br />

Dr. Lena Brundin seeks ways to<br />

diagnose and treat depression<br />

and suicidality by studying<br />

inflammation of the nervous<br />

system. Her findings may lead to earlier interventions<br />

for depressive patients and to the development of a new<br />

class of antidepressants that targets the immune system.<br />

She also investigates how inflammatory mechanisms can<br />

damage nerve cells in Parkinson’s disease.<br />

Hong-yuan Chu, Ph.D.<br />

Assistant Professor<br />

Dr. Hong-yuan Chu investigates<br />

how and why dopamineproducing<br />

cells die off in<br />

Parkinson’s, a process that<br />

underlies many of the disease’s<br />

hallmark symptoms. He plans to leverage this new<br />

knowledge to develop new, more precise ways to slow<br />

or stop disease progression.<br />

Gerhard Coetzee, Ph.D.<br />

Professor<br />

Dr. Gerhard Coetzee searches<br />

the human genome for<br />

minuscule changes that<br />

contribute to the onset,<br />

progression and drug resistance<br />

of many diseases, including cancer and Parkinson’s.<br />

His team deploys genome sequencing technologies<br />

and high-powered computational arrays to tease out<br />

patterns and interactions of markers and treatment<br />

targets from among the human genome’s more than<br />

three billion DNA base pairs.<br />

Rita Guerreiro, Ph.D.<br />

Associate Professor<br />

Dr. Rita Guerreiro parses<br />

the genetic variations that<br />

contribute to neurodegenerative<br />

diseases such as Parkinson’s,<br />

Alzheimer’s, dementia with<br />

Lewy bodies and frontotemporal dementia. Her<br />

research has led to new insights into the genetic<br />

contributors to these diseases, which currently have<br />

no cure and no treatments that slow progression.<br />

RESEARCH<br />

1923

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