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ABOUT
As part of the Sticht Center for Healthy Aging and Alzheimer's Disease Prevention at Wake Forest School of Medicine, the Macauley Lab focuses on the role of metabolic dysfunction in Alzheimer's disease. According to the Alzheimer’s Association, 1 in 8 Americans over the age of 65 has Alzheimer’s disease, nearly 1 in 2 has AD by the age of 85, and AD accounted for an estimated $183 billion in health care costs to Americans in 2011. Similarly, type-2-diabetes is metabolic disorder that affects approximately 346 million people worldwide, with an estimated 3.4 million dying from diabetes in 2004 alone. Since recent studies demonstrate that patients with type-2-diabetes have an increased risk for developing AD, the goal of our research is to understand how metabolic disruption affects Alzheimer's disease and whether shared mechanisms between type-2-diabetes and Alzheimer's disease can be targeted therapeutically.
LAB MEMBERS

Shannon L. Macauley, PhD
Principal Investigator
Dr. Macauley's CV
Associate Professor, Physiology & Pharmacology, Wake Forest School of Medicine
Education/Training: BA, Middlebury College; PhD, Washington University School of Medicine; Postdoctoral Fellowship, Washington University School of Medicine
Shannon L. Macauley earned her BA in Biology and Psychology from Middlebury College (Middlebury, VT) and worked in translational neuroscience at Genzyme Corporation (Boston, MA) prior to graduate school. Dr. Macauley completed her Ph.D. in Neuroscience at Washington University (St. Louis, MO) with Dr. Mark Sands and her postdoctoral training in Alzheimer’s disease in the laboratory of Dr. David Holtzman at Washington University (St. Louis, MO). Dr. Macauley joined the Sticht Center for Healthy Aging and Alzheimer’s Prevention at Wake Forest Baptist Health as an Assistant Professor in August 2017. The goal of Dr. Macauley’s research is to understand central nervous system (CNS) disease and how mechanistic drivers of neuronal dysfunction, such as metabolic dysfunction, sleep impairment, vascular damage, and neuroinflammation, can be targeted therapeutically, To date, her work has focused on two main areas: first, the study of mechanisms underlying neurodegenerative disease and the development of CNS therapeutics as it relates to lysosomal storage diseases. Second, the exploration of the link between type 2 diabetes and Alzheimer’s disease, how metabolic challenges affect normal brain function in health and disease, and how metabolic dysfunction can be targeted as a therapeutic approach for treatment of Alzheimer’s disease and diabetes.
Current Members

Andy
Snipes
Research Assistant/
Lab Manager Extraordinaire

Sarah
Kaye
4th year PhD student
Neuroscience

Nick
Constantino
2nd year PhD student
Neuroscience

Riley
Irmen, MS
Incoming PhD student
Neuroscience

Stephen
Gironda, MS
3rd year PhD student
Neuroscience
F31 Fellow

Zhen
Lin, MS
2nd year PhD student
BME

Ryan
Pettit-Mee, MS, PhD
Postdoctoral Fellow
Past Members

Dave
Rubinow, MS
Masters Student
Neuroscience
Current: Kallyope Inc.

Khadijah
Winkey Lewis, MS
Masters Student
Neuroscience
Current: Clinical Coordinator ADRC

Charlotte Hollingsworth
Lab Manager

Lily
Deitelzweig
High School Student intern
Current: Undergrad UT-Austin

Caitlin
Carroll, PhD
Neuroscience PhD Student
F31 awardee
Current: T32 PostDoc
with Dr. Ruth Benca, Wake Forest

Matthew
Parker
WSSU, ENGAGED Scholar
Current: Master's Student

John
Grizzanti, PhD
Postdoctoral Fellow
T32 fellow

Stephen
Day, PhD
Postdoctoral Fellow
T32 fellow
Current: Research Track,
Assistant Prof, SUNY Binghamtom

Sami
Vincent
Wake Forest, Honors Thesis
Current: Masters in Bioethics &
Wake Forest Law Student

Morgan
Pait, PhD
IPP PhD Student
F31 Awardee