Dr. Cynthia Bulik of UNC leads multinational anorexia genetics project

The Anorexia Nervosa Genetics Initiative (ANGI) will collect DNA samples from more than 8,000 people with anorexia nervosa (AN) and those without an eating disorder in an effort to detect genes that contribute to this potentially life-threatening illness.

Dr. Cynthia Bulik of UNC leads multinational anorexia genetics project click to enlarge ANGI team (L-R), Chris Hilliard, Laura M. Thornton, PhD, Cynthia M. Bulik, PhD, Lauren Metzger, MSW, LCSWA, and Jessica Baker, PhD

Media contacts:
Tom Hughes, 919-966-6047, Thomas.Hughes@unchealth.unc.edu , Stephanie Mahin, 919-951-4758,


Thursday, March 27, 2014
ANGI graphic
CHAPEL HILL, N.C. – University of North Carolina School of Medicine researcher Cynthia Bulik, PhD, FAED, Distinguished Professor of Eating Disorders, is the lead investigator of the largest and most rigorous genetic initiative in eating disorders ever undertaken.

The Anorexia Nervosa Genetics Initiative (ANGI) will collect clinical information and blood samples from more than 8,000 females and males who have had anorexia nervosa at any point in their lives and those without an eating disorder in an effort to detect genes that contribute to this potentially life-threatening illness.

“Genome-wide association studies have been enormously successful in identifying genes that contribute to a range of medical and psychiatric conditions. These discoveries have opened up new avenues of understanding of both cause and cure,” said Bulik. “Once we identify genetic associations in ANGI, we will use the information to develop better strategies to detect, treat, and prevent anorexia nervosa. If our project is successful, it will change the life course of millions of individuals with anorexia and their families.”

Each person's complete set of DNA, or genome, will be purified from a blood sample, placed on tiny chips and scanned on automated laboratory machines. The machines quickly survey each participant's genome for strategically selected markers of genetic variation, which are called single nucleotide polymorphisms, or SNPs.  If certain genetic variations are found to be significantly more frequent in people with anorexia compared with people without anorexia, the variations are said to be "associated" with the disease. The associated genetic variations can serve as powerful pointers to the region of the human genome where the disease-causing problem resides.

Cynthia Bulik, PhD, director of the UNC Center of Excellence for Eating Disorders, is the lead principal investigator for ANGI, which also includes researchers from the Karolinska Institutet in Stockholm, Sweden, the Queensland Institute of Medical Research in Brisbane, Australia, and Aarhus University in Aarhus, Denmark.

Joining Bulik at UNC are Patrick Sullivan, MD, a professor in the departments of genetics and psychiatry and director of UNC’s Center for Psychiatric Genomics and Laura Thornton, PhD, associate professor in the department of psychiatry.

ANGI team
ANGI team (L-R), Chris Hilliard, Laura M. Thornton, PhD, Cynthia M. Bulik, PhD, Lauren Metzger, MSW, LCSWA, and Jessica Baker, PhD

ANGI was established in 2013 by the Klarman Family Foundation — a private foundation based in Boston, Mass.

ANGI investigators from the Karolinska Institutet are Mikael Landén, MD, PhD; Andreas Birgegård, PhD; Claes Norring, PhD; and Paul Lichtenstein, PhD.

ANGI investigators from the Queensland Institute of Medical Research are Nicholas Martin, PhD; Grant Montgomery, PhD; and Tracey Wade, PhD (Flinders University).

The ANGI investigator at Aarhus University is Preben Bo Mortensen, MD, PhD.

Anyone interested in participating in ANGI, or seeking additional information can visit www.unceatingdisorders.org/angi or the ANGI Facebook page (https://www.facebook.com/angi.unc), or call 919-966-3065.





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