in early heart disease
Yale School of Medicine researchers have identified a rare defect in a single gene that poses a substantial risk for metabolic syndrome and early heart disease, the leading cause of death worldwide.
The international study -- led by Dr. Arya Mani, assistant professor of cardiology, and Dr. Richard Lifton, chair of genetics at Yale -- identifies a new pathway implicated in heart disease. Even though the genetic mutation is very rare, these findings point to new approaches for improving this aspect of health.
"These findings indicate that altered activity of a well-known signaling pathway, Wnt, has large effects on multiple metabolic pathways that contribute to cardiovascular disease," says Mani.
Coronary artery disease (CAD) is commonly caused by metabolic syndrome, which includes a constellation of risk factors such as high levels of low-density lipoprotein (LDL) cholesterol and triglycerides, low levels of high-density lipoprotein (HDL) cholesterol, hypertension and diabetes.
This study, published in Science on March 2, was based on a large family of Iranian ancestry that had an extraordinary prevalence of early CAD. Among 58 blood relatives, 28 were diagnosed with early CAD at or before age 50 for the men, and 55 for the women. Twenty-three of the 28 died from CAD at young ages. In contrast, relatives without early CAD died at an average age of 81. The relatives with CAD had high LDL, high triglycerides, hypertension and diabetes, while their unaffected relatives did not. The relatives with CAD also were predisposed to osteoporosis, which the scientists say is particularly interesting given recent evidence of osteoporosis' association with CAD.
By comparing the inheritance of CAD to the inheritance of each chromosome segment in the pedigree, the team narrowed the location of the disease-causing gene to a short segment of chromosome 12. In this region, they found a single mutation in a gene called LRP6, which acts in the Wnt signaling pathway and which was previously known to be involved in development and in certain forms of cancer. The mutation changed one amino acid in the protein, which the team showed altered the activity of the protein encoded by LRP6.
"The reason for the observed association of multiple risk factors with one another has been a mystery," Lifton says. "Our findings have implicated the Wnt signaling pathway in the development of many risk factors and early CAD. We expect that studies of the Wnt signaling pathway in patients with early CAD and metabolic syndrome will provide new insight into the basic biology of disease causation and allow new approaches to disease prevention."
-- By Jacqueline Weaver
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IN MEMORIAM
B. Davie Napier: Former Yale trustee, professor and preacher
James B. Crowley: Specialist in the history of modern Japan
Paul Sevier Minear: A leading scholar of the New Testament
Kathryn Perrone: Assistant to the president
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