Mitochondrial mutation linked to blood pressure and cholesterol problems

Researchers at Yale and Syracuse Universities found the first direct evidence for a mutation in mitochondrial DNA that
directly affects blood pressure and cholesterol levels.


It has long been known that several metabolic traits including high cholesterol and hypertension cluster in individuals more
frequently than by chance, but the underlying causes were unknown. This study, published early in Science Express on line,
suggests that altered mitochondria may account for the clustering as well as the disorders.



"Looking further, this finding raises the possibility that all features of the metabolic syndrome may be attributable to
altered mitochondrial function," said Richard T. Lifton, Sterling Professor and Chair of Genetics at Yale and research team
leader.


Metabolic syndrome is an emerging problem in industrial societies and. epidemic in the United States. The symptoms include
high blood pressure, cholesterol and triglycerides, insulin resistance, obesity, and low HDL. There is independent evidence
that altered mitochondrial function plays a role in insulin resistance and high triglyceride level, and the current finding
indicates that these other components of metabolic syndrome may also linked to mitochondrial disfunction.



The clear correlation of mutation and disorder in this study was made possible by the evaluation of 142 people in four
generations of an affected family. Although family members with each disorder - hypertension, hypercholesterolemia and
hypermagnesemia - have the same mitochondrial mutation, the presence of the mutation does not produce all of the symptoms in
each individual.


While this study focuses on a rare mutation in mitochondria that provides a clear link to specific disorders, mitochondrial
function is known to decline with age in normal people and may be contributing to these common traits in the general
population.


Other researchers included Frederick H. Wilson, Ali Hariri, Anita Farhi, Hongyu Zhao, Kitt Falk Petersen, Hakan R. Toka,
Carlo Nelson-Williams, Michael Kashgarian, and Gerald I. Schulman at Yale, and Khalid M. Raja and Steven J. Scheinman at
Syracuse University. Grants from the National Institutes of Health the Howard Hughes Medical Institute and the American Heart
Association supported this research.


Citation: Science Express (October 21, 2004).


Contact: Janet Rettig Emanuel

janet.emanuelyale

203-432-2157

Yale University