Mind and Body
Living Longer Linked to Gene VariationsEnvironment and family history are factors in healthy aging, but genetic “variants” play an important role in living to be very old. ![]() In a study reported in the journal Science, researchers say that genetic variants can predict exceptional longevity in humans with 77 percent accuracy. The study was funded by the National Institute on Aging (NIA) and the National Heart, Lung, and Blood Institute (NHLBI). The series of genetic variants can suggest whether or not a person will live to 100 years of age. They say this is a breakthrough in understanding the role of genes in determining human lifespan. Dr. Robert Marion, at Montefiore Medical Center in the Bronx, New York, says experts probably could have predicted life span with even greater accuracy had they asked people how long their parents had lived. But, this study has paved the way for advances in science to also help determine lifespan. He says that eventually, if you can identify early in life those individuals who have a predisposition to die young, you might actually be able to approach their care to help them to live longer. "One of the big benefits of the new genomic medicine is that we're going to be able to do personalized medicine, and this is one way to approach that," explains Dr. Marion. Who Lives to Be 100?Right now, people in industrialized nations live an average of 80 to 85 years. About one in 6,000 people in this group achieves centenarian status. Supercentenarians - those who live to 110 or beyond - occur at a rate of only about one in 7 million. Senior study author Dr. Thomas Perls, says, "We have about 80,000 centenarians alive at any time. The oldest person right now is about 116, in Japan." And, he notes, the majority of people living to 100 and beyond are women. "Centenarians are indeed a model of aging," says Dr. Perls, at Boston University School of Medicine. "A lot of people would not want to live to 100 because they think they would have every age-related disease under the sun and are on death's doorstep, but this isn't true. We have noted in previous work that 90 percent of centenarians are disability-free at an average age of 93,” he explains. “They compress their diseases towards the very end of their lives." Genes an Obvious Area of StudyGiven that long life spans tend to run in families, researchers have long suspected that genetics play a big role in this trait. In this study, the researchers conducted a genome-wide association study with two groups - in 1,055 centenarians and 1,267 non-centenarians participating in the New England Centenarian Study, founded and directed by Dr. Perls. The team identified 19 genetic clusters or "genetic signatures" of exceptional longevity that described 90 percent of the centenarians studied. The different signatures correlated with differences in the prevalence and age-of-onset of diseases such as dementia and hypertension, and may help identify key subgroups of healthy aging, says Dr. Perls. Notably, the team found that 45 percent of the oldest centenarians - those 110 years and older - had a genetic signature with the highest proportion of longevity-associated genetic variants. "I think a lot of study needs to be done as to what guidance physicians and health care providers can give to individuals as to what they do with this information," says Dr. Perls said. In particular, there could be implications from an insurance point of view. Always consult your physician or other healthcare provider for more information. |
September 2010Understanding Genes in MedicineGenetics is the study of the patterns of inheritance - how traits and characteristics are passed from parents to their children. Genes are formed from segments of DNA (deoxyribonucleic acid), the molecule that encodes genetic information in the cells. DNA controls the structure, function, and behavior of cells and can create exact copies of itself. Humans have an estimated 70,000 different genes that contain specific genetic information. These genes are located on chromosomes (stick-like structures in the nucleus of cells). Every cell contains 46 chromosomes grouped in 23 pairs. Medical genetics is the branch of medicine concerned with how hereditary and genetic factors play a role in causing a disease, birth defect, or inherited susceptibility to a health problem. The Human Genome Project began in 1990 with the goal of mapping the location of all of the genes on the chromosomes. This huge achievement has given scientists the building blocks to determine how diseases are caused, how to possibly treat them and, ultimately, prevent them. Research in medical genetics has given us information about the genetic mechanisms that can result in disease. Common examples of genetic conditions have been included, but are not meant to be comprehensive. Genetic tests use blood and other tissue to identify genetic disorders. The National Institutes of Health (NIH) says that about 900 such tests are available. Genetic testing is commonly used for:
There are many reasons for being tested or not being tested. For many people, knowing whether or not a disease can be prevented or treated is important. Always consult your physician or other healthcare provider for more information. Online Resources(Our Organization is not responsible for the content of Internet sites.) American Federation for Aging Research Human Genome Project Information National Heart, Lung, and Blood Institute (NHLBI) National Institutes of Health (NIH) Science - Genetic Signatures of Exceptional Longevity in Humans |
Disclaimer - This content is reviewed periodically and is subject to change as new health information becomes available. The information provided is intended to be informative and educational and is not a replacement for professional evaluation, advice, diagnosis or treatment by a healthcare professional. © 2009 Staywell Custom Communications.




