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Genetic Finding May Provide a Test for Longevity


 
  
Scientists studying the genomes of centenarians found a set of genetic variants that predicts extreme longevity with 77 percent accuracy.


Date:

New York Times, By NICHOLAS WADE, July 1, 2010

When it becomes affordable to have one's genome sequenced, perhaps in a few years, a longevity test, though not a foolproof one, may be feasible, if a new claim holds up. Scientists studying the genomes of centenarians in New England say they have identified a set of genetic variants that predicts extreme longevity with 77 percent accuracy.

The centenarians had just as many disease-associated variants as shorter-lived mortals, so their special inheritance must be genes that protect against disease, said the authors of the study, a team led by Paola Sebastiani and Thomas T. Perls of Boston University. Their report appears in Thursday's issue of Science.

The finding, if confirmed, would complicate proposals for predicting someone's liability to disease based on disease-causing variants in the person's genome, since much would depend on whether or not an individual possessed protective genes as well.

Read more in New York Times.

Abstract from

Genetic Signatures of Exceptional Longevity in Humans, Science DOI: 10.1126/science.1190532

Healthy aging is thought to reflect the combined influence of environmental factors (lifestyle choices) and genetic factors. To explore the genetic contribution, we undertook a genome-wide association study of exceptional longevity (EL) in 1055 centenarians and 1267 controls. Using these data, we built a genetic model that includes 150 single-nucleotide polymorphisms (SNPs) and found that it could predict EL with 77% accuracy in an independent set of centenarians and controls. Further in silico analysis revealed that 90% of centenarians can be grouped into 19 clusters characterized by different combinations of SNP genotypes - or genetic signatures - of varying predictive value. The different signatures, which attest to the genetic complexity of EL, correlated with differences in the prevalence and age of onset of age-associated diseases (e.g., dementia, hypertension, and cardiovascular disease) and may help dissect this complex phenotype into subphenotypes of healthy aging.

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