Article Synopsis

  • The study analyzed data from 1 million parental lifespans to validate previous findings and discover new genetic associations related to lifespan, focusing on specific loci.
  • It confirmed that certain genes linked to lifespan variation are notably expressed in fetal brain cells and the adult dorsolateral prefrontal cortex, as well as in pathways related to lipid proteins, vesicle transport, and synaptic function.
  • The research found that genetic variants linked to dementia, cardiovascular disease, and lung cancer significantly contribute to lifespan differences, with a polygenic score indicating a mean lifespan variation of about five years among different genetic profiles.

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Article Abstract

Unlabelled: We use a genome-wide association of 1 million parental lifespans of genotyped subjects and data on mortality risk factors to validate previously unreplicated findings near , , , , , and 13q21.31, and identify and replicate novel findings near , , and . We also validate previous findings near 5q33.3/ and , whilst finding contradictory evidence at other loci. Gene set and cell-specific analyses show that expression in foetal brain cells and adult dorsolateral prefrontal cortex is enriched for lifespan variation, as are gene pathways involving lipid proteins and homeostasis, vesicle-mediated transport, and synaptic function. Individual genetic variants that increase dementia, cardiovascular disease, and lung cancer - but not other cancers - explain the most variance. Resulting polygenic scores show a mean lifespan difference of around five years of life across the deciles.

Editorial Note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333444PMC
http://dx.doi.org/10.7554/eLife.39856DOI Listing

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