Copy number variation associates with mortality in long‐lived individuals: a genome‐wide assessment. Issue 1 (8th October 2015)

• Record Type: Journal Article
• Authors: Nygaard, Marianne; Debrabant, Birgit; Tan, Qihua; Deelen, Joris; Andersen‐Ranberg, Karen; de Craen, Anton J.M.; Beekman, Marian; Jeune, Bernard; Slagboom, Pieternella E.; Christensen, Kaare; Christiansen, Lene
• Is Part Of: Aging cell. Volume 15:Issue 1(2016)
• Page Start: 49
• Page End: 55
• Publication Date: 2015-10-08
• Subjects: aging -- copy number variation -- deletions -- genetics -- long‐lived individuals -- mortality; Cells -- Aging -- Periodicals; 571.8783605
• DOI: 10.1111/acel.12407
• Languages: English
• ISSNs: 1474-9718

Abstract

Summary: Copy number variants (CNVs) represent a significant source of genetic variation in the human genome and have been implicated in numerous diseases and complex traits. To date, only a few studies have investigated the role of CNVs in human lifespan. To investigate the impact of CNVs on prospective mortality at the extreme end of life, where the genetic component of lifespan appears most profound, we analyzed genomewide CNV data in 603 Danish nonagenarians and centenarians (mean age 96.9 years, range 90.0–102.5 years). Replication was performed in 500 long‐lived individuals from the Leiden Longevity Study (mean age 93.2 years, range 88.9–103.4 years). First, we assessed the association between the CNV burden of each individual (the number of CNVs, the average CNV length, and the total CNV length) and mortality and found a significant increase in mortality per 10 kb increase in the average CNV length, both for all CNVs (hazard ratio (HR) = 1.024, P = 0.002) and for duplications (HR = 1.011, P = 0.005), as well as per 100 kb increase in the total length of deletions (HR = 1.009, P = 0.0005). Next, we assessed the relation between specific deletions and duplications and mortality. Although no genome–wide significant associations were discovered, we identified six deletions and one duplication that showed consistent association with mortality in both or either of the sexes across both study populations. These results indicate that the genome–wide CNV burden, specifically the average CNV length and the total CNV length, associates with higher mortality in long‐lived individuals.