Mosaic loss of Y chromosome and the association to mortality in Danish men aged 56–100 years

Mosaic loss of the Y chromosome (mLOY) is a common somatic mutation in the blood of elderly men and several studies have found mLOY in blood cells to be associated with an increased risk of various diseases and mortality. However, most of these studies have focused on middle-aged and older adults, meaning that mLOY in extremely old individuals like centenarians is understudied. To explore mLOY across a wider age range compared to earlier studies and to specifically focus on centenarians, mLOY was estimated in 917 Danish men aged 56-100 years. We found that the percentage of men with LOY increased with age until age 85, after which it plateaued at around 40 %. Consistently, a longitudinal comparison of mLOY revealed that mLOY predominantly increased with age, although inter-individual variation was seen. Using a twin sub-sample, the broad-sense heritability of mLOY was estimated at 72 %, indicating a substantial genetic influence. Supporting previous findings, mLOY was found to associate with increased mortality across all study participants and in men younger than 80 years. In centenarians, however, a higher level of mLOY associated with better survival, most likely due to selection, although confirmation of our findings in larger studies is needed.

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Publication Details

Journal
Mechanisms of Ageing and Development
Published
2024-09-16
DOI
https://doi.org/10.1016/j.mad.2024.111979
Citations
9
Primary Topic
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Type
article
Field-Weighted Citation Impact
4.95

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article

Mosaic loss of Y chromosome and the association to mortality in Danish men aged 56–100 years

Jacob Krabbe Pedersen, Dominika Marzena Hozakowska-Roszkowska, Karen Andersen‐Ranberg, Jonas Mengel‐From et al.
9 citations
Mechanisms of Ageing and Development
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
4.95
article

Mosaic loss of Y chromosome and the association to mortality in Danish men aged 56–100 years

Jacob Krabbe Pedersen, Dominika Marzena Hozakowska-Roszkowska, Karen Andersen‐Ranberg, Jonas Mengel‐From, Kaare Christensen, Marianne Nygaard, Jacob Hjelmborg, Teodora K Hristozova, Bernard Jeune, Richard Röttger
article en
9 citations

Abstract

Mosaic loss of the Y chromosome (mLOY) is a common somatic mutation in the blood of elderly men and several studies have found mLOY in blood cells to be associated with an increased risk of various diseases and mortality. However, most of these studies have focused on middle-aged and older adults, meaning that mLOY in extremely old individuals like centenarians is understudied. To explore mLOY across a wider age range compared to earlier studies and to specifically focus on centenarians, mLOY was estimated in 917 Danish men aged 56-100 years. We found that the percentage of men with LOY increased with age until age 85, after which it plateaued at around 40 %. Consistently, a longitudinal comparison of mLOY revealed that mLOY predominantly increased with age, although inter-individual variation was seen. Using a twin sub-sample, the broad-sense heritability of mLOY was estimated at 72 %, indicating a substantial genetic influence. Supporting previous findings, mLOY was found to associate with increased mortality across all study participants and in men younger than 80 years. In centenarians, however, a higher level of mLOY associated with better survival, most likely due to selection, although confirmation of our findings in larger studies is needed.

Mechanisms of Ageing and DevelopmentVol. 222
University of Southern Denmark (DK), Odense University Hospital (DK)
European Commission, National Research Foundation, Danmarks Grundforskningsfond, AXA Research Fund, Science for Life Laboratory, National Institutes of Health, Forsknings- og Innovationsstyrelsen, Danish Agency for Science and Higher Education, European Regional Development Fund, Interreg
Good health and well-being
Openalex Percentile: Top 5%
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
4.95
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