Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Ben Hollis
  • Felix R. Day
  • Alexander S. Busch
  • Deborah J. Thompson
  • Ana Luiza G. Soares
  • Paul R.H.J. Timmers
  • Alex Kwong
  • Doug F. Easton
  • Peter K. Joshi
  • Nicholas J. Timpson
  • Rosalind A. Eeles
  • Brian E. Henderson
  • Christopher A. Haiman
  • Zsofia Kote-Jarai
  • Fredrick R. Schumacher
  • Ali Amin Al Olama
  • Sara Benlloch
  • Kenneth Muir
  • Sonja I. Berndt
  • David V. Conti
  • Fredrik Wiklund
  • Stephen Chanock
  • Susan Gapstur
  • Victoria L. Stevens
  • Catherine M. Tangen
  • Jyotsna Batra
  • Judith Clements
  • Henrik Gronberg
  • Nora Pashayan
  • Johanna Schleutker
  • Demetrius Albanes
  • Alicja Wolk
  • Catharine West
  • Lorelei Mucci
  • Géraldine Cancel-Tassin
  • Stella Koutros
  • Karina Dalsgaard Sorensen
  • Eli Marie Grindedal
  • David E. Neal
  • Freddie C. Hamdy
  • Jenny L. Donovan
  • Ruth C. Travis
  • Robert J. Hamilton
  • Sue Ann Ingles
  • Barry S. Rosenstein
  • Yong Jie Lu
  • Graham G. Giles
  • Adam S. Kibel
  • Ana Vega
  • Nordestgaard, Børge
  • Australian Prostate Cancer BioResource (APCB)
  • The Practical Consortium
  • 23andMe Research Team

The timing of puberty is highly variable and is associated with long-term health outcomes. To date, understanding of the genetic control of puberty timing is based largely on studies in women. Here, we report a multi-trait genome-wide association study for male puberty timing with an effective sample size of 205,354 men. We find moderately strong genomic correlation in puberty timing between sexes (rg = 0.68) and identify 76 independent signals for male puberty timing. Implicated mechanisms include an unexpected link between puberty timing and natural hair colour, possibly reflecting common effects of pituitary hormones on puberty and pigmentation. Earlier male puberty timing is genetically correlated with several adverse health outcomes and Mendelian randomization analyses show a genetic association between male puberty timing and shorter lifespan. These findings highlight the relationships between puberty timing and health outcomes, and demonstrate the value of genetic studies of puberty timing in both sexes.

OriginalsprogEngelsk
Artikelnummer1536
TidsskriftNature Communications
Vol/bind11
Udgave nummer1
ISSN2041-1723
DOI
StatusUdgivet - 2020

Antal downloads er baseret på statistik fra Google Scholar og www.ku.dk


Ingen data tilgængelig

ID: 249105595