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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

Research output: Contribution to journalArticle

  • Felix R Day
  • et al.
  • John R B Perry
Original languageEnglish
Pages (from-to)834-841
Number of pages11
JournalNature Genetics
Volume49
Issue number6
Early online date24 Apr 2017
DOIs
DateAccepted/In press - 17 Mar 2017
DateE-pub ahead of print - 24 Apr 2017
DatePublished (current) - Jun 2017

Abstract

The timing of puberty is a highly polygenic childhood trait that is epidemiologically associated with various adult diseases. Using 1000-Genome imputed genotype data in up to ~370,000 women, we identify 389 independent signals (P<5×10-8) for age at menarche, a notable milestone in female pubertal development. In Icelandic data from deCODE, these signals explain ~7.4% of the population variance in age at menarche, corresponding to ~25% of the estimated heritability. We implicate ~250 genes via coding variation or associated expression, demonstrating significant enrichment in neural tissues. Rare variants near imprinted genes MKRN3 and DLK1 were identified, exhibiting large effects only when paternally inherited. Mendelian randomization analyses indicate causal inverse associations, independent of BMI, between puberty timing and risks for breast and endometrial cancers in women, and prostate cancer in men. In aggregate, our findings reveal new complexity in the genetic regulation of puberty timing and support causal links with cancer susceptibility.

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    Rights statement: This is the author accepted manuscript (AAM). The final published version (version of record) is available online via Nature at http://www.nature.com/ng/journal/vaop/ncurrent/full/ng.3841.html. Please refer to any applicable terms of use of the publisher.

    Accepted author manuscript, 585 KB, PDF document

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