Understanding the genetic complexity of puberty timing across the allele frequency spectrum
Pubertal timing varies considerably and is associated with later health outcomes. We performed multi-ancestry genetic analyses on ~800,000 women, identifying 1,080 signals for age at menarche. Collectively, these explained 11% of trait variance in an independent sample. Women at the top and bottom 1...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
July 2024
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| In: |
Nature genetics
Year: 2024, Volume: 56, Issue: 7, Pages: 1397-1411 |
| ISSN: | 1546-1718 |
| DOI: | 10.1038/s41588-024-01798-4 |
| Online Access: | Verlag, kostenfrei, Volltext: https://doi.org/10.1038/s41588-024-01798-4 Verlag, kostenfrei, Volltext: https://www.nature.com/articles/s41588-024-01798-4 
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| Author Notes: | Katherine A. Kentistou, Lena R. Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Andrea Messina, Robin G. Walters, Xiaoxi Liu, Alexander S. Busch, Hannes Helgason, Deborah J. Thompson, Federico Santoni, Konstantin M. Petricek, Yassine Zouaghi, Isabel Huang-Doran, Daniel F. Gudbjartsson, Eirik Bratland, Kuang Lin, Eugene J. Gardner, Yajie Zhao, Raina Y. Jia, Chikashi Terao, Marjorie J. Riggan, Hermann Brenner, Frederico Canzian, Jenny Chang-Claude, Ute Haman [und 193 weitere] ; the Lifelines Cohort Study, the Danish Blood Donor Study, the Ovarian Cancer Association Consortium, the Breast Cancer Association Consortium, the Biobank Japan Project, the China Kadoorie Biobank Collaborative Group |
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| 245 | 1 | 0 | |a Understanding the genetic complexity of puberty timing across the allele frequency spectrum |c Katherine A. Kentistou, Lena R. Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Andrea Messina, Robin G. Walters, Xiaoxi Liu, Alexander S. Busch, Hannes Helgason, Deborah J. Thompson, Federico Santoni, Konstantin M. Petricek, Yassine Zouaghi, Isabel Huang-Doran, Daniel F. Gudbjartsson, Eirik Bratland, Kuang Lin, Eugene J. Gardner, Yajie Zhao, Raina Y. Jia, Chikashi Terao, Marjorie J. Riggan, Hermann Brenner, Frederico Canzian, Jenny Chang-Claude, Ute Haman [und 193 weitere] ; the Lifelines Cohort Study, the Danish Blood Donor Study, the Ovarian Cancer Association Consortium, the Breast Cancer Association Consortium, the Biobank Japan Project, the China Kadoorie Biobank Collaborative Group |
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| 500 | |a Online verfügbar: 01. Juli 2024 | ||
| 500 | |a Gesehen am 02.05.2025 | ||
| 520 | |a Pubertal timing varies considerably and is associated with later health outcomes. We performed multi-ancestry genetic analyses on ~800,000 women, identifying 1,080 signals for age at menarche. Collectively, these explained 11% of trait variance in an independent sample. Women at the top and bottom 1% of polygenic risk exhibited ~11 and ~14-fold higher risks of delayed and precocious puberty, respectively. We identified several genes harboring rare loss-of-function variants in ~200,000 women, including variants in ZNF483, which abolished the impact of polygenic risk. Variant-to-gene mapping approaches and mouse gonadotropin-releasing hormone neuron RNA sequencing implicated 665 genes, including an uncharacterized G-protein-coupled receptor, GPR83, which amplified the signaling of MC3R, a key nutritional sensor. Shared signals with menopause timing at genes involved in DNA damage response suggest that the ovarian reserve might signal centrally to trigger puberty. We also highlight body size-dependent and independent mechanisms that potentially link reproductive timing to later life disease. | ||
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| 787 | 0 | 8 | |i Errata |a Kentistou, Katherine A. |t Publisher correction: understanding the genetic complexity of puberty timing across the allele frequency spectrum |d 2024 |w (DE-627)1924278073 |
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