Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility
Spontaneous dizygotic (DZ) twinning occurs in 1%–4% of women, with familial clustering and unknown physiological pathways and genetic origin. DZ twinning might index increased fertility and has distinct health implications for mother and child. We performed a GWAS in 1,980 mothers of spontaneous DZ...
Published in: | The American Journal of Human Genetics |
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Online Access: | https://kclpure.kcl.ac.uk/portal/en/publications/identification-of-common-genetic-variants-influencing-spontaneous-dizygotic-twinning-and-female-fertility(59c0be68-bba9-45ce-ad2e-090541b38684).html https://doi.org/10.1016/j.ajhg.2016.03.008 |
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ftkingscollondon:oai:pure.atira.dk:publications/59c0be68-bba9-45ce-ad2e-090541b38684 2023-05-15T16:48:33+02:00 Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility Mbarek, Hamdi Steinberg, Stacy Nyholt, Dale R. Gordon, Scott D. Miller, Michael B. McRae, Allan F. Hottenga, Jouke Jan Day, Felix R. Willemsen, Gonneke de Geus, Eco J. Davies, Gareth E. Martin, Hilary C. Penninx, Brenda W. Jansen, Rick McAloney, Kerrie Vink, Jacqueline M. Kaprio, Jaakko Plomin, Robert Spector, Tim D. Magnusson, Patrik K. Reversade, Bruno Harris, R. Alan Aagaard, Kjersti Kristjansson, Ragnar P. Olafsson, Isleifur Eyjolfsson, Gudmundur Ingi Sigurdardottir, Olof Iacono, William G. Lambalk, Cornelis B. Montgomery, Grant W. McGue, Matt Ong, Ken K. Perry, John R.B. Martin, Nicholas G. Stefánsson, Hreinn Stefánsson, Kari Boomsma, Dorret I. 2016-05 https://kclpure.kcl.ac.uk/portal/en/publications/identification-of-common-genetic-variants-influencing-spontaneous-dizygotic-twinning-and-female-fertility(59c0be68-bba9-45ce-ad2e-090541b38684).html https://doi.org/10.1016/j.ajhg.2016.03.008 eng eng info:eu-repo/semantics/closedAccess Mbarek , H , Steinberg , S , Nyholt , DR , Gordon , SD , Miller , MB , McRae , AF , Hottenga , JJ , Day , FR , Willemsen , G , de Geus , EJ , Davies , GE , Martin , HC , Penninx , BW , Jansen , R , McAloney , K , Vink , JM , Kaprio , J , Plomin , R , Spector , T D , Magnusson , PK , Reversade , B , Harris , R A , Aagaard , K , Kristjansson , RP , Olafsson , I , Eyjolfsson , GI , Sigurdardottir , O , Iacono , WG , Lambalk , CB , Montgomery , GW , McGue , M , Ong , KK , Perry , JR B , Martin , NG , Stefánsson , H , Stefánsson , K & Boomsma , DI 2016 , ' Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility ' , American Journal of Human Genetics , vol. 98 , no. 5 , pp. 898-908 . https://doi.org/10.1016/j.ajhg.2016.03.008 article 2016 ftkingscollondon https://doi.org/10.1016/j.ajhg.2016.03.008 2022-10-14T10:29:50Z Spontaneous dizygotic (DZ) twinning occurs in 1%–4% of women, with familial clustering and unknown physiological pathways and genetic origin. DZ twinning might index increased fertility and has distinct health implications for mother and child. We performed a GWAS in 1,980 mothers of spontaneous DZ twins and 12,953 control subjects. Findings were replicated in a large Icelandic cohort and tested for association across a broad range of fertility traits in women. Two SNPs were identified (rs11031006 near FSHB, p = 1.54 × 10−9, and rs17293443 in SMAD3, p = 1.57 × 10−8) and replicated (p = 3 × 10−3 and p = 1.44 × 10−4, respectively). Based on ∼90,000 births in Iceland, the risk of a mother delivering twins increased by 18% for each copy of allele rs11031006-G and 9% for rs17293443-C. A higher polygenic risk score (PRS) for DZ twinning, calculated based on the results of the DZ twinning GWAS, was significantly associated with DZ twinning in Iceland (p = 0.001). A higher PRS was also associated with having children (p = 0.01), greater lifetime parity (p = 0.03), and earlier age at first child (p = 0.02). Allele rs11031006-G was associated with higher serum FSH levels, earlier age at menarche, earlier age at first child, higher lifetime parity, lower PCOS risk, and earlier age at menopause. Conversely, rs17293443-C was associated with later age at last child. We identified robust genetic risk variants for DZ twinning: one near FSHB and a second within SMAD3, the product of which plays an important role in gonadal responsiveness to FSH. These loci contribute to crucial aspects of reproductive capacity and health. Article in Journal/Newspaper Iceland King's College, London: Research Portal The American Journal of Human Genetics 98 5 898 908 |
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Open Polar |
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King's College, London: Research Portal |
op_collection_id |
ftkingscollondon |
language |
English |
description |
Spontaneous dizygotic (DZ) twinning occurs in 1%–4% of women, with familial clustering and unknown physiological pathways and genetic origin. DZ twinning might index increased fertility and has distinct health implications for mother and child. We performed a GWAS in 1,980 mothers of spontaneous DZ twins and 12,953 control subjects. Findings were replicated in a large Icelandic cohort and tested for association across a broad range of fertility traits in women. Two SNPs were identified (rs11031006 near FSHB, p = 1.54 × 10−9, and rs17293443 in SMAD3, p = 1.57 × 10−8) and replicated (p = 3 × 10−3 and p = 1.44 × 10−4, respectively). Based on ∼90,000 births in Iceland, the risk of a mother delivering twins increased by 18% for each copy of allele rs11031006-G and 9% for rs17293443-C. A higher polygenic risk score (PRS) for DZ twinning, calculated based on the results of the DZ twinning GWAS, was significantly associated with DZ twinning in Iceland (p = 0.001). A higher PRS was also associated with having children (p = 0.01), greater lifetime parity (p = 0.03), and earlier age at first child (p = 0.02). Allele rs11031006-G was associated with higher serum FSH levels, earlier age at menarche, earlier age at first child, higher lifetime parity, lower PCOS risk, and earlier age at menopause. Conversely, rs17293443-C was associated with later age at last child. We identified robust genetic risk variants for DZ twinning: one near FSHB and a second within SMAD3, the product of which plays an important role in gonadal responsiveness to FSH. These loci contribute to crucial aspects of reproductive capacity and health. |
format |
Article in Journal/Newspaper |
author |
Mbarek, Hamdi Steinberg, Stacy Nyholt, Dale R. Gordon, Scott D. Miller, Michael B. McRae, Allan F. Hottenga, Jouke Jan Day, Felix R. Willemsen, Gonneke de Geus, Eco J. Davies, Gareth E. Martin, Hilary C. Penninx, Brenda W. Jansen, Rick McAloney, Kerrie Vink, Jacqueline M. Kaprio, Jaakko Plomin, Robert Spector, Tim D. Magnusson, Patrik K. Reversade, Bruno Harris, R. Alan Aagaard, Kjersti Kristjansson, Ragnar P. Olafsson, Isleifur Eyjolfsson, Gudmundur Ingi Sigurdardottir, Olof Iacono, William G. Lambalk, Cornelis B. Montgomery, Grant W. McGue, Matt Ong, Ken K. Perry, John R.B. Martin, Nicholas G. Stefánsson, Hreinn Stefánsson, Kari Boomsma, Dorret I. |
spellingShingle |
Mbarek, Hamdi Steinberg, Stacy Nyholt, Dale R. Gordon, Scott D. Miller, Michael B. McRae, Allan F. Hottenga, Jouke Jan Day, Felix R. Willemsen, Gonneke de Geus, Eco J. Davies, Gareth E. Martin, Hilary C. Penninx, Brenda W. Jansen, Rick McAloney, Kerrie Vink, Jacqueline M. Kaprio, Jaakko Plomin, Robert Spector, Tim D. Magnusson, Patrik K. Reversade, Bruno Harris, R. Alan Aagaard, Kjersti Kristjansson, Ragnar P. Olafsson, Isleifur Eyjolfsson, Gudmundur Ingi Sigurdardottir, Olof Iacono, William G. Lambalk, Cornelis B. Montgomery, Grant W. McGue, Matt Ong, Ken K. Perry, John R.B. Martin, Nicholas G. Stefánsson, Hreinn Stefánsson, Kari Boomsma, Dorret I. Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
author_facet |
Mbarek, Hamdi Steinberg, Stacy Nyholt, Dale R. Gordon, Scott D. Miller, Michael B. McRae, Allan F. Hottenga, Jouke Jan Day, Felix R. Willemsen, Gonneke de Geus, Eco J. Davies, Gareth E. Martin, Hilary C. Penninx, Brenda W. Jansen, Rick McAloney, Kerrie Vink, Jacqueline M. Kaprio, Jaakko Plomin, Robert Spector, Tim D. Magnusson, Patrik K. Reversade, Bruno Harris, R. Alan Aagaard, Kjersti Kristjansson, Ragnar P. Olafsson, Isleifur Eyjolfsson, Gudmundur Ingi Sigurdardottir, Olof Iacono, William G. Lambalk, Cornelis B. Montgomery, Grant W. McGue, Matt Ong, Ken K. Perry, John R.B. Martin, Nicholas G. Stefánsson, Hreinn Stefánsson, Kari Boomsma, Dorret I. |
author_sort |
Mbarek, Hamdi |
title |
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
title_short |
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
title_full |
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
title_fullStr |
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
title_full_unstemmed |
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
title_sort |
identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility |
publishDate |
2016 |
url |
https://kclpure.kcl.ac.uk/portal/en/publications/identification-of-common-genetic-variants-influencing-spontaneous-dizygotic-twinning-and-female-fertility(59c0be68-bba9-45ce-ad2e-090541b38684).html https://doi.org/10.1016/j.ajhg.2016.03.008 |
genre |
Iceland |
genre_facet |
Iceland |
op_source |
Mbarek , H , Steinberg , S , Nyholt , DR , Gordon , SD , Miller , MB , McRae , AF , Hottenga , JJ , Day , FR , Willemsen , G , de Geus , EJ , Davies , GE , Martin , HC , Penninx , BW , Jansen , R , McAloney , K , Vink , JM , Kaprio , J , Plomin , R , Spector , T D , Magnusson , PK , Reversade , B , Harris , R A , Aagaard , K , Kristjansson , RP , Olafsson , I , Eyjolfsson , GI , Sigurdardottir , O , Iacono , WG , Lambalk , CB , Montgomery , GW , McGue , M , Ong , KK , Perry , JR B , Martin , NG , Stefánsson , H , Stefánsson , K & Boomsma , DI 2016 , ' Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility ' , American Journal of Human Genetics , vol. 98 , no. 5 , pp. 898-908 . https://doi.org/10.1016/j.ajhg.2016.03.008 |
op_rights |
info:eu-repo/semantics/closedAccess |
op_doi |
https://doi.org/10.1016/j.ajhg.2016.03.008 |
container_title |
The American Journal of Human Genetics |
container_volume |
98 |
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5 |
container_start_page |
898 |
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908 |
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