The genetic architecture of sporadic and multiple consecutive miscarriage

Triin Laisk; Ana Luiza G Soares; Teresa Ferreira; Jodie N Painter; Jenny C Censin; Samantha Laber; Jonas Bacelis; Chia-Yen Chen; Maarja Lepamets; Kuang Lin; Siyang Liu; Iona Y Millwood; Avinash Ramu; Jennifer Southcombe; Marianne S Andersen; Ling Yang; Christian M Becker; Anders D Børglum; Scott D Gordon; Jonas Bybjerg-Grauholm; Øyvind Helgeland; David M Hougaard; Xin Jin; Stefan Johansson; Julius Juodakis; Christiana Kartsonaki; Viktorija Kukushkina; Penelope A Lind; Andres Metspalu; Grant W Montgomery; Andrew P Morris; Ole Mors; Preben B Mortensen; Pål R Njølstad; Merete Nordentoft; Dale R Nyholt; Margaret Lippincott; Stephanie Seminara; Andres Salumets; Harold Snieder; Krina Zondervan; Thomas Werge; Zhengming Chen; Donald F Conrad; Bo Jacobsson; Liming Li; Nicholas G Martin; Benjamin M Neale; Rasmus Nielsen; Robin G Walters; Ingrid Granne; Sarah E Medland; Reedik Mägi; Deborah A Lawlor; Cecilia M Lindgren

doi:10.1038/s41467-020-19742-5

The genetic architecture of sporadic and multiple consecutive miscarriage

Triin Laisk, Ana Luiza G Soares, Teresa Ferreira, Jodie N Painter, Jenny C Censin, Samantha Laber, Jonas Bacelis, Chia-Yen Chen, Maarja Lepamets, Kuang Lin, Siyang Liu, Iona Y Millwood, Avinash Ramu, Jennifer Southcombe, Marianne S Andersen, Ling Yang, Christian M Becker, Anders D Børglum, Scott D Gordon, Jonas Bybjerg-GrauholmØyvind Helgeland, David M Hougaard, Xin Jin, Stefan Johansson, Julius Juodakis, Christiana Kartsonaki, Viktorija Kukushkina, Penelope A Lind, Andres Metspalu, Grant W Montgomery, Andrew P Morris, Ole Mors, Preben B Mortensen, Pål R Njølstad, Merete Nordentoft, Dale R Nyholt, Margaret Lippincott, Stephanie Seminara, Andres Salumets, Harold Snieder, Krina Zondervan, Thomas Werge, Zhengming Chen, Donald F Conrad, Bo Jacobsson, Liming Li, Nicholas G Martin, Benjamin M Neale, Rasmus Nielsen, Robin G Walters, Ingrid Granne, Sarah E Medland, Reedik Mägi, Deborah A Lawlor, Cecilia M Lindgren

66 Citationer (Scopus)

Abstract

Miscarriage is a common, complex trait affecting ~15% of clinically confirmed pregnancies. Here we present the results of large-scale genetic association analyses with 69,054 cases from five different ancestries for sporadic miscarriage, 750 cases of European ancestry for multiple (≥3) consecutive miscarriage, and up to 359,469 female controls. We identify one genome-wide significant association (rs146350366, minor allele frequency (MAF) 1.2%, P = 3.2 × 10-8, odds ratio (OR) = 1.4) for sporadic miscarriage in our European ancestry meta-analysis and three genome-wide significant associations for multiple consecutive miscarriage (rs7859844, MAF = 6.4%, P = 1.3 × 10-8, OR = 1.7; rs143445068, MAF = 0.8%, P = 5.2 × 10-9, OR = 3.4; rs183453668, MAF = 0.5%, P = 2.8 × 10-8, OR = 3.8). We further investigate the genetic architecture of miscarriage with biobank-scale Mendelian randomization, heritability, and genetic correlation analyses. Our results show that miscarriage etiopathogenesis is partly driven by genetic variation potentially related to placental biology, and illustrate the utility of large-scale biobank data for understanding this pregnancy complication.

Originalsprog	Engelsk
Tidsskrift	Nature Communications
Vol/bind	11
Udgave nummer	1
Sider (fra-til)	5980
ISSN	2041-1722
DOI	https://doi.org/10.1038/s41467-020-19742-5
Status	Udgivet - 25 nov. 2020

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10.1038/s41467-020-19742-5

Citationsformater

Laisk, T., Soares, A. L. G., Ferreira, T., Painter, J. N., Censin, J. C., Laber, S., Bacelis, J., Chen, C.-Y., Lepamets, M., Lin, K., Liu, S., Millwood, I. Y., Ramu, A., Southcombe, J., Andersen, M. S., Yang, L., Becker, C. M., Børglum, A. D., Gordon, S. D., ... Lindgren, C. M. (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11(1), 5980. https://doi.org/10.1038/s41467-020-19742-5

Laisk, T, Soares, ALG, Ferreira, T, Painter, JN, Censin, JC, Laber, S, Bacelis, J, Chen, C-Y, Lepamets, M, Lin, K, Liu, S, Millwood, IY, Ramu, A, Southcombe, J, Andersen, MS, Yang, L, Becker, CM, Børglum, AD, Gordon, SD, Bybjerg-Grauholm, J, Helgeland, Ø, Hougaard, DM, Jin, X, Johansson, S, Juodakis, J, Kartsonaki, C, Kukushkina, V, Lind, PA, Metspalu, A, Montgomery, GW, Morris, AP, Mors, O, Mortensen, PB, Njølstad, PR, Nordentoft, M, Nyholt, DR, Lippincott, M, Seminara, S, Salumets, A, Snieder, H, Zondervan, K, Werge, T, Chen, Z, Conrad, DF, Jacobsson, B, Li, L, Martin, NG, Neale, BM, Nielsen, R, Walters, RG, Granne, I, Medland, SE, Mägi, R, Lawlor, DA & Lindgren, CM 2020, 'The genetic architecture of sporadic and multiple consecutive miscarriage', Nature Communications, bind 11, nr. 1, s. 5980. https://doi.org/10.1038/s41467-020-19742-5

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title = "The genetic architecture of sporadic and multiple consecutive miscarriage",

abstract = "Miscarriage is a common, complex trait affecting ~15% of clinically confirmed pregnancies. Here we present the results of large-scale genetic association analyses with 69,054 cases from five different ancestries for sporadic miscarriage, 750 cases of European ancestry for multiple (≥3) consecutive miscarriage, and up to 359,469 female controls. We identify one genome-wide significant association (rs146350366, minor allele frequency (MAF) 1.2%, P = 3.2 × 10-8, odds ratio (OR) = 1.4) for sporadic miscarriage in our European ancestry meta-analysis and three genome-wide significant associations for multiple consecutive miscarriage (rs7859844, MAF = 6.4%, P = 1.3 × 10-8, OR = 1.7; rs143445068, MAF = 0.8%, P = 5.2 × 10-9, OR = 3.4; rs183453668, MAF = 0.5%, P = 2.8 × 10-8, OR = 3.8). We further investigate the genetic architecture of miscarriage with biobank-scale Mendelian randomization, heritability, and genetic correlation analyses. Our results show that miscarriage etiopathogenesis is partly driven by genetic variation potentially related to placental biology, and illustrate the utility of large-scale biobank data for understanding this pregnancy complication.",

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author = "Triin Laisk and Soares, {Ana Luiza G} and Teresa Ferreira and Painter, {Jodie N} and Censin, {Jenny C} and Samantha Laber and Jonas Bacelis and Chia-Yen Chen and Maarja Lepamets and Kuang Lin and Siyang Liu and Millwood, {Iona Y} and Avinash Ramu and Jennifer Southcombe and Andersen, {Marianne S} and Ling Yang and Becker, {Christian M} and B{\o}rglum, {Anders D} and Gordon, {Scott D} and Jonas Bybjerg-Grauholm and {\O}yvind Helgeland and Hougaard, {David M} and Xin Jin and Stefan Johansson and Julius Juodakis and Christiana Kartsonaki and Viktorija Kukushkina and Lind, {Penelope A} and Andres Metspalu and Montgomery, {Grant W} and Morris, {Andrew P} and Ole Mors and Mortensen, {Preben B} and Nj{\o}lstad, {P{\aa}l R} and Merete Nordentoft and Nyholt, {Dale R} and Margaret Lippincott and Stephanie Seminara and Andres Salumets and Harold Snieder and Krina Zondervan and Thomas Werge and Zhengming Chen and Conrad, {Donald F} and Bo Jacobsson and Liming Li and Martin, {Nicholas G} and Neale, {Benjamin M} and Rasmus Nielsen and Walters, {Robin G} and Ingrid Granne and Medland, {Sarah E} and Reedik M{\"a}gi and Lawlor, {Deborah A} and Lindgren, {Cecilia M}",

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doi = "10.1038/s41467-020-19742-5",

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journal = "Nature Communications",

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T1 - The genetic architecture of sporadic and multiple consecutive miscarriage

AU - Laisk, Triin

AU - Soares, Ana Luiza G

AU - Ferreira, Teresa

AU - Painter, Jodie N

AU - Censin, Jenny C

AU - Laber, Samantha

AU - Bacelis, Jonas

AU - Chen, Chia-Yen

AU - Lepamets, Maarja

AU - Lin, Kuang

AU - Liu, Siyang

AU - Millwood, Iona Y

AU - Ramu, Avinash

AU - Southcombe, Jennifer

AU - Andersen, Marianne S

AU - Yang, Ling

AU - Becker, Christian M

AU - Børglum, Anders D

AU - Gordon, Scott D

AU - Bybjerg-Grauholm, Jonas

AU - Helgeland, Øyvind

AU - Hougaard, David M

AU - Jin, Xin

AU - Johansson, Stefan

AU - Juodakis, Julius

AU - Kartsonaki, Christiana

AU - Kukushkina, Viktorija

AU - Lind, Penelope A

AU - Metspalu, Andres

AU - Montgomery, Grant W

AU - Morris, Andrew P

AU - Mors, Ole

AU - Mortensen, Preben B

AU - Njølstad, Pål R

AU - Nordentoft, Merete

AU - Nyholt, Dale R

AU - Lippincott, Margaret

AU - Seminara, Stephanie

AU - Salumets, Andres

AU - Snieder, Harold

AU - Zondervan, Krina

AU - Werge, Thomas

AU - Chen, Zhengming

AU - Conrad, Donald F

AU - Jacobsson, Bo

AU - Li, Liming

AU - Martin, Nicholas G

AU - Neale, Benjamin M

AU - Nielsen, Rasmus

AU - Walters, Robin G

AU - Granne, Ingrid

AU - Medland, Sarah E

AU - Mägi, Reedik

AU - Lawlor, Deborah A

AU - Lindgren, Cecilia M

PY - 2020/11/25

Y1 - 2020/11/25

N2 - Miscarriage is a common, complex trait affecting ~15% of clinically confirmed pregnancies. Here we present the results of large-scale genetic association analyses with 69,054 cases from five different ancestries for sporadic miscarriage, 750 cases of European ancestry for multiple (≥3) consecutive miscarriage, and up to 359,469 female controls. We identify one genome-wide significant association (rs146350366, minor allele frequency (MAF) 1.2%, P = 3.2 × 10-8, odds ratio (OR) = 1.4) for sporadic miscarriage in our European ancestry meta-analysis and three genome-wide significant associations for multiple consecutive miscarriage (rs7859844, MAF = 6.4%, P = 1.3 × 10-8, OR = 1.7; rs143445068, MAF = 0.8%, P = 5.2 × 10-9, OR = 3.4; rs183453668, MAF = 0.5%, P = 2.8 × 10-8, OR = 3.8). We further investigate the genetic architecture of miscarriage with biobank-scale Mendelian randomization, heritability, and genetic correlation analyses. Our results show that miscarriage etiopathogenesis is partly driven by genetic variation potentially related to placental biology, and illustrate the utility of large-scale biobank data for understanding this pregnancy complication.

AB - Miscarriage is a common, complex trait affecting ~15% of clinically confirmed pregnancies. Here we present the results of large-scale genetic association analyses with 69,054 cases from five different ancestries for sporadic miscarriage, 750 cases of European ancestry for multiple (≥3) consecutive miscarriage, and up to 359,469 female controls. We identify one genome-wide significant association (rs146350366, minor allele frequency (MAF) 1.2%, P = 3.2 × 10-8, odds ratio (OR) = 1.4) for sporadic miscarriage in our European ancestry meta-analysis and three genome-wide significant associations for multiple consecutive miscarriage (rs7859844, MAF = 6.4%, P = 1.3 × 10-8, OR = 1.7; rs143445068, MAF = 0.8%, P = 5.2 × 10-9, OR = 3.4; rs183453668, MAF = 0.5%, P = 2.8 × 10-8, OR = 3.8). We further investigate the genetic architecture of miscarriage with biobank-scale Mendelian randomization, heritability, and genetic correlation analyses. Our results show that miscarriage etiopathogenesis is partly driven by genetic variation potentially related to placental biology, and illustrate the utility of large-scale biobank data for understanding this pregnancy complication.

KW - Abortion, Habitual/epidemiology

KW - Abortion, Spontaneous/epidemiology

KW - Adult

KW - Aged

KW - Case-Control Studies

KW - Datasets as Topic

KW - European Continental Ancestry Group/genetics

KW - Female

KW - Gene Frequency

KW - Genetic Predisposition to Disease

KW - Genome-Wide Association Study

KW - Humans

KW - Inheritance Patterns

KW - Medical History Taking

KW - Middle Aged

KW - Placenta/physiopathology

KW - Polymorphism, Single Nucleotide

KW - Pregnancy

KW - Young Adult

U2 - 10.1038/s41467-020-19742-5

DO - 10.1038/s41467-020-19742-5

M3 - Journal article

C2 - 33239672

SN - 2041-1722

VL - 11

SP - 5980

JO - Nature Communications

JF - Nature Communications

IS - 1

ER -

The genetic architecture of sporadic and multiple consecutive miscarriage

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