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GWAS Study

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.

Warrington NM, Beaumont RN, Horikoshi M et al.

31043758 PubMed ID
GWAS Study Type
230069 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WN
Warrington NM
BR
Beaumont RN
HM
Horikoshi M
DF
Day FR
Helgeland Ø
LC
Laurin C
BJ
Bacelis J
PS
Peng S
HK
Hao K
FB
Feenstra B
WA
Wood AR
MA
Mahajan A
TJ
Tyrrell J
RN
Robertson NR
RN
Rayner NW
QZ
Qiao Z
MG
Moen GH
VM
Vaudel M
MC
Marsit CJ
CJ
Chen J
NM
Nodzenski M
ST
Schnurr TM
ZM
Zafarmand MH
BJ
Bradfield JP
GN
Grarup N
KM
Kooijman MN
LR
Li-Gao R
GF
Geller F
AT
Ahluwalia TS
PL
Paternoster L
RR
Rueedi R
HV
Huikari V
HJ
Hottenga JJ
LL
Lyytikäinen LP
CA
Cavadino A
MS
Metrustry S
CD
Cousminer DL
WY
Wu Y
TE
Thiering E
WC
Wang CA
HC
Have CT
VN
Vilor-Tejedor N
JP
Joshi PK
PJ
Painter JN
NI
Ntalla I
MR
Myhre R
PN
Pitkänen N
VL
van Leeuwen EM
JR
Joro R
LV
Lagou V
RR
Richmond RC
EA
Espinosa A
BS
Barton SJ
IH
Inskip HM
HJ
Holloway JW
SL
Santa-Marina L
EX
Estivill X
AW
Ang W
MJ
Marsh JA
RC
Reichetzeder C
ML
Marullo L
HB
Hocher B
LK
Lunetta KL
MJ
Murabito JM
RC
Relton CL
KM
Kogevinas M
CL
Chatzi L
AC
Allard C
BL
Bouchard L
HM
Hivert MF
ZG
Zhang G
ML
Muglia LJ
HJ
Heikkinen J
MC
Morgen CS
VK
van Kampen AHC
VS
van Schaik BDC
MF
Mentch FD
LC
Langenberg C
LJ
Luan J
SR
Scott RA
ZJ
Zhao JH
HG
Hemani G
RS
Ring SM
BA
Bennett AJ
GK
Gaulton KJ
FJ
Fernandez-Tajes J
VZ
van Zuydam NR
MC
Medina-Gomez C
DH
de Haan HG
RF
Rosendaal FR
KZ
Kutalik Z
MP
Marques-Vidal P
DS
Das S
WG
Willemsen G
MH
Mbarek H
MM
Müller-Nurasyid M
SM
Standl M
AE
Appel EVR
FC
Fonvig CE
TC
Trier C
VB
van Beijsterveldt CEM
MM
Murcia M
BM
Bustamante M
BS
Bonas-Guarch S
HD
Hougaard DM
MJ
Mercader JM
LA
Linneberg A
SK
Schraut KE
LP
Lind PA
MS
Medland SE
SB
Shields BM
KB
Knight BA
CJ
Chai JF
PK
Panoutsopoulou K
BM
Bartels M
SF
Sánchez F
SJ
Stokholm J
TD
Torrents D
VR
Vinding RK
WS
Willems SM
AM
Atalay M
CB
Chawes BL
KP
Kovacs P
PI
Prokopenko I
TM
Tuke MA
YH
Yaghootkar H
RK
Ruth KS
JS
Jones SE
LP
Loh PR
MA
Murray A
WM
Weedon MN
TA
Tönjes A
SM
Stumvoll M
MK
Michaelsen KF
EA
Eloranta AM
LT
Lakka TA
VD
van Duijn CM
KW
Kiess W
KA
Körner A
NH
Niinikoski H
PK
Pahkala K
RO
Raitakari OT
JB
Jacobsson B
ZE
Zeggini E
DG
Dedoussis GV
TY
Teo YY
SS
Saw SM
MG
Montgomery GW
CH
Campbell H
WJ
Wilson JF
VT
Vrijkotte TGM
VM
Vrijheid M
DG
de Geus EJCN
HM
Hayes MG
KH
Kadarmideen HN
HJ
Holm JC
BL
Beilin LJ
PC
Pennell CE
HJ
Heinrich J
AL
Adair LS
BJ
Borja JB
MK
Mohlke KL
EJ
Eriksson JG
WE
Widén EE
HA
Hattersley AT
ST
Spector TD
KM
Kähönen M
VJ
Viikari JS
LT
Lehtimäki T
BD
Boomsma DI
SS
Sebert S
VP
Vollenweider P
ST
Sørensen TIA
BH
Bisgaard H
BK
Bønnelykke K
MJ
Murray JC
MM
Melbye M
NE
Nohr EA
MD
Mook-Kanamori DO
RF
Rivadeneira F
HA
Hofman A
FJ
Felix JF
JV
Jaddoe VWV
HT
Hansen T
PC
Pisinger C
VA
Vaag AA
PO
Pedersen O
UA
Uitterlinden AG
JM
Järvelin MR
PC
Power C
HE
Hyppönen E
SD
Scholtens DM
LW
Lowe WL
DS
Davey Smith G
TN
Timpson NJ
MA
Morris AP
WN
Wareham NJ
HH
Hakonarson H
GS
Grant SFA
FT
Frayling TM
LD
Lawlor DA
NP
Njølstad PR
JS
Johansson S
OK
Ong KK
MM
McCarthy MI
PJ
Perry JRB
ED
Evans DM
FR
Freathy RM
Chapter II

Abstract

Summary of the research findings

Birth weight variation is influenced by fetal and maternal genetic and non-genetic factors, and has been reproducibly associated with future cardio-metabolic health outcomes. In expanded genome-wide association analyses of own birth weight (n = 321,223) and offspring birth weight (n = 230,069 mothers), we identified 190 independent association signals (129 of which are novel). We used structural equation modeling to decompose the contributions of direct fetal and indirect maternal genetic effects, then applied Mendelian randomization to illuminate causal pathways. For example, both indirect maternal and direct fetal genetic effects drive the observational relationship between lower birth weight and higher later blood pressure: maternal blood pressure-raising alleles reduce offspring birth weight, but only direct fetal effects of these alleles, once inherited, increase later offspring blood pressure. Using maternal birth weight-lowering genotypes to proxy for an adverse intrauterine environment provided no evidence that it causally raises offspring blood pressure, indicating that the inverse birth weight-blood pressure association is attributable to genetic effects, and not to intrauterine programming.

210,267 European ancestry individuals, 19,802 individuals

Chapter III

Study Statistics

Key metrics and study information

230069
Total Participants
GWAS
Study Type
No
Replicated
European, South East Asian, Greater Middle Eastern (Middle Eastern, North African or Persian), Other, East Asian, Hispanic or Latin American, African American or Afro-Caribbean
Ancestry
Canada, Australia, Netherlands, Denmark, Finland, Norway, U.K., Philippines, Thailand, U.S., Germany, Switzerland, Greece, Spain, Singapore, Barbados
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.