Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother–infant pairs
Year: 2020
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Many maternal traits are associated with a neonate's gestational duration, birth weight, and birth length. These birth outcomes are subsequently associated with late-onset health conditions. The causal mechanisms and the relative contributions of maternal and fetal genetic effects behind these observed associations are unresolved. METHODS AND FINDINGS: Based on 10,734 mother-infant duos of European ancestry from the UK, Northern Europe, Australia, and North America, we constructed haplotype genetic scores using single-nucleotide polymorphisms (SNPs) known to be associated with adult height, body mass index (BMI), blood pressure (BP), fasting plasma glucose (FPG), and type 2 diabetes (T2D). Using these scores as genetic instruments, we estimated the maternal and fetal genetic effects underlying the observed associations between maternal phenotypes and pregnancy outcomes. We also used infant-specific birth weight genetic scores as instrument and examined the effects of fetal growth on pregnancy outcomes, maternal BP, and glucose levels during pregnancy. The maternal nontransmitted haplotype score for height was significantly associated with gestational duration (p = 2.2 × 10-4). Both maternal and paternal transmitted height haplotype scores were highly significantly associated with birth weight and length (p < 1 × 10-17). The maternal transmitted BMI scores were associated with birth weight with a significant maternal effect (p = 1.6 × 10-4). Both maternal and paternal transmitted BP scores were negatively associated with birth weight with a significant fetal effect (p = 9.4 × 10-3), whereas BP alleles were significantly associated with gestational duration and preterm birth through maternal effects (p = 3.3 × 10-2 and p = 4.5 × 10-3, respectively). The nontransmitted haplotype score for FPG was strongly associated with birth weight (p = 4.7 × 10-6); however, the glucose-increasing alleles in the fetus were associated with reduced birth weight through a fetal effect (p = 2.2 × 10-3). The haplotype scores for T2D were associated with birth weight in a similar way but with a weaker maternal effect (p = 6.4 × 10-3) and a stronger fetal effect (p = 1.3 × 10-5). The paternal transmitted birth weight score was significantly associated with reduced gestational duration (p = 1.8 × 10-4) and increased maternal systolic BP during pregnancy (p = 2.2 × 10-2). The major limitations of the study include missing and heterogenous phenotype data in some data sets and different instrumental strength of genetic scores for different phenotypic traits. CONCLUSIONS: We found that both maternal height and fetal growth are important factors in shaping the duration of gestation: genetically elevated maternal height is associated with longer gestational duration, whereas alleles that increase fetal growth are associated with shorter gestational duration. Fetal growth is influenced by both maternal and fetal effects and can reciprocally influence maternal phenotypes: taller maternal stature, higher maternal BMI, and higher maternal blood glucose are associated with larger birth size through maternal effects; in the fetus, the height- and metabolic-risk-increasing alleles are associated with increased and decreased birth size, respectively; alleles raising birth weight in the fetus are associated with shorter gestational duration and higher maternal BP. These maternal and fetal genetic effects may explain the observed associations between the studied maternal phenotypes and birth outcomes, as well as the life-course associations between these birth outcomes and adult phenotypes.
Source: PLoS Medicine
Institutions: Cincinnati Children's Hospital Medical Center, University of Cincinnati, Sahlgrenska University Hospital, Region Västra Götaland, University of Gothenburg, March of Dimes Prematurity Research Center Ohio Collaborative, Oulu University Hospital, University of Oulu, University of Helsinki, Helsinki University Hospital, Statens Serum Institut, University of Copenhagen, Stanford Medicine, Stanford University, University of Exeter, University of Bristol, NIHR Bristol Biomedical Research Centre, MRC Integrative Epidemiology Unit, University of Iowa, Case Western Reserve University, Norwegian Institute of Public Health
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,732
Funders: Burroughs Wellcome Fund, Bill and Melinda Gates Foundation, March of Dimes Foundation, Oak Foundation, Cincinnati Children's Hospital Medical Center, Wellcome Trust, National Institute for Health and Care Research, British Heart Foundation, University of Bristol, Helse- og Omsorgsdepartementet, Norges Forskningsråd, National Institutes of Health, Medical Research Council, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke, National Institute of Environmental Health Sciences, H2020 European Research Council
Awards: G1112915806, G1192034430, G12365209, Reproductive and cardio-metabolic health, G1602760451, G1605161196, G1653514516, G1756123706, G1795185051, G1795554050, G1922679944, G1930730855, G1977033855, G2047650810, G207808720, G2315532689, G2538597952, G2716889063, G2786058305, The Avon Longitudinal Study of Parents and Children (ALSPAC): A multi-generation, longitudinal resource, G3193858039, G3206767929, G3330779559, G3345452146, G3370464334, The Avon Longitudinal Study of Parents and Children (ALSPAC): A multi- generation, longitudinal resource focusing on life course health and well- being., Gene-Environment Interactions in an Autism Birth Cohort, G3831911591, Using genetics to understand how the maternal intrauterine environment influences fetal growth., G3998038441, G4004514323, G4129682460, G4257455355, G4344264865, G4418645022, The Avon Longitudinal Study for Parents and Children: An international resource for population genomic and lifecourse epidemiology. Core programme support 2014-2019., G4597593161, G4715994284, G4758008823, G4794356421, The Avon Longitudinal Study of Parents and Children: An international resource for population
genomics and lifecourse epidemiology. Core Programme Support 2011-2015 and Core programme support 2014-2019, G5171609179, G5260012927, G5287754643, G5482967079, G5562631338, G5607908600, NIHR Senior Investigator Award, G5661482178, NORWAY MOTHER AND CHILD COHORT STUDY: CONTINUED SPECIMEN, G5964956942, G648019732, G6543882502, G6605167459, Mendelian randomization to hypothesis-free causal inference, G6910425605, Effects of maternal gestational adiposity on fetal development and perinatal, postnatal and next generation health., G7239951043, Metabolomic and Epigenomic Mechanisms in Developmental Overnutrition., G7385418751, G7828794151, G8201869620, G8340598841, G8486009620, G8502142660, G86128987, G8613471032, G8850960788
OpenAlex ID: W3080851942
