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      Maternal Body Mass Index, Early-Pregnancy Metabolite Profile, and Birthweight

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          Abstract

          Context

          Maternal prepregnancy body mass index (BMI) has a strong influence on gestational metabolism, but detailed metabolic alterations are unknown.

          Objective

          First, to examine the associations of maternal prepregnancy BMI with maternal early-pregnancy metabolite alterations. Second, to identify an early-pregnancy metabolite profile associated with birthweight in women with a higher prepregnancy BMI that improved prediction of birthweight compared to glucose and lipid concentrations.

          Design, Setting, and Participants

          Prepregnancy BMI was obtained in a subgroup of 682 Dutch pregnant women from the Generation R prospective cohort study.

          Main Outcome Measures

          Maternal nonfasting targeted amino acids, nonesterified fatty acid, phospholipid, and carnitine concentrations measured in blood serum at mean gestational age of 12.8 weeks. Birthweight was obtained from medical records.

          Results

          A higher prepregnancy BMI was associated with 72 altered amino acids, nonesterified fatty acid, phospholipid and carnitine concentrations, and 6 metabolite ratios reflecting Krebs cycle, inflammatory, oxidative stress, and lipid metabolic processes ( P-values < 0.05). Using penalized regression models, a metabolite profile was selected including 15 metabolites and 4 metabolite ratios based on its association with birthweight in addition to prepregnancy BMI. The adjusted R 2 of birthweight was 6.1% for prepregnancy BMI alone, 6.2% after addition of glucose and lipid concentrations, and 12.9% after addition of the metabolite profile.

          Conclusions

          A higher maternal prepregnancy BMI was associated with altered maternal early-pregnancy amino acids, nonesterified fatty acids, phospholipids, and carnitines. Using these metabolites, we identified a maternal metabolite profile that improved prediction of birthweight in women with a higher prepregnancy BMI compared to glucose and lipid concentrations.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Regression Shrinkage and Selection Via the Lasso

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              The Generation R Study: design and cohort update 2017

              The Generation R Study is a population-based prospective cohort study from fetal life until adulthood. The study is designed to identify early environmental and genetic causes and causal pathways leading to normal and abnormal growth, development and health from fetal life, childhood and young adulthood. This multidisciplinary study focuses on several health outcomes including behaviour and cognition, body composition, eye development, growth, hearing, heart and vascular development, infectious disease and immunity, oral health and facial growth, respiratory health, allergy and skin disorders of children and their parents. Main exposures of interest include environmental, endocrine, genomic (genetic, epigenetic, microbiome), lifestyle related, nutritional and socio-demographic determinants. In total, 9778 mothers with a delivery date from April 2002 until January 2006 were enrolled in the study. Response at baseline was 61%, and general follow-up rates until the age of 10 years were around 80%. Data collection in children and their parents includes questionnaires, interviews, detailed physical and ultrasound examinations, behavioural observations, lung function, Magnetic Resonance Imaging and biological sampling. Genome and epigenome wide association screens are available. Eventually, results from the Generation R Study contribute to the development of strategies for optimizing health and healthcare for pregnant women and children.
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                Author and article information

                Journal
                J Clin Endocrinol Metab
                J Clin Endocrinol Metab
                jcem
                The Journal of Clinical Endocrinology and Metabolism
                Oxford University Press (US )
                0021-972X
                1945-7197
                January 2022
                14 August 2021
                14 August 2021
                : 107
                : 1
                : e315-e327
                Affiliations
                [1 ] The Generation R Study Group, Erasmus MC, University Medical Center , Rotterdam,the Netherlands
                [2 ] Department of Pediatrics, Sophia’s Children’s Hospital, Erasmus MC, University Medical Center , Rotterdam, the Netherlands
                [3 ] Department of Clinical Genetics, Center for Lysosomal and Metabolic Disease, Erasmus MC, University Medical Center , Rotterdam, the Netherlands
                [4 ] Division of Metabolic and Nutritional Medicine, Dept. Paediatrics, Dr. von Hauner Children’s Hospital, LMU University Hospitals , Munich, Germany
                Author notes
                Correspondence: Romy Gaillard, MD, PhD, The Generation R Study Group, Erasmus University Medical Center, PO Box 2040, 3000 CA Rotterdam, the Netherlands. Email: r.gaillard@ 123456erasmusmc.nl .
                Author information
                https://orcid.org/0000-0002-7967-4600
                Article
                dgab596
                10.1210/clinem/dgab596
                8684472
                34390344
                6482f70f-b113-4ec0-b29c-a9a398d648ec
                © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 21 May 2021
                : 09 August 2021
                : 20 September 2021
                Page count
                Pages: 13
                Funding
                Funded by: Erasmus Medical Center, DOI 10.13039/501100003061;
                Funded by: Erasmus University Rotterdam, DOI 10.13039/501100001828;
                Funded by: Netherlands Organization for Health Research and Development;
                Award ID: 543003109
                Funded by: Dutch Heart Foundation;
                Award ID: 2017T013
                Funded by: Dutch Diabetes Foundation;
                Award ID: 2017.81.002
                Funded by: European Research Council, DOI 10.13039/501100000781;
                Award ID: ERC-2014-CoG-648916
                Award ID: 322605
                Funded by: European Union’s Horizon;
                Award ID: 727565
                Funded by: European Joint Programming Initiative;
                Award ID: 529051022
                Funded by: ZonMW the Netherlands;
                Award ID: 529051026
                Funded by: German Ministry of Education and Research, Berlin;
                Award ID: 01 GI 0825
                Funded by: German Research Council;
                Award ID: 409/224-1 FUGG
                Categories
                Online Only Articles
                Clinical Research Articles
                AcademicSubjects/MED00250

                Endocrinology & Diabetes
                pregnancy,obesity,metabolomics,birth complications
                Endocrinology & Diabetes
                pregnancy, obesity, metabolomics, birth complications

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