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Maternal plasma metabolic markers of neonatal adiposity and associated maternal characteristics: The GUSTO study

Abstract

Infant adiposity may be related to later metabolic health. Maternal metabolite profiling reflects both genetic and environmental influences and allows elucidation of metabolic pathways associated with infant adiposity. In this multi-ethnic Asian cohort, we aimed to (i) identify maternal plasma metabolites associated with infant adiposity and other birth outcomes and (ii) investigate the maternal characteristics associated with those metabolites. In 940 mother-offspring pairs, we performed gas chromatography-mass spectrometry and identified 134 metabolites in maternal fasting plasma at 26–28 weeks of gestation. At birth, neonatal triceps and subscapular skinfold thicknesses were measured by trained research personnel, while weight and length measures were abstracted from delivery records. Gestational age was estimated from first-trimester dating ultrasound. Associations were assessed by multivariable linear regression, with p-values corrected using the Benjamini-Hochberg approach. At a false discovery rate of 5%, we observed associations between 28 metabolites and neonatal sum of skinfold thicknesses (13 amino acid-related, 4 non-esterified fatty acids, 6 xenobiotics, and 5 unknown compounds). Few associations were observed with gestational duration, birth weight, or birth length. Maternal ethnicity, pre-pregnancy BMI, and diet quality during pregnancy had the strongest associations with the specific metabolome related to infant adiposity. Further studies are warranted to replicate our findings and to understand the underlying mechanisms.

Introduction

Being born too early, too small, or too large is associated with impaired development and chronic diseases later in life1,2,3. Infants of similar weight often differ in adiposity4, and given the increasing trend of childhood obesity globally, investigation of infant adiposity is crucial in order to understand the early-life determinants of metabolic health5.

Metabolomics is the study of low molecular weight metabolites (<1000 Daltons)6 downstream from the omics cascade (genomics, transcriptomics, and proteomics) and most closely reflects the metabolic phenotype7. Maternal metabolite profiling is of interest and value in perinatology, because it provides a snapshot of the maternal physiological status. It therefore reflects both genetic and lifestyle (environmental) influences, thus allowing elucidation of metabolic pathways associated with birth outcomes8,9,10. While studies among non-pregnant populations have reported variations in metabolomic profiles associated with ethnicity, diet, adiposity, and smoking status11,12,13,14, it is unclear whether similar associations are observed during pregnancy, when the maternal body undergoes major physiological adaptions to support fetal development and growth15.

Several studies have demonstrated associations between maternal metabolite profiling during pregnancy and infant birth outcomes, based on biospecimens such as plasma16,17,18,19,20,21,22, urine22,23,24,25,26, amniotic fluid26,27,28, serum29,30,31,32, cervicovaginal fluid33,34,35, and hair36. Blood plasma is clinically accessible37 and potentially reflects processes in all organ systems. Compared to other biofluids, it is more comprehensive and contains the broadest array of metabolites6. Plasma metabolite profiles were typically analysed by liquid chromatography-mass spectrometry (LC-MS)16,17,19,21, flow injection analysis mass spectrometry (FIA-MS)20, or nuclear magnetic resonance (NMR)18, but none by gas chromatography-mass spectrometry (GC-MS), which has been regarded as the gold standard for metabolite profiling of volatile, low molecular weight metabolites due to its greater chromatographic resolution8.

In addition, most previous studies were conducted in Western countries16,17,18,19,20,21,22 and had sample sizes under 100 participants17,18,19, with minimal or no adjusment for confounders16,17,18. Larger multi-ethnic studies are therefore warranted. In our multiethnic Asian mother-offspring cohort study, we aimed to (i) identify maternal plasma metabolites associated with gestational duration and offspring birth size and adiposity and (ii) investigate the maternal characteristics associated with those metabolites to examine the potential sources of metabolic variation.

Methods

Study participants

First-trimester pregnant women aged 18–50 y were recruited from the National University Hospital and KK Women’s and Children’s Hospital between June 2009 and September 2010 to participate in the GUSTO (Growing Up in Singapore Towards healthy Outcomes) mother-offspring cohort38. Women were ineligible if their parents and spouses’ parents had different ethnicity (i.e., Chinese, Malay, or Indian descent), received chemotherapy or psychotropic drugs, or had type 1 diabetes. This study was approved by the National Health Care Group Domain Specific Review Board (reference D/09/021) and the SingHealth Centralized Institutional Review Board (reference 2009/280/D). All research was performed in accordance with the relevant guidelines and informed consent was obtained from all participants upon recruitment.

Maternal metabolite assessment

Plasma sample preparation

We collected fasting blood samples at 26–28 week of gestation, processed within 4 h, and stored at −80 °C. Plasma samples were analysed in random order, and laboratory staff were blinded to birth outcomes. A 200 µL aliquot of plasma was spiked with two internal standard mixes: 20 µL of mix 1 prepared by dissolving 36 mg citric acid-d4, 34 mg alanine-d4, 26 mg tryptophan-d5, 23 mg hexanoic-d11 acid, 21 mg phenylalanine-d5, and 15 mg tyrosine-d2 in 36 ml of milli-Q water; and 20 µL of mix 2 prepared by dissolving 29 mg octanoic-d15 acid and 58 mg stearic-d35 acid in 36 ml of methanol. Quality control (QC) samples were prepared from a pool created from 40 µL aliquots of all samples. The samples were dried using a SpeedVac Concentrator (Thermo Scientific) at 80 Pa with no heating and stored at −80 °C.

Extraction of metabolites and derivatization (to increase compound volatility) were based on a published protocol39. Dried samples were suspended in 500 µL cold methanol-water solution (50% vol/vol), vortexed, centrifuged at 3500 rpm for 5 min at −4 °C, and the supernatant was collected. The same extraction process was repeated for methanol-water (80% vol/vol) and methanol solutions. The pooled supernatants were dried using a SpeedVac Concentrator and stored at −80 °C.

Dried samples were suspended in 400 µL sodium hydroxide (1 mol/L), 334 µL methanol and 68 µL pyridine in a silanized glass tube to reduce compound adherence to the glass wall (Thermo Scientific). The derivatization was initiated by adding 40 µL methyl chloroformate, followed by vigorous vortexing for 30 s. This process was repeated before adding 400 µL chloroform and 800 µL sodium bicarbonate (50 mmol/L), vortexing for 10 s after each addition. Derivatised samples were centrifuged at 2000 rpm for 3 min; the aqueous layer was removed and dehydrated with 300 mg anhydrous sodium sulphate before gas chromatography-mass spectrometry (GC-MS) analysis. Negative controls (without the addition of plasma and internal standards) underwent the same processing.

Gas chromatography-mass spectrometry (GC-MS) analysis

We analysed the samples on a GC-MS system—a GC7890B coupled to an MSD5977A operated at 70 eV electron ionization (Agilent Technologies)—equipped with a ZB-1701 column, 30 m × 0.25 mm × 0.15 μm with 5 m guard column (Phenomenex), at a constant flow rate of 1.0 mL/min of helium. Based on a published protocol39, samples (1 µL) were injected under pulsed splitless mode (for trace analyses) with the inlet at 290 °C (180 kPa for 1 min, 50 mL/min purge flow after 1 min). The GC oven temperature was initially held at 45 °C for 2 min, after which it was raised to 180 °C at 9 °C/min and held for 5 min. Subsequently, the temperature was raised to 220 °C at 40 °C/min and held for 5 min. The temperature was raised again to 240 °C at 40 °C/min and held for 11.5 min. Finally, the temperature was raised to 280 °C at 40 °C/min and held for 10 min. The interface was kept at 250 °C and the quadrupole at 130 °C. The detector operated in scan mode, started after 5.5 min with a mass range between 38–550 atomic mass units at 2.9 scans/s. Negative controls were injected at the beginning of each run and QCs were run every seventh sample.

Data processing

The GC-MS data were deconvoluted and metabolites were identified by the Automated Mass Spectral Deconvolution and Identification system software40 with the in-house methyl chloroformate39 and publicly available National Institute of Standards and Technology 14 mass spectra library41. We used the R Metab package for peak integration42. Features present in <5% of all samples and contaminants, identified by comparison with negative control samples, were excluded. Visual inspection of all extracted ion chromatograms was performed, and any integration errors were corrected. Each metabolite was normalised by one of the seven internal standards, chosen based on the highest linear correlation to the metabolite in the QC samples. All metabolites with an R2 < 0.75 with each and every internal standard were omitted from the analysis. We used median centering to align batches based on the correction factors derived from QCs in each of the batches43. Values below the limit of detection were assigned half of the minimum value for that metabolite44. We identified 134 metabolites; the median (IQR) coefficient of variation for all metabolites in the QC samples was 10.3 (8.2–13.4) and all were below the 30% threshold45. Metabolite values were log-transformed and centered before statistical analysis. Of the 134 metabolites, 43 were identified (80–100% match to a reference standard), 11 were putatively identified (80–100% mass spectral match), 38 were tentatively identified (60–79% mass spectral match), and 42 were unknown (<60% mass spectral match). We set the level of identification based on mass spectral matching levels and according to acceptable practices for chemical journals46.

Infant characteristics

Gestational age (GA) was estimated by a dating scan in the first trimester; preterm birth was defined as delivery of a live birth <37 weeks of gestation. Birth weight was measured shortly after birth to the nearest 1 g (SECA 334; SECA Corp.), and recumbent length measured to the nearest 0.5 cm from the top of the head to the soles of the feet (SECA 210). Sex-specific birth weight-for-GA z-scores were derived using a global birth weight reference47 adapted for the GUSTO population48. Triceps and subscapular skinfold thicknesses, which have greater discriminative power than other anthropometric measurements for neonatal total body adiposity49, were measured in triplicate to the nearest 0.2 mm on the right side of the body by anthropometrists and summed (Holtain Skinfold Caliper; Holtain Ltd.). All research personnel were trained according to standardized procedures obtained from the PhenX toolkit50. Infant sex was retrieved from birth delivery reports.

Maternal characteristics

Maternal age (in years, continuous), ethnicity (Chinese, Malay, or Indian), education (before secondary, postsecondary, or university), and self-reported pre-pregnancy weights were collected during recruitment. At 26–28 weeks’ gestation, maternal weight was measured to the nearest 0.1 kg (SECA 803) and standing height was measured in duplicate to the nearest 0.1 cm from the top of the head to the heels (SECA 213). Pre-pregnancy underweight (BMI < 18.5 kg/m2 or ≥18.5 kg/m2), pre-pregnancy overweight (BMI ≥ 23 kg/m2 or <23 kg/m2)51 was determined and weight gain until 26–28 weeks’ gestation (in kg, continuous) was calculated by subtracting pre-pregnancy weight from weight. Blood glucose levels were measured after fasting and two hours after a 75 g oral glucose load at 26–28 weeks’ gestation. Women were diagnosed with gestational diabetes (yes or no) if fasting glucose was ≥7.0 mmol/L and/or 2-hour post-glucose was ≥7.8 mmol/L according to the World Health Organization diagnostic criteria52. At 26–28 weeks’ gestation, information on diet quality during pregnancy (measured using the Healthy Eating Index for pregnant women in Singapore, continuous)53, physical activity (inactive, sufficiently active, or highly active)54, tobacco smoke exposure (plasma cotinine <0.17 ng/mL and no environmental tobacco smoke exposure, <0.17 ng/mL and self-reported environmental tobacco smoke exposure, 0.17–13.99 ng/mL, or ≥14 ng/mL)55, and alcohol consumption during pregnancy (yes or no) were also obtained. Parity (nulliparous or multiparous) and hypertensive disorders (yes or no) including chronic hypertension, pregnancy-induced hypertension, and pre-eclampsia were retrieved from delivery medical notes.

Statistical analysis

Among the 1152 spontaneously conceived singleton pregnancies, 940 mothers who provided their blood samples and had metabolite data and information on their offspring birth outcomes were included in the analysis (Supplemental Fig. 1).

Maternal and child characteristics were summarized according to quintiles of gestational age, birth weight, birth length, and sum of neonatal skinfold thicknesses. P values for trend were assessed by modelling the median value of the quintiles in linear regression for continuous variables or Cochran-Mantel-Haenszel tests for categorical variables.

The associations of 134 maternal metabolites with offspring birth outcomes (i.e. gestational duration, birth weight, birth length, and sum of skinfold thicknesses) were assessed by multiple linear regression using a separate model for each metabolite. We conducted sensitivity analysis on sex-specific birth weight-for-GA z-scores to examine the robustness of our study results. The models were adjusted for infant sex and maternal age, parity, education, ethnicity, pre-pregnancy BMI, weight gain until 26–28 weeks’ gestation, height, tobacco smoke exposure, physical activity, diet quality, and gestational diabetes. The analysis approach is adopted and supported by recently published studies21,31. Metabolites associated with birth outcomes with a Benjamini-Hochberg false discovery rate (FDR) corrected q-value <0.1056 were selected for the next step of analysis57.

For the second aim of the study, relationships between maternal characteristics and those selected metabolites were independently examined using multiple linear regression. Metabolite z-scores were modelled as dependent variables while the independent variables were maternal characteristics. To derive individual estimates for each ethnic group, we created three variables: Chinese (yes or no), Malay (yes or no), and Indian (yes or no) and fitted the model with one ethnic variable at a time while adjusting for other maternal characteristics.

Missing data (height (n = 9), diet quality (n = 9), physical activity (n = 10), education (n = 11), alcohol use (n = 25), gestational diabetes (n = 36), pre-pregnancy BMI (n = 66), weight gain until 26–28 weeks of gestation (n = 73), and prenatal tobacco smoke exposure (n = 73)) were estimated by 20 imputations by the Markov chain Monte Carlo method; the reported results are those from the pooled analysis. To evaluate whether the imputation of missing data may have affected the results, we carried out a sensitivity analysis on participants with no missing data (n = 722).

We investigated potential effect modification by ethnicity by including an interaction term (ethnicity x metabolite) in the regression models. Ethnic differences were further explored by stratified analyses if the interaction term was significant (q-value <0.05). We performed sensitivity analyses to restrict analysis to term births (except for the analysis of gestational age). We also limited the analysis to women without hypertensive disorders, pre-eclampsia, or gestational diabetes (n = 536) in a separate sensitivity analysis.

All statistical analysis was performed in Stata 14 (StataCorp LP, USA). We considered q-values <0.05 statistically significant and 0.05 < q-values <0.10 as trends.

Ethics approval and consent to participate

This study was approved by the National Health Care Group Domain Specific Review Board (reference D/09/021) and the SingHealth Centralized Institutional Review Board (reference 2009/280/D). All participants gave informed consent upon recruitment.

Results

Characteristics of participants and birth outcomes

This cohort comprised 55% Chinese, 26% Malays, and 19% Indians. The mean and standard deviation of maternal age was 30.5 ± 5.1 y, and 43% were overweight before pregnancy. Among the 940 infants, 7.6% were born preterm; the means and standard deviations of birth weight, birth length, and sums of neonatal skinfold thicknesses were 3094 ± 451 g, 48.6 ± 2.3 cm, and 10.3 ± 2.2 mm, respectively. Women with shorter gestational duration were more likely to have lower education, greater exposure to tobacco smoke during pregnancy, and hypertensive disorders. Heavier and longer infants were more likely to be born to mothers who were older, taller, had higher education, and had lower exposure to tobacco smoke. Infants with a lower sum of skinfold thicknesses were more likely to be born to mothers who were nulliparous and had higher education and higher diet quality. Mothers who were overweight before pregnancy and those of higher weight gain up to 26–28 weeks’ gestation were more likely to have infants who were heavier and have higher sum of skinfolds. Chinese infants were generally longer than Malay infants. Only results from the extreme quintiles are presented in Table 1 while all results are presented in Supplemental Table S1.

Table 1 Characteristics of participants according to quintiles of birth outcomes.

Associations of maternal metabolites and birth outcomes

Only metabolites associated with birth outcomes (q-value <0.05) are presented in Table 2, while all results are presented in Supplemental Table S2. One metabolite was found to be inversely associated with gestational duration, and another metabolite with birth weight; they were tentatively identified as pyrazole, 3-nitro- and 10-nonadecenoic acid, methyl ester respectively. There were trends toward association of four metabolites and birth length, of which two were related to branched chain amino acids (3-methyl-2-oxopentanoic acid and isoleucine).

Table 2 Associations between maternal plasma metabolite levels and infant birth outcomes (q-value <0.05).

We observed inverse associations between 28 metabolites and infants’ sum of skinfold thicknesses at birth — 13 amino acid-related, 4 fatty acids, 6 xenobiotics, and 5 unknown compounds. Branched-chain fatty acids, medium-chain fatty acids (C10:0 and C12:0), and omega-6 fatty acids (C20:2 and C22:4) showed inverse trends with sum of skinfolds while 2-hydroxybutyric acid and 2-hydroisobutyric acid showed positive trends.

Potential interactions between ethnicity and metabolite associations for birth weight (5 metabolites) and birth length (8 metabolites) but not gestational age or sum of skinfolds (Supplemental Table S3). Stratified analyses were conducted, and higher branched-chain fatty acids were associated with higher birth weight and longer birth length in Indians but not in Chinese and Malays.

Associations of maternal characteristics and infant adiposity-related metabolites

Figure 1 summarizes the relationships between maternal characteristics and the infant adiposity-related metabolites. All results and estimates are presented in Supplemental Table S4. Ethnicity had the highest number of significant and independent associations with metabolites related to infant adiposity (n = 26). Generally, Chinese and Indian women showed contrasting associations. For example, levels of branched chain amino acids and 2-hydroxybutyric acid were higher in Chinese women but lower in Indian women. Metabolite profiles of Chinese women shared similarities with those of women who were overweight before pregnancy (n = 16 metabolites showed concordant direction of effect estimates).

Figure 1
figure 1

Maternal characteristics and infant adiposity-related metabolites. Multiple linear regression was performed with metabolite z-scores modelled as dependent variables and maternal characteristics as independent variables. Each circle denotes negative log-transformed q-values derived by the Benjamini-Hochberg procedure. Larger circles represent a lower q-value (i.e., a lower false discovery rate). (description for ‘Positive association’, ‘Negative association’ and ‘Significant association’).

Among the modifiable factors, pre-pregnancy overweight and maternal diet quality had the strongest associations with the metabolome (n = 17 and n = 15 metabolites, respectively). Few significant associations were found with parity, maternal age, tobacco smoke exposure during pregnancy, and gestational diabetes, and none with pre-pregnancy underweight, physical activity, and alcohol consumption during pregnancy.

Branched chain fatty acids were associated with most maternal factors. Lower levels were observed in participants who were exposed to tobacco smoke during pregnancy, multiparous, overweight, or of Chinese ethnicity, but higher levels were seen in Malay and Indian women and women with better diet quality.

Sensitivity analysis

Results were largely consistent when we examined sex-specific birth weight-for-GA z-scores or adjusted for fasting or postprandial plasma glucose level instead of gestational diabetes. When we restricted our analysis of sum of skinfold thicknesses to participants with no missing data (n = 722), term births, or women without hypertensive disorders, or gestational diabetes (n = 536), results remained similar (data not shown).

Discussion

In this multi-ethnic Asian cohort of 940 mother-offspring pairs, maternal levels of amino acid-related metabolites, non-esterified fatty acids, and xenobiotics were associated with neonatal sum of triceps and subscapular skinfold thicknesses. Few associations were observed with gestational duration, birth weight, or birth length. Maternal ethnicity, pre-pregnancy BMI, and diet quality during pregnancy had the strongest associations with the specific metabolome related to infant adiposity.

We are aware of one study that has examined the association between the maternal plasma metabolome and infant adiposity at birth21. In that United States study (n = 121), alkyl-linked phosphatidylcholines containing fatty acid 20:4 in the third trimester were associated with lower newborn body fat. However, differences in the analytical approach (targeted versus untargeted) and analytical platform (LC-MS versus GC-MS) limit our ability to compare our results to those of the previous study.

We observed an inverse association between amino acid-related metabolites and infant skinfold thickness. This finding is in line with our previous work, which showed higher maternal protein intake associated with lower abdominal internal adiposity in neonates58. However, we cautioned that protein intake does not necessarily mirror plasma concentrations of amino acids59,60 and that metabolite levels are also influenced by other maternal factors (e.g., ethnicity and pre-pregnancy overweight; see Fig. 1).

Congruent with previous studies, we showed positive trends between maternal 2-hydroxybutyrate levels and infant skinfold thickness. 2-hydroxybutyrate is a known early biomarker of insulin resistance61 and maternal glucose intolerance has also been shown (in our cohort and others) to be strongly associated with higher skinfold thickness in infancy62,63.

Accumulating evidence shows that elevated fatty acid concentrations are not necessarily associated with increased adiposity and insulin resistance64. Some fatty acids play a vital role in fetal growth and development65. In particular, medium chain fatty acids, which were associated with lower infant skinfold thickness in our study, have been shown to be related to higher oxidative metabolism and reduced adiposity in both animal and human studies66.

Branched-chain fatty acids (BCFA) showed inverse trends with infant skinfold thickness. We also observed lower levels of BCFA in women exposed to tobacco smoke during pregnancy, and in women who were multiparous, overweight, or of Chinese ethnicity, while higher levels were observed in Malay and Indian women and in women with better diet quality (Fig. 1). BCFA can be synthesized de novo or obtained from ruminant fats and milk67. Recent studies have reported that BCFA levels are positively associated with insulin sensitivity and are lower in obese than in lean persons68,69. However, inadequate information on lipid metabolism during pregnancy limits our understanding of the underlying mechanisms.

Several xenobiotics were significantly associated with the sum of skinfolds. However, their precise function and origin are largely unknown, except for 2-hydroxyisobutyric acid (2-HIBA). 2-HIBA is a gut microbiota-associated metabolite70 and may also reflect environmental exposure of the fuel additive, methyl tert-butyl ether71. Higher levels of 2-HIBA, which was associated with higher infant skinfold thickness in our study, have been observed in the urine of obese people72 and identified as a metabolic signature of adiposity73 and diabetes mellitus74.

We observed trends toward higher levels of branched-chain amino acid-related metabolites and longer birth length. This finding is in line with a cohort in United States examining cord blood metabolite patterns75. Pyrazole, 3-nitro- was found to be inversely associated with gestational duration, and 10-Nonadecenoic acid, methyl ester with birth weight. Based on their tentative identities, these metabolites have not been reported in earlier studies16,17,18,19, likely due to differences in analytical techniques (GC-MS versus LC-MS or NMR). We found associations between higher branched chain fatty acids and higher birth weight and longer birth length in Indians, but this was not observed in Chinese and Malays. Ethnic-specific associations have not been reported in previous studies.

Maternal ethnicity had the strongest associations with the specific metabolome related to infant adiposity. Chinese and Indian women often showed contrasting associations; these ethnic differences were also observed in our earlier work in which Chinese infants, compared to Indians, were more susceptible to excessive neonatal adiposity from high maternal glycemia63. We also observed that metabolite profiles of Chinese women were similar to women who were overweight even though Chinese women had a lower mean BMI than Malay and Indians in our study (mean ± SD: 21.6 ± 3.4 in Chinese; 24.2 ± 5.4 in Malay, 23.9 ± 4.5 in Indian). This may explain why the impact of increasing BMI on insulin resistance, C-reactive protein, and adiponectin levels is more pronounced in Chinese than in the other ethnic groups in Singapore76.

Among the modifiable factors, pre-pregnancy overweight and maternal diet quality were strongly associated with the metabolic signature of infant adiposity. Metabolite profiles have been shown to be reflective of diet quality13, but we did not observe similar diet-metabolite associations in our study. This difference may be attributable to differences in study population (pregnant versus non-pregnant)13 or in socio-cultural dietary habits. Congruent with our findings, pre-pregnancy BMI has been identified as an important driver of metabolic variation in a United States cohort16, and metabolites we found to be associated with overweight status have also been reported in other cohorts14,66,68,77,78,79. If our findings are replicated in other cohorts, formal mediation analysis would help sort out the degree to which the associations shown in Table 1 are mediated by the maternal metabolites or through other causal pathways

Strengths of our study include its prospective design (which minimizes interviewer and recall bias), the metabolomic profiling of a large multi-ethnic Asian population, the collection of lifestyle and clinical data (which permit adjustment for confounding factors), and the assessment of infant skinfold thicknesses, in addition to more common measures such as birth weight, which has been strongly associated with infant adipose stores and highlighted as a strong predictor of later child obesity risk16.

Several limitations of our study are worth noting. First, we have explored only the maternal plasma metabolome and concentrated on GC-MS analysis with methyl chloroformate derivatization. Although this method has optimized the detection of compounds with amino and/or carboxyl groups (which includes most metabolites of central carbon metabolism and key intermediates of cell metabolism39), our work could be complemented by employing different analytical techniques such as a variation of sample extraction methods or the use of multiple analytical platforms to obtain a more comprehensive overview of the metabolome. Second, we assessed maternal metabolites at 26–28 weeks of gestation, which precludes analysis of changes in metabolite levels across pregnancy. Third, we did not examine fetal growth throughout pregnancy; as a consequence, the temporal sequence between the maternal metabolome and infant birth size is unclear. Maternal metabolite profiles could have bi-directional relationships with fetal growth, such that abnormal fetal growth (e.g., intrauterine growth restriction) could influence maternal metabolite levels. Future studies should examine serial fetal biometry to address this issue. Last, as in any observational study, our findings could still be influenced by residual confounding such as imprecise measurements or underlying medical conditions despite the many potential confounding factors we adjusted for, and causality cannot be inferred.

In conclusion, we observed links between amino acid-related metabolites, non-esterified fatty acids, and infant adiposity at birth measured by sum of skinfold thickness. Few associations were observed with gestational duration, birth weight, or birth length. Maternal ethnicity, pre-pregnancy BMI, and diet quality had the strongest associations with the metabolome. Further independent studies are warranted to replicate our findings and to understand the underlying mechanisms.

Data availability

Data are available upon request because data request for analysis must be assessed and approved by the executive committee of the GUSTO study and administered by the main GUSTO study team of data management, which is a third-party source. Any matter related to data request, please contact Mary Chong Foong Fong at mary_chong@nus.edu.sg

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Acknowledgements

All authors thank the GUSTO study group, GUSTO study team, Department of Diagnostic and Interventional Imaging, KKH, Department of Diagnostic Imaging, NUH and the study participants; parents and their neonates for their valuable contribution in this study. The GUSTO study group includes Allan Sheppard, Amutha Chinnadurai, Anne Eng Neo Goh, Anne Rifkin-Graboi, Anqi Qiu, Arijit Biswas, Bee Wah Lee, Birit F.P. Broekman, Boon Long Quah, Borys Shuter, Chai Kiat Chng, Cheryl Ngo, Choon Looi Bong, Christiani Jeyakumar Henry, Cornelia Yin Ing Chee, Yam Thiam Daniel Goh, Doris Fok, Fabian Yap, George Seow Heong Yeo, Helen Chen, Hugo P S van Bever, Iliana Magiati, Inez Bik Yun Wong, Ivy Yee-Man Lau, Jeevesh Kapur, Jenny L. Richmond, Jerry Kok Yen Chan, Joanna D. Holbrook, Joshua J. Gooley, Keith M. Godfrey, Kenneth Kwek, Kok Hian Tan, Krishnamoorthy Niduvaje, Leher Singh, Lin Lin Su, Lourdes Mary Daniel, Lynette Pei-Chi Shek, Marielle V. Fortier, Mark Hanson, Mary Foong-Fong Chong, Mary Rauff, Mei Chien Chua, Michael Meaney, Mya Thway Tint, Neerja Karnani, Ngee Lek, Oon Hoe Teoh, P. C. Wong, Peter D. Gluckman, Pratibha Agarwal, Rob M. van Dam, Salome A. Rebello, Seang-Mei Saw, Shang Chee Chong, Shirong Cai, Shu-E Soh, Sok Bee Lim, Chin-Ying Stephen Hsu, Victor Samuel Rajadurai, Walter Stunkel, Wee Meng Han, Wei Wei Pang, Yap-Seng Chong, Yin Bun Cheung, Yiong Huak Chan and Yung Seng Lee. This research is supported by the Singapore Institute for Clinical Sciences, Agency for Science Technology and Research (A*STAR), Singapore; and the Ministry of Business, Innovation, and Employment (MBIE), New Zealand, through the International Relationships Fund. GUSTO is financially supported under Translational Clinical Research (TCR) Flagship Programme on Developmental Pathways to Metabolic Disease (NMRC/TCR/004-NUS/2008; NMRC/TCR/012-NUHS/2014) funded by the National Research Foundation (NRF) and administered by the National Medical Research Council (NMRC), Singapore. Additional funding is provided by the Singapore Institute for Clinical Sciences, A*STAR, Singapore. K.M.G. is supported by the National Institute for Health Research through the NIHR Southampton Biomedical Research Centre and the European Union’s Erasmus+ Capacity-building ENeASEA Project and Seventh Framework Programme (FP7/2007–2013), projects EarlyNutrition and ODIN (grant numbers 289346 and 613977). Study sponsors were not involved in the design of the study, statistical analysis and results interpretation.

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M.F.-F.C., P.N.B. and N.K. designed the research; K.M.G., F.Y., K.H.T., L.P.-C.S. and Y.S.L. designed and led the GUSTO study; A-R.C. and J.V.d.S. performed the experiment and processed the metabolites data under the guidance of G.W., K.S., T.-L.H., and E.J.M.; I.M.A. contributed to birth data collection, cleaning, and analysis. A-R.C. performed the statistical analysis and drafted the manuscript. M.F.-F.C. and M.S.K. provided statistical input. All authors reviewed the manuscript for important intellectual content.

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Correspondence to Ai-Ru Chia or Mary Foong-Fong Chong.

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L.P.-C.S. and K.M.G. have received reimbursement for speaking at conferences sponsored by companies selling nutritional products. They are part of an academic consortium that has received research funding from Abbott Nutrition, Nestle, and Danone. The other authors have no potential conflicts of interest to disclose.

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Chia, AR., de Seymour, J.V., Wong, G. et al. Maternal plasma metabolic markers of neonatal adiposity and associated maternal characteristics: The GUSTO study. Sci Rep 10, 9422 (2020). https://doi.org/10.1038/s41598-020-66026-5

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