Umbilical cord plasma lysophospholipids and triacylglycerols associated with birthweight percentiles
Umbilical cord plasma lysophospholipids and triacylglycerols associated with birthweight percentiles
Dysregulated transplacental lipid transfer and fetal-placental lipid metabolism affect birthweight, as does maternal hyperglycemia. As the mechanisms are unclear, we aimed to identify the lipids in umbilical cord plasma that were most associated with birthweight. Seventy-five Chinese women with singleton pregnancies recruited into the GUSTO mother-offspring cohort were selected from across the glycemic range based on a mid-gestation 75 g oral glucose tolerance test, excluding pre-existing diabetes. Cord plasma samples collected at term delivery were analyzed using targeted liquid-chromatography tandem mass-spectrometry to determine the concentrations of 404 lipid species across 17 lipid classes. The birthweights were standardized for sex and gestational age by local references, and regression analyses were adjusted for the maternal age, BMI, parity, mode of delivery, insulin treatment, and fasting/2 h glucose, with a false discovery-corrected
p < 0.05 considered significant. Ten lysophosphatidylcholines (LPCs) and two lysophosphatidylethanolamines were positively associated with the birthweight percentiles, while twenty-four triacylglycerols were negatively associated with the birthweight percentiles. The topmost associated lipid was LPC 20:2 [21.28 (95%CI 12.70, 29.87) percentile increase in the standardized birthweight with each SD-unit increase in log
10-transformed concentration]. Within these same regression models, maternal glycemia did not significantly associate with the birthweight percentiles. Specific fetal circulating lysophospholipids and triacylglycerols associate with birthweight independently of maternal glycemia, but a causal relationship remains to be established.
fetal growth, GUSTO, lipidomics, lysophosphatidylcholine, triacylglycerol, umbilical cord blood
Wong, Gerard
e7bf15bb-66a6-4307-9dbf-1d7d31909604
Narasimhan, Kothandaraman
8e3b3155-7998-4a4d-9867-89bdaa176f37
Cheong, Wei Fun
9cbd3bcf-b57d-4942-a48f-f1ceac267274
Godfrey, Keith M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
17 January 2024
Wong, Gerard
e7bf15bb-66a6-4307-9dbf-1d7d31909604
Narasimhan, Kothandaraman
8e3b3155-7998-4a4d-9867-89bdaa176f37
Cheong, Wei Fun
9cbd3bcf-b57d-4942-a48f-f1ceac267274
Godfrey, Keith M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Wong, Gerard, Narasimhan, Kothandaraman and Cheong, Wei Fun
,
et al.
(2024)
Umbilical cord plasma lysophospholipids and triacylglycerols associated with birthweight percentiles.
Nutrients, 16 (2), [274].
(doi:10.3390/nu16020274).
Abstract
Dysregulated transplacental lipid transfer and fetal-placental lipid metabolism affect birthweight, as does maternal hyperglycemia. As the mechanisms are unclear, we aimed to identify the lipids in umbilical cord plasma that were most associated with birthweight. Seventy-five Chinese women with singleton pregnancies recruited into the GUSTO mother-offspring cohort were selected from across the glycemic range based on a mid-gestation 75 g oral glucose tolerance test, excluding pre-existing diabetes. Cord plasma samples collected at term delivery were analyzed using targeted liquid-chromatography tandem mass-spectrometry to determine the concentrations of 404 lipid species across 17 lipid classes. The birthweights were standardized for sex and gestational age by local references, and regression analyses were adjusted for the maternal age, BMI, parity, mode of delivery, insulin treatment, and fasting/2 h glucose, with a false discovery-corrected
p < 0.05 considered significant. Ten lysophosphatidylcholines (LPCs) and two lysophosphatidylethanolamines were positively associated with the birthweight percentiles, while twenty-four triacylglycerols were negatively associated with the birthweight percentiles. The topmost associated lipid was LPC 20:2 [21.28 (95%CI 12.70, 29.87) percentile increase in the standardized birthweight with each SD-unit increase in log
10-transformed concentration]. Within these same regression models, maternal glycemia did not significantly associate with the birthweight percentiles. Specific fetal circulating lysophospholipids and triacylglycerols associate with birthweight independently of maternal glycemia, but a causal relationship remains to be established.
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Accepted/In Press date: 11 January 2024
e-pub ahead of print date: 17 January 2024
Published date: 17 January 2024
Additional Information:
Funding: This research is supported by the Singapore National Research Foundation under its Translational and Clinical Research (TCR) Flagship Programme and administered by the Singapore Ministry of Health’s National Medical Research Council (NMRC), Singapore—NMRC/TCR/004-NUS/2008; NMRC/TCR/012-NUHS/2014. Additional funding is provided by the Singapore In�stitute for Clinical Sciences, Agency for Science Technology and Research (A*STAR), Singapore. The Singapore Lipidomics Incubator receives funding from the Life Sciences Institute, the National University of Singapore Yong Loo Lin School of Medicine, and the National Research Foundation (grant number NRFI2015-05). This research is also supported by a Clinician Scientist Award to
S.-Y.C. from the Singapore National Medical Research Council (NMRC/CSA-INV/0010/2016; MOH�CSAINV19nov-0002). K.M.G. is supported by the UK Medical Research Council (MC_UU_12011/4), the National Institute for Health Research (NIHR Senior Investigator (NF-SI-0515-10042) and the NIHR Southampton Biomedical Research Centre) and the European Union (Erasmus+ Programme ImpENSA 598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP).
Publisher Copyright:
© 2024 by the authors.
Keywords:
fetal growth, GUSTO, lipidomics, lysophosphatidylcholine, triacylglycerol, umbilical cord blood
Identifiers
Local EPrints ID: 486497
URI: http://eprints.soton.ac.uk/id/eprint/486497
ISSN: 2072-6643
PURE UUID: fd7e4b67-61fc-470b-b336-1209a2ca6865
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Date deposited: 24 Jan 2024 17:46
Last modified: 14 May 2024 01:33
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Author:
Gerard Wong
Author:
Kothandaraman Narasimhan
Author:
Wei Fun Cheong
Corporate Author: et al.
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