Please use this identifier to cite or link to this item: https://doi.org/10.2337/dc22-1892
Title: Plasma Amino Acids in Early Pregnancy and Midpregnancy and Their Interplay With Phospholipid Fatty Acids in Association With the Risk of Gestational Diabetes Mellitus: Results From a Longitudinal Prospective Cohort
Authors: Yang, Jiaxi 
Wu, Jing
Tekola-Ayele, Fasil
Li, Ling-Jun 
Bremer, Andrew A
Lu, Ruijin
Rahman, Mohammad L
Weir, Natalie L
Pang, Wei Wei 
Chen, Zhen
Tsai, Michael Y
Zhang, Cuilin 
Keywords: Science & Technology
Life Sciences & Biomedicine
Endocrinology & Metabolism
METABOLISM
METABOLOMICS
OBESITY
WOMEN
SERUM
Issue Date: Apr-2023
Publisher: AMER DIABETES ASSOC
Citation: Yang, Jiaxi, Wu, Jing, Tekola-Ayele, Fasil, Li, Ling-Jun, Bremer, Andrew A, Lu, Ruijin, Rahman, Mohammad L, Weir, Natalie L, Pang, Wei Wei, Chen, Zhen, Tsai, Michael Y, Zhang, Cuilin (2023-04). Plasma Amino Acids in Early Pregnancy and Midpregnancy and Their Interplay With Phospholipid Fatty Acids in Association With the Risk of Gestational Diabetes Mellitus: Results From a Longitudinal Prospective Cohort. DIABETES CARE 46 (4) : 722-732. ScholarBank@NUS Repository. https://doi.org/10.2337/dc22-1892
Abstract: OBJECTIVE We prospectively evaluated plasma amino acids (AAs) in early pregnancy and midpregnancy and their interplay with phospholipid fatty acids (FAs) in association with gestational diabetes mellitus (GDM) risk. RESEARCH DESIGN AND METHODS From a longitudinal pregnancy cohort of 2,802 individuals, concentrations of 24 plasma AAs at 10–14 and 15–26 gestational weeks (GW) were assessed among 107 GDM case subjects and 214 non-GDM control subjects. We estimated adjusted odds ratios (OR) and 95% CI for the associations of plasma AAs and the joint associations of plasma AAs and phospholipid FAs with GDM risk, adjusting for risk factors including age, prepregnancy BMI, and family history of diabetes. RESULTS Glycine at 10–14 GW was inversely associated with GDM (adjusted OR [95% CI] per SD increment: 0.55 [0.39–0.79]). Alanine, aspartic acid, and glutamic acid at 10–14 GW were positively associated with GDM (1.43 [1.08–1.88], 1.41 [1.11–1.80], and 1.39 [0.98–1.98]). At 15–26 GW, findings for glycine, alanine, aspartic acid, and the glutamine– to–glutamic acid ratio were consistent with the directions observed at 10–14 GW. Isoleucine, phenylalanine, and tyrosine were positively associated with GDM (1.64 [1.19–2.27], 1.15 [0.87–1.53], and 1.56 [1.16–2.09]). All P values for linear trend were <0.05. Several AAs and phospholipid FAs were significantly and jointly associated with GDM. For instance, the lowest risk was observed among women with higher glycine and lower even-chain saturated FAs at 10–14 GW (adjusted OR [95% CI] 0.15 [0.06, 0.37]). CONCLUSIONS Plasma AAs may be implicated in GDM development starting in early pregnancy. Associations of AAs with GDM may be enhanced in the copresence of phospholipid FA profile.
Source Title: DIABETES CARE
URI: https://scholarbank.nus.edu.sg/handle/10635/245737
ISSN: 0149-5992
1935-5548
DOI: 10.2337/dc22-1892
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