TY - JOUR
T1 - Plasma Amino Acids in Early Pregnancy and Midpregnancy and Their Interplay With Phospholipid Fatty Acids in Association With the Risk of Gestational Diabetes Mellitus
T2 - Results From a Longitudinal Prospective Cohort
AU - Yang, Jiaxi
AU - Wu, Jing
AU - Tekola-Ayele, Fasil
AU - Li, Ling Jun
AU - Bremer, Andrew A.
AU - Lu, Ruijin
AU - Rahman, Mohammad L.
AU - Weir, Natalie L.
AU - Pang, Wei Wei
AU - Chen, Zhen
AU - Tsai, Michael Y.
AU - Zhang, Cuilin
N1 - Funding Information:
Acknowledgments. The authors thank all the participants and staff at the participating clinical centers in the Eunice Kennedy Shriver NICHD Fetal Growth Studies–Singleton Cohort, including Christina Care Health Systems, University of California, Irvine, Long Beach Memorial Medical Center, Northwestern University, Medical University of South Carolina, Columbia University, New York Hospital Queens, St. Peter’s University Hospital, University of Alabama at Birmingham, Women and Infants Hospital of Rhode Island, Fountain Valley Regional Hospital and Medical Center, and Tufts University. We also acknowledge the C-TASC Corporation, which provided data coordination, and the Department of Laboratory Medicine and Pathology, University of Minnesota, which provided laboratory resources essential for biochemical analysis. Funding. This work was supported by Eunice Kennedy Shriver NICHD intramural funding and American Recovery and Reinvestment Act funding via contract numbers HHSN275200800013C, HHSN275200800002I, HHSN27500006, HHSN27 5200800003IC, HHSN275200800014C, HHSN275 200800012C, HHSN275200800028C, HHSN2752 01000009C, and HHSN275201000001Z. Duality of Interest. No potential conflicts of interest relevant to this article were reported. Authors Contributions. J.Y. and J.W. conducted statistical analysis and designed the figures. J.Y. drafted the manuscript. C.Z. conceptualized the study design. C.Z. obtained funding and supervised data collection for the Eunice Kennedy Shriver NICHD Fetal Growth Study. All authors contributed to the interpretation of the results and revision of the manuscript for important intellectual content and approved the final version of the manuscript. C.Z. and J.Y. are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Prior Presentation. Parts of this study were presented as an abstract during the American Society for Nutrition’s virtual Nutrition 2022 Live Online Conference, 14–16 June 2022.
Publisher Copyright:
© 2023 by the American Diabetes Association.
PY - 2023/4
Y1 - 2023/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85151042776&partnerID=8YFLogxK
U2 - 10.2337/dc22-1892
DO - 10.2337/dc22-1892
M3 - Article
C2 - 36701229
AN - SCOPUS:85151042776
SN - 0149-5992
VL - 46
SP - 722
EP - 732
JO - Diabetes care
JF - Diabetes care
IS - 4
ER -