妊娠早期和中期的妊娠糖尿病与不同的叶酸相关代谢物有关:一项前瞻性队列研究。

IF 4.6 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Wei Zheng, Yujie Zhang, Puyang Zhang, Tengda Chen, Xin Yan, Lin Li, Lijun Shao, Zhiru Song, Weiling Han, Jia Wang, Junhua Huang, Kaiwen Ma, Ruihua Yang, Yuru Ma, Lili Xu, Kexin Zhang, Xianxian Yuan, Guanghui Li
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引用次数: 0

摘要

目的:本研究旨在评估妊娠期糖尿病(GDM)与循环叶酸代谢物、叶酸摄入量以及亚甲基四氢叶酸还原酶(MTHFR)和蛋氨酸合成酶还原酶(MTRR)基因型之间的关系:一项前瞻性妊娠队列研究于 2022 年至 2023 年在中国北京进行。在妊娠 6-17 周和 20-26 周时测定循环叶酸代谢物,包括红细胞(RBC)5-甲基四氢叶酸(5-MTHF)、5,10-亚甲基四氢叶酸(5,10-CH2-THF)、5-甲酰四氢叶酸(5-CHO-THF)和未代谢叶酸(UMFA),以及血浆同型半胱氨酸(HCY)、5-MTHF 和甲基丙二酸(MMA)。此外,还检测了脂肪酸摄入量以及 MTHFR 和 MTRR 基因型。通过 75 克口服葡萄糖耐量试验(OGTT),在妊娠 24 至 28 周期间诊断出 GDM。使用多变量广义线性模型、逻辑回归模型和限制性三次样条回归确定叶酸状况与 GDM 之间的关系,并对潜在的混杂因素进行调整:研究共纳入 2032 名孕妇,其中 392 人(19.29%)罹患 GDM。孕早期 UMFA 高于第 75 百分位数(≥P75)[调整 OR (aOR) (95% 置信区间 [CI]) = 1.36 (1.01-1.84)],UMFA ≥ P90 [aOR (95% CI) = 1.82 (1.23-2.69)],HCY ≥ P75 [aOR (95% CI) = 1.40 (1.04-1. 88)]。88)],以及孕中期≥ P75 的 RBC 5-MTHF [aOR (95% CI) = 1.48 (1.10-2.00)]、RBC 5,10-CH2-THF [aOR (95% CI) = 1.55 (1.15-2.10)]和血浆 5-MTHF [aOR (95% CI) = 1.36 (1.00-1.86)]与 GDM 相关。孕早期较高的 UMFA 水平与 OGTT 期间的 1 小时和 2 小时血糖水平呈正相关,较高的 HCY 水平与 OGTT 期间空腹血糖水平升高相关。相比之下,妊娠中期的红细胞 5- MTHF 和 5,10-CH2-THF,以及血浆 5- MTHF 与 1-h 血糖水平呈正相关(p 结论):孕早期 UMFA 和 HCY 水平升高,以及孕中期红细胞 5- MTHF 和 5,10-CH2-THF 以及血浆 5- MTHF 水平升高,均与 GDM 有关。这些研究结果表明,不同的叶酸代谢物与 GDM 的发生之间存在明显的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gestational diabetes mellitus is associated with distinct folate-related metabolites in early and mid-pregnancy: A prospective cohort study

Aims

This study aimed to evaluate the association between gestational diabetes mellitus (GDM) and circulating folate metabolites, folic acid (FA) intake, and the methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) genotype.

Materials and Methods

A prospective pregnancy cohort study was conducted in Beijing, China, from 2022 to 2023. Circulating folate metabolites, including red blood cell (RBC) 5-methyltetrahydrofolate (5-MTHF), 5, 10-methylene-tetrahydrofolate (5,10-CH2-THF), 5- formyltetrahydrofolate (5-CHO-THF), and unmetabolised folic acid (UMFA), and plasma homocysteine (HCY), 5-MTHF, and methylmalonic acid (MMA), were determined at 6–17 weeks and 20–26 weeks of gestation. FA intake and the MTHFR and MTRR genotype were also examined. GDM was diagnosed between 24 and 28 weeks of pregnancy by a 75-g oral glucose tolerance test (OGTT). The association between the folate status and GDM was ascertained using multivariate generalised linear models, logistic regression models, and restricted cubic spline regression, adjusting for potential confounders.

Results

The study included 2032 pregnant women, of whom 392 (19.29%) developed GDM. UMFA above the 75th percentile (≥P75) [adjusted OR (aOR) (95% confidence interval [CI]) = 1.36 (1.01–1.84)], UMFA ≥ P90 [aOR (95% CI) = 1.82 (1.23–2.69)], and HCY ≥ P75 [aOR (95% CI) = 1.40 (1.04–1.88)] in early pregnancy, and RBC 5-MTHF [aOR (95% CI) = 1.48 (1.10–2.00)], RBC 5,10-CH2-THF [aOR (95% CI) = 1.55 (1.15–2.10)], and plasma 5-MTHF [aOR (95% CI) = 1.36 (1.00–1.86)] in mid-pregnancy ≥ P75 are associated with GDM. Higher UMFA levels in early pregnancy show positive associations with the 1-h and 2-h glucose levels during the OGTT, and higher HCY levels are associated with increased fasting glucose levels during the OGTT. In comparison, RBC 5- MTHF and 5,10-CH2-THF, and plasma 5- MTHF in mid-pregnancy are positively associated with the 1-h glucose level (p < 0.05). The MTHFR and MTRR genotype and FA intake are not associated with GDM.

Conclusions

Elevated levels of UMFA and HCY during early pregnancy, along with elevated RBC 5-MTHF and 5,10-CH2-THF and plasma 5-MTHF during mid-pregnancy, are associated with GDM. These findings indicate distinct connections between different folate metabolites and the occurrence of GDM.

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来源期刊
Diabetes/Metabolism Research and Reviews
Diabetes/Metabolism Research and Reviews 医学-内分泌学与代谢
CiteScore
17.20
自引率
2.50%
发文量
84
审稿时长
4-8 weeks
期刊介绍: Diabetes/Metabolism Research and Reviews is a premier endocrinology and metabolism journal esteemed by clinicians and researchers alike. Encompassing a wide spectrum of topics including diabetes, endocrinology, metabolism, and obesity, the journal eagerly accepts submissions ranging from clinical studies to basic and translational research, as well as reviews exploring historical progress, controversial issues, and prominent opinions in the field. Join us in advancing knowledge and understanding in the realm of diabetes and metabolism.
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