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Article

The Association between Maternal B Vitamins in Early Pregnancy and Gestational Diabetes Mellitus: A Prospective Cohort Study

1
Nursing Department, Obstetrics and Gynaecology Hospital of Fudan University, Shanghai 200090, China
2
School of Nursing, Fudan University, Shanghai 200032, China
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Nutrients 2022, 14(23), 5016; https://doi.org/10.3390/nu14235016
Submission received: 26 October 2022 / Revised: 17 November 2022 / Accepted: 22 November 2022 / Published: 25 November 2022
(This article belongs to the Special Issue Nutrition in Pregnancy and Child)

Abstract

:
Background: This study evaluated the association between maternal B vitamins in early pregnancy and gestational diabetes mellitus (GDM) risk. Methods: A cohort of 1265 pregnant women was recruited at 8–15 weeks of gestation in 2021–2022 (Shanghai, China). Pregnancies with both serum B vitamin measurements at recruitment and glucose measurements at 24–28 weeks of gestation were included in the final analysis. Results: Of the 1065 pregnancies, in the final analysis, GDM occurred in 121 women (11.36%). In multivariate logistic models, an increased risk trend across serum vitamin B1 quartiles with GDM was observed (p-Trend = 0.001). Compared with women in the lowest quartile of serum vitamin B6, those in the upper two quartiles had approximately twofold higher odds of GDM. Moreover, compared with women with vitamin B12 levels < 150 pmol/L, those with vitamin B12 levels > 150 pmol/L had lower odds of GDM (p = 0.005). The restricted cubic spline regression models also revealed that serum vitamin B6 and vitamin B12 were associated with an increased risk of GDM in a nonlinear fashion. Conclusions: Our study shows that higher maternal serum vitamin B1 and B6 levels in early pregnancy are associated with increased GDM risk, while sufficient vitamin B12 status is associated with lower GDM risk.

Graphical Abstract

1. Introduction

Gestational diabetes mellitus (GDM) is one of the most common metabolic disorders during pregnancy, affecting 16.7% of pregnancies worldwide [1]. The prevalence is 14.8% in China [2]. GDM is related to higher short-term and long-term adverse outcomes in both mothers and offspring [3,4,5]. In addition, adverse metabolic programming of offspring may exist prior to the diagnosis of GDM [6]. Thus, identifying modifiable risk factors for GDM would be useful for the prevention of this disease.
Balanced nutrition is important for pregnant women. During pregnancy, severe micronutrient deficiency or excess can have negative impacts on both the fetus (including low birth weight, intrauterine growth retardation or congenital malformations) and the pregnant women (hypertensive disorders or gestational diabetes) [7,8,9]. Group B vitamins, particularly thiamine (B1), riboflavin (B2), niacin (B3), pyridoxine (B6), folate and cobalamin (B12), have important roles in glucose metabolism and most have been linked to type 2 diabetes [10,11]. Folate and vitamin B12 are essential nutrients for the metabolism of the one-carbon unit involved in the DNA methylation and synthesis of amino acids, lipids and nucleic acids [12]. In order to prevent neural tube defects, supplementation of 400 µg folic acid daily is routinely recommended for women of childbearing age from at least 3 months before conception and during pregnancy [13,14].
Recently, folate and vitamin B12 have been studied regarding their relationship with GDM risk, but conflicting results have been reported [15,16]. In several studies, vitamin B12 insufficiency and folate excess were common in early pregnancy, and a higher serum folate/vitamin B12 ratio was associated with an elevated risk of GDM [16,17]. These findings highlight the detrimental effects of maternal imbalance of these two vitamins. Vitamin B12 is also a coenzyme involved in the degradation of odd-chain fatty acids and branched-chain amino acids (BCAAs) [18]. Elevated BCAA levels play a role in the onset of type 2 diabetes [19].
Today, increasing numbers of pregnant women are taking compound vitamin supplements mainly containing folic acid and other B-group vitamins. In fact, B vitamins are often metabolically entwined and some of the mechanisms of their roles could contribute to glucose homeostasis. For example, vitamin B6 is also involved in one-carbon and homocysteine metabolism, and it can promote the absorption of vitamin B12 [20]. Vitamin B1 is involved in many redox reactions in glucose and BCAA metabolism [21]. Vitamin B1 homeostasis disturbance is prevalent in type 1 and type 2 diabetes [21,22], but its role in glucose metabolism during pregnancy is unclear. Although several B vitamins (such as vitamin B1, vitamin B2 and vitamin B6) are included in dietary supplements, their individual metabolic roles are not well specified in pregnancy [23].
To our knowledge, limited studies have investigated the relationship between B vitamins other than folate and vitamin B12 in early pregnancy and GDM. Therefore, the aims of this prospective cohort study were to (1) describe the serum levels of B vitamins including folate and vitamins B1, B2, B6 and B12 in early pregnancy; and (2) investigate whether serum B vitamins in early pregnancy are associated with glucose levels and the risk of GDM.

2. Materials and Methods

2.1. Study Population

A prospective cohort study to investigate the influences of maternal dietary supplements and nutritional biomarkers on blood glucose levels and GDM during pregnancy was conducted among pregnant women in a hospital in Shanghai, China. The Research Committee of the study hospital approved this study (No. 202123), and all participants gave written informed consent to participate. In brief, all participants were recruited from a maternity hospital, which is a tertiary university-affiliated hospital located in Shanghai. Annually, the total number of births is about 12,000 in the hospital. From March 2021 to March 2022, two research nurses enrolled women at their first antenatal visits. Participants were eligible for our study if they (1) had a live singleton pregnancy at 8–15 weeks’ gestation and (2) had registered and planned to give birth in the study hospital. The exclusion criteria were (1) pre-existing diabetes or a diagnosis of GDM before 24 weeks of gestation; (2) a previous pregnancy with a neural tube defect; (3) chronic viral hepatitis, cirrhosis or severe liver disease; and (4) multiple gestation. In total, 1800 pregnant women were approached and 1265 women were recruited after assessing their eligibility. We restricted our study sample to pregnant women with complete measurements of folate and vitamins B1, B2, B6 and B12 at 8–15 weeks of gestation and three glucose measurements by oral glucose tolerance test (OGTT) at 24–28 weeks of gestation. These inclusion criteria resulted in 1065 participants in the final analysis.

2.2. Data Collection

Baseline data were collected via face-to-face interviews using a self-reported questionnaire. The data collected included the following: demographics (age, educational background and monthly personal income), lifestyle characteristics (smoking, passive smoking, alcohol consumption and physical activity), supplement intake (brand, type and duration), and medical, reproductive and family history. The medical histories of the participants were cross-checked with the electronic medical records from the hospital. Weights were measured at recruitment and OGTT visits. We calculated weight gain by subtracting self-reported pre-pregnancy weight from the weight measured at each visit. Pre-conceptional body mass index (BMI) was calculated through self-reported pre-pregnancy weight and height and divided into four categories: underweight (BMI below 18.5 kg/m2), normal weight (BMI of 18.5 to 23.9 kg/m2), overweight (BMI of 24.0 to 27.9 kg/m2) or obese (BMI of 28.0 kg/m2 or higher); these are the BMI cutoffs for Chinese individuals [24]. Physical activity level was assessed according to the International Physical Activity Questionnaire-Short Form [25], from which metabolic equivalent (MET)-min/week was calculated. Smoking exposure was defined as smoking or passive smoking 3 months before or during pregnancy. Alcohol consumption was defined as drinking any alcoholic beverages 3 months before or during pregnancy. B vitamin supplementation was regarded as regularly taking folic acid or compound vitamin supplements 3 months before and during pregnancy. In general, the folic acid supplement contains 0.4 mg/pill of folic acid, and the compound vitamin supplements contain 0.4 mg/pill or 0.8 mg/pill of folic acid, combined with other B vitamins depending on the brands.

2.3. Diagnosis of GDM

In accordance with the criteria developed by the International Association of Diabetes and Pregnancy Study Groups, participants underwent a 75 g OGTT between 24 weeks and 28 weeks of gestation and GDM was diagnosed if any of the following criteria were met: fasting glucose ≥5.1 mmol/L, 1 h glucose ≥10.0 mmol/L, 2 h glucose ≥8.5 mmol/L, or any combination of these [26].

2.4. Biochemical Analysis

As part of routine antenatal care, blood samples were collected at recruitment and at 24–28 weeks of gestation from all participants by trained nurses. Samples were centrifuged at 3000 rpm for 5 min to separate serum or plasma for biochemical analysis. B vitamin levels were measured immediately on a vitamin analyzer (VSS-A-01, Chongqin, China) using electro-chemiluminescent assays (Synovie). Plasma glucose levels were measured by the electrochemical glucose oxidase method using an automatic biochemical analyzer (Hitachi 7600, Tokyo, Japan). All measurements were conducted by the professional staff in the biochemical laboratory of the study hospital. The inter-assay coefficients of variation were <10% for the entire measurements.

2.5. Statistical Analysis

R 4.2.1 and Stata 16.0 (Stata Corp., College Station, TX, United States) were used for all the analyses. Categorical variables were described as frequencies and percentages. Continuous data were summarized as means and standard deviations or medians and interquartile ranges. Comparisons between groups for categorical variables were performed using χ2 tests. Comparisons between groups for continuous variables with normal distribution were analyzed using analysis of variance (ANOVA) or unpaired Student t-tests, and continuous variables with skewed distributions were performed by Kruskal–Wallis tests. Vitamin B12 insufficiency was defined as <150 pmol/L, which is often used to define vitamin B12 deficiency in pregnant women [27]. Folate insufficiency was defined as <5.9 nmol/L, which is suggested to define folate deficiency in the first trimester of pregnancy [28]. Other serum B vitamins were only placed into quartiles because there are no specified cut-off values for pregnant women. Correlation analysis was performed to investigate the relationship among serum B vitamins, fasting, 1 h and 2 h plasma glucose. Multivariable logistic regression models were used to explore the associations of these serum B vitamins with GDM, with adjustment for age, education, parity, first-degree family history of diabetes, smoking exposure, alcohol consumption, pre-conceptional BMI, gestational weight gain at OGTT visit and physical activity levels. Odds ratios (OR) and 95% confidence intervals (CI) were reported. Moreover, restricted cubic spline (RCS) regression models with assumed three knots were used to outline the potential nonlinear relationships between continuous serum B vitamins and GDM risk. A two-tailed p value of <0.05 was regarded as statistically significant.

3. Results

3.1. Baseline Characteristics

Table 1 shows the demographic characteristics and the biochemical measurements of the study population, according to GDM status. Among 1065 pregnancies, GDM occurred in 121 women (11.36%). The mean (standard deviation) age was 30.8 (3.7) years. Of the 1065 participants, 89.1% were nulliparous, with more than 90% having a college or above degree. Overweight and obese women accounted for 16.9% while 14.9% of the women were found to be underweight. B-vitamin supplement intake was found in 94.3% of pregnant women, of which 68.4% took multivitamin supplements. The median (interquartile range) concentrations of serum vitamin B1, vitamin B2, vitamin B6, folate and vitamin B12 were 86.5 (75.1–98.5) pmol/L, 13.5 (12.3–14.9) pmol/L, 27.2 (24.2–35.7) pmol/L, 11.8 (10.1–13.9) nmol/L and 174.8 (132.6–210.3) pmol/L. Compared with women without GDM, women with GDM were more likely to be older (p < 0.001) and multiparous (p = 0.037), overweight or obese before pregnancy (p < 0.001), and have a higher first-degree family history of diabetes (p < 0.001). In addition, women with GDM had significantly higher levels of serum vitamin B1 (p < 0.001) and lower levels of vitamin B12 (p = 0.038), and more had vitamin B12 insufficiency (p = 0.003).

3.2. Correlations between Serum B Vitamins and Glucose Levels

Table 2 shows the correlations between serum B vitamins and blood glucose levels at OGTT. Serum vitamin B1 was positively correlated with fasting, 1 h and 2 h plasma glucose, with Pearson correlation coefficients of 0.062, 0.123 and 0.111, respectively (Figure 1). Moreover, significant positive correlations were found between serum levels of vitamin B1 and vitamin B6, whereas negative correlations were found between serum levels of folate and vitamin B12 (Table 3).

3.3. Associations between Serum B Vitamins and GDM Risk

Table 4 shows the adjusted ORs (aOR) and 95% CIs estimated based on the quartiles of serum B vitamins and GDM risks. An obvious positive increased risk trend across vitamin B1 quartile groups with GDM risk was observed (p-Trend = 0.001). Furthermore, high serum levels of vitamin B6 were associated with an increased risk of GDM. Compared with women in the lowest quartile of vitamin B6, those in the upper two quartiles had approximately twofold higher odds of GDM (aOR 1.93 [95% CI 1.08–3.43], p = 0.026; aOR 1.84 [95% CI 1.03–3.29], p = 0.040). However, no obvious increased risk trend with GDM was found across vitamin B6 quartile groups (p-Trend = 0.054). Compared with vitamin B12 levels < 150 pmol/L, levels > 150 pmol/L were associated with a lower risk of GDM (aOR 0.57 [95% CI 0.38–0.84]; p = 0.005). No significant associations were found between serum vitamin B2, folate levels or the ratio of folate and vitamin B12 and GDM risks. RCS regression models revealed that serum vitamin B6 (p = 0.048) and vitamin B12 (p = 0.033) were associated with an increased risk of GDM in a nonlinear fashion. No significant associations were found between serum vitamin B2 and folate levels and GDM risks in RCS regression models (Figure 2).

4. Discussion

In this prospective cohort study, we investigated the association between serum levels of B vitamins in early pregnancy and the incidence of GDM at 24–28 weeks of gestation. We found that the risk of GDM increased in a dose–response manner across serum vitamin B1 quartiles one to four during early pregnancy, after comprehensively adjusting for a number of covariables. Consistent with this, positive correlations between serum vitamin B1 levels as a continuous variable with plasma fasting, OGTT 1 h and 2 h glucose levels were observed in the present study. Moreover, women in the upper two quartiles of serum vitamin B6 levels had higher odds of GDM. In addition, serum vitamin B12 levels > 150 pmol/L had a protective effect on GDM incidence. However, the associations between serum folate or the serum folate/vitamin B12 and GDM risks were not detected in the present study.
Vitamin B1 is an essential micronutrient involved in glucose metabolism in almost all living organisms. The Chinese dietary guidelines recommend a dietary reference intake of 1.2 mg per day for healthy adult women and pregnant women in the first trimester, and 1.4 mg and 1.5 mg per day in the second and third trimesters, respectively [29]. This recommendation reflects increased requirements for energy and carbohydrates during pregnancy. Vitamin B1 levels are often reduced in individuals with dietary patterns rich in carbohydrates and in those with diabetic neuropathy. Routine intake of vitamin B1 supplements for disease prevention is not recommended during pregnancy.
To date, only a few studies have evaluated the associations between vitamin B1 (including food intake or body status) and the risks of diabetes, and inconsistent findings have been reported. Recently, a national prospective study in the Chinese population has revealed a U-shaped association between dietary vitamin B1 intake and new-onset diabetes [30]. Furthermore, an ecological study revealed that the increased prevalence of diabetes in an American population was significantly and positively correlated with an increased consumption of vitamin B1 [31]. However, Thornalley reported that a low level of plasma vitamin B1 was prevalent in diabetes patients [32]. These conflicting findings may result from different study designs and populations, especially cohorts with particular diseases and dietary patterns. Therefore, the association between vitamin B1 intake and vitamin B1 body status and the risk of diabetes remains uncertain. These findings also imply an important role of population background in determining health consequences. As far as we know, our study provides the first data that a high serum vitamin B1 concentration in early pregnancy may bring about a subsequent risk of GDM. However, the exact mechanisms linking optimal vitamin B1 intake and serum vitamin B1 levels and the risk of GDM are still not clear. More studies are needed to confirm our findings and explore the underlying mechanisms among pregnant women.
Vitamin B6 functions as a coenzyme for many of the enzymes involved in the metabolism of glucose, lipids, amino acids, DNA and neurotransmitters [33]. In addition, vitamin B6 can quench reactive oxygen species as an antioxidant molecule [34]. It can be found in several foods including fish, meat, nuts and fresh vegetables, with recommendations of 1.4 mg daily for adults and 2.2 mg daily for pregnant women in the Chinese dietary guidelines [29]. In clinical practice, vitamin B6 has been used to alleviate nausea and vomiting caused by pregnancy status [35]. Plasma levels of pyridoxal 5-phosphate, an active metabolite of vitamin B6, are decreased in conditions with elevated alkaline phosphatase such as liver and bone diseases, diabetes and cancer; therefore, the measurement of total B6 (as in our study) has been recommended as a direct marker of B6 status in pregnant women [20].
Animal studies have shown that vitamin B6 deficiency in pregnancy may increase the risk of glucose intolerance by disturbing the catabolism of tryptophan into serotonin, which is critical for β-cell proliferation during pregnancy [36]. However, one study revealed that in mice with vitamin B6 deficiency, insulin levels remained intact, though insulin resistance increased [37]. In addition, vitamin B6 administration does not affect blood glucose levels in women with GDM [38]. Our study showed a nonlinear association between serum vitamin B6 levels and the risk of GDM, with women in the upper two quartiles having a higher risk of GDM. Of note, we found a positive relationship between vitamin B1 and vitamin B6 (r = 0.063, p < 0.05) and the former was positively correlated with GDM risk as previously mentioned. One possible explanation is that high vitamin B6 level was related to elevated appetite, energy intake and body weight. Additional research is required to investigate the underlying mechanisms involved in the relationship between vitamin B6 and GDM.
Vitamin B6, folate and vitamin B12 are of great importance in fetal development because of their role in one-carbon metabolism, which is crucial for the synthesis of DNA, the conversion of homocysteine to methionine, neurological function, and the formation of red blood cells [12,39]. Folate is a key nutrient for pregnant women. Recommendations for synthetic folic acid supplementation in pregnant women and women preparing for pregnancy are part of public health strategies to prevent birth defects [14]. A deficiency of vitamin B12 in pregnancy can induce anemia, homocysteinemia, cardiovascular dysfunction, neurological disorders and oxidative stress [40]. Vitamin B12 is only present in animal sources; therefore, vegans, vegetarians and pregnant women who suffer from pregnancy-associated nausea and vomiting are at risk of B12 deficiency [40]. A recent meta-analysis found that vitamin B12 insufficiency was common in pregnant women, with pooled estimates of 21%, 19% and 29% in the first, second and third trimesters, respectively. Furthermore, geographic differences in the maternal prevalence of vitamin B12 deficiency were observed, with the highest prevalence reported in India (70–74%) [41].
In our study population, 32.9% (350/1065) of women had vitamin B12 insufficiency. Previous evidence suggests that vitamin B12 deficiency increases the risk of GDM, which was in line with our findings [42,43]. The relationship between serum B12 levels and GDM was nonlinear with our RCS model, and a serum vitamin B12 level of ≥150 pmol/L reduced the risk of GDM by 43%. Several mechanisms have been proposed to explain the protective effects of vitamin B12 on diabetes; although, none have been proven. Vitamin B12 has a negative effect on homocysteine metabolism, and an association exists between hyperhomocysteinemia and insulin resistance; furthermore, oxidative stress is caused by vitamin B12 deficiency [44]. In animal studies, low levels of vitamin B12 increase lipid accumulation in adipocytes and trigger dyslipidemia, leading to β-cell lipotoxicity [45]. Vitamin B12 is a coenzyme involved in the degradation of odd-chain fatty acids and BCAAs [18]. Increased dietary and plasma levels of BCAAs are correlated with obesity, insulin resistance and diabetes [46].
Vitamin B12 has a close metabolic inter-relationship with folate. It is required for the conversion of N5-methyl-tetrahydrofolate into tetrahydrofolate, which is the active form of folate involved in the synthesis of DNA and the methionine cycle [12]. The levels of these two biomarkers were significantly and inversely correlated in our population (r = −0.087, p < 0.05). The ratio of folic acid/vitamin B12 and GDM risk has been investigated in several studies [15,16,17] and analyzed in a meta-analysis [47]. Nevertheless, these studies have yielded contradictory results with negative, positive and no link detected. No association between this ratio in early pregnancy and the risk of GDM was detected in the current study. Possible reasons for the contradictory findings include differences in the following: study design, vitamin supplements used in different populations, and gestational age at the time of sampling (e.g., early pregnancy vs. middle or late pregnancy). Intriguingly, the serum levels of vitamin B12 were highest in women who took folic acid supplements in our study (Supplementary Materials Table S1). Further large-scale longitudinal studies and trials on vitamin B12 supplementation are necessary to clarify the relationships between folic acid/vitamin B12 status and GDM risk. The aim will be to determine the dose of these two vitamins to achieve an optimum balance throughout pregnancy.
Several limitations of this study should be noted. First, we controlled for a number of covariates; however, residual confounding may not be eliminated as we had no information on diet and liver function tests. Second, this study was conducted in Shanghai; therefore, whether the findings observed here can be translated to other populations needs further verification. Third, the lack of pre-specified power calculations for sample size in the study might limit the strength of the evidence regarding the association between B vitamins and GDM.

5. Conclusions

This cohort study in China showed that higher maternal serum vitamin B1 and vitamin B6 levels in early pregnancy are significantly associated with increased GDM risk. In addition, sufficient vitamin B12 status is significantly associated with a lower GDM risk. Our findings suggest that the body status of B vitamins in early pregnancy is a potential predictive biomarker of GDM. Further research is necessary to determine the appropriate levels of B vitamins in early pregnancy to optimize maternal and offspring health.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/nu14235016/s1, Table S1: Serum levels of B vitamins according to B-vitamin supplements intake in the cohort.

Author Contributions

Conceptualization, N.W. and Y.D.; methodology, N.W. and T.Z.; software, N.W. and T.Z.; validation, N.W. and Y.D.; formal analysis, N.W. and T.Z.; investigation, T.Z., X.M. and Y.L.; data curation, T.Z. and N.W.; writing—original draft preparation, N.W. and T.Z.; writing—review and editing, Y.D.; supervision, Y.D.; project administration, T.Z. and N.W.; funding acquisition, N.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Shanghai Municipal Commission of Health Foundation (grant number: 202150050); the Obstetrics and Gynecology Hospital, Fudan University (grant number: FC2021CR203_ZC).

Institutional Review Board Statement

The research was conducted according to the Declaration of Helsinki, and the Ethics Committee of the Obstetrics and Gynecology Hospital, Fudan University approved the study (NO. 202123).

Informed Consent Statement

Written informed consent was obtained from each participant involved in the study.

Data Availability Statement

The data used in this study can be acquired on request from the corresponding author.

Acknowledgments

We are grateful to all the participants who took part in this study and the study hospital for supporting this work. We appreciate the help from Weihong Hu and Xinli Zhu for participant recruitment.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. International Diabetes Federation. Global Diabetes Data Report 2000–2045. Available online: https://diabetesatlas.org/data/en/world/ (accessed on 30 September 2022).
  2. Gao, C.; Sun, X.; Lu, L.; Liu, F.; Yuan, J. Prevalence of gestational diabetes mellitus in mainland China: A systematic review and meta-analysis. J. Diabetes Investig. 2019, 10, 154–162. [Google Scholar] [CrossRef]
  3. Vounzoulaki, E.; Khunti, K.; Abner, S.C.; Tan, B.K.; Davies, M.J.; Gillies, C.L. Progression to type 2 diabetes in women with a known history of gestational diabetes: Systematic review and meta-analysis. BMJ 2020, 369, m1361. [Google Scholar] [CrossRef]
  4. Ye, W.; Luo, C.; Huang, J.; Li, C.; Liu, Z.; Liu, F. Gestational diabetes mellitus and adverse pregnancy outcomes: Systematic review and meta-analysis. BMJ 2022, 377, e67946. [Google Scholar] [CrossRef]
  5. Lowe, W.J.; Scholtens, D.M.; Lowe, L.P.; Kuang, A.; Nodzenski, M.; Talbot, O.; Catalano, P.M.; Linder, B.; Brickman, W.J.; Clayton, P.; et al. Association of Gestational Diabetes with Maternal Disorders of Glucose Metabolism and Childhood Adiposity. JAMA 2018, 320, 1005–1016. [Google Scholar] [CrossRef] [Green Version]
  6. Venkataraman, H.; Ram, U.; Craik, S.; Arungunasekaran, A.; Seshadri, S.; Saravanan, P. Increased fetal adiposity prior to diagnosis of gestational diabetes in South Asians: More evidence for the ‘thin-fat’ baby. Diabetologia 2017, 60, 399–405. [Google Scholar] [CrossRef] [Green Version]
  7. Kanasaki, K.; Kumagai, A. The impact of micronutrient deficiency on pregnancy complications and development origin of health and disease. J. Obstet. Gynaecol. Res. 2021, 47, 1965–1972. [Google Scholar] [CrossRef]
  8. Santander, B.S.; Gimenez, C.M.; Ballestin, B.J.; Luesma, B.M. Is Supplementation with Micronutrients Still Necessary during Pregnancy? A Review. Nutrients 2021, 13, 3134. [Google Scholar] [CrossRef]
  9. Li, Q.; Zhang, Y.; Huang, L.; Zhong, C.; Chen, R.; Zhou, X.; Chen, X.; Li, X.; Cui, W.; Xiong, T.; et al. High-Dose Folic Acid Supplement Use from Prepregnancy Through Midpregnancy Is Associated with Increased Risk of Gestational Diabetes Mellitus: A Prospective Cohort Study. Diabetes Care 2019, 42, e113–e115. [Google Scholar] [CrossRef] [Green Version]
  10. Deshmukh, S.V.; Prabhakar, B.; Kulkarni, Y.A. Water Soluble Vitamins and their Role in Diabetes and its Complications. Curr. Diabetes Rev. 2020, 16, 649–656. [Google Scholar] [CrossRef]
  11. Zhu, J.; Chen, C.; Lu, L.; Yang, K.; Reis, J.; He, K. Intakes of Folate, Vitamin B6, and Vitamin B12 in Relation to Diabetes Incidence Among American Young Adults: A 30-Year Follow-up Study. Diabetes Care 2020, 43, 2426–2434. [Google Scholar] [CrossRef]
  12. Finer, S.; Saravanan, P.; Hitman, G.; Yajnik, C. The role of the one-carbon cycle in the developmental origins of Type 2 diabetes and obesity. Diabet. Med. 2014, 31, 263–272. [Google Scholar] [CrossRef]
  13. Tamura, T.; Picciano, M.F. Folate and human reproduction. Am. J. Clin. Nutr. 2006, 83, 993–1016. [Google Scholar] [CrossRef] [Green Version]
  14. Chitayat, D.; Matsui, D.; Amitai, Y.; Kennedy, D.; Vohra, S.; Rieder, M.; Koren, G. Folic acid supplementation for pregnant women and those planning pregnancy: 2015 update. J. Clin. Pharmacol. 2016, 56, 170–175. [Google Scholar] [CrossRef]
  15. Chen, X.; Zhang, Y.; Chen, H.; Jiang, Y.; Wang, Y.; Wang, D.; Li, M.; Dou, Y.; Sun, X.; Huang, G.; et al. Association of Maternal Folate and Vitamin B12 in Early Pregnancy with Gestational Diabetes Mellitus: A Prospective Cohort Study. Diabetes Care 2021, 44, 217–223. [Google Scholar] [CrossRef]
  16. Saravanan, P.; Sukumar, N.; Adaikalakoteswari, A.; Goljan, I.; Venkataraman, H.; Gopinath, A.; Bagias, C.; Yajnik, C.S.; Stallard, N.; Ghebremichael-Weldeselassie, Y.; et al. Association of maternal vitamin B12 and folate levels in early pregnancy with gestational diabetes: A prospective UK cohort study (PRiDE study). Diabetologia 2021, 64, 2170–2182. [Google Scholar] [CrossRef] [PubMed]
  17. Lai, J.S.; Pang, W.W.; Cai, S.; Lee, Y.S.; Chan, J.; Shek, L.; Yap, F.; Tan, K.H.; Godfrey, K.M.; van Dam, R.M.; et al. High folate and low vitamin B12 status during pregnancy is associated with gestational diabetes mellitus. Clin. Nutr. 2018, 37, 940–947. [Google Scholar] [CrossRef]
  18. Green, C.R.; Wallace, M.; Divakaruni, A.S.; Phillips, S.A.; Murphy, A.N.; Ciaraldi, T.P.; Metallo, C.M. Branched-chain amino acid catabolism fuels adipocyte differentiation and lipogenesis. Nat. Chem. Biol. 2016, 12, 15–21. [Google Scholar] [CrossRef] [Green Version]
  19. De Almeida-Pititto, B.; Dualib, P.M.; Jordao, M.C.; Izar, H.F.M.; Jones, S.R.; Blaha, M.J.; Toth, P.P.; Santos, R.D.; Bensenor, I.M.; Ferreira, S.; et al. Branched-chain amino acids predict incident diabetes in the Brazilian Longitudinal Study of Adult Health—ELSA-Brasil. Diabetes Res. Clin. Pract. 2021, 174, 108747. [Google Scholar] [CrossRef] [PubMed]
  20. Mascolo, E.; Verni, F. Vitamin B6 and Diabetes: Relationship and Molecular Mechanisms. Int. J. Mol. Sci. 2020, 21, 3669. [Google Scholar] [CrossRef] [PubMed]
  21. Eshak, E.S.; Arafa, A.E. Thiamine deficiency and cardiovascular disorders. Nutr. Metab. Cardiovasc. Dis. 2018, 28, 965–972. [Google Scholar] [CrossRef] [PubMed]
  22. Anwar, A.; Ahmed, A.M.; Siddiqui, J.A.; Panhwar, G.; Shaikh, F.; Ariff, M. Thiamine Level in Type I and Type II Diabetes Mellitus Patients: A Comparative Study Focusing on Hematological and Biochemical Evaluations. Cureus 2020, 12, e8027. [Google Scholar] [CrossRef]
  23. Gernand, A.D.; Schulze, K.J.; Stewart, C.P.; West, K.J.; Christian, P. Micronutrient deficiencies in pregnancy worldwide: Health effects and prevention. Nat. Rev. Endocrinol. 2016, 12, 274–289. [Google Scholar] [CrossRef] [Green Version]
  24. Zhou, B. Cooperative meta-analysis group of China obesity task force. Predictive values of body mass index and waist circumference to risk factors of related disease in Chinese adult population. Zhonghua Liu Xing Bing Xue Za Zhi 2002, 1, 5–10. [Google Scholar]
  25. Bassett, D.J. International physical activity questionnaire: 12-country reliability and validity. Med. Sci. Sports Exerc. 2003, 35, 1396. [Google Scholar] [CrossRef] [PubMed]
  26. Metzger, B.E.; Gabbe, S.G.; Persson, B.; Buchanan, T.A.; Catalano, P.A.; Damm, P.; Dyer, A.R.; Leiva, A.; Hod, M.; Kitzmiler, J.L.; et al. International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care 2010, 33, 676–682. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Behere, R.V.; Deshmukh, A.S.; Otiv, S.; Gupte, M.D.; Yajnik, C.S. Maternal Vitamin B12 Status During Pregnancy and Its Association with Outcomes of Pregnancy and Health of the Offspring: A Systematic Review and Implications for Policy in India. Front. Endocrinol. 2021, 12, 619176. [Google Scholar] [CrossRef]
  28. Abbassi-Ghanavati, M.; Greer, L.G.; Cunningham, F.G. Pregnancy and laboratory studies: A reference table for clinicians. Obstet. Gynecol. 2009, 114, 1326–1331. [Google Scholar] [CrossRef]
  29. Chinese Nutrition Society. Chinese Dietary Guidelines; People’s Medical Publishing House Press: Beijing, China, 2022. [Google Scholar]
  30. Liu, C.; Meng, Q.; Zu, C.; Li, R.; Yang, S.; He, P.; Li, H.; Zhang, Y.; Zhou, C.; Liu, M.; et al. U-Shaped association between dietary thiamine intake and new-onset diabetes: A nationwide cohort study. QJM 2022, hcac159. [Google Scholar] [CrossRef]
  31. Zhou, S.S.; Li, D.; Zhou, Y.M.; Sun, W.P.; Liu, Q.G. B-vitamin consumption and the prevalence of diabetes and obesity among the US adults: Population based ecological study. BMC Public Health 2010, 10, 746. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Thornalley, P.J.; Babaei-Jadidi, R.; Al, A.H.; Rabbani, N.; Antonysunil, A.; Larkin, J.; Ahmed, A.; Rayman, G.; Bodmer, C.W. High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease. Diabetologia 2007, 50, 2164–2170. [Google Scholar] [CrossRef] [Green Version]
  33. Di Salvo, M.L.; Contestabile, R.; Safo, M.K. Vitamin B(6) salvage enzymes: Mechanism, structure and regulation. Biochim. Biophys. Acta 2011, 1814, 1597–1608. [Google Scholar] [CrossRef] [PubMed]
  34. Dalto, D.B.; Matte, J.J. Pyridoxine (Vitamin B(6)) and the Glutathione Peroxidase System; a Link between One-Carbon Metabolism and Antioxidation. Nutrients 2017, 9, 189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Pecriaux, C. Interest of vitamin b6 for treatment of nausea and/or vomiting during pregnancy. Gynecol. Obstet. Fertil. Senol. 2020, 48, 840–843. [Google Scholar] [PubMed]
  36. Kim, H.; Toyofuku, Y.; Lynn, F.C.; Chak, E.; Uchida, T.; Mizukami, H.; Fujitani, Y.; Kawamori, R.; Miyatsuka, T.; Kosaka, Y.; et al. Serotonin regulates pancreatic beta cell mass during pregnancy. Nat. Med. 2010, 16, 804–808. [Google Scholar] [CrossRef]
  37. Fields, A.M.; Welle, K.; Ho, E.S.; Mesaros, C.; Susiarjo, M. Vitamin B6 deficiency disrupts serotonin signaling in pancreatic islets and induces gestational diabetes in mice. Commun. Biol. 2021, 4, 421. [Google Scholar] [CrossRef]
  38. Mooradian, A.D.; Failla, M.; Hoogwerf, B.; Maryniuk, M.; Wylie-Rosett, J. Selected vitamins and minerals in diabetes. Diabetes Care 1994, 17, 464–479. [Google Scholar] [CrossRef]
  39. Khare, A.; Lopez, M.; Gogtay, J. Homocysteine, B vitamins, and cardiovascular disease. N. Engl. J. Med. 2006, 206, 209–211. [Google Scholar]
  40. Shipton, M.J.; Thachil, J. Vitamin B12 deficiency—A 21st century perspective. Clin. Med. 2015, 15, 145–150. [Google Scholar] [CrossRef] [Green Version]
  41. Sukumar, N.; Rafnsson, S.B.; Kandala, N.B.; Bhopal, R.; Yajnik, C.S.; Saravanan, P. Prevalence of vitamin B-12 insufficiency during pregnancy and its effect on offspring birth weight: A systematic review and meta-analysis. Am. J. Clin. Nutr. 2016, 103, 1232–1251. [Google Scholar] [CrossRef] [Green Version]
  42. Sukumar, N.; Venkataraman, H.; Wilson, S.; Goljan, I.; Selvamoni, S.; Patel, V.; Saravanan, P. Vitamin B12 Status among Pregnant Women in the UK and Its Association with Obesity and Gestational Diabetes. Nutrients 2016, 8, 768. [Google Scholar] [CrossRef]
  43. Krishnaveni, G.V.; Hill, J.C.; Veena, S.R.; Bhat, D.S.; Wills, A.K.; Karat, C.L.; Yajnik, C.S.; Fall, C.H. Low plasma vitamin B12 in pregnancy is associated with gestational ‘diabesity’ and later diabetes. Diabetologia 2009, 52, 2350–2358. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Zhang, X.; Qu, Y.Y.; Liu, L.; Qiao, Y.N.; Geng, H.R.; Lin, Y.; Xu, W.; Cao, J.; Zhao, J.Y. Homocysteine inhibits pro-insulin receptor cleavage and causes insulin resistance via protein cysteine-homocysteinylation. Cell Rep. 2021, 37, 109821. [Google Scholar] [CrossRef] [PubMed]
  45. Ghosh, S.; Sinha, J.K.; Putcha, U.K.; Raghunath, M. Severe but Not Moderate Vitamin B12 Deficiency Impairs Lipid Profile, Induces Adiposity, and Leads to Adverse Gestational Outcome in Female C57BL/6 Mice. Front. Nutr. 2016, 3, 1. [Google Scholar] [CrossRef] [Green Version]
  46. Giesbertz, P.; Daniel, H. Branched-chain amino acids as biomarkers in diabetes. Curr. Opin. Clin. Nutr. Metab. Care 2016, 19, 48–54. [Google Scholar] [CrossRef] [PubMed]
  47. Wang, L.; Hou, Y.; Meng, D.; Yang, L.; Meng, X.; Liu, F. Vitamin B12 and Folate Levels During Pregnancy and Risk of Gestational Diabetes Mellitus: A Systematic Review and Meta-Analysis. Front. Nutr. 2021, 8, 670289. [Google Scholar] [CrossRef]
Figure 1. Scatter plot of serum vitamin B1 and glucose levels at OGTT: (a) fasting glucose; (b) 1 h glucose; (c) 2 h glucose. The lines indicate the straight-line correlations, and the grey–shaded areas represent 95% confidence intervals (CI).
Figure 1. Scatter plot of serum vitamin B1 and glucose levels at OGTT: (a) fasting glucose; (b) 1 h glucose; (c) 2 h glucose. The lines indicate the straight-line correlations, and the grey–shaded areas represent 95% confidence intervals (CI).
Nutrients 14 05016 g001
Figure 2. Restricted cubic spline (RCS) regression analysis of group B vitamins including (a) serum vitamin B1, (b) serum vitamin B2, (c) serum vitamin B6, (d) serum folate, and (e) serum vitamin B12 with GDM risk. The median of vitamin B1 86.5 pmol/L, B2 13.5 pmol/L, B6 27.2 pmol/L, folate 11.8 nmol/L and B12 174.8 pmol/L was selected as the reference levels, respectively. The lines indicate estimated ORs, and the light-blue–shaded areas represent 95% CI.
Figure 2. Restricted cubic spline (RCS) regression analysis of group B vitamins including (a) serum vitamin B1, (b) serum vitamin B2, (c) serum vitamin B6, (d) serum folate, and (e) serum vitamin B12 with GDM risk. The median of vitamin B1 86.5 pmol/L, B2 13.5 pmol/L, B6 27.2 pmol/L, folate 11.8 nmol/L and B12 174.8 pmol/L was selected as the reference levels, respectively. The lines indicate estimated ORs, and the light-blue–shaded areas represent 95% CI.
Nutrients 14 05016 g002aNutrients 14 05016 g002b
Table 1. The basic characteristic of the study population by gestational diabetes mellitus (GDM) status (N = 1065).
Table 1. The basic characteristic of the study population by gestational diabetes mellitus (GDM) status (N = 1065).
CharacteristicsAllGDM (n = 121)Non-GDM (n = 944)p-Value
Age30.8 ± 3.732.2 ± 3.830.6 ± 3.6<0.001
Education background (n (%)) 0.381
 ≤Senior high school68 (6.4)12 (9.9)56 (5.9)
 College693 (65.1)76 (62.8)617 (65.4)
 ≥Postgraduate degree304 (28.5)33 (27.3)271 (28.7)
Smoking exposure (n (%))131 (12.3)19 (15.7)112 (11.9)0.226
Alcohol drinking (n (%))108 (10.1)9 (7.4)99 (10.5)0.296
Pre-conceptional body mass index (kg/m2) (n (%)) <0.001
 <18.5159 (14.9)9 (7.4)150 (15.9)
 18.5–24726 (68.2)76 (62.8)650 (68.9)
 >24180 (16.9)36 (29.8)144 (15.3)
First-degree family history of diabetes (n (%)) <0.001
 Yes136 (12.8)24 (19.8)112 (11.9)
 No906 (85.1)90 (74.4)816 (86.4)
 Unclear23(2.2)7 (5.8)16 (1.7)
Primiparity (n (%))874 (82.1)91 (75.2)783 (82.9)0.037
Gestational weight gain at OGTT visits (kg)7.9 ± 3.88.2 ± 3.67.9 ± 3.80.478
Physical activity level ≥ 600 MET (n (%))346 (32.5)45 (37.2)301(31.9)0.241
B-vitamin supplements (n (%)) 0.671
 Folate supplements276 (25.9)28 (23.1)248 (26.3)
 Multivitamin supplements728 (68.4)87 (71.9)641 (67.9)
 No61(5.7)6 (5.0)55 (5.8)
Biochemical characteristics
 B1 (pmol/L)86.5 (75.1–98.5)95.9 (78.5–110.2)86.1 (74.7–97.5)<0.001
 B2 (pmol/L)13.5 (12.3–14.9)13.2 (11.9–14.7)13.5 (12.3–14.9)0.406
 B6 (pmol/L)27.2 (24.2–35.7)28.9 (24.8–37.4)26.9 (24.1–35.4)0.069
 Folate (nmol/L)11.8 (10.1–13.9)11.7 (10.3–14.0)11.8 (10.1–13.9)0.952
 Folate insufficiency at <5.9 nmol/L14 (1.3)2 (1.7)12 (1.3)0.729
 B12 (pmol/L)174.8(132.6–210.3)160.0 (124.7–194.8)176.1 (134.5–211.1)0.038
 B12 insufficiency at <150 pmol/L350 (32.9)54 (44.6)296 (31.4)0.003
 Homocysteine (umol/L)6.6 (6.0–7.5)6.7 (5.9–7.7)6.6 (6.0–7.5)0.828
OGTT, oral glucose tolerance test; MET, metabolic equivalent.
Table 2. The correlation of serum B vitamins and glucose levels in the cohort study 1.
Table 2. The correlation of serum B vitamins and glucose levels in the cohort study 1.
OGTTVitamin B1Vitamin B2Vitamin B6FolateVitamin B12
Fasting0.062 *−0.0380.048−0.0100.051
1 h0.123 *0.0030.0110.025−0.027
2 h0.111 *0.0300.0360.0120.010
1 Pearson correlation coefficient was shown, * p < 0.05.
Table 3. The correlation of various serum B vitamins in the cohort study 1.
Table 3. The correlation of various serum B vitamins in the cohort study 1.
Vitamin B1Vitamin B2Vitamin B6Vitamin B12Folate
Vitamin B11.000
Vitamin B2−0.0081.000
Vitamin B60.063 *−0.0371.000
Vitamin B120.038−0.055−0.0031.000
Folate−0.0520.032−0.022−0.087 *1.000
1 Pearson correlation coefficient was shown, * p < 0.05.
Table 4. Association of maternal serum vitamin B1, vitamin B2, vitamin B6, folate, and vitamin B12 in early pregnancy with GDM risk (N = 1065).
Table 4. Association of maternal serum vitamin B1, vitamin B2, vitamin B6, folate, and vitamin B12 in early pregnancy with GDM risk (N = 1065).
VariablesGDM/Total (%)Model 1 Model 2
OR95% CIp-ValueOR 95% CIp-Value
Vitamin B1
Q123/276 (8.33) reference reference
Q221/266 (7.89)0.910.50–1.690.7630.930.49–1.770.831
Q330/266 (11.28)1.350.76–2.390.3051.490.82–2.690.188
Q447/266 (17.67)2.281.34–3.870.002 2.201.27–3.820.005
p-Trend   <0.001
Vitamin B2
Q134/268 (12.69) reference reference
Q230/266 (11.28)0.870.52–1.480.6170.880.51–1.500.631
Q329/267 (10.86)0.840.49–1.420.5130.910.53–1.570.738
Q428/264 (10.61)0.820.48–1.390.4550.730.42–1.280.276
p-Trend 0.435 0.310
Vitamin B6
Q122/267 (8.24) reference reference
Q227/266 (10.15)1.260.70–2.270.4461.270.69–2.330.437
Q336/266 (13.53)1.741.00–3.050.0521.931.08–3.430.026
Q436/266 (13.53)1.741.00–3.050.0521.841.03–3.290.040
p-Trend 0.069 0.054
Folate
Q127/267(10.11) reference reference
Q238/269 (14.13)1.460.86–2.470.1561.550.90–2.680.112
Q322/263 (8.37)0.810.45–1.460.4880.900.49–1.660.745
Q434/266 (12.78)1.300.76–2.230.3341.410.81–2.450.225
p-Trend 0.697 0.499
Vitamin B12
Q137/267(13.86) reference reference
Q234/266 (12.78)0.910.55–1.500.7150.900.54–1.510.697
Q326/266 (9.77)0.670.40–1.150.1460.710.41–1.230.219
Q424/266 (9.02)0.620.36–1.060.0820.630.36–1.110.110
p-Trend 0.050 0.079
<150 pmol/L54/350 (15.43) reference reference
≥150 pmol/L67/715 (9.37)0.570.39–0.830.0040.570.38–0.840.005
Folate/B12
Q128/267 (10.49) reference reference
Q223/266 (8.65)0.810.45–1.440.4710.810.45–1.470.497
Q335/265 (13.21)1.300.77–2.200.3321.230.71–2.120.464
Q435/267 (13.11)1.290.76–2.190.3491.370.79–2.360.258
p-Trend 0.176 0.121
Univariate model. Adjusted for age, education, parity, first-degree family history of diabetes, smoking exposure, alcohol drinking, pre-conceptional body mass index, gestational weight gain at OGTT visits and physical activity levels. OR, odds ratio; Q, quartile.
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Wang, N.; Zhou, T.; Ma, X.; Lin, Y.; Ding, Y. The Association between Maternal B Vitamins in Early Pregnancy and Gestational Diabetes Mellitus: A Prospective Cohort Study. Nutrients 2022, 14, 5016. https://doi.org/10.3390/nu14235016

AMA Style

Wang N, Zhou T, Ma X, Lin Y, Ding Y. The Association between Maternal B Vitamins in Early Pregnancy and Gestational Diabetes Mellitus: A Prospective Cohort Study. Nutrients. 2022; 14(23):5016. https://doi.org/10.3390/nu14235016

Chicago/Turabian Style

Wang, Na, Tianchun Zhou, Xiaoxia Ma, Yuping Lin, and Yan Ding. 2022. "The Association between Maternal B Vitamins in Early Pregnancy and Gestational Diabetes Mellitus: A Prospective Cohort Study" Nutrients 14, no. 23: 5016. https://doi.org/10.3390/nu14235016

APA Style

Wang, N., Zhou, T., Ma, X., Lin, Y., & Ding, Y. (2022). The Association between Maternal B Vitamins in Early Pregnancy and Gestational Diabetes Mellitus: A Prospective Cohort Study. Nutrients, 14(23), 5016. https://doi.org/10.3390/nu14235016

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