Journal of Diabetes Research

Journal of Diabetes Research / 2020 / Article
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Diabetes Mellitus and its Cardiovascular Complications: New Insights into an Old Disease 2020

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Research Article | Open Access

Volume 2020 |Article ID 4085757 | https://doi.org/10.1155/2020/4085757

Man Sun, Baihui Zhao, Sainan He, Ruopeng Weng, Binqiao Wang, Yunping Ding, Xinwen Huang, Qiong Luo, "The Alteration of Carnitine Metabolism in Second Trimester in GDM and a Nomogram for Predicting Macrosomia", Journal of Diabetes Research, vol. 2020, Article ID 4085757, 12 pages, 2020. https://doi.org/10.1155/2020/4085757

The Alteration of Carnitine Metabolism in Second Trimester in GDM and a Nomogram for Predicting Macrosomia

Guest Editor: Markus Wallner
Received07 May 2020
Revised20 Jun 2020
Accepted13 Jul 2020
Published11 Aug 2020

Abstract

Objective. The metabolism of three major nutrients (sugar, lipid, and protein) will change during pregnancy, especially in the second trimester. The present study is aimed at evaluating carnitine alteration in fatty acid metabolism in the second trimester of pregnancy and the correlation between carnitine and GDM. Methods. 450 pregnant women were recruited in the present prospective study. Metabolic profiling of 31 carnitines was detected by LC-MS/MS in these women. Correlation between carnitine metabolism and maternal and neonatal complication with GDM was analyzed. Results. We found the levels of 7 carnitines increased in , , , and ART pregnant groups, but the level of free carnitine (C0) decreased. Nine carnitines were specific metabolites of GDM. Prepregnancy BMI, weight gain, and carnitines (C0, C3, and C16) were independent risk factors associated with GDM and related macrosomia. C0 was negatively correlated with FBG, LDL, TG, and TC. A nomogram was developed for predicting macrosomia in GDM based on carnitine-related metabolic variables. Conclusion. The carnitine metabolism in the second trimester is abnormal in GDM women. The dysfunction of carnitine metabolism is closely related to the abnormality of blood lipid and glucose in GDM. Carnitine metabolism abnormality could predict macrosomia complicated with GDM.

1. Introduction

Pregnancy is a complex process accompanied by substantial changes in sugar, protein, and lipid metabolism [1]. Maternal lipid and protein metabolism of the second trimester is an anabolic state combined with accelerating maternal fat stores and increasing protein synthesis [2]. Dyslipidemia is associated with maternal metabolic disorder (GDM, hyperlipemia, and hypertension) and adverse neonate outcomes (macrosomia, fetal growth restriction) [3]. Fatty acid oxidation decreases in obesity during pregnancy and has linked to GDM development [4].

GDM is a common metabolic disorder during pregnancy and occurs in approximately 10–15% of pregnancies globally [5]. Pregnant women with GDM are more prone to hypertension and metabolic syndrome. The risks to the fetus include macrosomia, respiratory distress syndrome, childhood obesity, and type 2 diabetes mellitus (T2DM) in adults [6]. GDM is associated with profound changes in metabolism. Free carnitine (C0) has a critical role in energy metabolism of transporting long-chain fatty acid from the cytosol into the mitochondria, which results in C0 transforming into acylcarnitine (AC) [7, 8]. Carnitine deficiency is defined as a serum C0 μmol/L [9]. C0 deficiency might impair lipid metabolism resulting in GDM [10]. Evaluated circulating AC (such as C3 and C5) is associated with GDM and induces pancreatic β-cell dysfunction [11]. A previous study proposed that C0 and AC decreased in pregnancy in the first trimester compared with nonpregnancy [12]. However, studies of metabolic profiling of carnitine in the second trimester among diverse pregnant women are rare. Herein, we provide a study of the metabolism of carnitine to investigate the potential risk factors in GDM.

In the present study, a LC–MS/MS-based metabolomics approach was used to quantify the maternal plasma level of AC in order to identify the correlation between nonglucose metabolism abnormalities and pregnancy metabolic diseases during the second trimester. We analyzed metabolic alteration in the second trimester and detected the independent risk factors of GDM. Moreover, we established a prognostic nomogram of incorporating AC for predicting GDM macrosomia.

2. Method

2.1. Subject

This study was a prospective study. Between June 2017 and April 2018, 450 pregnant women in the second trimester were recruited in this study at Women’s Hospital, School of Medicine, Zhejiang University, in Hangzhou. The study design has been approved by the Ethics Committee of the hospital. All participants were of Chinese Han ethnicity. We obtain maternal characteristic information as follows: gravidity, parity, age, height, prepregnancy BMI, weight gain during pregnancy, use of assisted reproductive technique (ART), and method of pregnancy termination. The following information of the offspring was collected: termination of pregnancy weeks, sex, birth length, actual birth weight, head circumference, abdomen circumference, and abdomen minus head circumference (data from fetal growth measurement ultrasound before labor).

GDM was defined according to the Chinese Current Care Guidelines for GDM as one or more pathological glucose values in a standard oral glucose tolerance test (OGTT) [13]. The diagnostic thresholds were fasting plasma glucose: 5.1 mmol/L, 1 h 10.0 mmol/L, and 2 h 8.5 mmol/L [14]. According to the guideline, 64 GDM cases were diagnosed. The control group was composed of 128 randomly sampled women without GDM from residual pregnant women participating in this study matched by birthday, age, delivery mode, and number of fetuses with 2 : 1 ratio. The 2 : 1 design can eliminate the interference of many factors (such as age, height, and gestational week at delivery) in the study, and a double sample has good statistical performance. The common definition of macrosomia is birth weight over 4000 g [15]. Biochemical status of the GDM and control groups was also collected and analyzed.

2.2. Metabolic Profiling Detection by LC-MS/MS

We used the method of LC-MS/MS to investigate the level of 31 plasma carnitines of pregnant women in the second trimester. We also obtain their neonate blood plasma sample. Blood samples were taken via venipuncture, using 4 mL Vacutainer Tubes containing K2-EDTA as anticoagulant centrifuged at 2500 g for 15 min; then, samples of plasma were stored at – 20°C and detected monthly. For plasma analysis, plasma was pipetted into a 2.0 mL 96-deep-well plate. To this, internal standard solution was added, and the plate was vortex mixed for 1 min. Proteins were precipitated by adding 0.3 M zinc sulfate in methanol (1 : 5 ), and the plate was vortexed again for 1 min. Water was added, and the plate was sealed and centrifuged. Following centrifugation, supernatant was injected for analysis [16]. Furthermore, sample preparation used in tandem mass spectrometry (4000 QTrap™; AB Sciex, Darmstadt, Germany) test the concentration. The method used in the present study was essentially a modification of the procedure described elsewhere [17]. AA and AC were quantified using appropriate isotope-labelled standards. LC separation was performed on an Acquity UPLC HSS T3 column ( mm, 100 Å, 1.8 lm particle size; Waters Corporation, MA) using water with 0.1% formic acid, 5 mM ammonium acetate, and 0.015% heptafluorobutyric acid as solvent A and methanol with 0.1% formic acid and 5 mM detected with a Xevo-G2-QTOF MS (Waters Corporation) operating in a positive mode. Raw data was processed using Targetlynx as described previously. Accuracy of quantification was below 6% for all quantified metabolites except glutamic acid (13.9%). Quantitative data was obtained using MetIDQTM Software [18].

2.3. Statistical Analysis

Data distributed normally were expressed as . The statistical method used for testing difference between two groups was Student’s-test. One-way ANOVA was used in more than two groups. For correlation analysis, the Spearman correlation coefficient was calculated in the level of AA and AC between the mothers in the second trimester and their neonates. In PLS-DA, metabolomics data were log-transformed to ensure a normally distributed data set; (goodness of fitness) and (goodness of prediction) were assessed in the PLS-DA models. Multivariate logistic regression analysis was used to determine the association of GDM and macrosomia with prepregnancy BMI, weight gain, and ACs. Odds ratios (ORs) and 95% confidence intervals (CIs) were reported per standard deviation. All statistical analysis was performed using IBM SPSS 23.0 edition, SIMCA 14.0, and R vision 3.6.0. A significance level of 0.05 was used for all statistical tests.

3. Results

The study setup is illustrated in Figure 1. We identified the metabolic alternation in 450 pregnant women of the second trimester. We also investigated the metabolic risk factors in GDM and established a prognostic nomogram based on AC risk factors for predicting macrosomia.

3.1. Maternal Plasma AC Levels of the Second Trimester in 450 Pregnant Women

The baseline characteristics of 450 study participants divided into different categories according to natural conditions of pregnant women such as gravidity, parity, age, height, prepregnancy BMI, weight gain, ART, and method of pregnancy termination. The statistically significant results are shown in Table 1 and Figure 2. In the age subgroup, there was a trend that the level of AC (C2, C3, C4DC+C5OH, C16, C18, and C18:1) was higher in the group, whereas the level of C0 in the group was lower. In and 30 subgroups, several ACs (C2, C3, C5, C16, and C18:1) were higher, whereas the level of C0 was lower. In the weight gain group, C3, C5, C16, and C18:1 were higher in the  kg group than the other groups, while C0 was lower. In the ART group, C2, C3, and C5 were higher while C0 was lower. There was no statistical difference in gravity, parity, height, and method of pregnancy termination subgroups (data not shown).


Age valuePrepregnancy BMI valueWeight gain (kg) valueART value
<2525-35>35<18.518.5-24.925.0-29.9≥30<12.512.5-1515-20>20NoYes

12247191925315335971471505637674
C00.0350.0380.0160.002
C20.0430.0170.6400.016
C30.0420.0150.0350.042
C4DC+C5OH0.0140.2900.4900.185
C50.5240.0270.0380.035
C160.0190.0260.0290.338
C180.0320.5100.5600.483
C18:10.0170.0190.0450.467

Additionally, we investigated the maternal level AC in second trimester pregnancy under the different neonate subgroups (termination of pregnancy weeks, sex, birth length, birth weight, head circumference, abdomen circumference, and abdomen minus head circumference). The results are shown in Table 2 and Figure 3. In the  g group, we found that ACs (C2, C3, C5, C16, and C18:1) were higher; these metabolites increased with birth weight, while C0 was lower. In the  cm group, several ACs (C2, C3, C5, and C16) were higher; C0 was lower. In the abdomen minus circumference subgroup, the metabolite characteristics have a similar trend with the  cm subgroup.


Birth weight (g) valueAbdomen circumference (cm) valueAbdomen-head circumference (cm) value
<28002800-35003500-4000 g>4000 g<3232-35>35<22-55

C00.0260.0180.014
C20.0230.0230.033
C30.0140.0240.013
C50.0370.0250.026
C160.0270.0260.015
C18:10.0170.2070.123

3.2. Specific AC Distribution in GDM

We examined the serum metabolite in 64 GDM patients and 128 matched patients without GDM. Our study used the PLS-DA model (, ) to analyze differences between two groups. The PLS-DA scatterplot showed a clear class separation with GDM at the left and the control group at the right (Figure 4(a)). Furthermore, we used variable importance in projection (VIP) to estimate the contribution of every AC to class separation (GDM vs. control). A was considered with a high contribution to class separation. The VIP analysis (Figure 4(b)) showed that C0 () plays the main role in class separation.

3.3. Clinical Characteristics and AC Plasma Level of GDM

Table 3 shows the characteristics of GDM patients and control. The prepregnancy BMI, weight gain, ART, and the serum levels of C2, C3, C4DC+C5OH, C6DC, C8, C16, C18, and C18:1 were higher, while those of C0 was lower in the GDM group.


GDMControl value

Total64128
Maternal age (years)0.28
Height (cm)0.35
Prepregnancy weight (kg)0.21
Prepregnancy BMI (kg/m2)0.03
Weight gain (kg)0.02
Gestational week at delivery (weeks)0.54
Nulliparous76.4080.200.64
ART19.614.20.04
Smoker7.18.00.35
Birth weight (g)0.03
C0 (μmol/L)0.03
C20.03
C30.02
C4DC+C5OH0.01
C6DC0.03
C80.04
C160.04
C180.02
C18:10.04

3.4. Multiple Logistic Regression Analysis of the Association between GDM and Other Factors

We selected significant factors from univariate analysis to enter multiple logistic regression analysis to examine whether acting independently. Prepregnancy BMI (, ), weight gain (, ), C0 (, ), C3 (, ), C16 (, ), and C18 (, ) were statistically associated with GDM. These factors can work as independent risk factors involve in the process of GDM (Table 4).


OR95% CI value

Prepregnancy BMI (kg/m2)1.151.06-1.780.03
Weight gain (kg)1.181.03-1.640.03
ART1.241.00-1.390.73
C0 (μmol/L)0.700.60-0.830.02
C21.320.65-4.370.32
C31.031.02-2.080.01
C4DC+C5OH1.011.01-2.480.81
C6DC1.931.20-3.720.93
C81.261.10-4.350.56
C161.301.12-3.280.03
C181.271.00-3.010.04
C18:11.171.13-2.760.17

3.5. Association of C0 Deficiency and Blood Glucose and Lipid in GDM and Control

When divided into two groups according to the C0 level (<20 μmol/L or ≥20 μmol/L), we found that 81.25% of GDM women of the second trimester pregnancy are in C0 deficiency status. In GDM women, FBG, TG, TC, LDL, and homocysteine (HCY) were significantly higher in the μmol/L group. Similar results were also seen in the control group of μmol/L (Table 5). In GDM and control groups, C0 was negatively correlated with FBG, LDL, TG, TC, and HCY and positively correlated with HDL. There were no significant correlations between C0 and OGTT-1 h and OGTT-2 h (Figure 5).


GDM valueControl value

52 (81.25%)12 (128.75)96 (75%)32 (25%)
FBG (mmol/L)0.020.03
OGTT-1 h (mmol/L)0.430.36
OGTT-2 h (mmol/L)0.390.28
TG (mmol/L)0.020.02
TC (mmol/L)0.030.03
HDL (mmol/L)0.390.04
LDL (mmol/L)0.020.02
HCY (μmol/L)0.030.03

3.6. Cluster Correlation Heat Map

The heat map depicting the internal correlations between metabolites revealed the predominant clusters of intercorrelated metabolites: C2, C4, C6, and C8 (Figure 6). The four metabolites included in the final model showed strongly internal correlations. There were no strong intercorrelations in others.

3.7. Clinical Characteristics and AC Plasma Level and a Nomogram of Prediction of Macrosomia

Here, we investigated the clinical characteristics and AC metabolite between GDM with macrosomia and GDM without macrosomia (Table 6). We found that prepregnancy weight, BMI, weight gain, C0, C2, C3, C16, and C18 were higher in GDM with macrosomia (). In the multiple logistic regression analysis, we found that prepregnancy BMI, weight gain, C0, C3, and C16 were also evaluated (Table 7, ). These factors are independent risk factors involved in the process of GDM-induced macrosomia. The nomogram of predicting GDM-induced macrosomia had incorporated these significant variables. Among these metabolites, C0 deficiency showed the highest OR (, ). Vertical lines should be drawn from the correct location from each independent risk factor. “Total points” which could be obtained by adding all points of the axis to the bottom axes made the conversion into a macrosomia probability. The accuracy of the model was well assessed by the AUC equal to 0.78 (Figure 7).


MacrosomiaNonmacrosomia value

1252
Maternal age (years)0.79
Height (cm)0.33
Prepregnancy weight (kg)0.04
Prepregnancy BMI (kg/m2)0.03
Weight gain (kg)0.02
Gestational week at delivery (weeks)0.83
Nulliparous (%)74.262.50.82
ART19.614.20.55
Smoker7.48.20.96
Birth weight (g)0.02
C0 (μmol/L)0.03