<i>APOC3</i> rs2070667 Associates with Serum Triglyceride Profile and Hepatic Inflammation in Nonalcoholic Fatty Liver Disease

Xu, Qing-Yang; Li, Han; Cao, Hai-Xia; Pan, Qin; Fan, Jian-Gao

doi:https://doi.org/10.1155/2020/8869674

BioMed Research International

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Abstract Introduction Materials and Methods Results Discussion Conclusion Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 8869674 | https://doi.org/10.1155/2020/8869674

APOC3 rs2070667 Associates with Serum Triglyceride Profile and Hepatic Inflammation in Nonalcoholic Fatty Liver Disease

Qing-Yang Xu,¹Han Li,¹Hai-Xia Cao,¹Qin Pan,¹and Jian-Gao Fan^1,2,3

Academic Editor: Zhanjun Jia

Received01 Sept 2020

Revised02 Nov 2020

Accepted10 Nov 2020

Published27 Nov 2020

Abstract

Single-nucleotide polymorphisms (SNPs) of apolipoprotein C3 (APOC3) play important role in lipid metabolism, and dyslipidemia underlies nonalcoholic fatty liver disease (NAFLD). But the correlation of serum lipidomics, APOC3 SNPs, and NAFLD remains limited understood. Enrolling thirty-four biopsy-proven NAFLD patients from Tianjin, Shanghai, Fujian, we investigated their APOC3 genotype and serum lipid profile by DNA sequencing and ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), respectively. Scoring of hepatocyte steatosis, ballooning, lobular inflammation, and liver fibrosis was then performed to reveal the role of lipidomics-affecting APOC3 SNPs in NAFLD-specific pathological alterations. Here, we reported that APOC3 SNPs (rs4225, rs4520, rs5128, rs2070666, and rs2070667) intimately correlated to serum lipidomics in NAFLD patients. A allele instead of G allele at rs2070667, which dominated the SNPs underlying lipidomic alteration, exhibited downregulatory effect on triacylglycerols (TGs: TG 54 : 7, TG 54 : 8, and TG 56 : 9) containing polyunsaturated fatty acid (PUFA). Moreover, subjects with low-level PUFA-containing TGs were predisposed to high-grade lobular inflammation (TG 54 : 7, and ; TG 54 : 8, and P =0.016; TG 56 : 9, and ). The significant correlation of APOC3 rs2070667 and inflammation grading [G/G vs. G/A+A/A: 0.00 (0.00 and 1.00) vs. 1.50 (0.75 and 2.00), ] further confirmed its pathological action on the basis of lipidomics-impacting activity. These findings suggest an inhibitory effect of A allele at APOC3 rs2070667 on serum levels of PUFA-containing TGs, which are associated with high-grade lobular inflammation in NAFLD patients.

1. Introduction

Nonalcoholic fatty liver disease (NAFLD) reflects an important pathological syndrome demonstrating hepatocyte steatosis, ballooning, and lobular inflammation, with clinical outcomes of liver fibrosis/cirrhosis, hepatocellular carcinoma, and related mortality [1–8]. By its rapid growing incidence in the recent decades, NAFLD has already been a leading cause of chronic liver diseases worldwide [9–13]. Aberrant lipid metabolism, which facilitates the hepatocyte steatosis, oxidative stress, hepatic injury, and inflammation [12, 14–16], is now widely accepted to serve as a fundamental etiology that results in the NAFLD-inducing “multiple hits” [10, 17, 18].

Nowadays, multiple studies reveal an intimate association of single-nucleotide polymorphisms (SNPs) in the lipometabolism-related genes [19–24] and the genetic susceptibility of NAFLD [25–32]. Among these genes, APOC3 encodes apolipoprotein C3 (apoC3), which is the critical inhibitor of lipoprotein lipase (LPL) in chylomicron (CM) remnants and very-low-density lipoprotein (VLDL) [33–35]. The modulatory effect of apoC3 on LDL receptor (LDLR) activation causes the reduction of uptake and integration of triglyceride- (TG-) rich particles in hepatocytes [33–35]. Loss-of-function mutations of APOC3 (R19X, IVS2+1G→A, IVS3+1G→T, A43T, and V50M) [33, 36] have been well described to correlate to plasma triglycerides [37] and related cardiovascular diseases (coronary heart disease, ischemic cardiovascular disease, etc.) in heterozygous carriers [33, 36]. The critical role of APOC3 in lipid metabolism, together with the dyslipidemia caused by APOC3 mutations [38, 39] and apolipoprotein C3 deficiency [33, 36], suggests an association of APOC3 SNPs and dyslipidemia-based NAFLD. However, this APOC3 SNPs and NAFLD association remains limited, yet controversial, understood [32, 40–43]. In brief, APOC3 variants (C-482T or T-455C) in the promoter are reported to predispose subjects to NAFLD by Petersen et al. [32], but this observation was disproved by Kozlitina et al. [41]. Thus, the correlation of APOC3 SNPs, serum lipids, and NAFLD needs further exploration.

We, therefore, performed APOC3 sequencing, serum lipidomic detection, and pathological evaluation in Chinese Han patients with biopsy-proven NAFLD. The association among APOC3 SNPs, serum lipid profile, and pathological scoring was then investigated to uncover the lipidomics-based intervention of APOC3 polymorphisms on NAFLD.

2. Materials and Methods

2.1. Study Subjects

Thirty-four () Chinese Han patients with biopsy-proven NAFLD were recruited from Xinhua Hospital, Shanghai (); Tianjin Hospital of Infectious Diseases, Tianjin (); and Zhengxing Hospital, Zhangzhou, Fujian () during January 2012 and June 2013 in this cross-sectional study (Table 1). The following criteria were employed for patient exclusion: (1) drinking history or excessive alcohol consumption, (2) virus hepatitis, (3) steatosis-related chronic liver diseases, and (4) liver transplantation [44–47]. Each participator provides 1 mL total blood for further detection. Institutional approval of this study was obtained from Xinhua Hospital Research Ethics Committee, and informed consent was issued by each participant. All methods in this study were conducted in accordance with the approved guidelines and the Declaration of Helsinki.

2.2. DNA Isolation and Genotyping of APOC3 SNPs

After centrifugation of 500 μl total blood, DNA was extracted from peripheral mononuclear cells by QiAamp DNA Mini Kit (Qiagen, Venlo, Netherlands). The concentration and quality of DNA were verified using NanoDrop® ND-1000 (Thermo Fisher Scientific, Waltham, MA, USA) and 0.8% agarose gel electrophoresis. Thereafter, primers of five APOC3 SNPs (rs4225, rs4520, rs5128, rs2070666, and rs2070667) were designed on the basis of dbSNP database (https://www.ncbi.nlm.nih.gov/snp/) to construct a custom Ion AmpliSeq panel (Thermo Fisher Scientific, Waltham, MA, USA). The emulation polymerase chain reaction (PCR) of the template DNA was processed using the Ion OneTouch 2 System (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instructions. APOC3 SNPs were successively genotyped according to the following procedures: (1) DNA sequencing by Ion 318 Chip on the Ion PGM™ System (Thermo Fisher Scientific, Waltham, MA, USA) and (2) data analysis by the Auto-user software (Life Technology, Gaithersburg, MD, USA) [48].

2.3. Lipidomics Analysis

Serum sample (40 μl) from each NAFLD patient was subjected to serum lipidomic analysis using Triple TOF 5600 mass spectrometer (AB SCIEX, Framingham, MA, USA) by means of untargeted ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Firstly, a Waters BEH C8 column ( and 1.7 μm) was used for lipid separation. The mobile phases were composed of 3 : 2 (v/v) ACN/O (10 mM AcAm, phase A) and 9 : 1 (v/v) IPA/ACN (10 mM AcAm, phase B). A 20-minute elution gradient program was run at the flow rate of 0.26 mL/min and the column temperature of 55°C. The elution gradient stared with 32% B for 1.5 min and rose up linearly to 85% B at 14 min, then reached 97% B at 15.5 min for 2.5 min. It returned to 32% B within 0.1 min and held for 1.9 min for column equilibration.

The UPLC-MS/MS parameters conducted for lipid detection were summarized as follows: temperature of interface heater, 600°C in electrospray ionization (ESI) (–) and 500°C in ESI (+); ion spray voltage of MS: 4500 V in ESI (–) and 5500 V ESI (+); declustering potential: 100 V ESI (–) and 100 V ESI (+); collision energy: 10 V ESI (–) and 10 V ESI (+). Thirteen quality control (QC) samples were randomly inserted into the testing sequence.

Raw data obtained was identified using LipidView/PeakView (AB SCIEX, Framingham, MA, USA) and quantified using MultiQuant 2.0 (AB SCIEX, Framingham, MA, USA). The relative standard deviation of 239 serum lipids in QC samples was measured against the internal standards [49].

2.4. Hepatic Histopathologic Assessment

Liver specimens from each patient were obtained by ultrasound-guided needle biopsy. Each sample was then treated by 10% formalin fixing, paraffin embedding, slicing, and hematoxylin & eosin (HE) and Masson’s trichrome staining in succession. Three pathologists who were not aware of the study assessed the NAFLD-related pathological characteristics according to the steatosis, activity, and fibrosis (SAF) scoring method as follows: (1) steatosis (S0, <5%; S1, 5-33%; S2, 34-66%; S3, >66%); (2) activity: sum of lobular inflammation (0, no foci per 200× field; 1, <2 foci per 200× field; 2, 2-4 foci per 200× field; 3, >4 foci per 200× field) and ballooning (0, none; 1, few balloon cells; 2, many cells/prominent ballooning); (3) fibrosis (F0, none; F1, perisinusoidal or portal fibrosis; F2, perisinusoidal and periportal fibrosis without bridging; F3, bridging fibrosis; F4, cirrhosis) [1, 50–52].

2.5. Statistical Analysis

All data were expressed as (SD). Unpaired Student’s independent -test was used to investigate the differences in serum lipidomics after examining the normality of data () by Kolmogorov-Smirnov test. Spearman’s correlation was performed to evaluate the association of serum lipid profile and hepatic histological parameters. Differences in histological parameters were analyzed by Mann-Whitney test. Analyses were performed using SPSS21.0 (SPSS Inc., Chicago, IL, USA) with a two-side significant criterion at .

3. Results

3.1. APOC3 SNPs Correlated with Serum Lipidomics in NAFLD Patients

Detecting APOC3 SNPs and 239 serum lipids, the effect of APOC3 polymorphisms on serum lipidomics was subjected to evaluation. Dramatically, there was a distinct correlation between APOC3 SNPs (rs4225, rs4520, rs5128, rs2070666, and rs2070667) and serum lipidomics in our NAFLD cohort (Table 2). APOC3 SNP-related lipids, including ceramide (Cer), diacylglycerol (DG), choline plasmalogen (PCO), phosphatidylethanolamine (PE), ethanolamine plasmalogen (PEO), phosphatidylinositol (PI), and triacylglycerol (TG), characterized the lipidomic alteration (Table 2).

3.2. G/A or A/A Genotype of APOC3 rs2070667 Exhibited Downregulatory Effect on Serum Lipid Profile

In contrast to most APOC3 SNPs exhibiting limited-scale lipidomic association, APOC3 rs2070667 exerted wide-range impacts on serum lipids of Cer, DG, PCO, and TG with statistical significance (Table 2). When compared to those with G/G genotype, NAFLD patients carrying G/A+A/A genotypes at APOC3 rs2070667 demonstrated statistically lowered levels of TGs (TG 54 : 7, TG 54 : 8, and TG 54 : 9), whereas obvious higher levels of Cer (Cer 42 : 1; 2), DG (DG 36 : 4), and PCO (PCO 38 : 4 and PCO 40 : 4) (Table 2).

3.3. APOC3 rs2070667-Dependent Low-Level TGs Associated with High-Grade Lobular Inflammation

To shed light on the interaction between serum lipidomics and NAFLD, we further investigated the association of APOC3 rs2070667-related differential serum lipids and NAFLD-specific pathological disorders (hepatocyte steatosis, lobular inflammation, ballooning, and liver fibrosis). Interestingly, polyunsaturated fatty acid- (PUFA-) containing TGs among these ones showed a negative correlation with lobular inflammation in similar Spearman coefficients (TG 54 : 7, and ; TG 54 : 8, and P =0.016; TG 56 : 9, and P =0.004) (Figure 1(b)). Being compared to those carrying G/G at APOC3 rs2070667, the NAFLD patients with G/A or A/A genotype were characterized by low serum levels of PUFA-containing TGs and high-grade lobular inflammation (Figure 1(b)). Other pathological characteristics of NAFLD, especially hepatocyte steatosis, shared the mild correlation of serum PUFA-containing TGs in an inverse manner (Figures 1(a), 1(c), and 1(d)).

Figure 1

Lower-level TGs were correlated with higher-grade lobular inflammation in nonalcoholic fatty liver disease patients. Scatters reflected the serum levels of TGs (TG 54 : 7, TG 54 : 8, and TG 56 : 9) and pathologic scoring (steatosis, lobular inflammation, ballooning, and fibrosis) in patients with nonalcoholic fatty liver disease. Linear fit lines were presented with rho corresponding to the correlation of TGs and pathological characteristics. Inverse correlation between TG 54 : 7, TG 54 : 8, and TG 56 : 9 and lobular inflammation was observed with statistical significance. The rho values of fit lines in (b) were similar.

3.4. NAFLD Patients Carrying A Allele at APOC3 rs2070667 Showed Severe Lobular Inflammation

By scoring hepatocyte steatosis, lobular inflammation, ballooning, and liver fibrosis, we assessed the role of APOC3 rs2070667 in NAFLD-related pathological characteristics. An aggravation of lobular inflammation and, to less extent, steatosis was documented in the NAFLD patients carrying A allele (G/A and A/A) at APOC3 rs2070667 in comparison to those with G allele (lobular inflammation: G/G vs. G/A+A/A: 0.00 (0.00 and 1.00) vs. 1.50 (0.75 and 2.00), ; hepatocyte steatosis: G/G vs. G/A+A/A: 2.00 (1.00 and 2.00) vs. 2.00 (1.75 and 3.00), ) (Figures 2(a) and 2(b)). However, different alleles at APOC3 rs2070667 showed insignificant effect on ballooning (G/G vs. G/A+A/A: 2.00 (1.00 and 2.00) vs. 1.50 (1.00 and 2.00), ) and liver fibrosis (G/G vs. G/A+A/A: 2.00 (1.00 and 3.00) vs. 1.00 (0.00 and 3.00), ) (Figures 2(c) and 2(d)). Thus, A allele at APOC3 rs2070667 is suggested to underlie severe lobular inflammation in the NAFLD patients with close association of lowered levels of PUFA-containing TGs.

(a)

(b)

(c)

(d)

Figure 2

Nonalcoholic fatty liver disease patients carrying G/G vs. G/A+A/A genotype at APOC3 rs2070667 demonstrated higher-grade lobular inflammation. Box plots indicated the differences in pathological characteristics of steatosis, lobular inflammation, ballooning, and fibrosis between nonalcoholic fatty liver disease patients with G/G vs. G/A+A/A genotype at APOC3 rs2070667. An aggravation of lobular inflammation was documented in the NAFLD patients carrying A allele (G/A and A/A) at APOC3 rs2070667 in comparison to those with G allele. Mild upregulated steatosis was also presented in the patients carrying A allele. Results were presented as medians and interquartile range. .

4. Discussion

Multiple researches have shed light on the versatile actions of APOC3 in lipid metabolism [35, 38, 39, 53–56]. apoC3 within CM is capable of inhibiting the LPL-dependent CM-TG hydrolysis and the hepatic CM intake on a basis of apoE and LDL receptor-related protein (LRP) combination [35, 53]. Upregulated apoC3 in VLDL also retards its clearance [38, 39, 54–56]. In addition, plasma level of apoC3 exhibited a correlation to HDL lipids of cholesterol ester (CE), TG, free cholesterol (FC), phosphatidylcholine (PC), PCO, sphingomyelin (SM), DG, Cer, and LPC [37]. This lipometabolic activity of apoC3 suggests an association of APOC3 SNPs and lipid metabolic traits [20, 23, 35, 37–39, 53–56].

Indeed, subjects with APOC3 -2854 G/T demonstrate higher serum TG [57], whereas -482C>T in APOC3 is related to the serum levels of TG and other lipids in the Chinese population [57]. An important role of polymorphisms tagging APOC3 is further convinced in the occurrence of dyslipidemia by Genome-Wide Association Studies (GWAS) [58–60]. Integrating DNA sequencing and UPLC-MS/MS analysis, our study presented novel findings that a group of APOC3 SNPs (rs4225, rs4520, rs5128, rs2070666, and rs2070667) exerted global impact on serum lipidomics in NAFLD patients. Moreover, APOC3 rs2070667 among these ones was statistically associated with 7 differential serum lipids, including Cer, DG, PCO, and TGs.

Nowadays, there are growing evidences highlighting a crucial effect of serum lipids on NAFLD [61–64]. Relying on the lipidomics-based evolutionary algorithm, serum lipids of TG (16 : 0, 18 : 0, and 18 : 1), PC (18 : 1 and 22 : 6), and PCO (24 : 1 and 20 : 4) are put forward to be predictive biomarkers of NAFLD [61]. On the contrary, both serum LPCs and PUFA-containing phospholipids associate with the liver fat content in an inverse manner [61]. Decrease in serum palmitoyl-, stearoyl-, and oleoyl-LPC characterizes the mice with experimental nonalcoholic steatohepatitis (NASH) [62]. Nevertheless, FFA released from circulating TG and adipose tissue has been reported to contribute to hepatocellular FFA accumulation and steatosis [63, 64]. APOC3 SNPs, therefore, are proposed to interfere in the NAFLD by lipidomic modulation.

When compared to those with G/G genotype, we documented significantly lowered levels of TGs (TG 54 : 7, TG 54 : 8, and TG 54 : 9) in NAFLD patients with G/A or A/A genotype at APOC3 rs2070667. Moreover, there was a negative correlation between these PUFA-containing TGs and NAFLD-specific pathological characteristics, including lobular inflammation and steatosis, in comparable Spearman coefficients. In contrast to saturated fatty acids that upregulate the levels of proinflammatory cytokines, n-3 PUFAs have been described to attenuate the inflammation activity of liver by the reduction of proinflammatory cytokine (e.g., TNF-α, IL-1β, and IL-6) secretion, as well as the increase of anti-inflammatory cytokine (e.g., adiponectin) [65–67]. Their incorporation into the phospholipids of inflammatory cells may underlie these pharmacological actions, resulting in the improved membrane fluidity and modified lipid derivatives [65]. On the other hand, PUFAs prevent the liver from steatosis on a basis of SREBP-1c and lipogenic gene (e.g., FAS, ACC, and SCD-1) downregulation [68] and then alleviate the hepatic inflammation by an amelioration of oxidative stress [69, 70].

In the present study, we verified much higher SAF grade of lobular inflammation in NAFLD patients carrying A allele at APOC3 rs2070667 in comparison to those with G allele. By the mild increase in their steatosis scoring, an association was highlighted between APOC3 rs2070667 and hepatocyte steatosis. In result, APOC3 rs2070667 is indicated to be responsible for the deteriorated pathological characteristics in NAFLD patients by, to a large extent, its inhibitory impact on the serum levels of PUFA-containing TGs. Contrastively, there are some literatures deny the role of APOC3 SNPs in NAFLD [40, 71]. This disagreement may be partially attributed to the test of blood lipids in routine method, which is insufficient to distinguish numerous components and their alterations in serum lipidomics.

Being contrast to most filtered SNPs locating in the exons of APOC3, rs2070667 is found to be an intron-resided SNP with probably intact structure and catalytic activity of apoC3. Its effects on serum lipidomics and NAFLD could be attributed to the epigenetic regulations, such as DNA methylation and miRNA-based expressive tuning [72–75]. Furthermore, transcriptional regulation reflects another potential mechanism of its lipidomic and pathological roles because approximately 40% of transcription factor (TF) binding sites have been identified in the introns [76].

However, there are some limitations in the present study. First, lacking of quantitative apoC3 test remains a shortcoming in highlighting the mechanisms underlying effects of APOC3 SNPs. In addition, untargeted UPLC-MS/MS instead of targeted UPLC-MS/MS was employed to investigate the effect of APOC3 on serum lipidomics. Thus, number of unsaturated bonds, but not their location, in serum lipids could be identified in our experiments.

5. Conclusion

APOC3 SNPs exhibit impact on the serum lipidomics of NAFLD patients. A allele at APOC3 rs2070667 demonstrates predominantly downregulatory effect on the serum lipid profile. Low-level PUFA-containing TGs (54 : 7, 54 : 8, and 56 : 9) among these differential lipids display significant association with high-grade lobular inflammation. Therefore, NAFLD patients carrying A instead of G allele at APOC3 rs2070667 may susceptible to hepatic inflammation upon the rs2070667-based alteration of serum TGs.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

Authors’ Contributions

Qing-Yang Xu and Han Li contributed equally to this work.

Acknowledgments

This work is supported by the National Key R&D Program of China (2017YFC0908903) and the National Natural Science Foundation of China (81270492, 81470859, and 81600464). We thank Guo-Wang Xu and Chun-Xiu Hu of Dalian Institute of Chemical Physics, Chinese Academy of Sciences.

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