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The role of PNPLA3 and TM6SF2 polymorphisms on liver fibrosis and metabolic abnormalities in Brazilian patients with chronic hepatitis C

BMC Gastroenterology volume 21, Article number: 81 (2021) Cite this article

Abstract

Background

Despite the growing body of knowledge about TM6SF2 and PNPLA3 polymorphisms in non-alcoholic fatty liver disease, their influence in the spectrum of HCV liver disease is not yet fully defined. Besides that, admixed populations, such as Brazilians, were not included in most of the studies.

Methods

This cross-sectional study enrolled 365 treatment-naïve patients with HCV and 134 healthy individuals. TM6SF2 (rs58542926 c.499C > T) and PNPLA3 (rs738409 c.444C > G) polymorphisms were evaluated regarding their association with clinical and laboratory data, histological liver steatosis and fibrosis, and with components of the metabolic syndrome.

Results

In HCV subjects, the frequencies of TM6SF2 CC and CT + TT were 89% and 11%, while PNPLA3 frequencies of CC and CG + GG were 51.4% and 48.6%. In the univariate logistic regression analysis, the TM6SF2 CT + TT genotype in HCV was associated with significant liver fibrosis (p = 0.047; OR 1.953; 95% CI 1.009–3.788). In comparison to the CT + TT genotype, the TM6SF2 CC genotype in HCV was associated with older age (p = 0.002), higher frequency of arterial hypertension (p = 0.032), obesity (p = 0.030), metabolic syndrome (p = 0.014) and lower total cholesterol levels (p = 0.036). The PNPLA3 GG subjects had lower body mass index than CG/ CC individuals (p = 0.047). None of the polymorphisms, or their combinations, was independently associated with hepatic steatosis or fibrosis. On the other hand, older age, lower serum levels of total cholesterol, and higher serum levels of alanine aminotransferase and alkaline phosphatase were associated with liver fibrosis in the multivariate logistic regression analysis.

Conclusion

In this evaluation of an admixed HCV population, neither TM6SF2 nor PNPLA3 polymorphisms were independently associated with hepatic steatosis or fibrosis. Other factors seem more influential than these specific polymorphisms in isolation. More studies are warranted to clarify the role of the TM6SF2 and PNPLA3 polymorphisms in Brazilians with HCV.

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Background

Chronic hepatitis C virus (HCV) infection affects about 1% of the world population and remains one of the main causes of liver disease worldwide [1]. In Brazil, it is estimated that 0.53% of the total population is anti-HCV positive [2]. Between 55 and 85% of patients exposed to the virus develop chronic liver disease, and 15 to 20% of these will reach the stage of cirrhosis [3]. HCV is the leading cause of death among viral hepatitis in Brazil, and it remains a public health problem: in 2019, it was estimated that 22,747 individuals were infected with HCV [4].

Persistent HCV infection leads to the induction of pro-inflammatory cytokine production by Kupffer cells, activation of hepatic stellate cells, and development of liver fibrosis and cirrhosis [5]. Liver disease progression with accelerated fibrosis and cirrhosis is also associated with other factors, such as insulin resistance, obesity, non-alcoholic fatty liver disease (NAFLD), alcohol consumption, and coinfections with HIV or hepatitis B virus [6]. Indeed, metabolic syndrome (MetS) features, such as obesity and diabetes mellitus can negatively impact chronic HCV infection [7]. In addition, liver steatosis is another frequent complication in HCV-infected patients, affecting 50 to 72% of this population [8].

With the advent of genome-wide association studies (GWAS), the influence of genetic factors in the development of steatosis and progression of chronic liver disease has gained evidence, mainly in NAFLD [9,10,11]. In this context, the single nucleotide (SNP) polymorphisms E167K of the Transmembrane 6 Superfamily Member 2 (TM6SF2) gene, and the polymorphisms I148M of the Patatin-like Phospholipase-3 (PNPLA3) gene, are two of the most frequently studied polymorphisms across populations [9, 11].

Experimental and observational studies have shown that the E167K variant (T allele) is associated with TM6SF2 functional loss, with consequent decreased VLDL secretion and increased intrahepatic fat aggregation, conferring an increased risk for NAFLD [12,13,14]. The common allele (C allele), in turn, seems to be associated with a lower risk of steatosis, but with higher serum levels of total cholesterol, LDL, and triglycerides (TG), and increased risk of cardiovascular disease [15]. In patients with chronic hepatitis C, TM6SF2 is believed to regulate the interaction between viral glycoproteins and the host’s lipid metabolism, with potentially deleterious consequences for the liver [16]. Despite this theoretical association, studies on hepatitis C have shown inconsistent results [16,17,18].

The I148M variant of PNPLA3 has shown an association with the progression of liver fibrosis and steatosis, and in the occurrence of hepatocellular carcinoma [9, 19, 20]. The strongest associations with the severity of liver disease were seen in patients with NAFLD, including the Brazilians [21,22,23]. Studies on chronic hepatitis C corroborate the relationship of this polymorphism with liver disease progression and steatosis [19, 24, 25]. However, other studies with a predominance of Asian populations have shown divergent results [26, 27].

Despite the growing investigational experience with TM6SF2 and PNPLA3 polymorphisms in NAFLD, their role in the spectrum of liver disease by the hepatitis C virus is not yet fully defined. Also, there is little data in mixed populations, such as among Brazilians [28]. In this context, the aim of this study is to describe the prevalence of TM6SF2 and PNPLA3 polymorphisms in Brazilian patients with chronic hepatitis C naïve for antiviral therapy, and to evaluate their association with liver fibrosis, steatosis, and other components of the metabolic syndrome.

Methods

Clinical Design and Patients’ Selection

This was a single-center cross-sectional study conducted in healthy subjects and in patients with chronic hepatitis C, followed between 2014 and 2016 at the Outpatient Units of the Departments of Gastroenterology and Infectious Diseases at the Hospital das Clinicas of the University of Sao Paulo School of Medicine, Brazil. PNPLA3 (rs738409 c.444 C > G) and TM6SF2 (rs58542926 c.499C > T) polymorphisms were investigated in 365 patients with chronic hepatitis C naïve to antiviral therapy and in 134 unrelated healthy volunteers without chronic hepatitis B, C, or liver enzyme abnormalities.

The inclusion criteria for the HCV group were age ≥ 18 years old, presence of chronic hepatitis C, defined by HCV polymerase chain reaction (PCR) RNA positivity for at least 6 months, with histopathological diagnosis of chronic HCV, and naïve to antiviral therapy. All patients with chronic hepatitis C had liver histology evaluated by an experienced liver pathologist. The exclusion criteria were any other diagnosed chronic liver disease, significant alcohol intake (> 100 g/week), HIV or hepatitis B infection, previous liver transplantation, or refusal to participate in the study. The healthy volunteers’ group consisted of subjects without chronic hepatitis B, C, or liver enzyme abnormalities, selected from among the general population. This group was used only to describe the frequency of the PNPLA3 and TM6SF2 polymorphisms in healthy individuals in Brazil. No statistical analyses were performed between this group and patients with HCV.

Variables evaluated

Demographic and anthropometric data (age, gender, self-reported ethnicity, and body mass index) were obtained from the medical charts, as well as the presence of comorbidities [arterial hypertension, diabetes mellitus, dyslipidemia, MetS, previous cardiovascular event (CVE), and hypotireoidism]. CVE was defined as any one of the following: previous acute myocardial infarction, stroke, or diagnosed peripheral arterial disease. Alcohol consumption was also registered.

Diagnosis of metabolic syndrome was based on the recommendations of the Adult Treatment Panel III Report. It was made when three or more of the following criteria were met: triglycerides ≥ 150 mg/dL, high-density lipoproteins (HDL) < 40 mg/dL (men) or < 50 mg/dL (women), fasting glucose ≥ 110 mg/dL, systolic blood pressure ≥ 130 mm Hg, and diastolic blood pressure ≥ 85 mm Hg and abdominal obesity [29]. The definition of insulin resistance was based on the calculation of the Homeostatic Model of Assessment (HOMA-IR), with insulin resistance defined by a HOMA-IR when ≥ 2.5 [30].

Serum biochemistry included: alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase, gamma-glutamyl transferase (GGT), creatinine, total cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), and triglycerides. These were collected after a 12-h overnight fasting period at the time of the liver biopsy.

The serum HCV-RNA real-time PCR was made with the Amplicor HCV Monitor 2.0 test (Diagnostic Systems, Branchburg, NJ, USA, detection limit: 50 IU/ml). HCV genotyping was performed using the Versant® HCV Genotype 2.0 (LiPA) test (Immunogenetics, Ghent, Belgium).

Liver histology was assessed by blinded experienced liver pathologists and considered the METAVIR classification for fibrosis and inflammation [31]. The evaluation of fibrosis (F) and inflammatory activity (A) was according to the following parameters: Fibrosis: F0 (absent), F1 (portal fibrosis without septa), F2 (portal fibrosis with rare septa), F3 (numerous septa without cirrhosis) and F4 (cirrhosis); inflammatory activity: A0 (absent), A1 (mild activity), A2 (moderate activity) and A3 (intense activity) [31]. Steatosis was classified as absent (affecting less than 5% of liver parenchyma) or present (more than 5%).

DNA extraction and genotyping

Genomic DNA was isolated from 200 μl of blood and analyzed by QIAamp DNA Blood Mini Kit (QIAGEN, Hilden, Germany). Briefly, as previously described [22], PNPLA3 (rs738409 c.444 C > G) and TM6SF2 (rs58542926 c.499C > T) polymorphisms were genotyped using TaqMan primers and probes for allelic discrimination (7500 Fast Real-Time PCR system, Applied Biosystems, Thermo Fisher Brand, Foster City, California, USA) as per the manufacturer’s recommendations. Direct genotyping in random samples was conducted to validate the results. Quality control was conducted to check the reproducibility of the results.

Ethical considerations

The Ethics Committee of the Hospital das Clinicas of the University of Sao Paulo School of Medicine has approved this study (numbered 1,531,382 and 2,676,105). The protocol followed the 1975 Declaration of Helsinki. Informed consent was obtained from participants.

Statistical analysis

The data were compiled in a Windows Excel table for statistical analysis. Descriptive statistics (means, standard deviations) were calculated. The chi-square test and Fisher’s exact test were used to compare the categorical variables; Mann–Whitney and Kruskal–Wallis tests were used for numerical variables, since these did not have a normal distribution. The maximum percentage of missing values for any clinical/ biochemical covariate was 1.9%. Regarding liver histology covariates, we had one missing value for fibrosis, 11 for steatosis, and 65 for inflammation. To evaluate factors associated with liver fibrosis, inflammation, and steatosis, logistic regression analysis was used. In the multivariate logistic regression analysis, a stepwise variable selection criterion was used. Odds ratio (OR) and 95% confidence interval (CI) were calculated to evaluate the impact of these factors. Hardy–Weinberg equilibrium was evaluated. Heterozygosity and the polymorphic information content (PIC) in the studied groups were calculated [32]. The combination effect of TM6SF2 and PNPLA3 polymorphisms was evaluated on logistic regression analyses. A probability value of < 0.05 was considered significant. The Statistical Analysis System (SAS) for Windows software package, version 9.4 (SAS Institute Inc, 2002–2008, Cary, NC, USA) was used for the statistical analyses conducted by biomedical statisticians from the Statistics Service at School of Medical Sciences of the University of Campinas.

Results

We included 365 patients with chronic hepatitis C and 134 healthy individuals in the study. Among the patients with HCV, 55.1% were women, the mean BMI was 27.57, and the mean age was 54.54 ± 12.7 years. The most frequent self-reported ethnicity was white (76.7%), and 23.18% of the subjects fulfilled the MetS criteria. Regarding HCV infection, the most prevalent genotype was 1 (79.4%), followed by genotype 3 (17.9%). All stages of liver fibrosis were represented in this cohort, with cirrhosis predominating (30.5%). The main characteristics of the included patients are detailed in Table 1.

Table 1 Demographic, clinical and biochemical characteristics of patients with HCV
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TM6SF2 and PNPLA3 polymorphisms were in Hardy–Weinberg equilibrium among all groups. In the HCV group, TM6SF2 and PNPLA3 heterozygosity were 0.20 and 0.56, and the PIC were 0.18 and 0.56, respectively. Among healthy subjects, the TM6SF2 and PNPLA3 heterozygosity were 0.13 and 0.58, and the PIC were 0.12 and 0.50, respectively. In healthy subjects, the frequencies of TM6SF2 CC and CT + TT were 93.3% and 6.7%, respectively. In patients with HCV, these frequencies were 89% and 11% (Table 2). Regarding PNPLA3 polymorphisms in healthy subjects, the frequencies of CC and CG + GG were 49.3% and 50.7%, respectively, and 51.4% and 48.6% in patients with HCV (Table 2). Analyzing the associations of PNPLA3 polymorphisms in patients with HCV, we found that GG subjects had lower BMI than CG/ CC individuals (25.19 ± 3.7 vs. 27.9 ± 5.24 vs. 27.67 ± 4.94, p = 0.046), and that the presence of MetS was more frequent in CC/CG subjects (p = 0.013) (Table 3). No differences were observed regarding any other clinical, biochemical, or liver histology variables related to PNPLA3 genotypes (Table 3), or with the presence/absence of the G allele (data not shown). On the other hand, when analyzing TM6SF2 polymorphisms in patients with HCV, the CC genotype was associated with older age (p = 0.002), higher frequency of arterial hypertension (p = 0.032), obesity (p = 0.030), MetS (p = 0.014), and higher serum levels of alkaline phosphatase (p = 0.041) and total cholesterol (p = 0.036), relative to the CT/TT genotype. Also, the presence of the TM6SF2 T allele was associated with significant liver fibrosis (≥ stage 2 fibrosis; p = 0.044) (Table 4).

Table 2 PNPLA3C > G and TM6SF2C > T frequencies in healthy subjects and in patients with HCV
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Table 3 Characteristics of patients with HCV according to PNPLA3 polymorphisms (n = 364)
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Table 4 Characteristics of patients with HCV according to TM6SF2 polymorphisms (n = 362)
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On the univariate logistic regression analyses, older age, diabetes/ insulin resistance, dyslipidemia, arterial hypertension, MetS, higher serum levels of AST, ALT, alkaline phosphatase, GGT, and lower serum levels of total cholesterol and LDL were associated with significant liver fibrosis (≥ stage 2 fibrosis) (Table 5). Interestingly, the TM6SF2 CT/TT genotype was associated with a 1.95-fold increased finding of significant liver fibrosis among patients with HCV (p = 0.047, OR 1.953, 95% CI 1.009–3.788) (Table 5). In a stepwise multivariate logistic regression analysis, older age (p < 0.0001, OR 1.103, 95% CI 1.073–1.134), lower serum levels of total cholesterol (p < 0.0001, OR 1.026, 95% CI 1.016–1.036), higher serum levels of ALT (p < 0.0001, OR 1.028, 95%CI 1.017–1.038), and alkaline phosphatase (p = 0.004, OR 1.019, 95% CI 1.006–1.032) remained independently associated with significant liver fibrosis (Table 5). The TM6SF2 CT genotype was not associated with liver steatosis (p = 0.524, OR 1.243, 95% CI 0.636–2.428), or with moderate to intense liver inflammatory activity (p = 0.689, OR 1.152, 95%CI 0.575–2.307) on the univariate logistic regression analyses. The same was true for the presence of the G allele of PNPLA3 (p = 0.097, OR 1.422, 95% CI 0.937–2.155, and p = 0.564, OR 1.143, 95% CI 0.725–1.803, respectively). On the other hand, the presence of MetS (p = 0.003, OR 2.227, 95% CI 1.217–4.077), insulin resistance (p = 0.025, OR 1.720, 95% CI 1.070–2.756), and higher GGT levels (p = 0.013, OR 1.003, 95% CI 1.000–1.006) were independently associated with liver steatosis. The HCV genotype was not associated with any of the liver histology parameters evaluated. In addition, the combination of TM6SF2 and PNPLA3 was not associated with significant liver fibrosis or steatosis (p = 0.079 and p = 0.161, respectively) on logistic regression analyses.

Table 5 Factors associated with significant liver fibrosis in patients with HCV (n = 365)
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Discussion

The present study included the largest sample of Brazilians with chronic hepatitis C assessed for the TM6SF2 and PNPLA3 polymorphisms to date. In addition, it added a healthy group to describe these polymorphisms frequencies in subjects without this viral infection. In this cross-sectional clinical study, we could demonstrate that, in this cohort of patients naïve to antiviral therapy, with all stages of hepatic fibrosis, the PNPLA3 GG subjects had lower BMI than CG/CC individuals, and the presence of MetS was more frequent in CC/CG subjects, without any other clinical, biochemical or histological associations. In contrast, in comparison to the CT/TT genotype, the TM6SF2 CC genotype was associated with older age, higher frequency of arterial hypertension, obesity, MetS, higher serum levels of alkaline phosphatase and total cholesterol. Interestingly, the presence of the T allele of TM6SF2 was associated with a 1.95-fold increased finding of significant liver fibrosis in these patients. However, none of the polymorphisms were independently associated with hepatic steatosis or fibrosis.

The TM6SF2 genotypes distribution among patients with HCV was 89% of CC and 11% of CT/TT; results comparable with previously reported data from Milano et al. (2015), whose analysis of 815 subjects with HCV revealed 91.5% for CC and 8.5% for CT/TT [18]. The PNPLA3 CC, CG, and GG genotype frequencies in chronic hepatitis C patients were 51.4%, 41.2%, and 7.4%, respectively. These frequencies were similar to those in the healthy subjects and to previously published data from hepatitis C patients [33]. The distribution of PNPLA3 genotypes among healthy individuals (49.3% CC, 41% CG, and 9.7% GG) was comparable with data obtained from an anterior large systematic review that included 2,504 individuals of different ethnicities, which found frequencies of 56.9%, 33.8%, and 9.3%, respectively [10]. A recent Brazilian study in patients with HCV showed an unusual distribution of PNPLA3 genotypes, with 45.9% CC, 21% CG, and 34.4% GG [28]. The high reported frequency of the G allele in this sample and the discrepancy in the findings of the association of this allele with liver fibrosis in relation to our study may result, at least in part, from the population representativeness of the selected sample, or even that its genetic configuration was undergoing evolution for this specific polymorphism.

Experimental and clinical studies in NAFLD show that the TM6SF2 T allele is associated with decreased TM6SF2 gene expression and consequent hepatic accumulation of lipids and triglycerides. The C allele, on the other hand, plays the opposite role, protecting against liver steatosis, as it stimulates VLDL secretion and increases serum cholesterol levels and cardiovascular risk [11, 15, 34, 35]. Our results were in line with these concepts and with previous publications, with the T allele associated with significant liver fibrosis [18, 28, 36,37,38]. However, in the multivariate logistic regression analysis, older age and elevated ALT levels (as a surrogate marker of liver inflammation) remained drivers of hepatic fibrosis in this cohort [5]. On the other hand, the relationship of the CC genotype with higher serum total cholesterol levels, arterial hypertension, obesity, and MetS in the present study was compatible with the expected effect of the C allele in the stimulation of hepatic secretion of VLDL [12, 13, 36]. However, we could not analyze the association of the polymorphisms on previous cardiovascular events due to the small number of patients with this feature (only 17 subjects).

When analyzing PNPLA3 polymorphisms, we found no association with liver steatosis or fibrosis in our cohort, despite other compelling data in this direction [24, 25, 39,40,41]. Huang et al. (2017), found no significant association with the degree of liver fibrosis in 1,080 Asians with HCV [27]. Other studies have also found diverging results [26, 42]. Brazilians are an admixed population, and this could justify our results. However, even in Brazil, the PNPLA3 polymorphisms have also been implicated in liver fibrosis in patients with NAFLD [22, 23, 43] and chronic hepatitis C [28, 38]. However, data from these HCV studies reveal an unexpectedly high frequency of the PNPLA3 G allele [28, 38], and in the report of Magri et al. (2020), the PNPLA3 gene was not in Hardy–Weinberg equilibrium, which might preclude firm conclusions [38]. The differences in the finding of an association of PNPLA3 polymorphisms with liver fibrosis in HCV patients between previously published data [28, 38] and the present study with a larger cohort emphasizes the importance of further investigations on the role of these polymorphisms in chronic hepatitis C patients in Brazil.

In the era of direct-acting antiviral agents with high SVR rates, the identification of genetic polymorphisms and other metabolic characteristics of HCV patients might be of utility for risk stratification after treatment, as in previous studies with interferon based therapy [44, 45]. Indeed, it is important to highlight that the influence of TM6SF2 in the development of significant fibrosis and its association with factors of the MetS might occur independently of the presence of HCV, which demands attention even after the eradication of the virus [36, 46].

The present study has some limitations. The moderate sample size of patients with HCV is a weakness. The lack of information about the participants’ genetic ancestry and other factors, such as the distribution of body fat, may affect results. Also, the single-center cross-sectional study design limits the possibility of external validation of the results and hampers causality assumptions. Lastly, the low number of healthy individuals evaluated for the polymorphisms may not reflect the real frequency of the SNPs in the Brazilian general population.

In conclusion, we demonstrate that, in the univariate logistic regression analysis, the TM6SF2 CC genotype was associated with older age, higher frequency of arterial hypertension, obesity, MetS, higher serum levels of alkaline phosphatase and total cholesterol in comparison to the CT/TT genotype, in the largest sample of Brazilian individuals with chronic hepatitis C to date. Also, the presence of the T allele of TM6SF2 was associated with a 1.95-fold increased finding of significant liver fibrosis in this admixed population. Despite this, neither studied polymorphisms were independently associated with liver steatosis or fibrosis. On the other hand, older age, lower serum levels of total cholesterol and higher serum levels of ALT and alkaline phosphatase were independently associated with liver fibrosis. Other factors seem more influential than these specific polymorphisms in isolation. More studies are warranted to clarify the role of PNPLA3 and TM6SF2 polymorphisms in Brazilians with HCV.

Availability of data and materials

The datasets analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

AST:

Aspartate aminotransferase

ALT:

Alanine aminotransferase

BMI:

Body mass index

CI:

Confidence interval

CVE:

Cardiovascular event

GGT:

Gamma glutamyl transferase

GWAS:

Genome wide association studies

HCV:

Hepatitis C virus

HDL:

High-density lipoproteins

HSCs:

Hepatic stellate cells

HOMA-IR:

Homeostatic model of assessment

MetS:

Metabolic syndrome

NAFLD:

Non-alcoholic fatty liver disease

OR:

Odds ratios

PCR:

Polymerase chain reaction

PIC:

Polymorphic information content

PNPLA3:

Patatin-like phospholipase domain containing 3

SD:

Standard deviation

SNPs:

Single nucleotide polymorphisms

TM6SF2:

Transmembrane 6 superfamily member 2

VLDL:

Very low density lipoprotein

References

  1. Spearman CW, Dusheiko GM, Hellard M, Sonderup M. Hepatitis C. Lancet. 2019;394:1451–66.

    Article  Google Scholar 

  2. Benzaken AS, Girade R, Catapan E, et al. Hepatitis C disease burden and strategies for elimination by 2030 in Brazil A mathematical modeling approach. Braz J Infect Dis 2019;23:182–190.

  3. Westbrook RH, Dusheiko G. Natural history of hepatitis C. J Hepatol. 2014;61:S58-68.

    Article  Google Scholar 

  4. Ministério da Saúde do Brasil. Secretaria de Vigilância em Saúde. Boletim Epidemiológico de Hepatites Virais - 2020. Brasilia, Brazil, 2020. Available at: http://www.aids.gov.br/pt-br/pub/2020/boletim-epidemiologico-hepatites-virais-2020

  5. Khatun M, Ray RB. Mechanisms Underlying Hepatitis C Virus-Associated Hepatic Fibrosis. Cells. 2019;8:1249.

    Article  CAS  Google Scholar 

  6. Basit H, Tyagi I, Koirala J. Hepatitis C. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020.

  7. Wong RJ, Gish RG. Metabolic manifestations and complications associated with chronic Hepatitis C virus infection. Gastroenterol Hepatol (N Y). 2016;12:293–9.

    Google Scholar 

  8. Cardoso AC, Perez RM, de Figueiredo-Mendes C, Carvalho Leite N, Moraes-Coelho HS, Villela-Nogueira CA. Prevalence and predictive factors of moderate/severe liver steatosis in chronic hepatitis C (CHC) infected patients evaluated with controlled attenuation parameter (CAP). J Viral Hepat. 2018;25:1244–50.

    Article  CAS  Google Scholar 

  9. Romeo S, Kozlitina J, Xing C, et al. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat Genet. 2008;40:1461–5.

    Article  CAS  Google Scholar 

  10. Severson TJ, Besur S, Bonkovsky HL. Genetic factors that affect nonalcoholic fatty liver disease: a systematic clinical review. World J Gastroenterol. 2016;22:6742–56.

    Article  CAS  Google Scholar 

  11. Kozlitina J, Smagris E, Stender S, et al. Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease. Nat Genet. 2014;46:352–6.

    Article  CAS  Google Scholar 

  12. Holmen OL, Zhang H, Fan Y, et al. Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nat Genet. 2014;46:345–51.

    Article  CAS  Google Scholar 

  13. Dongiovanni P, Petta S, Maglio C, et al. Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease. Hepatology. 2015;61:506–14.

    Article  CAS  Google Scholar 

  14. Roh YS, Loomba R, Seki E. The TM6SF2 variants, novel genetic predictors for nonalcoholic steatohepatitis. Gastroenterology. 2015;148:252–4.

    Article  Google Scholar 

  15. Pirola CJ, Sookoian S. The dual and opposite role of the TM6SF2-rs58542926 variant in protecting against cardiovascular disease and conferring risk for nonalcoholic fatty liver: a meta-analysis. Hepatology. 2015;62:1742–56.

    Article  CAS  Google Scholar 

  16. Coppola N, Rosa Z, Cirillo G, et al. TM6SF2 E167K variant is associated with severe steatosis in chronic hepatitis C, regardless of PNPLA3 polymorphism. Liver Int. 2015;35:1959–63.

    Article  CAS  Google Scholar 

  17. Basyte-Bacevice V, Skieceviciene J, Valantiene I, et al. TM6SF2 and MBOAT7 gene variants in liver fibrosis and cirrhosis. Int J Mol Sci. 2019;20:1277.

    Article  CAS  Google Scholar 

  18. Milano M, Aghemo A, Mancina RM, et al. Transmembrane 6 superfamily member 2 gene E167K variant impacts on steatosis and liver damage in chronic hepatitis C patients. Hepatology. 2015;62:111–7.

    Article  CAS  Google Scholar 

  19. Bruschi FV, Tardelli M, Claudel T, Trauner M. PNPLA3 expression and its impact on the liver: current perspectives. Hepat Med. 2017;9:55–66.

    Article  Google Scholar 

  20. Yang J, Trépo E, Nahon P, et al. PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases. Int J Cancer. 2019;144:533–44.

    Article  CAS  Google Scholar 

  21. Rotman Y, Koh C, Zmuda JM, Kleiner DE, Liang TJ; NASH CRN. The association of genetic variability in patatin-like phospholipase domain-containing protein 3 (PNPLA3) with histological severity of nonalcoholic fatty liver disease. Hepatology 2010;52:894–903.

  22. Mazo DF, Malta FM, Stefano JT, et al. Validation of PNPLA3 polymorphisms as risk factor for NAFLD and liver fibrosis in an admixed population. Ann Hepatol. 2019;18:466–71.

    Article  CAS  Google Scholar 

  23. Lisboa QC, Nardelli MJ, Pereira PA, et al. PNPLA3 and TM6SF2 polymorphisms in Brazilian patients with nonalcoholic fatty liver disease. World J Hepatol. 2020;12:792–806.

    Article  Google Scholar 

  24. Crisan D, Grigorescu M, Crisan N, et al. Association between PNPLA3[G]/I148M variant, steatosis and fibrosis stage in hepatitis C virus - genetic matters. J Physiol Pharmacol 2019;70.

  25. Trépo E, Pradat P, Potthoff A, et al. Impact of patatin-like phospholipase-3 (rs738409 C>G) polymorphism on fibrosis progression and steatosis in chronic hepatitis C. Hepatology. 2011;54:60–9.

    Article  Google Scholar 

  26. Fan JH, Xiang MQ, Li QL, Shi HT, Guo JJ. PNPLA3 rs738409 polymorphism associated with hepatic steatosis and advanced fibrosis in patients with chronic hepatitis C virus: a meta-analysis. Gut Liver. 2016;10:456–63.

    Article  CAS  Google Scholar 

  27. Huang CM, Chang KC, Hung CH, et al. Impact of PNPLA3 and IFNL3 polymorphisms on hepatic steatosis in Asian patients with chronic hepatitis C. PLoS ONE. 2017;12:e0182204.

    Article  Google Scholar 

  28. Manchiero C, Nunes AKDS, Magri MC, et al. The rs738409 polymorphism of the PNPLA3 gene is associated with hepatic steatosis and fibrosis in Brazilian patients with chronic hepatitis C. BMC Infect Dis. 2017;17:780.

    Article  Google Scholar 

  29. Grundy SM, Brewer HB Jr, Cleeman JI, Smith SC Jr, Lenfant C; National Heart, Lung, and Blood Institute; American Heart Association. Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition. Arterioscler Thromb Vasc Biol 2004;24:e13–8.

  30. Vasques AC, Rosado LE, Cássia GAlfenas Rd, Geloneze B. Critical analysis on the use of the homeostasis model assessment (HOMA) indexes in the evaluation of the insulin resistance and the pancreatic beta cells functional capacity. Arq Bras Endocrinol Metabol 2008;52:32–9.

  31. The French METAVIR Cooperative Study Group. Intraobserver and interobserver variations in liver biopsy interpretation in patients with chronic hepatitis C. Hepatology. 1994;20:15–20.

    Article  Google Scholar 

  32. Botstein D, White RL, Skolnick M, Davis RW. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet. 1980;32:314–31.

    CAS  PubMed  PubMed Central  Google Scholar 

  33. Petta S, Vanni E, Bugianesi E, et al. PNPLA3 rs738409 I748M is associated with steatohepatitis in 434 non-obese subjects with hepatitis C. Aliment Pharmacol Ther. 2015;41:939–48.

    Article  CAS  Google Scholar 

  34. Boyer A, Park SB, de Boer YS, Li Q, Liang TJ. TM6SF2 Promotes Lipidation and Secretion of Hepatitis C Virus in Infected Hepatocytes. Gastroenterology. 2018;155(1923–1935):e8.

    Google Scholar 

  35. Mahdessian H, Taxiarchis A, Popov S, et al. TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content. Proc Natl Acad Sci USA. 2014;111:8913–8.

    Article  CAS  Google Scholar 

  36. Liu Z, Que S, Zhou L, et al. The effect of the TM6SF2 E167K variant on liver steatosis and fibrosis in patients with chronic hepatitis C: a meta-analysis. Sci Rep. 2017;7:9273.

    Article  Google Scholar 

  37. Eslam M, Mangia A, Berg T, et al. Diverse impacts of the rs58542926 E167K variant in TM6SF2 on viral and metabolic liver disease phenotypes. Hepatology. 2016;64:34–46.

    Article  CAS  Google Scholar 

  38. Magri MC, Manchiero C, Prata TVG, et al. The influence of gene-chronic hepatitis C virus infection on hepatic fibrosis and steatosis. Diagn Microbiol Infect Dis. 2020;97:115025.

    Article  CAS  Google Scholar 

  39. Cai T, Dufour JF, Muellhaupt B, et al. Viral genotype-specific role of PNPLA3, PPARG, MTTP, and IL28B in hepatitis C virus-associated steatosis. J Hepatol. 2011;55:529–35.

    Article  CAS  Google Scholar 

  40. Valenti L, Rumi M, Galmozzi E, et al. Patatin-like phospholipase domain-containing 3 I148M polymorphism, steatosis, and liver damage in chronic hepatitis C. Hepatology. 2011;53:791–9.

    Article  CAS  Google Scholar 

  41. Salameh H, Masadeh M, Al Hanayneh M, et al. PNPLA3 polymorphism increases risk for and severity of chronic hepatitis C liver disease. World J Hepatol. 2016;8:1584–92.

    Article  Google Scholar 

  42. Nakamura M, Kanda T, Nakamoto S, et al. No correlation between PNPLA3 rs738409 genotype and fatty liver and hepatic cirrhosis in Japanese patients with HCV. PLoS ONE. 2013;8:e81312.

    Article  Google Scholar 

  43. Machado CM, Leite NC, França PH, Cardoso CR, Salles GF, Villela-Nogueira CA. PNPLA3 gene polymorphism in Brazilian patients with type 2 diabetes: A prognostic marker beyond liver disease? Nutr Metab Cardiovasc Dis. 2019;29:965–71.

    Article  CAS  Google Scholar 

  44. Rembeck K, Lagging M. Impact of IL28B, ITPA and PNPLA3 genetic variants on therapeutic outcome and progression of hepatitis C virus infection. Pharmacogenomics. 2015;16:1179–88.

    Article  CAS  Google Scholar 

  45. Dunn W, Vittal A, Zhao J, et al. PNPLA3 gene predicts clinical recovery after sustained virological response in decompensated hepatitis C cirrhosis. BMJ Open Gastroenterol. 2019;6:e000241.

    Article  Google Scholar 

  46. Stevenson HL, Utay NS. Hepatic steatosis in HCV-infected persons in the direct-acting antiviral era. Trop Dis Travel Med Vaccines. 2016;2:21.

    Article  Google Scholar 

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Acknowledgements

We would like to thank Paulo Fanti for the agile statistical assistance.

Funding

Not applicable.

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Authors and Affiliations

  1. Division of Clinical Gastroenterology and Hepatology, LIM07, Department of Gastroenterology, University of São Paulo School of Medicine (FMUSP), Av. Dr. Enéas de Carvalho Aguiar no 255, Instituto Central, # 9159, São Paulo, 05403-900, Brazil

    Arthur Ivan N. Oliveira, Fernanda M. Malta, Patricia Momoyo Y. Zitelli, Ana Paula M. Salles, Michele S. Gomes-Gouvea, Joao Renato R. Pinho, Flair J. Carrilho, Claudia P. Oliveira, Mario G. Pessoa & Daniel F. Mazo

  2. Department of Infectious Diseases, University of São Paulo School of Medicine (FMUSP), Av. Dr. Enéas de Carvalho Aguiar no 255, São Paulo, 05403-900, Brazil

    Ana Catharina S. Nastri & Maria Cássia Mendes-Corrêa

  3. Division of Gastroenterology (Gastrocentro), School of Medical Sciences, University of Campinas (UNICAMP), Rua Carlos Chagas no 420, Campinas, 13083-878, Brazil

    Daniel F. Mazo

Authors
  1. Arthur Ivan N. Oliveira
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  2. Fernanda M. Malta
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  3. Patricia Momoyo Y. Zitelli
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Contributions

Oliveira AI worked on the data analysis and interpretation and wrote the manuscript. Mazo DF conceived and designed the study, contributed to the data analysis and interpretation and wrote the manuscript. Malta FM, Salles APM and Gomes-Gouvea MS performed the polymorphism genotyping. Oliveira AI, Zitelli PM, Nastri ACS, Pessoa MG and Mazo DF collected and assembled the data. Pinho JRR, Carrilho FJ, Oliveira CP, Mendes-Correa MC and Pessoa MG critically reviewed the manuscript. All authors read and approved the final version of the manuscript.

Corresponding author

Correspondence to Daniel F. Mazo.

Ethics declarations

Ethics approval and consent to participate

The Ethics Committee of the Hospital das Clinicas of the University of Sao Paulo School of Medicine has approved this study (numbered 1,531,382 and 2,676,105). The protocol followed the 1975 Declaration of Helsinki. Informed consent was obtained from participants.

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The authors declare that they have no competing interests.

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Oliveira, A.I.N., Malta, F.M., Zitelli, P.M.Y. et al. The role of PNPLA3 and TM6SF2 polymorphisms on liver fibrosis and metabolic abnormalities in Brazilian patients with chronic hepatitis C. BMC Gastroenterol 21, 81 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s12876-021-01654-3

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Keywords

BMC Gastroenterology

ISSN: 1471-230X

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