Transcription factor 7-like 2 gene- smoking interaction on the risk of diabetic nephropathy in Chinese Han population

Objectives To evaluate the relationship between transcription factor 7-like 2 (TCF7L2) gene polymorphism and diabetic nephropathy (DN) risk, as well as the effect of gene-environment interactions on DN risk in Chinese Han population. Methods The Hardy-Weinberg equilibrium (HWE) and the relationship between TCF7L2 gene single nucleotide polymorphism (SNPs) and DN susceptibility were evaluated by SNPStats. The interaction among four SNPs and environmental factors were tested by generalized multifactor dimensionality reduction (GMDR). The consistency of cross validation, accuracy of test balance and sign test were calculated to evaluate the interaction of each selection. The logistic regression was used to test the interaction between rs7903146 and current smoking by stratified analysis. Results Logistic regression analysis indicated that the DN risk of rs7903146-T allele carriers were obviously higher than that in CC genotype carriers (CT + TT versus CC), adjusted OR (95 %CI) = 1.64 (1.24–2.06). However, we also discovered that people with rs12255372, rs11196205 and rs290487 minor allele had non-significant difference risk of DN compared with people with major allele. The GMDR model found a significant two-locus model (p = 0.0100) including rs7903146 and current smoking, suggesting a potential gene–environment interaction between rs7903146 and current smoking. Compared with never smokers with rs7903146- CC genotype, current smokers with rs7903146- CT or TT genotype had the highest DN risk. After covariate adjustment, OR (95 %CI) was 2.15 (1.58–2.78). Conclusions We found a significant relationship of rs7903146-T alleles, and the interaction between rs7903146-T and current smoking with increased DN risk.


Introduction
Diabetic nephropathy (DN) is one of the most common chronic and progressive complications of diabetes. DN is associated with higher cardiovascular incidence rate and mortality and is the most common cause of end-stage renal disease (ESRD) in the world [1,2]. DN is also one of the important risk factors for the occurrence and development of chronic kidney disease and chronic cardiovascular disease [3], and one of the main causes of death in the world [4]. The pathogenesis of DN is complex and multifactorial, and the specific mechanism is still unclear. However, previous studies [5,6] have shown that the risk factors of DN include genetic factors and environmental factors, such as hypertension, hyperglycemia and hyperlipidemia.
The transcription factor 7-like 2 (TCF7L2), is a highly variable transcription factor, which plays an important role in regulating insulin secretion and maintaining glucose homeostasis in pancreatic β cells [7]. In addition, TCF7L2 protein, which is encoded by the TCF7L2 gene, is involved in regulation of endothelial cell growth and smooth muscle cell proliferation, and then affects vascular remodeling [8]. TCF7L2 gene is located on chromosome 10q25.3, which contains 215,863 bases, including 17 exons, encoding 596 amino acids. Previous epidemiological studies have indicated that the TCF7L2 gene single nucleotide polymorphisms (SNPs) were associated with common diseases, including type 2 diabetes mellitus (T2DM) [9] and DN [10][11][12]. The study on the relationship between single nucleotide polymorphism of TCF7L2 gene and DN risk in Chinese Han populations is very limited. Additionally, DN development has been proved to be the outcome of complicated interaction among genetic and environmental factors, up to now, limited researches focused on the association of interaction between TCF7L2 gene SNPs and environmental factors with DN risk. Therefore, the purpose of this study is to evaluate the relationship between TCF7L2 gene polymorphism and DN risk, as well as the effect of gene-environment interactions on DN risk in Chinese Han population.

Study population
Subjects were recruited continuously from our Hospital between June 2013 and July 2019. A total of 1083 subjects with an average age of 67.5 ± 13.9 years were selected, including 358 T2DM with DN cases and 720 T2DM without DN controls. All participants were selected from T2DM patients, and those T2DM with DN patients were included in case group, and those T2DM without DN patients were included in the control group. The diagnosis of T2DM and DN was diagnosed by two pathologists in our Hospital according to the World Health Organization diagnostic criteria [13]. Those patients with poor glycemic control, overt nephropathy, significant heart failure, treated by chemotherapy or radiotherapy (to ensure the accuracy of our information collection) or had any kinds of cancers were removed. The control group was matched to patients by sex, age and ethnic background, and those participants with family history of DN or others kidney disease were excluded. Current cigarette smoking was defined as those who self-reported smoking cigarettes at least once a day for 1 year or more.

The
TCF7L2 gene polymorphism (rs7903146, rs12255372, rs290487 and rs11196205) genotyping was performed by polymerase chain reaction (PCR) and following restriction fragment length polymorphism (RFLP). According to instructions of DNA Blood Mini Kit (Qiagen, Hilden, Germany), 3 ml EDTA-processed blood samples were extracted from all participants for DNA extraction, and DNA was preserved at -20°C before use. All primers applied in our research are shown in Table 1.

Statistical analysis
In our study, the mean and standard deviations (SDs) were calculated for continuous variables with normal distribution, and the percentages were calculated for categorical variables. The χ2 test was used for comparison for percentages and t test was used for comparison of means and SDs. The Hardy-Weinberg equilibrium (HWE) and the relationship between TCF7L2 gene SNPs and DN susceptibility were evaluated by SNPStats (https://www.snpstats.net/). The interaction among four SNPs and environmental factors were tested by generalized multifactor dimensionality reduction (GMDR) [14]. The consistency of cross validation, accuracy of test balance and sign test were calculated to evaluate the interaction of each selection. The logistic regression was used to test the interaction between rs7903146 and current smoking by stratified analysis.

Results
A total of 1083 subjects with an average age of 67.5 ± 13.9 years were selected, including 358 T2DM with DN cases and 720 T2DM without DN controls. The characteristics of subjects stratified by case and control are shown in Table 2. No statistically significant differences were observed between cases and controls in terms of age and proportion of males. The body mass index (BMI), smoking and alcohol drinking, fasting plasma glucose (FPG), duration of diabetes and hypertension rate in cases were significantly higher than that in controls.
HWE test was performed for controls, and we found that all genotypes were distributed according to HWE (all p values more than 0.05). The allele frequency of rs7903146-T and in DN group was significantly higher than that in control group (28.9 % vs19.7 %). Logistic regression analysis indicated that the DN risk of rs7903146-T allele carriers was obviously higher than that in CC genotype carriers (CT + TT versus CC), adjusted OR (95 %CI) = 1.64 (1.24-2.06). However, we also discovered that people with rs12255372, rs11196205 and rs290487 minor allele had non-significant difference risk of DN compared with people with major allele ( Table 3).
The GMDR model was used to evaluate the effect of SNP-SNP and gene-environmental factors interaction between 4 SNPs on DN risk. Table 4 shows the GMDR analysis results of SNP-SNP interaction and genecurrent smoking interaction. We found a significant two-locus model (p = 0.0100) including rs7903146 and current smoking, suggesting a potential gene-environment interaction between rs7903146 and current smoking. The cross-validation consistency of two-locus model was 9 of 10, and the testing accuracy was 0.5985. Compared with never smokers with rs7903146-CC genotype, current smokers with rs7903146-CT or TT genotype had the highest DN risk. After covariate adjustment, OR (95 %CI) was 2.15 (1.58-2.78) ( Table 5).

Discussion
In this study, we evaluated the effect SNPs of TCF7L2 on DN risk, and we found that the DN risk was obviously higher in rs7903146-T allele carriers than that in CC genotype carriers, However, we also discovered that people with rs12255372, rs11196205 and rs290487 minor allele had non-significant difference risk of DN compared with people with major allele. Previous studies have reported a statistically significant association between TCF7L2 gene polymorphism and DN and coronary atherosclerosis [15,16]. In recent years, the association between TCF7L2 gene polymorphism and DN has been reported in several studies [17][18][19][20]. However, there are few studies on the association between TCF7L2 mutation and DN risk in Chinese population.
TCF7L2 is a transcription factor containing DNA binding domain. Its coding gene is widely expressed in many organs of human body, mainly in adipose tissue and human pancreatic beta cells [21]. Previously, two studies conducted by Buraczynska et al. [17,22] has verified that the rs7903146-T allele of TCF7L2 gene was significantly associated with DN, especially in the early stage of diabetes. Zhuang et al. [18] carried out a case-control study in Chinese population, and found that TCF7L2 rs7903146 polymorphism had a significant impact on the susceptibility to DN in Chinese Han population, but rs290487 had no statistical association with DN. This was consistent with conclusions from Lewis et al. [23], Hussain et al. [12] and Sale et al. [24], But Fu et al. [25] concluded inconsistent results on relationship between TCF7L2 rs7903146 polymorphism and DN risk, in this study, just 248 DN patients were included in the analysis, so the limited sample size maybe the reason for inconsistent results between this study and our study. A case-control study conducted by Bodhini et al. [26] showed that rs12255372 polymorphism in TCF7L2 gene was associated with type 2 diabetes and DN, but its association with DN was affected by diabetes. However, study suggested that minor allele of rs12255372 had non-significant impact on risk of DN. DN susceptibility was influenced by too many risk factors, involving genetic factors, environmental factors, gene-gene and gene-environment interactions. In    current study, just one gene was investigated, therefore we could not estimate the gene-gene interaction on DN risk, just the SNP-SNP interaction was investigated. As we all known that smoking was a risk factor for DN risk [27,28], previous study has reported a significant geneenvironment interaction between MTHFR C677T polymorphism (rs1801133) and smoking on susceptibility to DN in Chinese men with T2DM. But to date, no study focused in the impact of interaction between TCF7L2 gene and smoking on DN risk. In this study, the current smoking rate was higher than that of control group, which means that the current smoking was a risk factor for DN susceptibility. Therefore, we also conducted TCF7L2 gene-environment interaction between fours SNPs and current smoking using GMDR model. We found a significant two-locus model including rs7903146 and current smoking. Compared with never smokers with rs7903146-CC genotype, current smokers with rs7903146-CT or TT genotype had the highest DN risk. The exact interaction mechanism for this gene-environment interaction is still unclear, but we believe that TCF7L2 gene and current smoking are related to DN risk factors, which might be the basis of gene-environment interaction. This research has some limitations. Firstly, just four SNPs of the TCF7L2 gene were selected for genotyping, and more SNPs within TCF7L2 gene should be included in future studies. Secondly, more environmental factors should be included in the GMDR model to investigate the gene-environment interaction. Lastly, the participants included in this study were all Chinese Han population, and the results obtained in our study should be verified in different ethnicities in China or different countries.

Conclusions
In summary, our research shows that rs7903146-T allele, interaction between rs7903146 and current smoking are all associated with increased susceptibility to DN. Although, previous studies have reported the relationship between rs7903146-T allele and DN risk, but these studies did not performed gene-smoking interaction analysis, and which was the new or additional finding on DN genetic association investigation.