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Genetic variation of Glucose Transporter-1 (GLUT1) and albuminuria in 10,278 European Americans and African Americans: a case-control study in the Atherosclerosis Risk in Communities (ARIC) Study

BMC Medical Genetics volume 12, Article number: 16 (2011) Cite this article

Abstract

Background

Evidence suggests glucose transporter-1(GLUT1) genetic variation affects diabetic nephropathy and albuminuria. Our aim was to evaluate associations with albuminuria of six GLUT1 single nucleotide polymorphisms(SNPs), particularly XbaI and the previously associated Enhancer-2(Enh2) SNP.

Methods

A two-stage case-control study was nested in a prospective cohort study of 2156 African Americans and 8122 European Americans with urinary albumin-to-creatinine ratio(ACR). Cases comprised albuminuria(N = 825; ≥ 30 μg/mg) and macroalbuminuria(N = 173; ≥ 300 μg/mg). ACR < 30 μg/mg classified controls(n = 9453). Logistic regression and odds ratios(OR) assessed associations. The evaluation phase(stage 1, n = 2938) tested associations of albuminuria(n = 305) with six GLUT1 SNPs: rs841839, rs3768043, rs2297977, Enh2(rs841847) XbaI(rs841853), and rs841858. Enh2 was examined separately in the replication phase(stage 2, n = 7340) and the total combined sample (n = 10,278), with all analyses stratified by race and type 2 diabetes.

Results

In European Americans, after adjusting for diabetes and other GLUT1 SNPs in stage 1, Enh2 risk genotype(TT) was more common in albuminuric cases(OR = 3.37, P = 0.090) whereas XbaI (OR = 0.94, p = 0.931) and remaining SNPs were not. In stage 1, the Enh2 association with albuminuria was significant among diabetic European Americans(OR = 2.36, P = 0.025). In African Americans, Enh2 homozygosity was rare(0.3%); XbaI was common(18.0% AA) and not associated with albuminuria. In stage 2(n = 7,340), Enh2 risk genotype had increased but non-significant OR among diabetic European Americans(OR = 1.66, P = 0.192) and not non-diabetics(OR = 0.99, p = 0.953), not replicating stage 1. Combining stages 1 and 2, Enh2 was associated with albuminuria(OR 2.14 [1.20-3.80], P = 0.009) and macroalbuminuria(OR 2.69, [1.02-7.09], P = 0.045) in diabetic European Americans. The Enh2 association with macroalbuminuria among non-diabetic European Americans with fasting insulin(OR = 1.84, P = 0.210) was stronger at the highest insulin quartile(OR = 4.08, P = 0.040).

Conclusions

As demonstrated with type 1 diabetic nephropathy, the GLUT1 Enh2 risk genotype, instead of XbaI, may be associated with type 2 diabetic albuminuria among European Americans, though an association is not conclusive. The association among diabetic European Americans found in stage 1 was not replicated in stage 2; however, this risk association was evident after combining all diabetic European Americans from both stages. Additionally, our results suggest this association may extend to non-diabetics with high insulin concentrations. Rarity of the Enh2 risk genotype among African Americans precludes any definitive conclusions, although data suggest a risk-enhancing role.

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Background

Glucose transporter 1(GLUT1) is the major facilitative glucose transporter in glomerular mesangial cells[1]. Studies show glucose transport as the rate limiting step in mesangial expansion, and alterations of GLUT1 activity may stimulate extracellular matrix(ECM) production [2] even under normoglycemic conditions [3]. Additionally, experimental evidence suggests GLUT1 may be associated with hypertensive glomerulopathy[4].

However, results of case-control studies of GLUT1 sequenece variations(the XbaI polymorphism, a C-to-A transversion in intron 2: see figure 1) and diabetic nephropathy have been inconsistent[5–11] with significant heterogeneity between studies[12]. Most studies demonstrated risk transmitted in a recessive fashion[5, 6, 8, 11, 13]. Few studies examined diabetic nephropathy in relation to GLUT1 SNPs other than XbaI[5, 11, 13]. A study of those with type 1 diabetes examined six GLUT1 single nucleotide polymorphisms(SNPs) and found homozygosity for the XbaI A allele was associated with diabetic nephropathy[5]. Additionally, putative human enhancer elements were identified [5], including the insulin-responsive enhancer-2(see figure 1), and homozygosity for the minor allele(C-to-T) of the enhancer-2 SNP1(Enh2 SNP) was also associated with type 1 diabetic nephropathy[5]. Though Enh2 SNP has strong linkage disequilibrium with XbaI SNP, more evidence suggests Enh2 SNP may be causally related to diabetic nephropathy[5]. More recently, a study extended the significant association of the Enh2 SNP risk genotype to those with type 2 diabetic nephropathy; however, a statistically significant association between XbaI genotypes and type 2 diabetic nephropathy was not demonstrated [11].

Figure 1
figure 1

GLUT1 is located on chromosome 1p34.2. The genomic structure of GLUT1 is illustrated with its 10 exons and three putative enhancers[5]. Genotyped polymorphisms located in intron 2 include the intron-2 SNP (rs841858), and the Enh2(rs841847) and XbaI (rs841853) SNPs which have been previously associated with diabetic nephropathy[5–7]. In the distal promoter region, the Promoter SNP (rs841839) was genotyped (located between putative enhancers 3 and 1). We also included two SNPs in intron 1, intron-1 SNP(rs3768043) and intron-2 SNP(rs2297977). No SNP was associated with albuminuria among all African Americans or among all European Americans, including XbaI (p = 0.08) and Enh2 (p = 0.08). None of the tagging SNPs were able to reach a Bonferroni adjusted level of statistical significance. †Bonferroni corrected level of statistical significance p = 0.01.

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There has been no investigation among non-diabetics or African Americans of albuminuria and GLUT1 genetic variation, especially for the Enh2 SNP. Additionally, the Enh2 SNP is not readily available on most candidate gene chips, with available proxy SNPs having low r2. We conducted a case-control study nested within a large biracial community-based middle-aged cohort to determine the risk of albuminuria associated with six GLUT1 SNPs by race and by type 2 diabetes status. We performed a two-stage analysis in our population(n = 10,278): 1) an initial evaluation of all six candidate GLUT1 SNPs among stage 1 participants(n = 2938), and 2) a subsequent phase (stage 2, n = 7340) to assess the likeliest stage 1 candidate SNP. Because enhancer-2 is a putative insulin-responsive element[5], we hypothesized insulin may interact with the Enh2 SNP to affect risk of albuminuria.

Methods

Study Design and Population

The study population consisted of African Americans and European Americans with and without type 2 diabetes in the Atheroslcerosis Risk in Communities (ARIC) Study, aged 45 to 64 years at baseline in 1987 through 1989, from 4 US communities: Forsyth County, NC; Jackson, MS; suburbs of Minneapolis, MN, and Washington Co., MD. Participants underwent four standardized examinations in field center clinics, scheduled approximately every three years[14] with approval of the institutional review boards.

Of the 11,625 African American and European American participants who attended visit four, urinary albumin and creatinine measurements were available for 11,447 participants. All measurements were from ARIC visit 4, as urine samples were only collected at this visit. We excluded those missing visit 4 serum creatinine (n = 182), information on diabetes, hypertension, systolic blood pressure (SBP), diastolic blood pressure (DBP), or body mass index (BMI) (n = 125), and those without available DNA (n = 69). For stage 1, we genotyped six GLUT1 SNPs (including Enh2 and XbaI) in a sample of the above participants (sample 1, n = 3,204), enriched for African Americans and people with type 2 diabetes, a convenience sample previously used for the study of genetic risk factors in cardiovascular disease and type 2 diabetes. Sample 1 was an otherwise unselected portion of the total population. We genotyped only the most likely candidate SNP (Enh2) from stage 1 in the remaining participants who met our inclusion criteria from ARIC visit 4, individuals who comprised stage 2 (sample 2, n = 7,867). Missing genotypes were excluded from stages 1(n = 266) and 2(n = 527). With exclusion criteria, of the total study population (n = 10,278), sample 1(n = 2938) was 28.6% and sample 2(n = 7340) was 71.4%. Participants from samples 1 and 2 were mutually exclusive.

Of those who attended visit 4, the 1,347 excluded individuals were older (63.1 vs. 62.8 years of age), more likely to be African American (37.7% vs. 21.0%), type 2 diabetic (22.5% vs. 16.2%), hypertensive (57.2% vs. 46.7%), and male (46.5% vs. 43.8%) compared to included participants.

Assessment of Clinical Characteristics

Clinical charcteristics were assessed during visit 4. A standardized interview, clinical examination, and laboratory investigation collected demographic, anthropometric, and cardiovascular risk factor data for participants [15]. Fasting blood sample collection and processing is described elsewhere [15]. Two standardized blood pressure measurements were performed by trained technicians, and their average was used. Hypertension was defined as a systolic blood pressure (SBP) ≥140 mmHg, a diastolic blood pressure (DBP) ≥90 mmHg, or the self-reported use of antihypertensive medication during the previous 2 weeks. Diabetes mellitus was defined as fasting glucose ≥ 126 mg/dL, nonfasting glucose ≥200 mg/dL, or self-reported history or treatment of type 2 diabetes. Visit 4 glomerular filtration rate (GFR) was estimated from calibrated serum creatinine using the simplified equation developed using data from the Modification of Diet in Renal Disease (MDRD) Study[16, 17] as follows:

GFR mL/min/1.73m2 = 186.3 * (SCr)-1.154 * (age)-0.203 * (0.742 if female) * (1.21 if African American)

Ascertainment of Albuminuria

An untimed urine sample was collected during visit 4. Aliquots were frozen within 12 hours and stored at -70°C. Albumin and creatinine concentrations were measured in the University of Minnesota Physicians Outreach Laboratories, Minneapolis, Minnesota, with albumin by a nephelometric method on the Dade Behring BN100 (assay sensitivity, 2.0 mg/L), and creatinine using the Jaffe method on a Beckman CX3 to determine albumin-to-creatinine ratios (ACR; ug/mg) for participants. Blinded samples (n = 516) analyzed for quality assurance showed a correlation coefficient® of the loge-transformed ACR as r = 0.95. ACR was used to determine levels of albuminuria according to American Diabetes Association [18] and National Kidney Foundation [19] recommendations: normoalbuminuria (ACR < 30 μg/mg), microalbuminuria (ACR 30-299 μg/mg), and macroalbuminuria (ACR ≥ 300 μg/mg). Normoalbuminuric participants were classified as controls. Albuminuria cases had either microalbuminuria or macroalbuminuria. Of the total study, there were 825 cases of albuminuria, 37.0%(n = 305) in sample 1 and 63.0%(n = 520) in sample 2. For sensitivity analysis, microalbuminuria and macroalbuminuria cases were examined separately, compared to controls.

GLUT1 Candidate SNP Selection and Genotyping

GLUT1 consists of 10 exons including three recently described putative human enhancers (see Figure 1)[5] with murine and rat homology[20, 21]. The XbaI SNP[5–7] and the Enh2 SNP[5, 11] were chosen as candidates for genotyping based on previous studies. Using the human GLUT1 genomic sequence(GenBank accession no. NT_032977) and the public SNP database dbSNP build 120, it was determined the XbaI SNP corresponds to rs841853 and the Enh2 SNP corresponds to rs841847. The dbSNP rs841839 C > A transversion(denoted Promoter SNP) was chosen for genotyping based on its proximity to both enhancers-3 and -1. At the time of genotyping, the Hap Map Phase II data were not available; therefore, 3 additional SNPs were chosen with an average distance between SNPs of 4.2 kb to provide coverage of the gene (76.8%). Three additional SNPs selected were: intron-1 SNP1(rs3768043), intron-1 SNP2(rs2297977), and intron-2 SNP(rs841858).

For the evaluation phase, genotypes in sample 1 were assessed by PCR amplification of genomic DNA and completed for rs841847(Enh2 SNP) using Pyrosequencing technology (Pyrosequencing, Uppsala, Sweden) as previously described [22]. For the SNPs rs841853 (XbaI), rs841839, rs3768043, rs2297977, and rs841858, genotypes were completed using Orchid SNPstream UHT genotyping system (Orchid Bioscience) as previously described[23]. For sample 1, the error rate on the basis of blind replicates (n = 444) for the Orchid SNPstream UHT genotyping system was 0.2%. For the replication phase, genotypes for rs841847 in sample 2 were assessed and completed using Pyrosequencing technology.

Statistical Analysis

For stage 1(n = 2938), genotype frequencies of all SNPs were tested for consistency with Hardy-Weinberg expectations by the χ2 test within race strata among controls consisting of non-diabetic individuals without albuminuria. Because allele frequencies differed by race, analyses were race-stratified. Tests of differences in clinical characteristics by case status included t-tests, ANOVA, and χ2 tests. Logistic regression models calculated the odds ratio (OR) and 95% confidence interval (95% CI) of albuminuria for each SNP, using either genotypic or recessive models for inheritance. Our genotypic associations of XbaI and Enh2 in European Americans suggest recessive modes of action, similar to previous findings [5, 6]. To differentiate the effects of the likely candidate from remaining GLUT1 SNPs, multivariate logistic regression was performed, adjusting for type 2 diabetes, XbaI, Enh2, rs841839, rs841858, rs2297977, and rs3768043 genotypes.

There was strong prior evidence for Enh2 (rs841847) as a functional candidate polymorphism, both in human and laboratory studies [5, 11, 24–29]. Based on this a priori determination of the status of Enh2 (rs841847) as a functional candidate SNP, we believed it was appropriate to keep the alpha for statistical significance of p < 0.05 for analyses focusing on Enh2 (rs841847) with further correction. However, given that the other 5 SNPs (rs841853, rs841839, rs3768043, rs2297977, rs841858) examined were largely meant to be tagging SNPs without any prior evidence to suggest function, we felt it necessary to correct for multiple testing errors by applying a Bonferroni correction[30], with the corrected alpha for statistical significance at the 0.05 level determined by dividing the significance level by the number of tagging SNPs, with adjusted p-value < 0.01.

Using the Bayesian method as implemented in PHASE v2.1[31, 32], haplotypes were inferred for all individuals with genotype data for at least five of the six SNPs (rs841847, rs841853, rs841839, rs3768043, rs2297977, rs841858) separately for African Americans (n = 1,036) and European Americans (n = 1638). Phase-formatted data were run as race-specific files which combined case and control subjects, a more conservative estimation of haplotype frequency than separate case and control sample analyses. Pairwise SNP linkage disequilibrium (LD) was measured with D' and r2[33] in HaploView(Cambridge, MA). Categorized by major haplotypes (> 5% frequency), haplotype frequency was compared between case and control groups with χ2 test. For haplotype analyses, a Bonferroni correction was also applied by dividing the significance level (0.05) by the number of major haplotypes (n = 4 for European Americans, n = 8 for African Americans) for haplotype-based association analysis (Bonferroni corrected level of statistical significance for European Americans p < 0.0125, for African Americans p < 0.00625). Associations with albuminuria for each diplotype (of major haplotypes) were examined separately using logistic regression. For diplotype analyses for European Americans, a Bonferroni correction was also applied by dividing the significance level by the number of diplotypes (n = 10) comprised of the major haplotypes, with adjusted level of statistical significance p < 0.005.

In stage 2 (n = 7340) the Enh2 SNP was genotyped. Associations of albuminuria/microabluminuria/macroalbuminuria and the Enh2 risk genotype were assessed using multivariate logistic regression models for the total study population, stratified by race and type 2 diabetes. Covariates included age, gender, systolic blood pressure, diastolic blood pressure, hypertension medication use, BMI, estimated GFR, and fasting glucose. Additionally, among non-diabetics, we examined interactions of albuminuria/macroalbuminuria for the Enh2 risk genotype with quartiles of fasting insulin, based on the Enh2 SNP location in the putative insulin-responsive enhancer 2[5]. Multivariate linear regression was used to assess associations between the Enh2 risk genotype with log-transformed ACR μg/mg (data log-transformed due to the skewed distribution) and also serum creatinine among European Americans, stratified by type 2 diabetes; these analyses were not performed among African Americans due to the rarity of the Enh2 risk genotype in that population.

Results

GLUT1SNPs

Six SNPs (average spacing 4.2 kb) of the GLUT1 genomic region (Promoter SNP, Intron-1 SNPs 1 and 2, Enhancer 2 SNP, XbaI SNP, and Intron 2 SNP) were genotyped in an unrelated sample of 1803 European Americans and 1135 African Americans in stage 1 (Figure 1). In European Americans, all SNPs were in Hardy-Weinberg Equilibrium (HWE). Among African Americans, the Promoter SNP was not in HWE (P < 0.05). XbaI minor allele(A) frequency in African Americans was higher than in European Americans (frequency = 0.42 versus 0.27). In European Americans, the XbaI A allele and the Enh2 T allele (frequency = 0.25) were comparable to previously published estimates[5, 6, 8, 9, 11]. However, minor allele of Enh2(T) was low in African Americans (frequency = 0.07).

The five SNPs (Intron-1 SNPs 1 and 2, Enh2 SNP, XbaI SNP, and Intron-2 SNP) downstream of Promoter SNP were in strong LD with each other (range of D' = 0.95 to 1.00 in European Americans and 0.96 to 1.00 in African Americans)[34]. The promoter SNP was separated from Intron-1 SNP1 by ~10 kb and was in greater LD among European Americans (D' = 0.69) than African Americans (D' = 0.09). Among both African Americans and European Americans, Enh2 and XbaI SNPs were in strong LD (D' = 0.96); however, the r 2was much lower in African Americans compared to European Americans (0.09 vs. 0.70) because frequencies of Enh2 and XbaI significantly differed in African Americans.

Clinical Characteristics

In both race groups in stage 1, the case subjects had worse risk factor profiles than controls (Table 1). Risk factor profiles were also worse for case subjects among participants from stage 2 (n = 7340).

Table 1 Baseline Characteristics. Clinical characteristics of study subjects by Race and Albuminuric Status
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Stage 1: Evaluation Phase of Six GLUT1 SNP Genotypes by Albuminuria Case Status

European Americans

Among European Americans in stage 1, GLUT1 SNP genotype distributions were not significantly different by case status, though the Enh2 SNP approached statistical significance (P = 0.08, figure 1). XbaI and other tagging SNPs did not approach the Bonferroni corrected level of statistical significance of p < 0.01. For Enh2 T allele, heterozygotes had an OR = 0.88, while homozygotes had OR = 1.77 (95% CI: 0.98 - 3.20). Similarly for the XbaI A allele, heterozygotes had OR 0.92 while homozygotes had OR 1.89 (95% CI: 1.01 - 3.55). Our genotypic associations of XbaI and Enh2 in European Americans suggest a recessive model, similar to previous findings [5, 6, 11].

Albuminuria was associated with the Enh2 TT risk genotype with OR 2.36 (95% CI: 1.09 - 5.09, P = 0.025) compared to those without the risk genotype (CC or CT) among those with type 2 diabetes. This association was not present among non-diabetics (OR 1.31, P = 0.574, Table 2). Similarly, the XbaI risk genotype (AA) had a larger association with albuminuria among those with type 2 diabetes rather than non-diabetics (OR 2.23 [P = 0.064] and 1.75 [P = 0.212], respectively), though associations were not statistically significant for XbaI and did not approach the Bonferroni corrected level of statistical significance (p < 0.01) (Table 2). Among European Americans stratified by diabetes, besides Enh2 no other GLUT1 polymorphisms were associated with albuminuria (results not shown). In all European Americans, multivariate analysis adjusting for diabetes simultaneously examined the association with albuminuria of all six GLUT1 SNPs, and the Enh2 risk genotype had an increased OR with albuminuria (OR = 3.37, 95% CI: 0.83 - 13.78, p = 0.090) whereas XbaI did not (OR = 0.94, 95% CI: 0.26-3.42, p = 0.931). For the four remaining SNPs, genotypic ORs ranged from 0.72 to 1.85 (all p-values > 0.17) with none of the SNPs approaching the Bonferroni adjusted statistical significance level of p < 0.01.

Table 2 Stage 1GLUT1 Enh2 and XbaI Risk genotype distributions among case and control subjects and odds ratio of albuminuria, by diabetes and race
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Similarly, detailed haplotype and diplotype analyses supported a potential role of the Enh2 TT genotype in raising the risk of albuminuria in a recessive fashion (Table 3). When the ten diplotypes associated with the major haplotypes A, B, C, and D (table 3) were examined among European Americans, only the BD diplotype was associated with albuminuria (OR 3.03, 95% CI 1.36 - 6.79, p = 0.007, compared to individuals without the BD diplotype). However, this approached but did not reach a Bonferroni corrected level of statistical significance of p < 0.005. Additionally, the diplotypes consisting of the B or D "risk" haplotypes were rare among European Americans, with BB, BD, and DD diplotypes accounting for 2.7%, 2.2%, and 0.5% of the 1663 European Americans with available diplotypes analyzed. Overall, haplotype diplotypes homozygous for the Enh2 T allele had an increased risk of albuminuria compared to all others combined (P = 0.014), though it did not reach the Bonferroni corrected level of statistical significance of p < 0.005.

Table 3 Major Haplotype Distribution in Case and Control Subjects by Race in stage 1†‡
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African Americans

Among African Americans, no GLUT1 SNP was significantly associated with case status. Frequency of the Promoter SNP genotype was slightly but not significantly different by case status (see figure 1). Enh2 TT genotype was rare (0.3% in controls, 0.0% in cases) and did not allow examination with case status. There was sufficient power to examine the XbaI SNP (with the minor A allele frequency of 42.4%) and case status in African Americans, which was not significant(P = 0.5). By diabetes status, the XbaI AA risk genotype was not associated with albuminuria either among those with type 2 diabetes (OR 1.05, 95% CI: 0.53 - 2.09) or without diabetes (OR 1.34, 95% CI: 0.70 - 2.56). Further detailed haplotype and diplotype analyses did not demonstrate any significant associations with albuminuria among African Americans (P = 0.877, table 3).

GLUT1 Enh2and Albuminuria in Samples from Stages 1 and 2

Based on stage 1, the Enh2 SNP appeared to be the risk polymorphism affecting albuminuria, particularly among European Americans with type 2 diabetes. The GLUT1 Enh2 polymorphism was genotyped in a separate stage 2 of European Americans (n = 6319; 374 cases) and African Americans (n = 1021, 146 cases), and the risk genotype tended towards an increased (but not statistically significant) OR among European Americans with diabetes (OR = 1.66, 95% CI: 0.77 - 3.57, p = 0.192) but not among non-diabetics (OR = 0.99, 95% CI: 0.61 - 1.59, p = 0.953). The risk association among European Americans with diabetes from stage 1 was not replicated in stage 2. In the stage 2 sample of African Americans, the GLUT1 Enh2 risk genotype was still rare (0.1% of controls and 1.4% of cases, Chi-square(2d.f.) P = 0.03) precluding informative analysis by diabetes status.

By race, we combined the samples from stages 1 and 2 for European Americans (n = 8,122) and African Americans (n = 2156) and examined risk-factor adjusted associations with albuminuria and the GLUT1 Enh2 risk genotype by diabetes status (Table 4). Among European Americans with diabetes, the Enh2 risk genotype had an increased risk-factor adjusted OR with albuminuria (OR 2.11, p = 0.010), microalbuminuria (OR 2.01, p = 0.034) and macroalbuminuria (OR 2.69, p = 0.045) (Model 1, Table 4). Further adjustment for BMI and estimated renal function (model 2) did not significantly affect the associations (with albuminuria OR 2.14, p = 0.009), nor did further adjustment for fasting glucose (OR 1.99, p = 0.029). However, among European Americans without type 2 diabetes, Enh2 was not associated with albuminuria (OR 1.01, p = 0.980) and was moderately but not significantly associated with macroalbuminuria (OR 1.64, 95% CI: 0.64-4.25, p = 0.305) (Model 1, Table 4). Additional adjustment for visit 2 hemoglobin A1C (HbA1C) in a sub-sample did not significantly change point estimates with albuminuria (OR = 1.87, 95% CI: 1.02 - 3.42 in diabetic individuals, OR = 1.25, 95% CI: 0.63 - 2.46 in non-diabetics). There was no evidence of interaction with hypertension (results not shown). Additionally, among European Americans, we also examined potential associations using multivariate linear regression with log-transformed ACR μg/mg (data log-transformed due to the skewed distribution) and also serum creatinine among European Americans, stratified by type 2 diabetes (see Table 5). Though the Enh2 risk genotype tended to be positively associated with worse ACR and higher serum creatinine only among type 2 diabetic European Americans, there were no statistically significant associations. We did not perform this analysis among African Americans given the low frequency of the Enh2 risk genotype among this population.

Table 4 Adjusted relative odds of albuminuria, microalbuminuria, and macroalbuminuria for Enh 2 in all genotyped European Americans and African Americans, by type 2 diabetes status.
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Table 5 Unadjusted and multivariate linear regression of ln (ACR) and serum creatinine for Enh 2 in all genotyped European Americans, by type 2 diabetes status.
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Among African Americans, after adjustment for model 2 covariates, the GLUT1 Enh2 risk genotype had a positive association with albuminuria and microalbuminuria among those with type 2 diabetes (OR = 4.36 and 6.39 with p = 0.321 and 0.203, respectively) and without diabetes (OR = 4.69 and 5.15 with p = 0.187 and 0.164, respectively), though it was not significant due to low frequency of the SNP.

The GLUT1Enh2 Risk Genotype and Insulin

To examine effects of insulin concentration on the association of GLUT1 Enh2 genotypes and albuminuria, we stratified by insulin concentrations excluding those with diabetes (to avoid confounding due to insulin treatment for diabetes). Due to the low frequency of the GLUT1 Enh2 risk genotype among African Americans, analysis was limited to European Americans. Among European Americans, (n = 6583 controls, 294 cases of microalbuminuria, and 46 cases of macroalbuminuria), the mean fasting insulin concentration was 10.9 μU/mL (S.D. = 7.5). Risk of albuminuria for Enh2 TT was OR 1.08 (95% CI: 0.70 - 1.67, p = 0.724), adjusting for age, gender, hypertension status, BMI, and GFR. Among individuals with insulin in the highest quartile (mean insulin 19.9 μU/mL, S.D. = 9.7), the adjusted OR of albuminuria for Enh2 TT was 1.25 (95% CI: 0.60 - 2.58, p = 0.547). Among individuals with insulin concentrations in the lower three quartiles (mean 7.9 μU/mL, S.D. = 2.9), the adjusted OR of albuminuria was 1.00 (95% CI: 0.58 - 1.72, p = 0.990) for Enh2 TT carriers. When we focused on the more specific outcome of macroalbuminuria as a phenotype and excluded patients with microalbuminuria, risk of macroalbuminuria for Enh2 TT was OR 1.84 (95% CI: 0.71 - 4.77, p = 0.210) as illustrated in figure 2. Among individuals with insulin in the highest quartile, the adjusted OR for Enh2 TT was 4.08 (95% CI: 1.06 - 15.61, p = 0.040). Among individuals with insulin concentrations in the lower three quartiles, the adjusted OR of macroalbuminuria was 1.00 (95% CI: 0.23 - 4.28; P = 0.995) for Enh2 TT carriers. Among non-diabetics, a formal test of interaction of the GLUT1 Enh2 risk genotype and the upper quartile of insulin was not significant for macroalbuminuria (P = 0.163).

Figure 2
figure 2

Macroalbuminuria, Enh2 risk genotypes and insulin concentrations among non-diabetic European Americans (n = 6629 (46 cases)). *P < 0.05. Among non-diabetic European Americans with fasting insulin, the risk of macroalbuminuria associated with the GLUT1 Enh2 TT risk genotype was 1.84, 95% CI: 0.71 - 4.77, P = 0.210, adjusting for age, gender, hypertension status, BMI, and GFR. For individuals in the upper quartile of insulin concentrations, the Enh2 TT genotype was associated with macroalbuminuria (OR 4.08, 95% CI: 1.06 - 15.61, p = 0.040) while it was not associated among those in the lower three quartiles (OR 1.00, 95% CI: 0.23 - 4.28, P = 0.995). There was no significant interaction between high concentrations of insulin and Enh2 TT genotypes on macroalbuminuria risk (P-interaction = 0.163).

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Discussion

Genetic variation of GLUT1 may be associated with the risk of micro- and macroalbuminuria in the general U.S. adult population of European Americans with type 2 diabetes. Though an association was seen when we combined European Americans with diabetes from stages 1 and 2, the findings of stage 1 were not replicated in stage 2. Both XbaI and Enh2 SNPs appeared to be associated in a recessive fashion with albuminuria, consistent with previous studies [5, 6, 8, 11, 13]. Further analysis showed Enh2 risk genotype (TT) increased risk independent of all other genotyped GLUT1 SNPs, including XbaI, suggesting that Enh2 is the causative GLUT1 SNP associated with albuminuria. Addtionally, no other GLUT1 SNPs besides Enh2 have been demonstrated to be located in a region with functional activity in vitro[5, 6, 8, 13]. By study stage, the Enh2 risk genotype was associated with diabetic albuminuria among European Americans only in stage 1 and in the total study population; these findings were not replicated when we examined stage 2. In the total study population of European Americans with type 2 diabetes, the risk effect of Enh2 on macroalbuminuria was independent of age, gender, and hypertension. Possession of the Enh2 risk genotype and high insulin concentrations particularly increased macroalbuminuria risk among non-diabetic European Americans. Among African Americans, XbaI was not associated with albuminuria. The association of the Enh2 risk genotype and albuminuria among African Americans was increased among individuals with and without type 2 diabetes but was not statistically significant. Despite having over 2000 African Americans in the present study, the low frequency of the Enh2 risk genotype in this population (0.3%) limited the power of our analysis and prevents us from making definitive conclusions about the role of GLUT1 genetic variation and albuminuria in African Americans. However, our results suggest that GLUT1 Enh2 may be associated with albuminuria.

In European Americans, our results extend the findings of a prior study by Ng et al. among type 1 diabetics[35], suggesting both XbaI and Enh2 homozygotes as having an increased risk of albuminuria. However, the authors could not examine the independent risk effect of Enh2 or XbaI separately; since no individuals in their study possessed the Enh2 risk genotype but not the XbaI risk genotype. Multivariate analysis in our study suggest the XbaI AA risk genotype by itself does not confer risk (OR = 0.94, p = 0.931), whereas the Enh2 TT risk genotype (OR = 3.37, p = 0.090) has a stronger association with albuminuria independent of XbaI. Our results extend the risk association of Enh2 to albuminuria in European Americans with type 2 diabetes. Additionally, a recent study in Tunisia of type 2 diabetics had similarly demonstrated an association of the Enh2 TT risk genotype with nephropathy (OR 8.4 (95% CI: 3.3-21.5)) while finding no association with XbaI[11].

Additionally, our results suggest that among non-diabetic European Americans with the Enh2 risk genotype, those with higher concentrations of insulin were at greater risk of having proteinuria. The putative human enhancer-2 is homologous with the murine enhancer-2 which was responsive to insulin in vitro[5, 24]. Furthermore, the Enh2 SNP is located within a binding site for the insulin-responsive transcription factor, the upstream stimulatory factor (USF) [5, 25, 26]. USF has been identified as a glucose-inducible transcription factor in mesangial cells [27, 28] and shown to regulate GLUT1 transcription[29]. The Enh2 SNP of GLUT1 is located within a USF responsive element in humans, suggesting the TT genotype might have altered gene expression of GLUT1 that contributes to diabetic nephropathy[36]. Additionally, the interaction of the Enh2 SNP and insulin supports the previously posited hypothesis[5] that in individuals with the Enh2 risk genotype, high intracellular glucose concentrations might increase in mesangial cells in response to insulin[37]. The high concentrations of intracellular glucose may contribute to mesangial matrix expansion and glomerulosclerosis through several pathologic cellular mechanisms including the polyol pathway, activation of protein kinase C, increased formation of advanced glycation end-products, and the hexosamine pathway[38, 39]. Additionally, there is evidence that podocytes are critical in maintaining the glomerular filtration barrier of the kidney and preventing albuminuria [40–42], and a recent study demonstrated that the glucose uptake of podocytes are insulin responsive and act via GLUT1, suggesting the insulin sensitivity of human podocytes resulting in urinary protein loss may act via these mechanisms [43]. Future studies should examine if the Enh2 SNP indeed modulates GLUT1 protein expression. Furthermore, most candidate gene chips (Affymetrix 5.0, 6.0, 500K, 100K; Illumina 550K, 650K) do not include Enh2 SNP. This suggests follow-up studies may need de-novo genotyping.

Previous studies of XbaI and diabetic nephropathy have had disparate results[12]. Our results for the XbaI risk genotype in European Americans are consistent with previous studies which demonstrated increased risk of type 1 diabetic nephropathy among those homozygous for the XbaI A allele[5, 6], suggesting recessive transmission of the phenotype. Inconsistent results in other studies of XbaI may be due to different patterns of disequilibrium with the Enh2 polymorphism [7–11].

Our study has several limitations. Its design is cross-sectional and the albuminuria classification is based on a spot urine ACR because urine which was only collected at one ARIC visit. A phenotype based on a single measurement of ACR could definitely lead to incorrect conclusions, particularly with potential misclassification of borderline values with a dichotomous outcome such as albuminuria. However, sensitivity analyses for macroalbuminuria demonstrated a significant risk association with the Enh2 risk genotype. Another limitation is that the Enh2 risk genotype was only significantly associated with diabetic albuminuria among European Americans from stage 1 and in the combined analysis. The findings of stage 1 were not replicated in stage 2. The samples from stage 1 and 2 were not randomly sampled, with stage 1 consisting of a convenience sample enriched for those with type 2 diabetes and African Americans, a sample previously used for the study of genetic risk factors in cardiovascular disease and type 2 diabetes. Participants comprising stage 2 consisted of the remaining ARIC visit 4 particpants not in sample 1. However, Enh2 TT still had an increased (but not statistically significant) association with albuminuria among European Americans with diabetes from stage 2, and had a significant and strong association with diabetic albuminuria when we combined both stages. Additionally, despite the fact that our study included 8122 European Americans, of whom there were 1095 type 2 diabetics, given the rarity of the Enh2 TT risk genotype among diabetics (6.6%), the size of our study precludes any definitive conclusions regarding the association of type 2 diabetic albuminuria and the Enh2 polymorphism of GLUT1. Given this limitation, our study can at best suggest an association between Enh2 and albuminuria among European American type 2 diabetics; however, due to the limitation in our number of subjects, we do not have sufficient power to make conclusive statements regarding this association. Perhaps a larger study of type 2 diabetic European Americans involving multiple cohorts may provide more power to definitively evaluate the role of the Enh2 risk genotype of GLUT1 and albuminuria. Furthermore, we did not have hemoglobin A1C (HbA1C) for all participants in our sample, though in our sub-sample, adjustment did not significantly affect results. Instead, we used fasting glucose as a marker of glycemic control. However, Ng et al. had previously found the strength of the association of the Enh2 risk genotype and diabetic albuminuria was independent of both HbA1C and duration of diabetes[5]. Ours is the largest study of GLUT1 genetic variation and albuminuria to date and the first to examine associations among non-diabetics and African Americans. We substantiate prievous findings and extend the association beyond type 1 diabetes, demonstrating a role for GLUT1 Enh2 and proteinuria among those with type 2 diabetes.

Conclusions

In summary, GLUT1 genetic variation of Enh2 may predict risk of micro- and macroalbuminuria among European Americans with type 2 diabetes. Though the Enh2 risk genotype was significantly associated with diabetic albuminuria among European Americans from stage 1 and in the combined analysis, the findings of stage 1 were not replicated in stage 2. Furthermore, the rarity of the Enh2 risk genotype among African Americans precludes any definitive conclusions, although data suggest a risk-enhancing role. Our results suggest the Enh2 SNP, and not XbaI, is the causative polymorphism associated with diabetic albuminuria. Additionally, the Enh2 risk genotype may interact with hyperinsulinemia to further increase susceptibility to albuminuria, consistent with hypotheses generated by laboratory data. Studying mechanisms mediating this association may shed light on novel pathways and therapeutic targets in the pathophysiology of albuminuria and nephropathy. The modest size of the risk associated with GLUT1 Enh2 variation limits utility for screening, risk stratification and individualized therapy. However, if multiple genes of small and moderate effect on nephropathy are identified, they may compose panels for risk assessment.

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Acknowledgements

The Atherosclerosis Risk in Communities Study is carried out as a collaborative study supported by National Heart, Lung, and Blood Institute contracts N01-HC-55015, N01-HC-55016, N01-HC-55018, N01-HC-55019, N01-HC-55020, N01-HC-55021, and N01-HC-55022. The American Diabetes Association and National Kidney Foundation of Maryland also provided support for C.C.H. The authors thank the staff and participants of the ARIC study for their important contributions.

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  1. Departments of Medicine and Epidemiology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA

    Charles C Hsu, Wenhong L Kao, Tejal Gambir, Frederick L Brancati, Charles W Heilig & Josef Coresh

  2. Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA

    Michael W Steffes

  3. Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA

    Alan R Shuldiner

  4. Human Genetics Center, University of Texas-Houston Health Science Center, Houston, Texas, USA

    Eric A Boerwinkle

  5. Department of Medicine, University of Chicago, Chicago, Illinois, USA

    Charles W Heilig

  6. Department of Radiation Oncology, University of California, San Francisco, California, USA

    Charles C Hsu

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CCH, WHLK, CWH, and JC designed the study. Laboratory work was undertaken by MWS, WHLK, TG, FLB, EB, and AS. Statistical analysis was done by CCH, WHLK, and JC. CCH wrote the first draft of the paper. All authors contributed to and approved of the final version of the manuscript.

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Hsu, C.C., Kao, W.L., Steffes, M.W. et al. Genetic variation of Glucose Transporter-1 (GLUT1) and albuminuria in 10,278 European Americans and African Americans: a case-control study in the Atherosclerosis Risk in Communities (ARIC) Study. BMC Med Genet 12, 16 (2011). https://doi.org/10.1186/1471-2350-12-16

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