Single-nucleotide polymorphisms of GSK3B, GAB2 and SORL1 in late-onset Alzheimer's disease: interactions with the APOE genotype

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Single-nucleotide polymorphisms of GSK3B, GAB2 and SORL1 in late-onset Alzheimer's disease: interactions with the APOE genotype

Giselle Izzo^I; Orestes V. Forlenza^{I, IV}; Bernardo dos Santos^{I, III}; Paulo H. F. Bertolucci^II; Elida B. Ojopi^I; Wagner F. Gattaz^{I, IV}; Daniel Shikanai Kerr^{I, IV}

^IFaculdade de Medicina da Universidade de São Paulo (Ipq-FMUSP), Department and Institute of Psychiatry), Laboratory of Neuroscience (LIM-27), São Paulo/SP, Brazil

^IIFederal University of Saio Paulo (UNIFESP), Faculty of Medicine, Department of Neurology, Nucleo De Envelhecimento Cerebral (NUDEC), Sao Paulo/SP, Brazil

^IIIUniversidade de São Paulo, Instituto de Matemática e Estatística (IME), São Paulo/SP, Brazil

^IVUniversidade São Paulo, Center for Interdisciplinary Research on Applied Neurosciences (NAPNA), São Paulo/SP, Brazil

ABSTRACT

In this study, we investigated the associations between single-nucleotide polymorphisms in GAB2 (rs2373115), GSK3B (rs6438552) and SORL1 (rs641120) and Alzheimer's disease (AD), both alone and in combination with the APOE*4 allele.

INTRODUCTION

Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder that is caused by the interaction of multiple genetic and environmental factors (1). In the early stages, Alzheimer's disease is clinically characterized by short-term memory impairment, which evolves to widespread cognitive decline and dementia. There is unequivocal evidence that genetic factors contribute to the pathogenesis of Alzheimer's disease, including the sporadic form (2). Currently, apolipoprotein E is the only well-established genetic risk factor for sporadic Alzheimer's disease, and the APOE*4 allele has been consistently shown to be associated with an increased risk of Alzheimer's disease (3,4). There is little doubt that other - most likely multiple - polymorphisms play an important role in the pathophysiology of Alzheimer's disease, given that the presence of one or even two copies of APOE*4 is neither a necessary nor sufficient condition for developing the disease.

Several new single-nucleotide polymorphisms (SNPs) associated with on Alzheimer's disease have recently been identified in genome-wide association studies, namely PICALM, CLU, CR1 and SORL1 (5-7). None of these SNPs can be regarded as etiological factors; rather, they serve as susceptibility modifiers, i.e., factors with independent or additive effects in the interactions among several genetic variants (mostly SNPs) at multiple genomic loci. These variants may not be deleterious per se, but they may modify disease outcomes as a result of direct and indirect interactions with other genetic and environmental factors (8,9).

Polymorphisms in the SORL1, GAB2 and GSK3B genes have been shown to be associated with Alzheimer's disease in recent studies. Association studies have yielded conflicting data regarding the role of SORL1 rs641120 in Alzheimer's disease (7,10,11-13). A recent study showed that there were age-dependent differences in SORL1 expression and promoter methylation in an AD cohort, with possible implications for the disease (14). Likewise, two studies suggested that there is an association between GAB2 polymorphisms and AD in Caucasians (15,16), but other studies failed to confirm this association in European (17) and Asiatic populations (18,19). Only one study to date has addressed the association between GSK3B polymorphisms and AD; the results of that study suggest that rs6438552 has a significant effect on disease risk (20). Therefore, the objective of the present study was to determine the effects of GAB2 (rs2373115), GSK3B (rs6438552) and SORL1 (rs641120) polymorphisms on the risk for AD and to investigate the interactions of these SNPs with APOE*4 in a sample of 201 older Brazilian adults.

MATERIALS AND METHODS

Subjects were recruited from two university-based memory clinics in Sao Paulo, Brazil. All participants underwent comprehensive clinical and neuropsychological evaluations. The diagnosis of probable AD (n = 130, mean age 77±8.3, 66% females) was established according to the NINCDS-ADRDA criteria (21). The comparison group included healthy volunteers (n = 71, mean age 71.8 + 6.7; 79% females) with no signs of cognitive or functional impairment. No relatives of AD patients were included in the control group. No statistically significant differences were observed with respect to the age distribution or self-reported ethnic background between the patients and controls, but there was a greater percentage of females in the control group. However, we believe that this gender difference should not negatively affect the findings, as similar results were obtained in a preliminary analysis of gender-matched samples.

The GSK3B, GAB2 and SORL1 SNPs were analyzed using a Real-Time PCR SNP genotyping system (TaqMan^® Assays - Applied Biosystems, CA, USA) TaqMan PCR Master Mix 1x, TaqMan SNP genotyping assay 1x, genomic DNA 10 ng/ µL and ultrapure water to a volume of 5 µL were mixed in each well of an optical plate. Allelic discrimination was performed using a 7500 Real-Time PCR system (Applied Biosystems, CA, USA) by comparing the fluorescence levels before and after amplification (45 cycles of 15 seconds at 95 C and 1 min at 60 °C). Two SNPs (rs7412 and rs429358) were evaluated to determine the APOE genotype, as previously described (22). The real-time PCR reactions were run using the protocol presented above.

Pearson's Chi-squared test with simulated p-values was used to compare the genotype distributions between cases and controls. The interactions between the GSK3B, GAB2 and SORL1 SNPs and APOE*4 were tested in two ways: first, each group was stratified into APOE*4-positive and APOE*4-negative subgroups, and the association between each SNP and the diagnosis of AD was assessed separately in each group. In the second step, a binomial logistic regression model was used to compare the interactions between APOE*4 and each of the three SNPs in the entire sample. The statistical analysis was conducted using R software version 2.12.2.

RESULTS AND DISCUSSION

Our results are consistent with the well-established role of the APOE*4 allele as a risk factor for sporadic AD (p<0.0001) (3, 5, 6, 23-25)(7). Data regarding the genetics of AD in the Brazilian population remain scarce (26, 27), underscoring the importance of our findings. We call attention to the positive association of all the studied SNPs, namely GAB2 rs2373115, GSK3B rs6438552 and SORL1 rs641120, with AD (Table 1). The association of the GG genotype of SORL1 with AD (p = 0.047, OR = 2.07, CI₉₅% [1.17 - 3.68]) was independent of APOE, and the binomial logistic regression analysis showed no interaction effect between APOE*4 and any of the SORL1 genotypes (Table 2). We conclude that SORL1 has an independent role in AD, irrespective of the presence of the APOE*4 allele.

We found a positive association between the GG genotype of GAB2 (rs2373115) and the diagnosis of AD (p=0.021, OR = 1.8, CI95% [1.01-3.18]). This genotype was associated with a greater odds ratio (OR) for AD in the APOE*4 carriers (p = 0.006, OR = 5.08, CI₉₅% [1.45-18.98]). We further used logistic regression to investigate the interaction between the APOE*4 and GAB2 polymorphisms (GG vs. non-GG genotypes, given the small proportion of individuals with the TT genotype in our sample), and we observed a robust increase in the effect as a result of the interaction between GAB2 GG and APOE*4 (p = 0.014, ORinteraction = 7.95, ORmain = 1.44) (Table 2).

With respect to the association between the GSK3B polymorphism (rs6438552) and AD diagnosis, we found that the GG genotype was approximately twice as common in the AD group (28.8%) than in the controls (13.8%) and that this genotype had a significant effect on the OR (p=0.018, OR=2.48, CI95% [1.19-5.20]). Interestingly, this effect was even more pronounced in the absence of APOE*4 (p = 0.003, OR = 4.45, CI₉₅% [1.47-16.39]). In contrast, the A allele was associated with a protective effect, irrespective of the APOE status (p = 0.018, OR = 0.40, CI₉₅% [0.19-0.84]); however, the logistic regression analysis showed that APOE*4-positive carriers of the AA genotype displayed an increased OR for AD (p = 0.024, OR_interaction = 1.10, ORmain = 0.19) (Table 2). This finding is noteworthy because it indicates that the A allele of the GSK3B gene may represent either a protective factor or a risk factor for AD, depending on the APOE genotype. We speculate that this dual role may occur because the rs6438552 polymorphism is intronic and may affect the transcription and splicing of GSK3B. In fact, splice variants of GSK3B arising from the AA genotype have been shown to favor Tau protein hyperphosphorylation, which is one of the pathological hallmarks of AD (28).

APOE*4 is involved in the abnormal cleavage of the amyloid-precursor protein (APP), leading to the accumulation of the amyloid-beta peptide, which in turn favors the hyperphosphorylation of Tau. These pathological changes ultimately disrupt axonal transport and neuronal viability (29, 30). GAB2 and GSK3B (rs6438552, AA genotype) have been shown to increase Tau phosphorylation (15, 28). The studied GSK3B and GAB2 polymorphisms are located in intronic regions of these genes and may thus have subtle effects on transcription, with biological consequences that are yet to be defined. It is also possible that these SNPs are in linkage disequilibrium with other polymorphisms that may contribute to the observed effects. GAB2 is a scaffolding protein with important roles in several growth and differentiation signaling pathways, including the phosphor-ylation of kinases that participate in core neurobiological pathways related to AD (15,16,31,32). GAB2 and presenilin 1 both activate PI3K, leading to the activation of PKB and the further inactivation of GSK3B (33). Because the inactivation of GSK3B prevents Tau hyperphosphorylation in neurons (34), it is reasonable to assume that any decrease in GAB2 expression and/or function would increase Tau phosphor-ylation (15). Supporting this hypothesis, in vitro studies have shown that the inhibition of GAB2 expression using siRNA increases Tau phosphorylation (15).

We conclude that interactions between the GAB2 and GSK3B polymorphisms and the well-established genetic factor APOE may modify the overall risk of AD. These effects are by no means linear or cumulative, given that the protective effect of a one studied polymorphism (e.g., the AA genotype of GSK3B) may increase the odds ratio for AD in the presence of APOE*4. Our results support the hypothesis that there is no single genetic cause for late-onset AD; instead, the development of AD depends on the interaction of several genes, environmental factors and age. Further evaluation of the interactions between distinct genes and of the respective implications on neuronal homeostasis may provide insight into the complex neurobiology of AD.

ACKNOWLEDGMENTS

We would like to thank CNPq, CAPES, FAPESP and ABADHS for financial support.

AUTHOR CONTRIBUTIONS

All authors contributed to the present work and consent to the publication of the findings. Gattaz WF and Ojopi EB were responsible for the initial concept. The patients were recruited by Bertolucci PHF, Forlenza OV and Gattaz WF. The experimental analyses were performed by Izzo G and

Kerr DS. The statistical analyses were performed by Santos B and Kerr DS. Izzo G wrote the first draft of the manuscript. The literature review was performed by by Izzo G and Kerr DS. The manuscript was prepared and formatted and the tables were prepared by Kerr DS and Forlenza OV. All authors have reviewed and approved the final manuscript.

No potential conflict of interest was reported.

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Publication Dates

• Publication in this collection
  18 Mar 2013
• Date of issue
  2013