Large Scale Association Analysis for Drug Addiction: Results from SNP to Gene

Guo, Xiaobo; Liu, Zhifa; Wang, Xueqin; Zhang, Heping

doi:https://doi.org/10.1100/2012/939584

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Volume 2012 | Article ID 939584 | https://doi.org/10.1100/2012/939584

Large Scale Association Analysis for Drug Addiction: Results from SNP to Gene

Xiaobo Guo,^1,2Zhifa Liu,¹Xueqin Wang,^2,3and Heping Zhang¹

Academic Editor: W. Tian, X. Zhao, J. Wan, R. Jiang

Received26 Sept 2012

Accepted25 Nov 2012

Published27 Dec 2012

Abstract

Many genetic association studies used single nucleotide polymorphisms (SNPs) data to identify genetic variants for complex diseases. Although SNP-based associations are most common in genome-wide association studies (GWAS), gene-based association analysis has received increasing attention in understanding genetic etiologies for complex diseases. While both methods have been used to analyze the same data, few genome-wide association studies compare the results or observe the connection between them. We performed a comprehensive analysis of the data from the Study of Addiction: Genetics and Environment (SAGE) and compared the results from the SNP-based and gene-based analyses. Our results suggest that the gene-based method complements the individual SNP-based analysis, and conceptually they are closely related. In terms of gene findings, our results validate many genes that were either reported from the analysis of the same dataset or based on animal studies for substance dependence.

1. Introduction

Genome-wide association studies (GWAS) have become a powerful tool in the identification of susceptible loci for numerous diseases [1]. A typical strategy in GWAS is to analyze single nucleotide polymorphisms (SNPs) individually and select the top SNPs by setting a stringent threshold for the value. Then the top SNPs were mapped into functional regions such as a gene or pathway to facilitate further investigation of the corresponding gene and disease. Based on SNP-based association analysis, many genetic variants underlying complex diseases or traits were detected [2, 3]. Due to the large number of SNPs with each of which entails an association test, it is essential to control the type I error or false discovery rate [4]. A predefined value is usually used as the threshold to declare a genome-wide significance SNP, which also limits the discoveries of the genes that are important to the disease. Also importantly, susceptible SNPs generally explain a small fraction of the risk—a phenomenon commonly referred to as the “missing heritability” [5, 6]. To alleviate this problem, alternative methods have emerged to complement the simple SNP-based methods. Among those methods, gene-based analysis [7–9], which jointly analyzes the SNPs within genes, is a promising solution to improve the power of GWAS. Compared with the SNP-based approach, gene-based association analysis has certain advantages. First, gene is a unit of heredity and function, and hence the gene-based association approaches can provide direct insights into the heredity and functional mechanisms of complex traits [10]. Second, from the statistical perspective, the gene-based association approaches reduce the number of association tests in the order of millions to about 20,000 gene-based tests, which dramatically reduces the chance of false discovery. In addition, the gene-based methods are not affected by the heterogeneity of a single locus. Hence, the results are highly consistent across populations [11], which enhances the likelihood of replication.

Gene-based methods have been successfully applied to GWAS of complex diseases, including Crohn’s disease [7], type 1 diabetes [12], and melanoma [8]. Despite the above-noted features of the gene-based association approach, there are few comparisons of genetic association analyses between SNP and gene-based methods. Here, we compare and relate these two approaches using the data from the Study of Addition: Genetics and Environment (SAGE) [13].

Recent studies show that there are many candidate genes associated with substance dependence. For example, GABRA2, CHRM2, ADH4, PKNOX2, GABRG3, TAS2R16, SNCA, OPRK1, and PDYN are well studied for alcohol addiction and have been replicated in many samples [13–28]. However, other candidate genes, such as KIAA0040, ALDH1A1, DKK2, and MANBA [25, 27, 29, 30], remain illusive. For addiction to nicotine, CHRNA5, CHRNA3, CHRNB4, and CSMD1 have been replicated in many studies [31–39].

Based on the analysis of the SAGE data, we report a number of susceptible loci at the SNP and/or gene levels, which validate many susceptibility loci that have been reported to be associated with substance dependence [13, 14, 25, 27, 29, 37, 38, 40–44]. Meanwhile, both SNP- and gene-based analyses reveal three novel risk genes: NCK2, DSG3, and PUSL1.

2. Materials and Methods

2.1. Dataset and Study Design

The dataset included 4,121 subjects in SAGE with six categories of substance dependence data: alcohol, cocaine, marijuana, nicotine, opiates, and other dependencies on drugs. The data were downloaded from dbGaP (study accession phs000092.v1.p1) [13]. SAGE [13] is a large case-control study which aims to detect susceptible genetic variants for addition. The subjects were recruited from eight study sites in seven states and the District of Columbia in the United States. All subjects’ life time dependencies on these six dependencies are diagnosed by using the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV). All samples were genotyped on ILLUMINA Human 1 M platform at the Center for Inherited Disease Research in Johns Hopkins University. In this paper, we strictly followed the quality control/quality assurance as we did in our previous analysis [14]. Genome-wide SNP data were filtered by setting thresholds: and . In addition, 60 duplicate genotype samples and 9 individuals with ethnic backgrounds other than African origin or European origin were excluded in our analysis. Finally, 3,627 unrelated samples with 859,185 autosomal SNPs passed the quality control procedures. To avoid population stratification, the dataset was stratified into four subsamples: 1,393 white women, 1,131 white men, 568 black women, and 535 black men. To capture most of the gene coding and regulatory variants, SNPs are considered being mapped to a gene if their physical locations are within 20 kilobases (kb) 5′ upstream and 10 kilobases (kb) 3′ downstream of gene coding regions [26]. In addition, SNPs are also assigned to a gene if they are in strong LD () with the initially assigned SNPs within the gene [10]. Together, around 533,639 SNPs were assigned to 18,699 protein coding genes (28.6 ± 47.7 (mean ± SD) SNPs per gene).

Following the conventional standards, we used and as the genome-wide significant thresholds for SNP-based and gene-based methods, respectively [4]. To increase the power of detecting potentially important SNPs that do not meet the stringent thresholds, we also considered relaxed thresholds. Specifically, SNPs with and genes were considered further. These values are referred to as relaxed significance thresholds below. The selected SNPs were then mapped into the corresponding genes by the mapping rule proposed above.

2.2. Genetic Association Test at SNP and Gene Levels

We took several steps in testing the associations between genetic variants (SNP or gene) and substance dependenice. First, the value of each SNP was evaluated by the logistic regression, and then the correlation coefficients () of all SNP pairs were calculated. The computation was performed in PLINK software (version 1.07) [45]. In the second step, we implemented the gene-based analysis in the open-source tool: Knowledge-Based Mining System for Genome-Wide Genetic Studies (KGG, version 2.0) [46] based on the association test results and LD files obtained from PLINK. Simes procedure (GATES) was employed in the gene-based association test [7]. Specifically, assume that SNPs are assigned to a gene; an association test such as through the traditional logistic regression or linear regression is used to examine the association between the phenotype and each single SNP. This step yields values for SNPs. GATES combines the available values within a gene by using a modified Simes test to give a gene-based value. The summary value is defined as where is the th smallest value among the SNPs; is the effective number of independent values among SNPs within the gene, and is the effective number of independent values among the top SNPs. The effective number of independent values was derived by accounting for the LD structure among the specified SNPs; we refer to [7] on the calculation.

In order to compare the performance of the SNP-based and gene-based methods, in the SNP-based method, we selected those SNPs whose values were less than and then mapped them into the corresponding genes. This allows us to compare the susceptible genes identified by both methods discussed above.

3. Results

3.1. Detecting Susceptibility Loci at the Relaxed Significance Level

Table 1 summarizes the susceptible genes identified by the SNP-based association test and gene-based association test at the relaxed significance level. In total, 207 genes passed the relaxed gene-based threshold, whereas only 64 genes with SNPs passed the relaxed SNP-based threshold.

Next, we performed a literature search on the genetic regions which contain the identified genes and filtered the susceptible genetic regions which have been reported to associate with substance dependence for further investigation. In Table 2, we listed the filtered genes, their associated substance dependence type, the values for the gene-based method, the minimal value of SNPs within a gene, and their literature references and reported substance dependence.

In Figure 1, we plot the filtered genes obtained from the SNP-based and gene-based analyses by the position on the chromosomes against their log-transformed values, . Each point for the SNP-based analysis in Figure 1 corresponds to the smallest SNP-based value within the gene.

Overall, five genes, NCK2 (opiates dependence in black men), SH3BP5 (cocaine dependence in white men), LRP5 (opiates dependence in white men), KIAA0040 (alcohol dependence in white women), and PKNOX2 (alcohol dependence in white women), were identified by both the SNP-based and gene-based methods as meeting either of the relaxed significance levels for a specific dependence and within a gender-racial group. Four genes, MAPK1 (marijuana dependence in black women), MANBA (alcohol dependence in white men), HAAO (cocaine dependence in white women), and IFNG (opiates dependence in white women), met the threshold by the gene-based method only. We found that the significant signal of gene MAPK1 was mainly driven by SNPs: rs7290469 (), rs9610271 (), rs9610417 (), and rs2876981 (). The values for these SNPs are slightly greater than the relaxed SNP-based threshold (), and hence the SNP-based method failed to detect them.

Furthermore, four other genes, FAM38B (cocaine dependence in black women), PTPRM (marijuana dependence in black women), CSMD1 (nicotine dependence in black women), and RELN (cocaine dependence in white men), contain at least one SNP that met the SNP-based relaxed threshold of significance. The gene-based values for FAM38B, PTPRM, and RELN are , , and , respectively, which are greater than yet at the same order as the relaxed threshold (value ). For CSMD1, 1,934 SNPs were mapped into it. Its signal was mainly determined by only five SNPs: rs2624087 (), rs4875371 (value ), rs2623607 (value ), rs10503267 (value), and rs4875372 (value). Because there were only 5.3% of the SNPs (103 SNPs) with value less than 0.05, the overall association from the gene became less significant.

3.2. Genome-Wide Significant Loci

Since none of the SNPs attained the genome-wide significance for any dependence by the SNP-based method, in this section we will only focus on the results from the gene-based method.

Table 3 presents the genes with gene-based value . This method identified one genome-wide significant gene, DSG3 ( value ) for nicotine dependence in white men. The value of gene NCK2: is very close to the genome-wide significant threshold, which provided very strong evidence for the association of opiates in black men. As shown in Table 3, both NCK2 and DSG3 contained SNPs with strong signals; they are rs2377339 ( value ) for NCK2 gene and rs6701037 ( value ) and rs1057302 ( value) for DSG3 gene. However, none of these SNPs reached genome-wide significance.

4. Discussion

In this paper, we thoroughly analyzed the SAGE data from the SNP-based and gene-based methods, and compared the results obtained from these two methods. Specifically, for each sex-racial group, we performed association analysis for the six categories of substance dependence separately. The gene-based method appears to be more powerful in detecting susceptibility loci.

Most of the genes identified in our study are supported by various reports in the literature related to the genetics of substance dependence [47, 48]. Based on some of the genes that we identified, here common genetic variants among different substance dependencies may exist [49].

Overall, we did not detect any genome-wide significant SNP when using the SNPs-based method. However, one gene, DSG3,is genome-wide significantly () associated with nicotine dependence in the white men, according to the gene-based method. Another gene, NCK2, is nearly genome-wide significant () in its association with substance dependence.

The SNP-based method and gene-based method are closely related. In fact, the SNP-based method can be viewed as a gene-based method using the extreme function, namely, the minimal value of the SNPs within a gene, whereas the typical gene-based method uses a weighted approach. The advantages and limitations of these two approaches are similar to those between the extreme function and a weighted average.

We should point out that both the SNP-based and gene-based methods have their own advantages and disadvantages. The SNP-based method has its unique strength in identifying genes with only a small number of significant SNPs. However, since the SNP-based method focuses on a single SNP at a time, it is less powerful to detect a gene whose SNPs have weak marginal effects, but a strong joint effect. In our analysis, 207 genes passed the relaxed gene-based threshold, whereas only 64 genes passed the relaxed SNP-based threshold.

Both the SNP-based and gene-based methods can be conducted conveniently in commonly available software, such as PLINK [45] for the SNP-based method and KGG [46] for the gene-based method. For the SNP-based analysis, PLINK is the most convenient platform. For the SAGE GWAS data, it took about 25 minutes to do a genome-wide SNP scan on a regular desktop computer (Intel Core 2, 4 GB Memory). In our gene-based analysis, we used the SNP-based association results and the linkage disequilibrium (LD) files from PLINK as the input to the KGG software. After this preparation, it took about 30 minutes to perform the gene-based association scan with the same desktop as mentioned above.

Authors’ Contributions

X. Guo and Z. Liu are contributed equally to this work.

Acknowledgments

This work was supported by Grant R01 DA016750-09 from the National Institute on Drug Abuse. Funding support for the Study of Addiction: Genetics and Environment (SAGE) was provided through the NIH Genes, Environment and Health Initiative (GEI) (U01 HG004422). SAGE is one of the genome-wide association studies funded as part of the Gene Environment Association Studies (GENEVA) under GEI. Assistance with phenotype harmonization and genotype cleaning, as well as with general study coordination, was provided by the GENEVA Coordinating Center (U01 HG004446). Assistance with data cleaning was provided by the National Center for Biotechnology Information. Support for the collection of datasets and samples was provided by the Collaborative Study on the Genetics of Alcoholism (COGA; U10 AA008401), the Collaborative Genetic Study of Nicotine Dependence (COGEND; P01 CA089392), and the Family Study of Cocaine Dependence (FSCD; R01 DA013423). Funding support for genotyping, which was performed at the Johns Hopkins University Center for Inherited Disease Research, was provided by the NIH GEI (U01HG004438), the National Institute on Alcohol Abuse and Alcoholism, the National Institute on Drug Abuse, and the NIH contract ‘‘High throughput genotyping for studying the genetic contributions to human disease’’ (HHSN268200782096C). The datasets used for the analyses described in this paper were obtained from dbGaP at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000092.v1.p1 through dbGaP accession number phs000092.v1.p. The authors have no conflict of interests.

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Copyright © 2012 Xiaobo Guo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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