Volume 9 Supplement 1

Selected articles from the 5th Translational Bioinformatics Conference (TBC 2015): medical genomics

Open Access

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

  • Anurag Verma1, 2Email author,
  • Shefali S. Verma1, 2Email author,
  • Sarah A. Pendergrass2,
  • Dana C. Crawford4,
  • David R. Crosslin5,
  • Helena Kuivaniemi3,
  • William S. Bush4,
  • Yuki Bradford1,
  • Iftikhar Kullo8,
  • Suzette J. Bielinski8,
  • Rongling Li9,
  • Joshua C. Denny6,
  • Peggy Peissig7,
  • Scott Hebbring7,
  • Mariza De Andrade8,
  • Marylyn D. Ritchie1, 2 and
  • Gerard Tromp3
BMC Medical GenomicsBMC series – open, inclusive and trusted20169(Suppl 1):32

https://doi.org/10.1186/s12920-016-0191-8

Published: 12 August 2016

Abstract

Background

We explored premature stop-gain variants to test the hypothesis that variants, which are likely to have a consequence on protein structure and function, will reveal important insights with respect to the phenotypes associated with them. We performed a phenome-wide association study (PheWAS) exploring the association between a selected list of functional stop-gain genetic variants (variation resulting in truncated proteins or in nonsense-mediated decay) and an extensive group of diagnoses to identify novel associations and uncover potential pleiotropy.

Results

In this study, we selected 25 stop-gain variants: 5 stop-gain variants with previously reported phenotypic associations, and a set of 20 putative stop-gain variants identified using dbSNP. For the PheWAS, we used data from the electronic MEdical Records and GEnomics (eMERGE) Network across 9 sites with a total of 41,057 unrelated patients. We divided all these samples into two datasets by equal proportion of eMERGE site, sex, race, and genotyping platform. We calculated single effect associations between these 25 stop-gain variants and ICD-9 defined case-control diagnoses. We also performed stratified analyses for samples of European and African ancestry. Associations were adjusted for sex, site, genotyping platform and the first three principal components to account for global ancestry. We identified previously known associations, such as variants in LPL associated with hyperglyceridemia indicating that our approach was robust. We also found a total of three significant associations with p < 0.01 in both datasets, with the most significant replicating result being LPL SNP rs328 and ICD-9 code 272.1 “Disorder of Lipoid metabolism” (pdiscovery = 2.59x10-6, preplicating = 2.7x10-4). The other two significant replicated associations identified by this study are: variant rs1137617 in KCNH2 gene associated with ICD-9 code category 244 “Acquired Hypothyroidism” (pdiscovery = 5.31x103, preplicating = 1.15x10-3) and variant rs12060879 in DPT gene associated with ICD-9 code category 996 “Complications peculiar to certain specified procedures” (pdiscovery = 8.65x103, preplicating = 4.16x10-3). 

Conclusion

In conclusion, this PheWAS revealed novel associations of stop-gained variants with interesting phenotypes (ICD-9 codes) along with pleiotropic effects.

Background

Genetic variations can result in changes in the success of transcription and translation, as well as modification of the structure and function of resulting proteins. These changes are also responsible for potential downstream effects across pathways and ultimately affecting phenotypic outcomes. Thus, exploring the associations between functional genetic variants and a number of phenotypes can be helpful in highlighting the impact of genetic architecture on outcomes in a more biologically interpretable manner. A number of resources for identifying the function of genetic variants on transcription, translation, protein structure and function have emerged, providing a way to highlight genetic variants that likely have an impact on protein structure or function. Loss-of-function or gain-of-function variants are responsible for changing the function of protein products, and these functional variants have been shown to be important for identifying clinically relevant associations in pharmacogenetic studies [1, 2]. Nonsense mutations result in premature termination of translation that result in the production of in non-functional polypeptides [3]. Variations that result in new stop-codon are referred to as stop-gain variants. Stop-gain variants have been shown to be associated with Mendelian diseases in the OMIM database [4]. Thus, there is the potential for stop-gain variants to explain stronger effects than other types of variants [5] In this study, we applied an approach to explore phenotypes conditional on genotypes, namely phenome wide association study (PheWAS).

PheWAS evaluates associations between selected genetic variants and an extensive set of phenotypes and thus is an effective approach. This approach has been successfully used to identify disease associations using EHR (Electronic Health Record) -based phenotype data [6, 7]. PheWAS has also been implemented within epidemiological and clinical trials datasets and has become an important tool for identifying novel associations as well as discovering pleiotropic effects [811]. PheWAS can identify associations across multiple phenotypes, where genetic variation is associated with more than one phenotype, some of which may be due to pleiotropy [12] and also some that are observed through multiple GWA studies can thus be identified with this approach. An example includes variation in the human leukocyte antigen (HLA) region known to be associated with variety of autoimmune diseases [13]. PheWAS has been shown to be effective at identifying cross-phenotype associations (pleiotropic associations) of functional variants [14]. In this study, we hypothesized that stop-gain variants are more likely to impact clinically relevant outcomes compared with the common variants targeted by genome-wide genotyping arrays. Therefore, to identify associations between EHR-based phenotypes and stop-gain variants, we performed a PheWAS between 25 selected stop-gain variants and multiple phenotypes in EHR data and to determine whether one or more of these putative functional variants are associated with any clinical conditions. Unlike GWAS studies where the clinical relevance of identified variants is difficult to explain, with this study we aimed at study only clinical or scientific relevant variants and its association with a comprehensive list of ICD-9 diagnoses codes. The Electronic MEdical Records and GEnomics (eMERGE) is a large dataset consisting of many sites where samples are also genotyped on various platforms. We provide a first of its kind approach to describe methods and challenges in investigating samples from various demographic regions within USA.

Methods

Study dataset

For the study we used the imputed genotype data available from the electronic medical records and genomics (eMERGE) network [15]. The eMERGE Network consists of 9 sites that are aimed at identifying genotype associations using phenotype data from the EHR [16]. The eMERGE Network consists of 55,289 samples genotyped across multiple platforms and imputed to 1000 Genomes reference panel covering ~18 million variants with age of participants ranging from infants to above 90 years of age. In order to identify relevant associations and replications, we used 41,057 adult samples (≥19 years of age) from the eMERGE Network. EHRs contain a variety of kinds of data, including International Classification of Diseases, Ninth Revision (ICD-9) codes, clinical lab variables, medication, demographics etc. ICD-9 codes classify variety of signs, symptoms, diseases, and injuries. In this study, we used ICD-9 diagnosis codes to define case/control status for a variety of conditions. Since samples in eMERGE were genotyped on several different platforms, genotypic imputation was performed on these datasets to combine them. eMERGE data were imputed using IMPUTE2 [17] with phasing done using SHAPEIT2 [16].

Discovery and replication dataset

To obtain highly robust results from this PheWAS, we divided the eMERGE dataset into a discovery and replication set using a random sampling approach. Samples in eMERGE are from diverse populations and several genotyping platforms were used in the analysis. Therefore, in order to consider confounding factors when dividing the data, we used a stratified sampling strategy to reduce the impact of potential biases that could arise after dividing the data due to extreme diversity in the dataset. We proportionately allocated samples by each stratum; where stratum is a class to which samples were distributed by sex, eMERGE site, genotyping platform, and race/ethnicity. We had a total of 21,085 samples in the discovery set and 21,065 samples in the replication dataset. Additional file 1: Table S1 shows the distribution of samples across each dataset by each stratum before quality control was performed on samples.

Quality control of genetic data

We used samples from eMERGE phase I and II. Samples from all sites in eMERGE I were genotyped on one of two platforms (Illumina 660 and 1 M) and in eMERGE-II, samples from all sites (9 sites) were genotyped on different platforms (a total of 9 different platforms) [15, 18, 19]. The overlap among the SNPs from different genotyping platforms was fairly small (about 20,000 SNPs), thus each dataset was imputed to enable robust combination of datasets. Described in detail in a previous publication, we imputed all samples using IMPUTE2 best practices guidelines and 1000 Genomes reference panel [20] which resulted in approximately 38 million variants across the entire dataset. Identity by decent (IBD) estimation was performed using PLINK’s method of moment in R package SNPrelate [21] in order identify and remove related samples from further analysis. The evaluation of relatedness was more appropriate after dividing the eMERGE dataset because there are known sample relationships from some sites and IBD estimation after randomly dividing the dataset dropped fewer samples. One member from a pair of individuals with kinship coefficient > 0.125 was removed which resulted in 20,526 and 20,531 unrelated samples in discovery and replication datasets respectively. Principal Component Analysis (PCA) was performed using smartpca program in Eigensoft package [22]. The first three principal components or eigenvectors were then used to adjust models for global ancestry.

Identifying stop-gain variants

To determine the functional impact of the all variants, we first annotated all SNPs that passed QC criteria with six bioinformatics annotation and prediction tools i.e., SNPeff [23], ANNOVAR [24], GEMINI [25], Variant effect predictor [26], VAT [27] and SeattleSeq [28]. The results of variant function predicted across these tools were quite different for the SNPs of this study as shown in Additional file 2: Table S2. As observed by others, functional prediction tools differ in their predictions [29]. To obtain a more robust measure of functionality of these eMERGE SNPs, we thus queried all genetic variants of this study against all stop-gain variants found in dbSNP137 and identified 225 stop-gain variants in our data. We then compared these dbSNP-annotated variants with the cross tissue average of every transcript generated from Illumina BodyMap 2.0 project data [30]. Within the Illumina BodyMap project there are 16 different tissues with RNAseq data and we considered the most widely expressed transcript as the most canonical transcript. After this filtering step, a total of 46 likely loss-of-function stop-gain variants were selected. To serve as positive controls, we included 9 additional SNPs with known association with traits. The list of 46 likely stop-gain variants and 9 proof-of-principle SNPs, were then extracted from both discovery and replication datasets. Variants below minor allele frequency (MAF) threshold of 0.005 were filtered out, thus resulting in total of 25 variants that were considered for association testing. Out of the 25 variants selected, 20 were identified through the annotation pipeline as stop-gain variants and five variants (Table 1) were used as positive controls for proof-of-concept validation.
Table 1

Proof of concept null variants. Note that ICD-9 codes are not shown for all traits because there is not a known association with an ICD-9 code for all traits

SNP

Gene

aTrait Previously Associated

rs328

LPL

Pure hyperglyceridemia (ICD9 272.1) [14]

rs2814778

DARC

White Blood Cell count [47]

rs1815739

ACTN3

Dystrophinopathy [48], type 2 diabetes [49]

rs16910526

CLEC7A

Inflammatory bowel disease [50], candidiasis [51], aspergillosis [52]

rs601338

FUT2

Gastroenteritis [53], Crohn’s disease [53]

aICD-9 codes are not shown for all traits because there is not a known association with an ICD-9 code based definition of the condition

Phenotype data

The phenotypic data consisted of 11,879 distinct ICD-9 codes for 41,057 individuals with genotype data. We defined case-control status for each ICD-9 code, where a case status is assigned when an individual has ≥ 3 instances of an ICD-9 code and control status is assigned based on the absence of an ICD-9 code. In cases of samples with more than one but fewer than three ICD-9 code instances, we removed them from analysis for that ICD-9 code. We further excluded the ICD-9 diagnoses that were present in fewer than 10 individuals. Using these filtering criteria on ICD-9 code data, there were 20,526 samples and 2,879 ICD-9 codes in the discovery dataset and 20,531 samples and 2,854 distinct ICD-9 codes in the replication dataset.

Association testing

We conducted standard and penalized regression in the discovery and replication dataset separately using PLATO (http://www.ritchielab.psu.edu/software/plato-download) and we adjusted the models for sex, site, platform, and the first three principal components to account for global ancestry. In the discovery dataset, we performed association testing with penalized logistic regression between 25 SNPs and 2,859 ICD-9 based case/control status and in the replication dataset 2,854 ICD-9 codes were included. Results of tests of association were visualized using Synthesis-View [31]. Because some of the SNPs might have shown association in one racial/ancestry group compared to another, and one of our proof-of-concept SNPs is more prevalent in people of African ancestry (DARC variant rs2814778) we also performed association testing stratified by the two largest racial/ethnic groups in the present study: European ancestry (EA) and African ancestry (AA).

ICD-9 codes classify diagnoses; there are three digit ICD-9 codes that specify disease categories (e.g. code 405 for “secondary hypertension”) that can are further be further subdivided using multiple four or five digit sub- ICD-9 codes (e.g. 405.1 for “benign secondary hypertension”, 405.11 “benign renovascular hypertension”). We therefore analyzed results based on replication requiring the exact ICD-9 code for more specific replication (three to five digit sub- ICD-9 codes), as well as evaluating results based on replication requiring only the same three digit ICD-9 code category, a more broad replication for a given case/control diagnosis. For seeking replication, we required a P < 0.01 with the same direction of genetic effect in both the testing discovery and replication dataset for the same SNP, and the same 3-digit ICD-9 code category as well as the exact same code (from three digit to 5 digit). Complete pipeline of the process from selecting of variants to running association analysis is shown in Fig. 1.
Fig. 1

Flowchart showing the analysis pipeline for PheWAS on functional variants in eMERGE data

Results

Association analyses for the discovery and replication datasets were performed independently. We performed both standardized and penalized regression analyses, however, standard regression failed due to complete or quasi-complete separation. Therefore, we describe results from only penalized logistic regression in the sections below. On the individual dataset level we identified 192 SNP-diagnoses associations in the discovery set and 195 SNP-diagnosis associations in replication dataset with a p < 0.01, at the 5-digit level ICD-9 code level (Additional file 3: Table S3 and Additional file 4: Table S4).

The most significant association in the discovery dataset was the association between ICD-9 coded 272.1 “Pure hyperglyceridemia” and the proof-of-principle LPL SNP rs328 (P = 2.59 × 10-6, OR = 0.52 [95 % CI: 0.39, 0.70]), replicating a previously published association for this SNP. The most significant association in the replication dataset was between the SNP rs601338 in CC2D2A gene with ICD-9 code 266.2 “B-complex deficiencies” with P = 3.73 × 10-5, OR = 0.74 [0.64, 0.85]. SNP rs601338 is in high LD with a non-synonymous common variant rs602662 which has a known association with plasma vitamin B12 [32].

We sought replication of results between the discovery and replication datasets at the three-digit level (more broad ICD-9 code level) as well as for the exact ICD-9 code (anywhere from the exact 3 digit to 5 digit code for a given association).

Only one association was found replicating at the 5-digit “exact” ICD-9 code level. A total of three associations replicated at the broader 3 digit ICD-9 level with P < 0.01 and same direction of genetic effect (Fig. 2).
Fig. 2

Synthesis-view plot for all replicating results based on 3 digit ICD-9 code category defined conditions from adults and EA for all adults tested and for European American (EA) adults analysis. Labels on the y-axis are SNP-ICD9 code category –Description of ICD9 code. This plot shows p-value in both datasets (discovery dataset in blue and replicating dataset in red) and the direction of triangle represents the direction of genetic effect of the association

We also included proof-of-principle variants that have known association with disease, and evaluated how well we replicated known associations for these variants. As previously mentioned, the most significant result in the discovery dataset was for LPL SNP rs328, and ICD9 code 272.1. This result replicated with P = 2.7 × 10-4. The SNP rs328 is a premature stop codon in gene LPL (lipoprotein lipase) known to be associated with lipid metabolism [33, 34]. In analyses including all adults, we did not find replication for any other proof-of-principle SNPs that were included in our list of variants. Among the novel results consistently associated in both the discovery and replication datasets at the 3-digit level was a variant in KCNH2 (rs1137617) a gene known to cause long QT syndrome with ICD-9 codes 244 “Acquired hypothyroidism” (Pdiscovery = 5.31x 10-3 and Preplication = 1.15x10-3).

Stratified analyses among European-American adults resulted in seven associations replicating by the 3 digit ICD-9 code category criteria (Fig. 1). Among the top associations was KCNJ11 SNP rs5219 and ICD-9 368 “Visual Disturbances” with discovery P = 6.6 × 10-4 and replication P =2.5 × 10-3. Interestingly, we observed that majority of the samples that were case for ICD-9 code 368 also had diagnosis for Diabetes Mellitus (ICD-9 code category 250). KCNJ11 rs5219 is known to be associated with Type 2 diabetes [3537], thus suggesting a potential interesting link between visual disturbances and diabetes. We found the association between LPL rs328 and disorders of lipid metabolism again in the European American adult analyses for both discovery and replication datasets (P = 2.8 × 10-3 and 9.91 × 10-5, respectively). We did not find any statistically significant associations replicating for the African Americans adult analyses.

Discussion

In this study, we focused on examining the effect of stop-gain variants on disease using a PheWAS approach. Stop-gain variants were selected for this analysis because these are high impact variants and they are expected to be clinically relevant [38, 39]. PheWAS has been proven as an effective approach in identifying already known associations as well as novel associations. We identified three novel associations along with replicating an already known association between a variant in LPL gene (rs328) and pure hyperglycedemia [33].

As mentioned above, we calculated associations by performing both standardized as well as penalized logistic regression in both discovery and replication dataset separately using PLATO after adjusting the models for sex, site, platform and the first 3 principal components. The reason behind conducting analyses by two methods is that none of the models from standardized regression converged. Non-convergence is an issue in logistic regression that occurs when likelihood maximization algorithm fails and the estimates from such regression are questionable [40]. The cause of non-convergence is due to certain data patterns leading to complete or quasi-complete separation [40] i.e. when the outcome variable completely separates the predictor variable. As described, the merged imputed data consisted of multiple sites and platforms. Therefore, we adjusted our regression model by site and platform to account for any confounding biases. Upon further investigation, we found that many ICD-9 codes had either “0” cases or “0” controls for one or more categories (site and platform), causing quasi-complete separation. A penalized maximum likelihood estimation approach proposed by David Firth allows solving separation problem and provides converged model [41]. Thus, we implemented Firth regression into PLATO and repeated the association testing with this new-method.

For our novel results meeting our criteria for replication across the two datasets with a match on ICD-9 codes category, we identified a novel association between KCNH2 SNP rs1137617 and acquired hypothyroidism (ICD-9 code 244). The KCNH2 gene is known to be associated with long QT syndrome. Prolonged QT intervals are also known to be affected due to thyroid stimulating hormone and it has also been observed that patients with hypothyroidism show higher QT dispersions [42, 43]. Thus, this association between KCNH2 and hypothyroidism is of potential interest.

In European Americans we identified seven associations that replicated. Among these, replicating results, we found potentially pleiotropic associations for SNP rs1861050 in CC2D2A gene and the diagnoses of osteoporosis and edema.

Another interesting association was between KCNJ11 gene and visual disturbances. KCJN11 gene is critical in regulation of insulin and is known to be associated with type 2 diabetes mellitus [44, 45]. Genome-wide association studies have found polymorphism in KCNJ11 (rs5219) to be associated with diabetic retinopathy [46] which may be related to the visual disturbances association identified in the current study.

PheWAS is a method to generate hypotheses by testing a selected set of SNPs and many phenotypes and thus there remains the challenge of correcting for multiple testing. One way to correct for multiple tests is by using Bonferroni correction; however, this is often not appropriate in PheWAS due to the non-independence of the SNPs as well as the phenotypes being tested. In order to address the challenge of multiple testing corrections without using a Bonferroni correction, we instead sought replication of associations by dividing the data into two independent dataset to identify consistent and replicating associations. A limitation of this study was the selection of only 25 null variants. An additional limitation is the selection of only ICD-9 codes. It is possible that with richer, more robust phenotypes, many novel associations would be identified.

Even with these shortcomings, this study design and analysis strategy may provide a more comprehensive exploration of the clinical relevance of known “functional” elements in the genome. Future work should include a substantial expansion of functional variants of interest, based on both protein coding and gene regulation relevance.

Declarations

Declaration

Publication of this article has been funded by eMERGE Network. The eMERGE Network was initiated and funded by NHGRI through the following grants: U01HG006828 (Cincinnati Children’s Hospital Medical Center/Boston Children’s Hospital); U01HG006830 (Children’s Hospital of Philadelphia); U01HG006389 (Essentia Institute of Rural Health, Marshfield Clinic Research Foundation and Pennsylvania State University); U01HG006382 (Geisinger Clinic); U01HG006375 (Group Health Cooperative/University of Washington); U01HG006379 (Mayo Clinic); U01HG006380 (Icahn School of Medicine at Mount Sinai); U01HG006388 (Northwestern University); U01HG006378 (Vanderbilt University Medical Center); U01HG006385 (Vanderbilt University Medical Center serving as the Coordinating Center); and U01HG004438 (CIDR) and U01HG004424 (the Broad Institute) serving as Genotyping Centers.

This article has been published as part of BMC Medical Genomics Volume 9 Supplement 1, 2016. Selected articles from the 5th Translational Bioinformatics Conference (TBC 2015): medical genomics. The full contents of the supplement are available online https://bmcmedgenomics.biomedcentral.com/articles/supplements/volume-9-supplement-1.

Availability of data and materials

Results are shared in the additional files.

Authors’ contributions

AV and SSV equally contributed in designing and performing analysis workflow and manuscript writing. SAP assisted with method design. DCC, HK, WSB assisted with selection of null variants. YB assisted with variant annotation software packages. DRC, IK, SJB, RL, JCD, PP, SH, MA assisted with data collection and data generation. MDR AND GT conceptualized and led the project. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interest.

Consent for publication

Not Applicable.

Ethics approval and consent to participate

Not Applicable.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Biochemistry and Molecular Biology, Center for Systems Genomics, Pennsylvania State University
(2)
Biomedical and Translational Informatics, Geisinger Health System
(3)
Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University
(4)
Case Western Reserve University
(5)
Department of Medicine, Division of Medical Genetics, University of Washington
(6)
Vanderbilt University
(7)
Marshfield Clinic
(8)
Mayo Clinic
(9)
National Human Genome Research Institute

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