Volume 3 Supplement 7
Genome-wide association study for empirically derived metabolic phenotypes in the Framingham Heart Study offspring cohort
© Wilcox et al; licensee BioMed Central Ltd. 2009
Published: 15 December 2009
We used data reduction and clustering methods to identify five phenotypically homogeneous groups of study participants with similar profiles for cardiovascular disease risk factors. We constructed both qualitative (binary subgroup membership) and quantitative traits (probability of subgroup membership) for each individual. The Cluster 1 comprised individuals who were generally healthy and had some history of smoking. Cluster 2 was dropped from the analyses due to the preponderance of missing data. Cluster 3 was used as the control group, healthy non-smokers. Members of Cluster 4 had features of the metabolic syndrome and were generally not as obese as Cluster 5. Obesity was the hallmark of Cluster 5, the members of which also had some features of the metabolic syndrome.
We then examined the genetic associations with both qualitative and quantitative representations of these empirically derived traits. Genetic analyses of the qualitative traits were conducted, comparing each of the affected groups with the unaffected cluster alone and, to increase statistical power, the unaffected group and healthy smokers combined. One single-nucleotide polymorphism on chromosome 4 met a conservative genome-wide significance level, but the effect was muted when we accounted for population stratification. The results for the quantitative traits were similar, with a small number of genome-wide significant findings muted by control for admixture. The directional findings will provide the basis for hypothesis generation for syndromes such as the metabolic syndrome and obesity.
The identification of subtypes of disease using data reduction and clustering methods has been helpful for identifying genetic associations in schizophrenia, rheumatoid arthritis, and other disorders [1–3].
The Framingham Heart Study (FHS) is an ongoing longitudinal study focusing on the development of coronary heart disease and associated risk factors in Framingham, MA. The long history of research conducted in Framingham has contributed to the contemporary understanding of cardiovascular and related diseases. One advantage of this study is that the ascertainment criteria do not require disease at the time of study entry. In addition, this is a random sample of households and not restricted to those seeking healthcare for any specific complaint.
Our analyses of the data made available to participants in the Genetic Analysis Workshop (GAW) 16 were restricted to members of the Offspring Cohort because some measures of metabolic function were not available in the Original Cohort and were not available for more than one measurement period in the Generation 3 Cohort.
The objectives of this study were 1) to identify subgroups of study participants with similar phenotypic characteristics (or syndromes) including patterns across measurements at multiple visits, and 2) to construct qualitative and quantitative representations of the new phenotypic subgroups, and 3) to conduct genome-wide association analyses of the quantitative traits; and for qualitative traits, to compare the newly identified affected phenotypic groups with unaffected controls.
We created categorical variables using the Centers for Disease Control (CDC) definitions for each of the following for each exam: body mass index (BMI; underweight, normal weight, overweight, or obese), high cholesterol (measured or on lipid lowering medication), low high-density lipoprotein (HDL), high triglycerides, and hypertension (measured or on medication) . These variables, along with categorical representations of smoking (current, ever, never), diabetes (yes, no), treatment for hypertension, treatment for high cholesterol, and heart disease (yes, no), were the basis for the data reduction and clustering.
The strategy for the development of qualitative traits included nonparametric data reduction, iterative two-staged clustering on the observed dimensions, and the assignment of binary membership in each cluster for each individual. Quantitative traits (probability of cluster membership) were estimated using logistic regression with cluster membership as the outcome and all variables used for clustering as predictor variables in the models.
We used multiple-correspondence analysis (MCA) for data reduction instead of the more traditional principal-components analysis (PCA). PCA is a method commonly used for data reduction. These data did not meet the distributional assumptions for a Pearson correlation, the basis for PCA. A similar method designed for use with categorical data was employed. MCA is a nonparametric data reduction method free of the assumptions underlying PCA and was developed for qualitative data. The objective of MCA is to identify a low-dimensional subspace that comes closest to all of the data points. It is analogous to graphing the results of a factor analysis in a multidimensional euclidean space. However, the space identified in MCA is not euclidian. The coordinates of each individual in the identified multi-dimensional space served as the basis for the identification of subgroups or clusters .
Each study participant with phenotype data on two or more visits was assigned a score on each of the 22 dimensions retained based upon the eigenvalues (data not shown). Next, a multi-staged clustering strategy was used to identify distinct subgroups . It is not unusual for groups identified with clustering techniques to be subject to the idiosyncrasies of the estimation data set. In an attempt to mitigate that difficulty, we first conducted repeated k-means clustering with different random cluster seeds and used a larger k (number of clusters) than we expected in the data. Groups that consistently clustered together across all of the initial analyses were identified as intact clusters. An agglomerative hierarchical clustering algorithm was then implemented using the intact clusters and the remaining individuals in the sample. An examination of the change in Ward's aggregation criterion and the nature of the groups was used to choose the final cluster structure [5, 6]. SPAD software  was used for both the MCA and the clustering algorithms. SAS software  was used to compute quantitative traits and for subgroup comparisons.
Genotype data preparation
There were 6,848 individuals with genotype data from Affymetrix 500 k platform (500,568 single-nucleotide polymophisms (SNPs)). Quality control for the genotype data was conducted at both subject and SNP level. At the subject level, we retained subjects with call rates greater than 0.90. Sex discrepancies were evaluated using the heterozygosity rate of X-chromosome SNPs and comparing with the phenotype data. Only subjects from the second generation were kept, and one subject from each pair of family members or cryptic relatedness was retained in the subsequent analysis. At the SNP level, we retained SNPs with a call rate greater than 0.90, a minor allele frequency of at least 0.01, and Hardy-Weinberg equilibrium p-value greater than 9.99 × 10-8 (i.e., 0.05/(no. of SNPs tested)). We also excluded SNPs that could not be mapped to reference genome assembly. After data quality control, there were 1,754 subjects and 418,411 SNPs retained in the final dataset.
PCA was used to examine population stratification. This analysis was performed using EIGENSOFT 2.0 [9, 10]. Theoretically, the leading principal component should reflect population structure. We noticed that some of the leading axes appeared to be dominated by a set of markers in a very small region that showed extended linkage disequilibrium. To deal with this problem, we applied a modified version of the PCA as described by Fellay et al. . The method we used is described in detail by Wang et al. .
PCA was performed in each of the analysis sets separately to derive significant principal components that represented the population structure in the analysis set. Population stratification (admixture) was controlled in subsequent analyses by including the final set of 18 significant components as covariates.
Genome-wide association (GWA) analyses
GWA analyses were performed using PLINK 1.03 . An additive genetic model was assumed for all GWA analyses. Each of the newly derived affected subgroups was compared with the identified control group separately using allelic chi-square tests in the absence of principal-component adjustment and logistic regression, including significant principal components derived above as covariates to control for admixture. A threshold of 4.2 × 10-7 was used for genome-wide significance based on a Bayesian formula as described by Lencz et al. .
Among the 2,760 study participants in the Offspring Cohort, five clusters were identified. Cluster 1 comprised individuals who were generally healthy and had some history (current or past) of smoking (n = 949, 34.4% [of the sample]). Cluster 2 (n = 365, 13.2%) comprised individuals who were missing information on two or more measurements. This group was omitted from the genetic analyses. Cluster 3 comprised healthy non-smokers (n = 597, 21.6%). This group served as the control group in our genetic association studies. Cluster 4 (n = 376, 13.6%) comprised individuals with features of the metabolic syndrome (MS) who were generally not obese (using the Centers for Disease Control definition of BMI of 30 or greater ). Obesity was the hallmark of the Cluster 5 (n = 473, 17.1%), the members of which also had some features of the MS. MS, as identified by the National Cholesterol Education Program's Adult Treatment Panel III, is a clustering of risk factors that can lead to cardiovascular disease (CVD). The risk factors include: abdominal obesity, atherogenic dyslipidemia, raised blood pressure, insulin resistance with or without glucose intolerance, proinflammatory state, and prothrombotic state .
We compared the MS and Obese groups with the healthy control group, and, to increase power (power calculations not shown), with the healthy control and healthy smokers combined. We used a fairly conservative approach to correct population stratification (18 principal components). Neither of the analyses using the controls alone revealed SNPs with p-values at or beyond the genome-wide significance level (data not shown). There was one genome-wide significant SNP on chromosome 4 when we used the larger comparison group. However, this finding was muted when we accounted for population stratification.
Our analyses of the 50 k chip showed similar results (data not shown). For the quantitative trait for the MS-like group there were five results across the genome with p < 1 × 10-5; similarly, there were eight for the Obese group. In both cases the findings were somewhat muted when we accounted for admixture.
We identified five phenotypic clusters using a limited set of measures pertaining to medical history, metabolic function, and environmental exposures. One group was omitted due to missing data. Two groups appeared to be relatively healthy, one of which was more inclined toward tobacco use than the other. The remaining two groups were characterized by elevated measures related to MS and obesity. Interestingly, those characterized by features of MS were not as heavy, nor did they gain weight as quickly over time as did the Obese group. Features associated with MS were not as prevalent in the group characterized by obesity as they were in the other affected cluster.
There are several limiting factors in our analyses. We used a conservative approach for the correction of population stratification. We also used a somewhat conservative approach for genome-wide significance levels. It would be interesting to see these results using an empirical p-value instead.
Next steps in these analyses will be to use the results for hypothesis generation and to also examine regions with suggestive findings for genes that have been implicated in metabolic disorders and obesity.
We identified distinct clusters of individuals with different manifestations of metabolic disorders. Genetic association analyses revealed several regions for further investigation.
List of abbreviations used
Body mass index
Framingham Heart Study
Genetic Analysis Workshop
High density lipoproteins
Multiple correspondence analysis
The Genetic Analysis Workshops are supported by NIH grant R01 GM031575 from the National Institute of General Medical Sciences.
This article has been published as part of BMC Proceedings Volume 3 Supplement 7, 2009: Genetic Analysis Workshop 16. The full contents of the supplement are available online at http://www.biomedcentral.com/1753-6561/3?issue=S7.
- Wilcox MA, Faraone SV, Su J, VanEerdewegh P, Tsuang MT: Genome scan of three quantitative traits in schizophrenia pedigrees. Biol Psych. 2002, 52: 847-854. 10.1016/S0006-3223(02)01465-8.View ArticleGoogle Scholar
- Wilcox MA, McAfee AT: Empirically derived subgroups in rheumatoid arthritis - association with SNPs on chromosome 6. BMC Proc. 2007, 1 (suppl 1): S20-10.1186/1753-6561-1-s1-s20.PubMed CentralView ArticlePubMedGoogle Scholar
- Kranzler HR, Wilcox MA, Weiss RD, Brady K, Hesselbrock V, Rounsaville B, Farrer L, Gelernter J: The validity of cocaine dependence subtypes. Addict Behav. 2008, 33: 41-53. 10.1016/j.addbeh.2007.05.011.PubMed CentralView ArticlePubMedGoogle Scholar
- Centers for Disease Control and Prevention: Overweight and Obesity. [http://www.cdc.gov/nccdphp/dnpa/obesity/defining.htm]
- Greenacre M: Theory and Applications of Correspondence Analysis. 1984, New York, WileyGoogle Scholar
- LeBart L, Morineau A, Warwick K: Multivariate Descriptive Statistical Analysis: Correspondence Analysis and Related Techniques for Large Matrices. 1984, New York, WileyGoogle Scholar
- CISIA: SPAD version 6. 2005, Paris, CISIAGoogle Scholar
- SAS Institute Inc: Program Guide. Version 9.2. 1989, Cary, NC, SAS Institute IncGoogle Scholar
- Patterson N, Price AL, Reich D: Population structure and eigenanalysis. PLoS Genet. 2006, 2: e190-10.1371/journal.pgen.0020190.PubMed CentralView ArticlePubMedGoogle Scholar
- Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet. 2006, 38: 904-909. 10.1038/ng1847.View ArticlePubMedGoogle Scholar
- Fellay J, Shianna KV, Ge D, Colombo S, Ledergerber B, Weale M, Zhang K, Gumbs C, Castagna A, Cossarizza A, Cozzi-Lepri A, De Luca A, Easterbrook P, Francioli P, Mallal S, Martinez-Picado J, Miro JM, Obel N, Smith JP, Wyniger J, Descombes P, Antonarakis SE, Letvin NL, McMichael AJ, Haynes BF, Telenti A, Goldstein DB: A whole-genome association study of major determinants for host control of HIV-1. Science. 2007, 317: 944-947. 10.1126/science.1143767.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang D, Sun Y, Stang F, Berlin JA, Wilcox MA, Li Q: Comparison of methods for correcting population stratification in a genome-wide association study of rheumatoid arthritis: principal-component analysis versus multidimensional scaling. BMC Proc. 2009, 3 (suppl 7): S109-10.1186/1753-6561-3-s7-s109.PubMed CentralView ArticlePubMedGoogle Scholar
- Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007, 81: 559-575. 10.1086/519795.PubMed CentralView ArticlePubMedGoogle Scholar
- Lencz T, Morgan TV, Athanasiou M, Dain B, Reed CR, Kane JM, Kucherlapati R, Malhotra AK: Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Molec Psych. 2004, 12: 572-580. 10.1038/sj.mp.4001983.View ArticleGoogle Scholar
- Grundy S, Brewer H, Cleeman J, Smith S, Lefant C: Definition of metabolic syndrome. Circulation. 2004, 109: 433-438. 10.1161/01.CIR.0000111245.75752.C6.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.