The genetic validation of heterogeneity in schizophrenia
© Tsutsumi et al; licensee BioMed Central Ltd. 2011
Received: 2 October 2010
Accepted: 7 October 2011
Published: 7 October 2011
Schizophrenia is a heritable disorder, however clear genetic architecture has not been detected. To overcome this state of uncertainty, the SZGene database has been established by including all published case-control genetic association studies appearing in peer-reviewed journals. In the current study, we aimed to determine if genetic variants strongly suggested by SZGene are associated with risk of schizophrenia in our case-control samples of Japanese ancestry. In addition, by employing the additive model for aggregating the effect of seven variants, we aimed to verify the genetic heterogeneity of schizophrenia diagnosed by an operative diagnostic manual, the DSM-IV.
Each positively suggested genetic polymorphism was ranked according to its p-value, then the seven top-ranked variants (p < 0.0005) were selected from DRD2, DRD4, GRIN2B, TPH1, MTHFR, and DTNBP1 (February, 2007). 407 Schizophrenia cases and 384 controls participated in this study. To aggregate the vulnerability of the disorder based on the participants' genetic information, we calculated the "risk-index" by adding the number of genetic risk factors.
No statistically significant deviation between cases and controls was observed in the genetic risk-index derived from all seven variants on the top-ranked polymorphisms. In fact, the average risk-index score in the schizophrenia group (6.5+/-1.57) was slightly lower than among controls (6.6+/-1.39).
The current work illustrates the difficulty in identifying universal and definitive risk-conferring polymorphisms for schizophrenia. Our employed number of samples was small, so we can not preclude the possibility that some or all of these variants are minor risk factors for schizophrenia in the Japanese population. It is also important to aggregate the updated positive variants in the SZGene database when the replication work is conducted.
Schizophrenia is a highly heritable disorder, but even its genetic architecture still remains unclear . In order to reveal the genetic involvement in the etiology, several research designs have been adopted. Linkage studies have not, however, found strongly linked loci . Alternatively, many association studies of schizophrenia have been performed because genetic association methods are a more powerful means for finding genes that are expected to have a small effect on risk for the disorder. Although many positive results were reported, most are never replicated extensively. To overcome this state of uncertainty, Bertram et al. assembled the SZGene database to aggregate the evidence for those genetic polymorphisms with the best, most reliable evidence for association with schizophrenia [3, 4]. SZGene is characterized by the inclusion of all published case-control genetic association studies appearing in peer-reviewed journals, and each association is evaluated using a uniform method of meta-analysis. This inclusive and consistent database renders sometimes ambiguous or amorphous bodies of evidence concrete, and highlights some of the most promising avenues for continued research by schizophrenia geneticists. From this database, we picked the most reliably associated variants, and sought to determine if these variants would be associated with risk for schizophrenia in our own case-control sample of Japanese ancestry. Consistent with a common-disease/common-variant hypothesis of the disorder, we would not hypothesize that each variant identified in SZGene would be a necessary component of the risk profile for schizophrenia in our sample, so we evaluated the independent and joint effects of the top seven variants. The objectives of this study were: 1) to determine if the top candidate genes for schizophrenia would show replicated evidence for a contribution to risk for the disorder; and 2) to see if the aggregate effect of these seven top variants was stronger than the individual effects of each variant alone.
Derived data from SZGene for investigated genes and polymorphisms
With regard to the genotyping procedure, Single nucleotide polymorphisms (SNPs) on the genomic DNA extracted from venous blood were identified by FRET method (Roche Diagnostics, Japan) according to the manufacture's protocol. The 120 bp Tandem Repeat polymorphism in DRD4 was detected by restriction fragment length polymorphism. Each primer and probe was provided on demand.
In addition to the analysis of each single polymorphism, we sought to aggregate the vulnerability of the disorder based on the participants' genetic information. The risk alleles of each of the seven top polymorphisms shown in SZGene were summated, such that an individual homozygous for a polymorphism's risk alleles was quantified as having a value of "2". The heterozygous genotype was given the value of "1", and the homozygote of non-risk alleles was coded "0". This scoring imparted an additive effect onto each variant, which was supported by the meta-analytic results in SZGene (although this may not be the true mode of inheritance of each gene's effect on risk, misspecification by an additive model is less costly than misspecification by other models). Each of the participants was additively scored from 0 to 14 according to their genetic vulnerability information from across all seven variants. This score was then entered as a predictor of case status in a logistic regression model, with the type-I-error rate fixed at 0.05.
P-value for the Individual SNPs and the Aggregation of Seven Variants
Individual SNPs(Fisher's exact test)
Aggregation of Seven SNPs(t-test)
p-value for Additive effect
p-value for Additive effect
Discussion and Conclusion
In this study, we utilized the evidence from the SZGene database to build very strong hypotheses of independent and joint effects of the top seven most strongly supported risk genes for schizophrenia. These hypotheses were roundly unsupported. While our results alone are not enough to invalidate the conclusions gleaned from the large body of evidence collated in SZGene, they do cast doubt about the strength of the documented associations. Several potential confounders may be able to explain our results.
The deviation from Hardy-Weinberg Equilibrium (X2, more than 3.84 represents the significant deviation from HWE at 0.05 p-value) and genetic power for investigated samples (prevalence = 0.008, type II error = 0.80, general 2df, alpha = 0.05)
Another caveat in interpreting our results regards the analytic models we employed. In the present study, in order to reduce the complexity, it was simply hypothesized that the attributable odds ratio for each polymorphism was 2, and we hypothesized that vulnerability could be calculated additively (however, we also evaluated a dominant model with similar negative results). It could be suspected that the mode of inheritance of schizophrenia is not simply additive, however no definitive model is identified so far [1, 5, 6]. Re-analyses of these data with other modes of inheritance specified (e.g., recessive, multiplicative) may have yielded different results more consistent with expectations based on SZGene.
A third caveat regarding interpretation of our study is the ancestry of our sample. All of our subjects were derived from a sample of Asian ancestry, Japanese, although the top seven variants were selected based on their collective evidence from all ancestral groups (though SZGene represents more Caucasian samples than Asian ones). Given the possibility that the current lack of detection derived from this discrepancy, we recalculated the top variants in SZGene from samples of only Asian ancestry. Within the seven variants, the majority of variants (four out of seven) were still significant in the Asian-only subsamples, and the other three variants had only been examined in Asian-ancestry samples once or twice previously, precluding definitive answers. These data imply that the investigated variants were deserving of further research both in general and in Asian samples specifically. Nevertheless our currently employed samples will not generalize to all samples evaluated by the schizophrenia geneticists so far.
With regard to the deviation from Hardy-Weinberg Equilibrium (HWE), the current result of genotyping in cases for 120bp Tandem Repeat in DRD4, and both in cases and controls for rs1801028 in DRD2 has shown the deviation from HWE (Table 4). Our finding on this article is not the simple positive association, therefore these deviations will not have a major influence on our overall conclusion. Although it is possible to expect that the deviated three group have false-negative association, we still conclude that our main finding will not be forced to change the fundamental direction.
Given these potential confounders it is keenly necessary to repeat this investigation in a larger, ethnically diverse population in order to validate (or invalidate) our model further. It is also important to aggregate the updated positive variants in the SZGene database when the replication work is conducted. Much work is needed in a collaborative effort in order to generate power to identify potential genetic markers for schizophrenia that transcend ethnicities and populations worldwide, if such exist. Studies of schizophrenia inevitably inherit the weaknesses of the current psychiatric nosology, which clinical observation (symptomatology) demands when we aimed to select the sample due to the lack of biological markers. Our current findings that there is no statistically significant deviation in the possession of "risk-conferring" alleles between schizophrenia and controls may have a chance to highlight the profound heterogeneity of the disorder of interest.
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