Introduction
Schizophrenia is a common and severely disabling psychiatric disorder where heritability is of considerable relevance in the aetiology of the disease [
9,
10,
43,
53]. One of the most replicated susceptibility genes for schizophrenia is the dysbindin-1 gene (
DTNBP1; OMIM *607145) on chromosome 6p22.3. Straub and collaborators first reported an association of
DTNBP1 (dystrobrevin-binding protein 1, or dysbindin) with schizophrenia in a family-based association analysis of High-Density Schizophrenia Families in Ireland ([
32], Irish Study of High-Density Schizophrenia Families ISHDSF) in 2002. Since then (and even before), numerous investigations have been realized to verify the role of
DTNBP1 as a schizophrenia susceptibility gene. While many genetic studies could replicate the association of
DTNBP1 with schizophrenia [
17,
34,
55,
61,
71,
74,
75,
83,
87], others failed to confirm the finding of Straub and colleagues [
50,
51,
67]. A meta-analysis authored by Li & He in 2007 only found a weak association of
DTNBP1 with schizophrenia [
36].
On the other hand, there is emerging evidence that
DTNBP1 might also play a role in the genetics of affective psychosis. Large genetic case–control association studies of European [
6,
19], Korean [
31,
56], and multiplex Ashkenazi Jewish family samples [
14] have shown a linkage of
DTNBP1 with bipolar disorder. However, in parallel to the state of research on schizophrenia, there are also negative association studies [
58].
So far, more than 20 different SNPs (single nucleotide polymorphisms) have been reported to be significantly associated with schizophrenia and/or bipolar disorder, either individually or within a haplotype [
19,
24]. However, there is widespread inconsistency among the associated
DTNPB1 haplotypes with a variety of combinations of SNPs and risk alleles reported throughout the literature [
82], complicated even more by large genetic differences between major geographic populations [
19,
24]. Thus, the question about the veritably underlying
DTNBP1 schizophrenia or other psychiatric susceptibility variants still remains [
82].
DTNBP1 encodes dysbindin-1 (β-dystrobrevin-binding protein or DTNBP1) [
4,
64], a 40- to 50-kDa protein expressed neuronally [
4] in many regions of the human brain [
66]. DTNBP1 binds both α- and β-dystrobrevin, which are components of the dystrophin glycoprotein complex [
4]. This complex is especially concentrated at postsynaptic densities [
4] in diverse brain areas [
4,
37], but only the β-dystrobrevin isoform is expressed in neurons [
4]. By means of binding β-dystrobrevin, DTNBP1 interacts with the dystrophin glycoprotein complex at postsynaptic sites and might thereby alter neuronal synaptic mechanisms. However, independent of β-dystrobrevin and the dystrophin glycoprotein complex, DTNBP1 has also been found to be presynaptically located in glutamatergic neurons in the hippocampus [
54,
69]. In this context, dysbindin-1 might play a role in glutamate signal transduction in the hippocampus formation [
54].
DTNBP1 is ubiquitously expressed throughout the brain [
70,
80] and corresponding to its primary localization to neurons,
DTNBP1 mRNA has predominantly been detected in grey matter areas [
80]. In the healthy adult brain,
DTNBP1 mRNA is most prominently expressed in the frontal cortex (especially in the dorsolateral prefrontal cortex), temporal cortex, hippocampus, caudate, putamen, nucleus accumbens, amygdala, thalamus, and midbrain [
80]. Post-mortem brain analyses of patients with schizophrenia showed significantly reduced
DTNBP1 mRNA and protein expression in the dorsolateral prefrontal cortex (DLPFC) and midbrain [
65,
66,
70] and in the hippocampal formation compared to healthy controls [
54,
79]. Weickert et al. [
79] reported a decrease in
DTNBP1 mRNA levels in schizophrenic patients particularly in the dentate gyrus and CA3 (cornu ammonis 3) of the hippocampus. This decline of mRNA was positively correlated with the expression of other synaptic markers known to be reduced in schizophrenia [
79].
Alterations in dopamine and glutamate signal transduction are considered to be the neurochemical basis of the pathophysiology of schizophrenia [
3,
12,
20,
47,
57,
73], but also play an important role in other psychiatric conditions [
16,
24,
39]. In this context, genetic variation in
DTNBP1 might confer the risk of schizophrenia or other psychiatric disorders by mediating effects on synaptic structure and function of glutamatergic neurons, particularly in the hippocampus [
48,
66].
Reductions in whole temporal lobe volumes and especially of the medial temporal lobe including the amygdala-hippocampus-complex are a major neuropathological finding in schizophrenia [
62,
68,
76]. Most of all, reduced bilateral hippocampal volumes have been reported for chronic schizophrenia patients, but also for first-episode patients with psychosis and for patients with bipolar affective disorder [
59,
68,
76]. Another principal neuropathological finding in schizophrenia is a reduced volume of prefrontal cortical regions [
7,
22], which has also been described in bipolar patients to a lesser extent [
49,
59]. Against this background, the aims of the present study were to directly investigate the effects of at-risk single nucleotide polymorphisms of the schizophrenia/psychiatric susceptibility gene
DTNBP1 on regional brain volumes in human subjects using structural MRI. We chose the two single nucleotide polymorphisms rs2619522 and rs1018381, which have been investigated in several genetic studies [
14,
17,
19,
38], and even referred to as a set for tagging a high-risk haplotype, reported by van den Oord et al. [
75] in the sample of the Irish study on high-density schizophrenia families. We hypothesized that there might be alterations in grey matter volume of the prefrontal cortex and hippocampal regions associated with the at-risk
DTNBP1 alleles.
Discussion
In the present study, we found variations of grey matter brain volumes independently associated with two different single nucleotide polymorphisms of the
DTNBP1 gene, both together characterized as a set for tagging a schizophrenia high-risk haplotype reported by van den Oord et al. [
75].
Regarding the SNP rs2619522, we found significantly higher grey matter volumes in several brain regions associated with the risk allele (G allele) [
6,
17,
19]. The major finding was in the left hippocampus, which was significant on a FDR-correction level. Contralaterally, the right hippocampus also was significantly enlarged, although on a slightly lower significance level. Besides this main finding, we observed significant volume increases associated with the G allele in frontal and parietal cortices as well as in lateral and medial temporal areas.
Concerning the SNP rs1018381, we also found significantly higher grey matter volumes in association with the reported risk allele (T allele) [
17]. Risk allele-carriers exhibited increased brain volumes bilaterally in frontal cortices, in the basal right thalamus/pulvinar and the left lingual gyrus.
Our results therefore complement the current state of research on schizophrenia and affective disorders with manifold findings relating to hippocampal and prefrontal morphology and function in the course of these psychiatric diseases [
60,
62]. Schizophrenia has been associated with reduced hippocampal volume in patients as well as in their biologic relatives [
5,
21,
28]. In bipolar disorder, findings of either enlarged [
30] or reduced hippocampal volumes [
13] have been described [
60]. In addition, there are also several reports of asymmetric hippocampal volume alterations with emphasis on the left hippocampus in schizophrenia and individuals at ultra-high risk for psychosis [
45,
77,
85], corresponding to our findings in association with rs2619522 (Table
2).
Hippocampal function, but also prefrontal and parietal cortical networks underlying higher cognitive functions, has been shown to be altered in schizophrenic and bipolar patients as well as in their healthy family members in several recent fMRI studies [
11,
18,
23,
25,
26]. Moreover, cognitive impairment and abnormal executive functioning in schizophrenia and bipolar disorder have been reported in association with
DTNBP1 risk genotypes [
8,
15], and deviating brain activation in prefrontal, temporal and parietal areas during cognitive and emotional tasks has been described in healthy carriers of
DTNBP1 risk alleles [
33,
41,
42,
72,
84].
With this in mind, our findings of increased grey matter volumes in association with the DTNBP1 risk alleles of both at-risk SNPs in the above-mentioned brain regions seem to be counterintuitive at first sight, especially with respect to the reported structural brain volume reductions in schizophrenia.
However, the pathophysiology of functional psychosis is still far from being understood in detail. According to the empirically well-supported dopamine hypothesis in schizophrenia [
27], productive psychotic states are associated with dopaminergic hyperactivity in subcortical regions [
29,
35,
44] and positive symptoms as well as memory deficits have been linked to dysfunctional hippocampal hyperactivity [
86]. Along with this, there is a body of evidence of dynamic structural brain alterations over the course of time in schizophrenia [
63], which applies to the hippocampal formation in particular [
45,
78].
Intriguingly, Nickl-Jockschat and co-workers recently reported reduced white matter fractional anisotropy in the right perihippocampal region in healthy T allele-carriers of
DTNBP1 SNP rs1018381 [
52]. At the same time, they also found elevated fibre tract integrity in bilateral frontal lobes in proximity to the bilateral medial frontal cortices, corresponding to our findings of higher grey matter volumes in association with the T allele (rs1018381) in these cortical brain areas.
Moreover, increased grey and white matter volumes in association with a schizophrenia risk allele-carrier status have also been described for a
Neuregulin-
1 at-risk SNP in childhood-onset schizophrenia [
1]. It is worth remarking that these risk allele-associated volumetric alterations were found equally in schizophrenia patients and healthy controls at the beginning of that prospective investigation, but differed in terms of structural neurodevelopment in the longitudinal course between groups to the detriment of the schizophrenia risk allele-carriers [
1].
In this sense, our findings of increased grey matter volumes in critical cerebral regions associated with the here-reported risk alleles of
DTNBP1 might represent an endophenotype of a compromised brain [
29], particularly vulnerable for developing further pathophysiological processes leading to clinical psychosis in the context of additional environmental stress. However, in which way and to what extent
DTNBP1 risk genotypes exactly modulate brain morphology and function still is a topic of current research.
It is noteworthy though that the present study, despite the relatively small sample size and its diagnostic heterogeneity, could provide such distinct findings on grey matter volumes in association with the two at-risk SNPs of
DTNBP1. Given the phenotypic and genetic overlap of schizophrenia with bipolar disorder [
40], the present results support existing evidence that genetic variation of
DTNBP1 may not only be a risk factor for schizophrenia, but also play a role in a broader context of psychiatric disorders including affective psychoses. Nevertheless, these results are limited by the diversity of the participating subjects and the findings will have to be replicated in a more homogeneous sample and with a higher number of subjects.
To conclude, compatible with previous reports on a role of the dysbindin-1 gene in hippocampal functions as well as in major psychoses, the present study provides first direct in vivo evidence that two risk alleles of DTNBP1 show linkage to altered grey matter volumes in the human brain. The risk alleles of rs2619522 and rs1018381 are significantly associated with variation of grey matter volumes in prefrontal areas and the latter (rs2619522) even with altered grey matter volumes in parietal cortices and bilaterally in the human hippocampus.