Brain vasculature disturbance in schizophrenia

Purpose of review The vascular hypothesis of schizophrenia (SZ) postulates that brain endothelial dysfunction contributes to brain pathophysiology. This review discusses recent evidence for and against this hypothesis, including data related to blood–brain barrier (BBB), brain endothelium, and brain blood supply, to provide a critical weighed update. Recent findings Different studies report a consistent proportion of SZ patients showing increased BBB permeability, reflected by higher levels of albumin in the cerebral spinal fluid. Of note, this was not a result of antipsychotic medication. The high inflammatory profile observed in some SZ patients is strongly associated with increased BBB permeability to circulating immune cells, and with more severe cognitive deficiencies. Also, sex was found to interact with BBB integrity and permeability in SZ. The strongest independent genetic association with SZ has been identified in FZD1, a hypoxia-response gene that is 600-fold higher expressed in early development endothelium as compared to adult brain endothelium. Regarding brain blood supply, there is evidence to suggest alterations in proper brain perfusion in SZ. Nonetheless, ex-vivo experiments suggested that widely used antipsychotics favor vasoconstriction; thus, alterations in cerebral perfusion might be related to the patients′ medication. Summary In some patients with SZ, a vulnerable brain endothelium may be interacting with environmental stressors, such as inflammation or hypoxia, converging into a more severe SZ symptomatology. Gene expression and performance of human brain endothelium could vary along with development and the establishment of the BBB; therefore, we encourage to investigate its possible contribution to SZ considering this dynamic context.

INTRODUCTION Schizophrenia (SZ) is a heterogeneous psychiatric disorder, affecting around 24 million people worldwide [1]. Although early death by suicide reduces life expectancy in SZ patients, the largest reduction comes from cardiovascular morbidity [2], illustrating the importance of the vasculature for them. Genome-wide association studies (GWAS) evidenced a polygenic architecture underlying SZ, with a few rare variants with large effects and hundreds of common genetic variants with small effects (reviewed in [3]). In addition, it has been described that genetic risk is better for predicting SZ in the presence of early life complications [4]. Therefore, an adverse environment, such as intrauterine hyp-oxia or obstetric complications [5], amongst others, interacting with multiple susceptible genes could trigger the disease during adulthood [6]. Accordingly, the neurodevelopmental hypothesis of SZ has been extended to a developmental risk factor model [7], and SZ is considered a multifactorial disease. The brain is a high-energy-and oxygendemanding organ. To meet these needs, it is highly vascularized and this vascular network develops in synchrony with the nervous system [8]. The blood vessels of the brain are structured within a multicellular niche called the neurovascular unit (NVU), composed of brain endothelial cells (BECs), smooth muscle cells, fibroblasts, pericytes, astrocytes, neurons, and microglia [9]. NVU cells secrete growth factors with neurotrophic, neuromodulator, and angiogenic effects [10] such as Vascular Endothelial Growth Factor (VEGF), Brain-Derived Neurotrophic Factor (BDNF) [11] and Nerve Growth factor (NGF) [12], among many others. In conjunction with other cellular components of the NVU, the brain endothelium contributes to regulating local blood flow based on neuronal activity changes; a phenomenon known as neurovascular coupling [13,14].
At the first stages of central nervous system (CNS) development, molecular signals from neural progenitor cells and neurons induce BECs to express a barrier phenotype. This blood-brain barrier (BBB) maintains a homeostatic CNS microenvironment and promotes neuronal activity by responding dynamically to the ongoing physiological demands [15]. Adherent (cadherins) and tight junction proteins (e.g., Claudins (CLDN) and Occludins (OCLN)) confer paracellular tightness between adjacent BECs, contributing to the barrier integrity and restricting the migration of cells and molecules across it [16]. ATP-driven transmembrane efflux pumps, such as ABC transporters, clear toxic material by removing it from the brain. Fetal astrocytes are also involved in BBB formation, through retinoic acid signaling [17,18], and contribute to the barrier maintenance throughout adulthood [13,19,20].
Alterations in BBB integrity due to down-regulation of tight or adherent junction proteins can trigger the loss of barrier function by enhancing general permeability (leakage) across brain endothelium. Some proteolytic enzymes, such as Matrix Metalloproteinase 9 (MMP9), can degrade blood vessels basement membrane and tight junction proteins. Therefore, MMP9 up-regulation can impair BBB integrity and increase its permeability [21,22]. Elevated albumin in cerebrospinal fluid (CSF), the most abundant protein in blood, is an indicator of increased BBB permeability to macromolecules [23]. Also, increased blood levels of brain-derived neuronal growth factors, such as S100 Calcium-Binding Protein (S100B), are potential biomarkers of BBB leakage.
BECs activation by systemic inflammatory challenges increases BBB selective permeability to circulating immune cells, through the up-regulation of Vascular and Intercellular Cell Adhesion molecules (VCAM1 and ICAM1, respectively), P-selectin and Eselectin [24][25][26]. Based on the aforementioned, a BBB function more sensitive to environmental stressors due to intrinsic alterations in BECs performance in SZ, could lead to neuroinflammation by allowing ingression of harmful material and infiltration of peripheral immune cells into the CNS. On the other hand, increased systemic inflammation may be a causal factor of increased BBB permeability in SZ patients. To study endothelial intrinsic mechanisms underlying SZ, human induced pluripotent stem cells (hiPSC)-derived BBB models have been employed [27 & ,28]. hiPSC are obtained from SZ and control subjects' somatic cells and differentiated to brain endothelium. Thereby, hiPSC-derived BBB models account for the patients' whole genetic information [27 & ,29-32] and allow to assess the performance of BBB isolated from other factors that might be present in SZ, such as inflammation and use of medication.
This review aims to summarize and discuss the latest findings related to impaired brain vascular function in SZ. As the brain vasculature is involved in the functioning of the BBB and in the regulation of local brain perfusion, the present review is divided into these two main topics. Data on structural and functional alterations of the cerebral vasculature, and how these features could be interacting with other altered phenotypes described in SZ, such as inflammation, will be covered. We will focus on the most recent literature.

Evidence from peripheral and cerebrospinal fluid markers
A meta-analysis found increased blood levels of S100B and MMP9, and increased CSF albumin ( ]. This might suggest that alterations in BBB integrity in SZ could be regional rather than widely distributed throughout the brain.

Evidence from in-vitro experiments
Deletion at the 22q11.2 chromosomal region (22qDS) is a relatively common chromosomal anomaly, which is associated with a 20-fold increase in SZ risk [44]. Interestingly, CLDN5 is located in this chromosomal region. In a matched-pair experimental design, hiPSC-derived BBB from 22qDS-SZ patients (5 SZ and 5 control cell lines) exhibited a disorganized CLDN5 expression pattern and higher expression of ICAM1, as compared to their matched controls. Furthermore, 22qDS-SZ-derived endothelium showed impaired barrier function, with reduced transendothelial electrical resistance and increased permissiveness to monocyte transmigration [27 & ]. These findings suggest intrinsic BECs dysfunction in 22qDS-SZ patients.
SEP-363856 is a Serotonin 1A receptor (5-HT1A) agonist and has been recently proposed as a promising potential drug for SZ treatment [45]. In 2021, Sugimoto et al. demonstrated that 5-HT1A is also expressed in human brain endothelium. Of note, serotonin signaling through 5-HT1A binding increased CLDN5 in cultured human BECs [46 && ].
Thus, SEP-363856 beneficial effects maybe partially related to BBB protection.
Inflammation and blood-brain barrier performance in schizophrenia According to the neuroinflammatory hypothesis of SZ, brain vasculature may be affected by chronic inflammation. Increased expression of pro-inflammatory genes in the brain is associated with SZ [47], as has been described for the complement pathway (discussed in Woo et al., (2020) [48]). Peripheral blood levels of pro-inflammatory cytokines, such as IL-6, IL-1, TNF, and IFN are also often reported to be increased [49]. Different studies suggested an association between BBB permeability and the inflammatory status of the patients; these are described below.

Evidence from peripheral and cerebrospinal fluid markers
The major histocompatibility complex locus, a chromosomal region coding for hundreds of genes and including the complement C4, carries a strong genetic association with SZ [50]. Increased plasma levels of C4-anaphylatoxin (C4-ana), a fragment of C4 released upon its activation, were reported in SZ (15 SZ and 14 controls ]. Summarizing, BBB leakage seems to be present in a consistent proportion of SZ cases, but its relationship with systemic or neuroinflammation is not yet clear. Aside from its possible involvement in BBB leakage, systemic inflammation in SZ could facilitate immune cells infiltration into the CNS through the up-regulation of cell adhesion molecules, such as ICAM1, VCAM1 and P-selectin, in BECs [24][25][26]54]. The soluble forms of these adhesion molecules serve as indicators of endothelial activation [55]. In 2020, a meta-analysis reported increased blood levels of soluble P-selectin in SZ (3 studies; 98 SZ and 72 control subjects). However, no differences were observed in blood sICAM1 or sVCAM1, nor in the CSF, between SZ and controls (2-12 studies; 56-833 SZ and 50-941 control subjects). Worth mentioning, heterogeneity was high across all these meta-analytic results (> 80%, except for CSF sICAM1) [33 && ]. Radu et al., (2020) reported lower sICAM1 and higher sVCAM1 plasma levels in first-episode SZ patients (50 SZ, 50 controls). sVCAM1 correlated positively with the severity of symptoms, suggesting an association between increased BBB permeability and worsening of the disease [56].
Plasminogen activator inhibitor-1 (PAI-1) is a pro-coagulant protein and its expression is enhanced in a pro-inflammatory environment [57], facilitating leukocyte migration across the endothe-lium [58]. Meixensberger et al., (2021) quantified CSF levels of endothelial cell adhesion molecules in SZ (40) and unipolar depression patients (39), and reported increased sICAM1, sVCAM1, and PAI-1 in SZ compared to the depressed patients. In SZ, CSF sICAM1 was also higher than reference control levels. Levels of these proteins were similar among first-episode and chronic SZ patients, suggesting that alterations were not a consequence of a degenerative process, nor of cumulative antipsychotic use [34 && ]. Elevated serum levels of PAI-1 and other pro-inflammatory cytokines were also reported in another study with large samples, and levels were even higher in SZ patients that had experienced Acute Ischemic Stroke (SZ-AIS) (150 SZ, 150 SZ-AIS, and 150 controls) [59]. The latter indicates a gradually increased inflammatory profile in SZ, exacerbated even further in SZ-AIS, along with the same trend in BBB permeability to circulating immune cells.
A cohort of 78 SZ patients and 73 controls was annotated into high and low inflammation groups based on circulating inflammatory cytokine transcripts. Plasma sICAM1 was elevated in the SZ-highinflammation group compared to the high-inflammation control group (number of high-inflamed subjects not reported). Leukocytes can also produce ICAM1; however, authors reported no differences in white blood cells ICAM1 expression between diagnostic, nor between inflammatory subgroups. Thus, suggesting that the source of increased sICAM1 is from the endothelium. Of note, high sICAM1 was associated with worse verbal memory

Evidence from postmortem studies
In 2020, Purves-Tyson et al. grouped SZ postmortem cases into 'SZ-high-inflammation 0 and 0 SZ-lowinflammation 0 , based on transcript measurements of inflammatory cytokines in brain tissue. Midbrain ICAM and the macrophage marker CD163 expression was substantially increased in the SZhigh-inflammation group, but no difference was observed in the SZ-low-inflammation compared to controls (13 SZ-high-inflammation, 15 SZ-lowinflamma-tion, 28 controls) [62 && ]. The same group also measured different brain endothelial transcripts in the dorsolateral prefrontal cortex (DLPFC). Considering the previously described 0 high 0 and 0 low inflammation 0 SZ biotypes, the authors found altered expression of structural and functional BECs markers such as increased CDH5 and OCLN, and decreased ABCG2 in the DLPFC of the SZ-high-inflammation group, as compared to controls (13 SZ-high-inflammation, 21 SZ-low-inflammation, 37 controls) [63 && ]. In addition, SZ-high-inflammation samples presented higher ICAM1 , along with an increased number of CD163þ macrophages [63 && ]. Thus, neuroinflammation, endothelial dysfunction, increased BBB permeability and more peripheral macrophages in cerebro are linked with the high inflammatory biotype in SZ patients. Expression of ICAM and classic BBB genes in cultured BECs was independent of therapeutic doses of different antipsychotics [63 && ]. SERPINA3 exerts antiangiogenic and antiinflammatory effects on the endothelium [64]. Its expression was increased in postmortem cerebral cortex of SZ subjects [65]. In 2020, high expression of SERPINA3 in SZ was replicated and was even higher in SZ-high-inflammation cases (14 SZ-high-inflammation, 23 SZ-low-inflammation, and 33 lowinflammation controls). Immunostainings indicated that blood-vessel-associated astrocytes are the major source of SERPINA3 increment in the SZ-high-inflammation group [66]. SERPINA3 upregulation in SZ could be a compensatory response to chronic inflammation [65]. However, SERPINA3 inhibits the catalytic activity of leukocyte elastase [67], a protease that cleaves ICAM1 which in turn favors attachment of leukocytes to endothelium [68]. Hence, elevated SERPINA3 in blood-vesselassociated astrocytes could be cooperating with CD163þ CNS infiltration in the SZ-high-inflammation group [63 && ].
Brain endothelial cells-and blood-brain barrier-related growth factors in schizophrenia Growth factors secreted by the cellular components of the NVU modulate different aspects of BECs performance, including growth, proliferation, and BBB establishment [10]. Recent data about BECsrelated growth factors in SZ are described below.

Evidence from peripheral and cerebrospinal fluid markers
Monocyte Chemoattractant Protein-1 (MCP1) is produced by different cells of the NVU, including BECs. It is involved in monocyte migration across endothelium [69] and can modulate BBB integrity [70]. In 2020, a meta-analysis reported unaltered MCP1 blood levels among drug-naive first-episode SZ ( ]. Glial Cell-derived Neurotrophic Factor (GDNF) is involved in BBB establishment [72,73]. Amyloid precursor protein (APP) is highly expressed in murine endothelium during the first stages of embryogenesis [74] and in-vitro studies indicated a positive effect of APP on endothelial cells migration, proliferation [75] and nitric oxide production [76]. CSF measurements of 11 different growth factors associated with neuro-plasticity indicated lower levels of APP and GDNF in SZ (94 SZ and 118 controls) [77 && ]. Of note, Human Umbilical Vein Endothelial Cells (HUVEC) lacking APP presented four times increase in permeability to FITC-dextran in the presence of an IL-1b stimulus compared to control HUVEC, suggesting a more sensitive endothelial barrier function to inflammation in the absence of APP [75].
NGF, VEGF, Insulin (INS), Insulin-like Growth Factor (IGF), Insulin-like Growth Factor 1 Receptor (IGF1R) and Insulin Receptor (INSR), are growth factors and receptors exerting powerful activities on BECs functioning. VEGF and NGF promote proliferation [12], whereas INS, IGF1R and INSR modulate nitric oxide production [78]. Interestingly, increased antibody reactivity for all these molecules was found in the CSF of SZ patients ( 81], respectively. In contrast with these findings, a study published in 2020 and not included in either of the two mentioned meta-analyses reported increased blood VEGF in SZ (79 SZ and 60 controls) [82].

Evidence from postmortem studies
Based on the heterogeneity of causes and symptomatology in SZ, Huang et al. (2020) applied a statistical methodology to identify genes with higher expression variance in SZ (212 SZ and 214 control postmortem samples). The authors describe a general over dispersion in gene expression among SZ brains and identified VEGFA as the most differentially variable expressed gene in SZ as compared to controls [83]. This finding allows reconciling different studies that point to such diverse results regarding the participation of VEGF in SZ. Variation in VEGF expression among patients may be related to a differential role in distinct stages of the disease.

Evidence from genetics
ALDH1A2 codes for aldehyde dehydrogenase that catalyzes a key step in retinoic acid synthesis by astrocytes, and retinoic acid is involved in the establishment of the BBB [17,18] and may prevent inflammation-induced increases in BBB permeability [84]. Methylome-wide association studies (MWAS) investigate correlations between a particular trait and the methylation state across different sites throughout the genome [85]. Interestingly, one of the most variably methylated site associated with SZ is located in the region of ALDH1A2 (744 SZ and 704 control subjects) [86 & ]. The AQP4 is expressed in brain perivascular astrocytic processes. It is a water channel protein involved in brain homeostasis and in BBB development and function [87]. In 2020, three different SNPs in AQP4 were associated with SZ risk (100 SZ and 100 control subjects) [88 & ].
Sex differences in blood-brain barrier integrity, permeability and brain endothelial cells functioning in schizophrenia Sex differences in prevalence and symptomatology are evident in SZ [89]. There are sex differences in the immune system, as sex hormones have opposite effects in particular on Th cells, leading to stronger (adaptive) immune activation in females [90], which might be contributing to the sex differences observed in the development of SZ. Additionally, recent data suggest interactions between sex and the performance of BECs in SZ. These findings are detailed below.

Evidence from mice models
As part of the renin-angiotensin system, angiotensinogen (AGT) is hydrolyzed into angiotensin I (ANG1), which is then converted into ANGII [97]. ANGII increases BBB permeability through its binding to AT1R, expressed in BECs [98,99]. Increased serum AGT was reported in SZ (111 SZ and 109 controls) [100]. Vasconcelos et al. (2021), studied the effectofperi-pubertaladministrationofanAT1R blocker, candesartan, in a two-hit mice model of SZ that combines a neonatal immune challenge with stressors during puberty. Low doses of candesartan prevented SZ-like behavior in female and male mice. But only males induced with the twohits had an increase in pro-inflammatory cytokines in the hippocampus that could be significantly reduced to control levels with the peri-pubertal administration of candesartan [101]. These results add novel evidence for differential sex contribution in SZ neurobiology, with different pathways possibly contributing to BBB susceptibility. Moreover, the administration of an AT1R blocker could help to reduce SZ risk, indirectly implying that protection of BBB could prevent stress-triggering SZ.

Brain blood supply in schizophrenia
Besides the relevance of BECs to the BBB, they are also involved in the regulation of local brain blood supply. Astrocytes, pericytes, and BECs sense changes in neuronal activity and modulate the diameter of the vessels, modifying the blood flow according to the metabolic and oxygen demands resulting from increased brain activity [102]. Oxygen diffuses freely from the blood to the brain across the BBB, as does carbon dioxide in the opposite direction [103], and diverse glucose transporters expressed in BECs ensure a continuous delivery of glucose to the brain [104]. Therefore, under physiological conditions, regional cerebral blood flow (CBF) is firmly coupled to cerebral glucose metabolism, and to brain activity [105,106]. Although, the vasculature density, the morphology of blood vessels, and their ability to dilate in response to brain activity are variables that may modulate the strength of this coupling and thus brain blood supply [107]. In the following lines, recent studies intended to evaluate brain blood perfusion in SZ will be detailed.

Evidence from different imaging techniques
Deviations in the brain vascular network structure may interfere with proper blood supply. Microtomographic images of the anterior cingulate cortex and the superior temporal gyrus showed strong correlations between neurite and capillaries curvatures in both SZ and controls (4 SZ and 4 control samples) [108], but higher neurite curvatures in the SZ group [109]. Capillary diameters did not differ between groups [108], whereas slices from SZ patients showed thinner neurites [109], leading to a volumetric mismatch between neurons and vessels.
SZ patients showed a deviant hemodynamic profile during cognitive challenges compared to control subjects, with a delay in mean flow velocity evolution in the middle cerebral artery (30 SZ and 15 controls). The delay was longer in patients with increased symptoms severity [110]. Frontal and temporal CBF variations have been associated with SZ [111]. Three months of treatment with long-acting injectable aripiprazole in 51 patients with first-episode of SZ, significantly increased regional CBF at the temporal and frontal right side of the brain. These improvements were accompanied by an enhancement in patients 0 cognitive functioning, suggesting a correlation between cognitive performance and CBF in SZ [112 & ]. Positron emission tomography (PET) and Arterial spin labeling (ASL) are imaging techniques that allow evaluation of regional CBF and cerebral glucose metabolism, respectively. In a recent bimodal neuroimaging meta-analysis combining data from whole brain PET and ASL, authors analyzed 'coupled' and 'uncoupled' deviations of these two parameters in SZ (557 SZ and 584 healthy controls). Authors reported 'coupled' reductions and 'coupled' increases of CBF and cerebral glucose metabolism across different brain regions in SZ respect to controls. Also, 'Uncoupled' changes were reported in the superior frontal gyrus and cerebellum of SZ patients [113 & ].

Evidence from animal experiments
Recent ex-vivo findings indicate inhibition of K þ rectifier currents in coronary arterial smooth muscle cells by olanzapine [114], ziprasidone [115], and ris-peridone [116]; widely used antipsychotic treatments for SZ. This leads to cell membrane depolarization and can promote vasoconstriction. Accordingly, brain perfusion in patients with SZ might be influenced by their treatment.

Retinal vasculature in schizophrenia
The retina and optic nerve are derived from the diencephalon during embryonic development and are components of the CNS [117]. Correspondingly, assessment of the retinal vasculature may serve as a reliable window to approach the cerebral vasculature of SZ patients. Recent studies that assessed the density and the morphology of retinal blood vessels in SZ are mentioned below.

Evidence from different imaging techniques
Fundus photography is a widely used method to obtain a two-dimensional representation of the retina and its vasculature [118]. Two studies using fundus photography indicated greater venular and narrower arterial diameters in SZ compared to control retinas ( combined fundus photography with brain magnetic resonance imaging to investigate the relationship between the diameter of retinal blood vessels and brain structure in SZ (20 SZ and 17 controls). They found a negative correlation between average vein diameters and mean cortical thickness; the correlation was absent in the control group [122 && ]. These results relate the decreased cerebral cortex thickness in SZ [123] with recent hypotheses implicating vasculature as an important factor in SZ pathophysiology.
Optical coherence tomography angiography (OCTA) is a more modern optical method that allows volumetric mapping of the retina. Four studies conducted during 2020 and 2021 provided evidence for decreased density of retinal blood vessels in SZ (22-39 patients and 15 -37 control subjects), in at least one region of the retina (macular or peripapillary area) [

].
A possible declined response to hypoxia in schizophrenia and the role ofearly development endothelium When cells are faced with limited oxygen levels, hypoxia-induced signaling pathways are activated to overcome these adverse conditions. BECs are sensitive to hypoxia and are relevant contributors to these adaptation processes [129]. Early life complications, including pre-and peri-natal hypoxia, are risk factors for SZ (discussed in [130]), and become stronger predictors when co-occurring with a high genetic risk for this disease [4]. Accordingly, a diminished or altered hypoxia-induced signaling might be contributing to SZ. Recent data related to hypoxia-induced response in SZ are described below.

Evidence from genetics
Hypoxia inducible factors (HIFs) up-regulate transcriptional cascades that induce adaptive responses to protect the hypoxic tissue [131]. In 2020, an analysis was conducted to better understand the biological relevance of 145 SZ-related loci [132], previously reported by a SZ GWAS [133], and 33 of the SZ-associated genes were identified as HIFsrelated genes. Also, SZ-mutation intolerant genes (112 genes) were enriched for three different gene sets related to hypoxia-response [132]. Comparisons of whole-genome transcriptomic data from mice embryonic periventricular endothelial cells (PVECs) and adult BECs showed that thousands of genes are differentially expressed. Early development brain endothelium indicated an increased sensitivity to hypoxia as compared to adult brain endothelium, reflected by the up-regulation of HIF-1 target genes in PVECs [134 & ]. Strikingly, the expression of WNT frizzled class receptor 1 (FZD1), an hypoxia-response gene [135][136][137] that carries the strongest independent genetic association with SZ (429 SZ and 255 control samples) [138], was 600-fold higher in the early development brain endothelium.
Taken together, these results suggest an altered response to hypoxia in SZ, with a contribution from BECs possibly during early development.

CONCLUSION
This review summarized many recent findings reflecting structure and function of the brain vasculature in SZ in general and that of the BBB in particular. Some findings were only reported in one or two small samples. Meta-analyses showed high heterogeneity among included studies. This is a clear indication that this field is still in its infancy and few conclusions can be drawn at this stage. Nevertheless, some findings derived either from large studies or replicated are discussed below.
A meta-analysis indicated BBB leak in SZ, reflected by higher levels of CSF  [75].
Multiple works indicate the presence of a SZ group associated with a pro-inflammatory immune status and increased BBB permeability to peripheral immune cells, reflected in higher brain or blood levels of ICAM [60 No recent studies using PET to assess BBB function in SZ have been reported. Clinical studies using novel hydrophilic radioactive tracers, unidirectionally transported from the blood to the brain and with low baseline brain uptake [139][140][141], would contribute with highly-sensitive and quantitative in-vivo measurements of BBB integrity in SZ patients.
Considering that BECs are also involved in the regulation of regional brain blood supply, we reviewed evidence related to CBF and blood vessels morphology in SZ. Reductions in brain perfusion and activity are jointly present in SZ [ ], suggesting deviations of the local vascular network structure. It is important to consider that widely used antipsychotics for SZ treatment promoted depolarization of arterial smooth muscle cells [114][115][116]; thus, may favor vasoconstriction. Hence, we cannot rule out that perfusion anomalies in SZ are related to its treatment. Brain irrigation measurements in drugnaïve SZ patients would help to better understand brain perfusion in SZ.
In summary, while the field is not very consistent and the number of methods applied are large, there is converging evidence that some of the patients with SZ have increased BBB permeability (potentially those with a pro-inflammatory signature) and altered brain perfusion. Astrocytes may be contributing to the pro-inflammatory signature [66] and to BBB dysfunction in some of the patients [86 & ,88 & ]. It is important to have in mind that gene expression along development can vary drastically within the same brain cell type [134 & ]. Accordingly, SZ genetic background may be differentially manifested along with the establishment of the BBB [134 & ,138]. Overlaying SZ-associated genes with the transcriptomic profile of different cellular components of the NVU at distinct neurodevelopmental stages could shed lights on particular cells, cellular states, and molecular pathways being altered during SZ etiology. Additionally, the sex of the patients should also be taken into account when evaluating BBB performance, due to potential sex interactions with brain barrier integrity and permeability in SZ Financial support and sponsorship This work is supported by a grant to I.E.C.S. from ZonMw mental health (GGZ) (ZonMw, project code: 63631 001 0) V.P. is recipient of a Fondecyt grant (# 1190083). S.P is a recipient of 'Graduated School of Medical Sciences, University of Groningen', and 'Agencia Nacional de Investigación y Desarrollo de Chile' fellowships for PhD studies (#21181102).
Conflicts of interest I.E.C.S. was a consultant to Gabather, received research support from Janssen Pharmaceuticals Inc. andSunovion Pharmaceuticals Inc. The rest of the authors do not have any conflicts of interest. In this study, the expression of the serotonin receptor 5-HT1A in human brain endothelium is demonstrated, together with the up-regulation of CLDN5 expression through serotonin binding to 5-HT1A in BECs. Therefore, suggesting that the beneficial effects of treatments with serotonin agonists in SZ might be partially related to BBB protection.  This is the only study that includes control subjects with a high inflammatory profile, and highlights that the increase in BBB permeability observed in SZ patients with high inflammation is not simply due to the inflammation, rather to an interaction of inflammation with a more vulnerable BBB in SZ.

REFERENCES AND RECOMMENDED READING
61.

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Klaus F, Mitchell K, Liou SC, et al. Chemokine MCP1 is associated with cognitive flexibility in schizophrenia: A preliminary analysis. J Psychiatr Res 2021; 138:139-145. This study reports increased blood ICAM1 in a SZ cohort with high levels of proinflammatory cytokines, supporting the associations between SZ, inflammation, and increased BBB permeability. 62.

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Purves-Tyson TD, Robinson K, Brown AM, et al. Increased macrophagesand C1qA, C3, C4 transcripts in the midbrain of people with schizophrenia. Front Immunol 2020; 11. This study links neuroinflammation with increased BBB permeability to circulating immune cells in SZ.

63.
Blokland GAM, Grove J, Chen C-Y, et al. Sex-dependent shared and nonshared genetic architecture across mood and psychotic disorders. Biol Psychiatry 2021. This article highlights a strong gene-sex interaction for SZ risk in the gene MOCOS, which is predominantly expressed in BECs.