Disease specific brain capillary angiopathy in schizophrenia, bipolar disorder, and Alzheimer's disease
Shinobu Hirai1, Atsuhiro Sakuma1, Yasuto Kunii2
1Brain Metabolic Regulation Group, Frontier Laboratory, Department of Psychiatry and Behavioral Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, 156-8506, Japan.
Insights
Brain capillary damage, indicated by fibrin accumulation, is common in schizophrenia and bipolar disorder. This finding offers new diagnostic and therapeutic avenues for these psychiatric conditions.
Area of Science:
- Neuroscience
- Pathology
- Vascular Biology
Background:
- Schizophrenia (SZ) and bipolar disorder (BD) share clinical symptoms.
- Brain capillary angiopathy, marked by fibrin accumulation, is a newly identified common feature in SZ and BD.
Purpose of the Study:
- To investigate similarities and differences in cerebral capillary injury across various brain diseases.
- To explore potential new diagnostic methods and therapeutic strategies for SZ and BD.
Main Methods:
- Postmortem brain tissue analysis was used to evaluate vascular damage.
- Fibrin accumulation in grey matter (GM) and white matter (WM) capillaries was quantified.
- Comparison was made between patients with SZ, BD, amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD), Alzheimer's disease (AD), and control subjects.
Main Results:
- Significant fibrin accumulation was observed in the GM capillaries of SZ and AD patients.
- Fibrin accumulation was noted in the WM capillaries of SZ, BD, and AD patients.
- ALS and PD brains showed no significant fibrin accumulation; AD brains exhibited fibrin leakage into the parenchyma.
Conclusions:
- Fibrin accumulation in brain capillaries is characteristic of SZ, BD, and AD.
- A non-disruptive fibrin-accumulating angiopathy distinguishes SZ and BD, with regional variations observed.
Abstract:
Schizophrenia (SZ) and bipolar disorder (BD), which are both psychiatric disorders, share some common clinical evidence. We recently discovered that brain capillary angiopathy is another common feature of these psychiatric disorders using fibrin accumulation in vascular endothelial cells as an indicator. This study aimed to characterize the similarities and differences in cerebral capillary injuries in various brain diseases to provide new diagnostic methods for SZ and BD and to develop new therapeutic strategies. We evaluated whether discrepancies exist in the degree of vascular damage among SZ and BD and other brain disorders (amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD), and Alzheimer's disease (AD)) using postmortem brains. Our results demonstrate that fibrin was strongly accumulated in the capillaries of the grey matter (GM) of brains of patients with SZ and AD and in the capillaries of the white matter (WM) in those of patients with SZ, BD, and AD when compared with control subjects without any psychiatric or neurological disease history. However, ALS and PD brains did not present a significant increase in the amount of accumulated fibrin, either in the capillaries of WM or GM. Furthermore, significant leakage of fibrin into the brain parenchyma, indicating a vascular physical disruption, was observed in the brains of patients with AD but not in the brains of other patients compared with control subjects. In conclusion, our work reveals that Fibrin-accumulation in the brain capillaries are observed in psychiatric disorders, such as SZ, BD, and AD. Furthermore, fibrin-accumulating, nonbreaking type angiopathy is characteristic of SZ and BD, even though there are regional differences between these diseases.
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