Abstract

Schizophrenia is a major health problem in which diversification and increase in the quality of antipsychotic molecules did not yield the anticipated results. that the etiopathogenesis of schizophrenia accounts for a combination of genetic factors forming the genetic spectrum of vulnerability for schizophrenia. The neurodevelopmental anomalies correlated with the gestational period and obstetric traumatisms raises major pharmacological management issues. The two levels of vulnerability (genetic and neurodevelopmental) are the basis of the pathogeny of side effects induced by antipsychotic medication. The most severe side effects are related to extrapyramidal symptoms, hyperhomocysteinemia, hypofrontality, impairment of the neurovascular unit and neuronal metabolic processes. Understanding these particular mechanisms will allow the clinician to identify the pathogenic model of schizophrenia, customized for each specific case. The adverse drug reaction decreases the compliance and adherence to the treatment, determining repeated discontinuations with psychotic relapses, and may trigger psychopathogenic bursts deteriorating the structural and cerebral functional balance. The type of psychotropic medication must be taken into account, as well as the concomitant medication administered for comorbidities associated with schizophrenia. The cerebral vascular modifications are correlated with the metabolic syndrome induced by antipsychotic medication. This complex syndrome, associated also with modifications in the homocysteine metabolism, determines weight gain, obesity, high blood pressure, ischemic cardiopathy, hyperglycemia and dyslipidemia. Identification of possible biological or neuroimaging markers helps and their early correction may prevent the onset of neurodegenerative evolution and irreversible cerebral atrophies, as well as decrease the risk of side effect that may endanger the life of the schizophrenic patient. The complexity of the pathogenic mechanisms requires a prophylactic behavior, not based on therapeutic switch, but on the proactive, customized pharmacologic intervention, addressing the pathogenic chains.

Highlights

  • White matter pathologyThe increase in stigma and social isolation amplifies the social stress, initiating secondary biological mechanisms dominated by episodic hyperactivation of the hypothalamic–pituitary–adrenal (HPA) axis, with increased cortisol release that disrupts the immune process (Chan et al, 2010)

  • Schizophrenia represents the most frightful psychotic disorder with an incidence rated at 0.34-0.85% in the general population (Simeone et al, 2015)

  • The diversification and increase in the quality of antipsychotic molecules did not yield the anticipated results. This context can be explained by the fact that the etiopathogenesis of schizophrenia accounts for a combination of genetic factors forming the genetic spectrum of vulnerability for schizophrenia

Read more

Summary

White matter pathology

The increase in stigma and social isolation amplifies the social stress, initiating secondary biological mechanisms dominated by episodic hyperactivation of the hypothalamic–pituitary–adrenal (HPA) axis, with increased cortisol release that disrupts the immune process (Chan et al, 2010). WMHs can be correlated with neurodevelopmental anomalies, especially hypoxic ischemic encephalopathy (HIE) In such cases, the white matter deterioration is located periventricular, (periventricular leukomalacia), and anticipates the risk of developing ventriculomegaly (VM), which is a neuroimaging indicator suggestive for schizophrenia with unfavorable evolution and therapeutic resistance. In the current medical practice, this type of neurodevelopmental disorder associated congenital cardiac anomalies The seriousness of these anomalies will determine the severity of cerebral hypoperfusion, which triggers apoptotic mechanisms. In the case of infectious pathogenic conditions in the current Coronavirus disease (COVID-19) pandemic, severe issues are raised due to maternal stress determining glucocorticoid release This context may lead to onset of gestational diabetes and hippocampal atrophy of the newborn due to the neurotoxic action of cortisol in the fetal brain. These mechanisms can endanger the life of the mother and the fetus

Extrapyramidal symptoms
Hypofrontality syndrome
Cerebellar dysfunction
Findings
10. Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call