Schizophrenia Clinical Trial
Official title:
The Antiatherogenic Properties of HDL in Psychiatric Patients With and Without Antipsychotic Therapy
Background:
Among individuals with schizophrenia, there is an increased prevalence of obesity,
dyslipidemia ,diabetes mellitus and related conditions such as cardiovascular disease.
People with severe mental illnesses, such as schizophrenia, depression or bipolar disorder,
have worse physical health and reduced life expectancy compared to the general population.
Number of epidemiological studies of patients with schizophrenia have documented a higher
incidence of cardiovascular disease than in the general population, and patients with
schizophrenia may be at an elevated risk for cardiovascular disease even in the absence of
antipsychotic treatment.
Affinity for the H1 receptor is most closely linked to increased weight gain, although
affinity for D2, 5-HT1A, 5-HT2C and a2-receptors may also be involved. Drug affinity for the
H1, M3 and 5-HT2C receptors is correlated with an increased risk of diabetes.
High-density lipoprotein cholesterol (HDL-C) concentration in the blood is independently and
inversely associated with an increased risk of cardiovascular disease(CVD). However many
patients with 'normal' or even 'elevated' plasma HDL experience clinical events. HDL may not
always be atheroprotective and in some conditions, it paradoxically enhances the process of
atherosclerosis. In addition to its role in reverse cholesterol transport, HDL shows many
other protective properties towards atherosclerosis. HDL inhibits the chemotaxis of
monocytes , prevents endothelial dysfunction and apoptosis, prohibit slow-density
lipoprotein (LDL ) oxidation, and stimulates the proliferation of endothelial cells and
smooth muscle cells. These anti-inflammatory, antioxidative, antiaggregatory, anti-coagulant,
and pro-fibrinolytic activities are exerted by different components of HDL
Aim of the study:
To investigate the functional properties of HDL in psychiatric patients before and during
antipsychotic therapy.
Patients and methods:
The blood will be drawn at baseline before the initiation of antipsychotic drugs and 2
months under the antipsychotic treatment.
Study procedures:
Full lipid profile including triglycerides, LDL-C, Total cholesterol, HDL-cholesterol, apo
AI, apoAII and apoB100.
Serum Paraoxanase Activity
LDL oxidation and resistance to oxidation (measured by conjugated diens formation during
incubation in the presence of copper).
HDL composition: total and unesterified cholesterol, triglycerides and phospholipids, TBARS
content before and after exposure to AAPH as a major indicator of oxidative stress, PON
activity using phenylacetate as a substrate, apoA1and PAF.
Serum parameters e.g. Diacyl glycerol acyltransferase activity, free ApoA1 and LCAT
activity.
3 [H]-Cholesterol efflux will be measured by incubating J744 macrophages with serum.
Radioactivity will measured by β counter in the cell lysate and the medium.
Statistical methods:
One-way AVOVA and Student's t-test for paired samples will be used for comparison of
multiple groups and paired samples, respectively. p<0.05 will be considered significant.
n/a
Observational Model: Cohort, Time Perspective: Prospective
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