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Lipid profile in schizophrenia: case control study
Insights
Schizophrenia patients exhibit higher cholesterol and LDL-C levels, increasing cardiovascular risk. Factors like age, male gender, and alcohol use worsen dyslipidemia, while depressive symptoms are linked to poorer lipid profiles.
Area of Science:
- Cardiovascular Health
- Psychiatric Disorders
- Metabolic Syndrome
Background:
- Cardiovascular diseases are a leading cause of mortality in schizophrenia patients.
- Dyslipidemia is a significant risk factor contributing to cardiovascular complications in this population.
- Understanding lipid profiles in schizophrenia is crucial for risk stratification and management.
Purpose of the Study:
- To compare lipid profiles (total cholesterol, triglycerides, HDL-C, LDL-C) between schizophrenia patients and healthy controls.
- To identify associations between lipid parameters and demographic, clinical, and treatment characteristics in schizophrenia patients.
Main Methods:
- A case-control study involving 78 schizophrenia patients and 68 healthy controls.
- Serum lipid parameters (TC, TG, HDL-C, LDL-C) were measured.
- Demographic data and clinical assessments using PANSS, CGI, GAF, and Calgary depression scale were collected.
Main Results:
- Schizophrenia patients showed significantly higher total cholesterol (TC) and LDL-C levels compared to controls.
- Prevalence of hypercholesterolemia and low-density hyperlipoproteinemia was significantly higher in patients.
- Age (≥35), male gender, and alcohol consumption were associated with dyslipidemia; cannabis use correlated with lower TG; depressive symptoms worsened lipid parameters.
Conclusions:
- Schizophrenia patients are at increased risk of dyslipidemia, exacerbated by alcohol and tobacco use, older age, and male gender.
- Paranoid schizophrenia and positive symptoms were associated with less dyslipidemia, whereas depressive symptoms indicated poorer lipid profiles.
- Regular lipid monitoring, lifestyle interventions, and tailored therapeutic strategies are essential to reduce cardiovascular morbidity and mortality in schizophrenia patients, with a focus on those with depressive symptoms.
Introduction:
Cardiovascular diseases are common co morbidities of schizophrenia and constitute the main factors of high mortality in this pathology. Cardiovascular damages are favored by some risk factors, of which one of the most important is dyslipidemia. In this context, a study of lipid profile in schizophrenia is interesting. The aims of this study were to compare the lipid profile of patients with schizophrenia to healthy controls and to investigate the associations between lipid parameters and demographics, clinical and treatment characteristics of the patients.
Methods:
We conducted a case-control study between April 2013 and March 2014 on 78 patients with schizophrenia and 68 healthy subjects who benefited from the dosage of four serum lipid parameters: total cholesterol (TC), triglycerides (TG), High-density lipoprotein Cholesterol (HDL-C) and Low-density lipoprotein cholesterol (LDL-C). For the socio-demographic and clinical assessments, we used an information sheet and the following psychometric scales: PANSS (Positive And Negative Syndrome Scale), CGI (Clinical Global Impressions), GAF (Global Assessment Functionning) and the Calgary scale for depression.
Results:
The comparative study showed that serum concentrations of TC and LDL-C were significantly higher for patients compared to healthy controls respectively with (t=2,83 ; p=0,008) and (t=9,35; p<0,001), the cholesterol ratio (TC / HDL-C) was also significantly higher for patients (t=2,23; p=0,033). The patients had significantly higher prevalence of hypercholesterolemia (OR = 2.96) and low density hyperlipoproteinemia (OR = 18.79). The analytical study in the population of patients showed that the age ≥35 year-old, male gender and alcohol consumption were associated with disturbances in lipid parameters. Cannabis consumption was associated with significantly lower concentrations in TG. Concerning clinical features, paranoid schizophrenia was associated with less dyslipidemia unlike the depressive dimension assessed by the Calgary scale. There was a negative correlation between plasmatic TG concentrations and doses of antipsychotics.
Conclusion:
The vast majority of the literature confirms that patients with schizophrenia are at greater risk of dyslipidemia. This high risk appears to be more important with the consumption of alcohol and tobacco. It seems also that age and masculine gender are dyslipidemia risk factors for schizophrenic patients. The paranoid type of schizophrenia and positive symptoms seem to be associated with less dyslipidemia while depressive symptoms worsen lipid parameters. It then follows that, clinical and regular monitoring of lipid profile, lifestyle recommendations (smoking cessation, exercise and balanced diet) and appropriate therapeutic choices could help reduce morbidity and mortality among patients with schizophrenia. A special focus should be accorded to patients with high negative and depression symptoms.
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