Magnesium Variations and Cardiometabolic Risk in Patients With Antipsychotic Drugs
Primary Purpose
Schizophrenia, Schizoaffective Disorder, Bipolar Disorder
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Blood sample
Sponsored by
About this trial
This is an interventional prevention trial for Schizophrenia focused on measuring Mental disorders, Antipsychotic agents, Magnesium, Cardiovascular risk factor, Metabolic syndrome
Eligibility Criteria
Inclusion criteria:
- Patient with severe mental illness (schizophrenia and other disorders chronic psychotic, schizoaffective disorder and bipolar disorder.
- Patient naive to antipsychotic treatment or stopped for more than 3 months (more than 6 months for antipsychotic action extended) and requiring the introduction of antipsychotic therapy
- Patient informed and accepting the proposed follow-up (himself or his/her legal representative)
- Patient available for one year monitoring
- Patient affiliated or beneficiary of a social security insurance
Exclusion criteria:
- patient's opposition
- Pregnant or breastfeeding patient
- Patients on anti-psychotic or treatment stopped for less than 3 months (6 months for antipsychotic prolonged action)
Sites / Locations
- Recruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
patient with antipsychotic/neuroleptic
Arm Description
Blood sample performed on patients requiring the establishment of treatment with antipsychotic / neuroleptic
Outcomes
Primary Outcome Measures
Proportion of patients with changes from baseline cardiometabolic risk
Changes from baseline cardiometabolic risk is defined the following composite outcome : 15% increase in fasting plasma glucose and/or 15% increase in plasma fasting insulin and/or 15% increase in HOMA-IR [Ins (uU / mL) x Gly (mmol / L) / 22.5] and/or 15% increase in total cholesterol levels, or LDL-cholesterol and/or reduction of 15% of HDL-cholesterol and/or 2 points increased in BMI and/or increase of 5 cm in waist circumference and/or 10 msec increase in the QTc interval of the ECG.
Secondary Outcome Measures
Proportion of patients with changes from baseline cardiometabolic risk
Proportion of patients with changes from baseline cardiometabolic risk
Proportion of patients with 15% increase in fasting plasma glucose
Proportion of patients with 15% increase in plasma fasting insulin
Proportion of patients with 15% increase in HOMA-IR [Ins (uU / mL) x Gly (mmol / L) / 22.5]
Proportion of patients with 15% increase in total cholesterol levels, or LDL-cholesterol and/or reduction of 15% of HDL-cholesterol
Proportion of patients with 2 points increased in BMI and/or increase of 5 cm in waist circumference
9. Proportion of patients with 10 msec increase in the QTc interval of the ECG
Change in zincemia
Change in zincemia
Change in zincemia
Full Information
NCT ID
NCT02986490
First Posted
July 8, 2016
Last Updated
December 5, 2016
Sponsor
University Hospital, Montpellier
1. Study Identification
Unique Protocol Identification Number
NCT02986490
Brief Title
Magnesium Variations and Cardiometabolic Risk in Patients With Antipsychotic Drugs
Official Title
Influence of Magnesium Variations (Serum and Intra-erythrocyte) on Markers of Cardiometabolic Risk in Long-term Prescription of Antipsychotic Drugs: a Prospective Cohort Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2016
Overall Recruitment Status
Unknown status
Study Start Date
September 2014 (undefined)
Primary Completion Date
January 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background: Antipsychotics can induce metabolic disorders such as obesity, hyperglycemia, dyslipidemia or metabolic syndrome. It has been observed that treatment with antipsychotic could be accompanied by a decrease in the concentration of serum magnesium. Low serum concentrations of magnesium are potentially a risk factor of cardiac sudden death (Peacock, 2010). Hypotheses linking magnesium and pathogenesis of cardiovacuscular diseases are multiple. Also, it seems to exist a close relationship between magnesium and carbohydrate metabolism. Most studies on the subject have generally studied plasmatic magnesium.
Objective : Describe the relationship between changes in serum and intra-erythrocyte magnesium and cardiometabolic risk in patients innitiating an antipsychotic treatment. A secondary objective is to specify the frequency, magnitude and time to onset of changes in plasma of magnesium levels under antipsychotic treatment.
Methods : This is a pilot single-center prospective cohort. After inclusion, patients status (including magnesium levels) will be evaluated (1 and 3 months of treatment) and that status will define the exposure criterion. Included patients will be followed for 1 year during which cardiometabolic markers will be measured.
Population : patients who are more than 18 years old with schizophrenia schizoaffective disorder or bipolar disorder, naive to antipsychotic treatment or off for more than 3 months and requiring the introduction of antipsychotic drug therapy. Patients will be recruited during consultations and stays in care units of Adult Psychiatry Unit of Montpellier University Hospital.
Factor studied: serum and intra-erythrocytic magnesium levels at beginning and during the antipsychotic treatment measured by a unique analyzer center. Changes in levels of hypomagnesemia expected during the treatment will determine exposure groups.
Outcome: cardiometabolic risk markers measured at the beginning and during the treatment will be fasting blood glucose, fasting plasma insulin, HOMA-IR [Ins (uU / mL) x Gly (mmol / L) / 22.5], lipid profile (total cholesterol, LDL, HDL), BMI, waist circumference and ECG (QTc).
Cofactors: age, sex, personal and family medical history, blood pressure, smoking, diet, physical activity, psychiatric disease, Global Impressions, anti-psychotic treatment and comedications.
Perspectives : to show that decreased in magnesium levels observed among patients starting antipsychotic treatment is associated with deterioration of cardiometabolic risk markers. The demonstration of this association could explain at least part the increased cardiovascular risk observed in this population. In the longer term, the results of this study would argue the implementation of an intervention research project studying magnesium supplementation to minimize the metabolic effects of antipsychotic medications.
Detailed Description
This is a pilot single-center prospective cohort. After inclusion, patients status (including magnesium levels) will be evaluated (1 and 3 months of treatment) and that status will define the exposure criterion. Included patients will be followed for 1 year during which cardiometabolic markers will be measured.
Patients will be recruited during consultations and stays in care units of Adult Psychiatry Unit of Montpellier University Hospital.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder, Bipolar Disorder
Keywords
Mental disorders, Antipsychotic agents, Magnesium, Cardiovascular risk factor, Metabolic syndrome
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
patient with antipsychotic/neuroleptic
Arm Type
Other
Arm Description
Blood sample performed on patients requiring the establishment of treatment with antipsychotic / neuroleptic
Intervention Type
Biological
Intervention Name(s)
Blood sample
Intervention Description
Blood sample
Primary Outcome Measure Information:
Title
Proportion of patients with changes from baseline cardiometabolic risk
Description
Changes from baseline cardiometabolic risk is defined the following composite outcome : 15% increase in fasting plasma glucose and/or 15% increase in plasma fasting insulin and/or 15% increase in HOMA-IR [Ins (uU / mL) x Gly (mmol / L) / 22.5] and/or 15% increase in total cholesterol levels, or LDL-cholesterol and/or reduction of 15% of HDL-cholesterol and/or 2 points increased in BMI and/or increase of 5 cm in waist circumference and/or 10 msec increase in the QTc interval of the ECG.
Time Frame
At 12 months
Secondary Outcome Measure Information:
Title
Proportion of patients with changes from baseline cardiometabolic risk
Time Frame
At 3 months
Title
Proportion of patients with changes from baseline cardiometabolic risk
Time Frame
At 6 months
Title
Proportion of patients with 15% increase in fasting plasma glucose
Time Frame
From baseline at 12 months
Title
Proportion of patients with 15% increase in plasma fasting insulin
Time Frame
From baseline at 12 months
Title
Proportion of patients with 15% increase in HOMA-IR [Ins (uU / mL) x Gly (mmol / L) / 22.5]
Time Frame
From baseline at 12 months
Title
Proportion of patients with 15% increase in total cholesterol levels, or LDL-cholesterol and/or reduction of 15% of HDL-cholesterol
Time Frame
From baseline at 12 months
Title
Proportion of patients with 2 points increased in BMI and/or increase of 5 cm in waist circumference
Time Frame
From baseline at 12 months
Title
9. Proportion of patients with 10 msec increase in the QTc interval of the ECG
Time Frame
From baseline at 12 months
Title
Change in zincemia
Time Frame
From baseline at 12 months
Title
Change in zincemia
Time Frame
From baseline at 3 months
Title
Change in zincemia
Time Frame
From baseline at 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Patient with severe mental illness (schizophrenia and other disorders chronic psychotic, schizoaffective disorder and bipolar disorder.
Patient naive to antipsychotic treatment or stopped for more than 3 months (more than 6 months for antipsychotic action extended) and requiring the introduction of antipsychotic therapy
Patient informed and accepting the proposed follow-up (himself or his/her legal representative)
Patient available for one year monitoring
Patient affiliated or beneficiary of a social security insurance
Exclusion criteria:
patient's opposition
Pregnant or breastfeeding patient
Patients on anti-psychotic or treatment stopped for less than 3 months (6 months for antipsychotic prolonged action)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Luc FAILLIE, MD PhD
Phone
+33 4 67 33 67 52
Email
jl-faillie@chu-montpellier.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Luc FAILLIE, MD PhD
Organizational Affiliation
Montpellier University Hospital
Official's Role
Principal Investigator
Facility Information:
City
Montpellier
ZIP/Postal Code
34295
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Luc FAILLIE, MD PhD
Phone
+33 4 67 33 67 52
Email
jl-faillie@chu-montpellier.fr
12. IPD Sharing Statement
Plan to Share IPD
No
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Magnesium Variations and Cardiometabolic Risk in Patients With Antipsychotic Drugs
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