Risks for Insulin Resistance and Metabolic Syndrome Between Major Depressive Disorder (MDD) or MDD With Psychotic Features
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
Studies have shown that people with certain disorders have an increased risk of developing a condition called Metabolic Syndrome (MS). In this study, the investigators want to learn more about MS among people staying in the hospital for treatment of Major Depressive Disorder (MDD) and also Major Depressive Disorder with Psychotic Features (MDpsy). The investigators also want to learn more about a stress hormone called cortisol that is made in the body. Those who take part in this study will answer some questionnaires, be given some psychiatric interviews, and have some blood taken along with a urine sample.
The investigators believe that patients in the hospital with MDpsy will have higher baseline rates of MS factors, cortisol levels, dexamethasone non-suppression, and insulin resistance, compared with MDD alone.
| Condition |
|---|
|
Major Depressive Disorder Major Depressive Disorder w/ Psychotic Features Metabolic Syndrome |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Comparative Risks for Insulin Resistance and Metabolic Syndrome (MS) Among Hospitalized Patients With Major Depressive Disorder With (MDpsy) or Without (MDD) Psychotic Features |
- The primary measure is any change in fasting insulin from admission to discharge while subjects are inpatient. [ Time Frame: Measure fasting insulin at two timepoints; to determine change from baseline (admission) and discharge ] [ Designated as safety issue: No ]To preserve statistical power, we will measure insulin as a continuous variable rather than dichotomizing participants into insulin sensitive vs insulin resistant.
- The first secondary measure is a fasting lipid panel, including fasting total cholesterol, fasting LDL, fasting HDL, and fasting triglycerides; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]
- Fasting glucose will be a separate secondary outcome measure; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]
- Waist Circumference; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]Waist circumference will be measured once at admission and once at discharge to determine if any changes have occurred throughout time of inpatient hospitalization
- Urine microalbumin; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]
- C-reactive Protein; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]
- Homocysteine; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]
- Blood pressure (supine & standing as available) [ Time Frame: We will be measuring this continuously throughout inpatient hospitalization, beginning at time of admission ] [ Designated as safety issue: No ]
- Cortisol; we want to measure a change in data from admission to discharge [ Time Frame: Two separate timepoints during inpatient hospitalization; first within 5 days of admission, and second within 72 hours of scheduled discharge ] [ Designated as safety issue: No ]Cortisol levels will be measured before and after a dexamethasone suppression test is administered at admission and discharge
| Enrollment: | 14 |
| Study Start Date: | January 2011 |
| Study Completion Date: | September 2012 |
| Groups/Cohorts |
|---|
| Major Depressive Disorder |
| Major Depressive Disorder with Psychotic Features |
Detailed Description:
Metabolic syndrome (MS) is a combination of medical problems that can increase the risk of heart disease and diabetes in some people. People with MS can have some or all of the following:
- High blood glucose
- High blood pressure
- Abdominal obesity
- Low levels of high-density lipoprotein (HDL) cholesterol
- High levels of triglycerides
Some studies have shown that people with certain disorders have a greater risk for developing MS. This may be because of a combination of factors, including but not limited to the type of medications used, age, and whether or not someone smokes. This study will also aim to learn more about a naturally-occurring stress hormone called cortisol that is made in the body.
In order to measure these factors, the following things will occur:
- administer a number of questionnaires
- gather information from medical history
- gather information about current psychiatric mood
- draw blood and collect a urine sample
To study the amount of cortisol in the body, a dexamethasone suppression test (DST) will be given. This test involves taking a single 1mg pill of dexamethasone, a steroid, and numerous blood draws. Like any drug, it has some risks, however it is unlikely any side effects will occur because of the low dose administered.
Eligibility| Ages Eligible for Study: | 18 Years to 85 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Eligible subjects are people who are inpatient in the medical-psychiatric unit at Massachusetts General Hospital. Included subjects have working diagnosis of major depressive disorder (MDD) or major depressive disorder with psychotic features (MDpsy).
Inclusion Criteria:
- Capable of giving informed consent
- DSM-IV TR diagnosis of Major Depressive Disorder with (MDpsy) or without (MDD) Psychotic Features
- Age between 18 and 85, inclusive
- Pre-existing Hyperlipidemia, Hypertension, and Diabetes must be stable with laboratory and clinical results within acceptable range; with or without medication for three months prior to admission
Exclusion Criteria:
- DSM-IV TR diagnosis of: schizophrenia, schizoaffective disorder, delusional disorder, bipolar disorder, organic mental disorder, substance use dependence including alcohol, that has been active within the past 6 months, acute bereavement, and psychotic disorder not elsewhere classified
- Subjects that meet criteria for substance or alcohol dependence more recently than three months prior to entering the study
- Subjects that meet criteria for substance or alcohol abuse more recently than four weeks prior to entering the study
- Pregnancy
- Unstable or inadequately treated pre-existing hyperlipidemia, hypertension, and diabetes
- Subjects who are involuntarily committed.
Contacts and Locations| United States, Massachusetts | |
| Massachusetts General Hospital | |
| Boston, Massachusetts, United States, 02114 | |
More Information
No publications provided
| Responsible Party: | John D. Matthews, Principal Investigator, Assistant Professor of Psychiatry, Harvard Medical School, Massachusetts General Hospital |
| ClinicalTrials.gov Identifier: | NCT01310140 History of Changes |
| Other Study ID Numbers: | 2009-P-002723 |
| Study First Received: | February 15, 2011 |
| Last Updated: | November 2, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Massachusetts General Hospital:
|
Metabolic Syndrome Insulin Resistance Massachusetts General Hospital Major Depressive Disorder |
Major Depressive Disorder with Psychotic Features Cortisol Dexamethasone Suppression Test |
Additional relevant MeSH terms:
|
Depressive Disorder Depression Insulin Resistance Mental Disorders Psychotic Disorders Depressive Disorder, Major Metabolic Syndrome X Mood Disorders Behavioral Symptoms |
Hyperinsulinism Glucose Metabolism Disorders Metabolic Diseases Schizophrenia and Disorders with Psychotic Features Insulin Hypoglycemic Agents Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 19, 2013