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Chronic stress has been proposed to be involved the development of western life-style diseases such as cardiovascular disease and type 2 diabetes (T2DM). At the same time chronic stress is also believed to cause psychiatric disease such as melancholic depression (MD)and anxiety disorders.
Accordingly, humans born with low birth weight (LBW) (ei. less than 5,0 LB) display an increased risk for T2DM and MD. Studies suggest stress and adrenal stress hormones (glucocorticoids) (GCC) might be involved in the development of both of these conditions.
Recent studies of animals born LBW suggest, that SSRI-compounds, usually employed in the treatment of MD-related diseases, reduces stress-responses and levels of stress hormones such adrenal steroids and at the same time has a positive influence on glucose metabolism.
In present study, the investigators aim to measure levels of GCC and stress and assess glucose metabolism in healthy young men (20-35 years) born LBW (40 subjects). The volume and structure of a certain brain area (ie. hippocampus) involved in regulation of adrenal GCC and known to be malfunctioning in chronically stressed individuals will be assessed by magnetic resonance imaging (MRI). Further metabolic examination will be accompanied by MRI spectroscopy of liver and muscle fat content as well as total fat content (Dexa-scanning) and contents of fat in the abdomen (by MRI) . Psychiatric well-ness and symptoms will be characterized by well-established questionnaires such as MDI and SCL-92 and responses as regards blood pressure, heart rate and changes in basal plasma concentrations of GCC and Epinephrine will be assessed while performing a Stroop Stress Test. Finally, a 24 hour blood pressure profile test will be included.
After this extensive examination program, subjects will be randomized to 3-4 months of treatment with either Escitalopram (an SSRI-compound) or Placebo. Subsequently, at the end of the treatment, the whole examination program will be repeated to detect potential beneficial changes.
A group of young normal birth weight men (20 subjects) will serve as a healthy baseline group for comparison and will not be exposed to any medical treatment.
This trial will add understanding to the mechanism underlying the development of type 2 diabetes and depression in LBW. Additionally, present trial might be capable of proposing a novel treatment strategy to prevent the development of these diseases in LBW man.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| escitalopram | Active Comparator | A pill containing Escitalopram |
|
| placebo | Placebo Comparator | a placebo pill |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Escitalopram | Drug | first week: 10mg/day. Then, treatment with 20mg/day is continued throughout a 3 months period of time. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes in rate of glucose dissappearance | Changes in LBW-subjects from baseline vs. post-treatment after 3 months treatment with placebo or Escitalopram | |
| Changes in the 24-hour AUC of free plasma cortisol | Changes in LBW-subjects from baseline vs. post-treatment after 3 months treatment with placebo or Escitalopram |
| Measure | Description | Time Frame |
|---|---|---|
| 24 hour basal plasma cortisol/ACTH profile as measured every 3rd hour. | before and after 3 months of treatment with placebo or Escitalopram | |
| hippocampic volume and structure as assessed by MRI | All limbic structures (amygdala, thalamus, hippocampus and ventromedial prefrontal cortex) were morphologically and volumetrically analyzed. |
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Inclusion Criteria:
Exclusion Criteria:
16/05-2011: Criterias updated - added 17 and adjusted 6. from BMI >25 to BMI >25.5
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Medical Dep M, Diabetes and Endocrinology Aarhus University Hospital, Aarhus Sygehus | Aarhus | 8000 | Denmark |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29053851 | Derived | Buhl CS, Stodkilde-Jorgensen H, Videbech P, Vaag A, Moller N, Lund S, Buhl ES. Escitalopram Ameliorates Hypercortisolemia and Insulin Resistance in Low Birth Weight Men With Limbic Brain Alterations. J Clin Endocrinol Metab. 2018 Jan 1;103(1):115-124. doi: 10.1210/jc.2017-01438. |
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| placebo | Drug | 1/2 pill pr day first week, then 1 pill pr. day throughout a 3 months treatment period (90-118 ± 7days) |
|
|
| before and after 3 months of treatment with placebo or Escitalopram |
| 24 hour bloodpressure profile | before and after 3 months of treatment with placebo or Escitalopram |
| MRI spectroscopy of fat in skeletal muscle tissue | Before and after 3 months of treatment with placebo or Escitalopram |
| MRI spectroscopy of fat in liver | Before and after 3 months of treatment with placebo or Escitalopram |
| Abdominal fat as assessed by MRI | Before and after 3 months of treatment with placebo or Escitalopram |
| MDI questionnaire scores | Before and after 3 months of treatment with placebo or Escitalopram |
| SCL-92 questionnaire scores | Before and after 3 months of treatment with placebo or Escitalopram |
| Fasting blood lipid profile | Before and after 3 months of treatment with placebo or Escitalopram |
| Ratio between insulin and glucose concentrations in blood during an oral glucose tolerance test (OGTT) | Before and after 3 months of treatment with placebo or Escitalopram |
| Whole body fat content as assessed by a dexa scanning | Before and after 3 months of treatment with placebo or Escitalopram |
| Hepatic insulin sensitivity as assessed suppression of endogenous glucose production (calculated by infusion of 3H-labelled glucose) | Before and after 3 months of treatment with placebo or Escitalopram |
| 10 pm to midnight basal plasma ACTH/cortisol concentration ratio as measured by blood sampling every 10th minute. | Before and after 3 months of treatment with placebo or Escitalopram |
| increase in blood pressure and heart rate during Stroops Stress test | Before and after 3 months of treatment with placebo or Escitalopram |
| Increase in plasma ACTH, cortisol and epinephrine concentrations during Stroops Stress Test | before and after 3 months of treatment with placebo or Escitalopram |
| SRPAS questionnaire scores | Self Reported Physical Activity Questionaire | Before and after 3 months of treatment with placebo or Escitalopram |
| Actigraph GT3X activity monitoring | Objective measurements of physical activity in 96 hours at home | Before and after 3 months of treatment with placebo or Escitalopram |
| Whole body bone mass density and T-/Z-scores as assessed by a dexa scanning | Before and after 3 months of treatment with placebo or Escitalopram |
| Plasma-Inflammation markers | Before and after 3 months of treatment with placebo or Escitalopram |
| ID | Term |
|---|---|
| D007333 | Insulin Resistance |
| D003924 | Diabetes Mellitus, Type 2 |
| D002318 | Cardiovascular Diseases |
| D003866 | Depressive Disorder |
| D001008 | Anxiety Disorders |
| ID | Term |
|---|---|
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D003920 | Diabetes Mellitus |
| D004700 | Endocrine System Diseases |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D000089983 | Escitalopram |
| ID | Term |
|---|---|
| D011437 | Propylamines |
| D000588 | Amines |
| D009930 | Organic Chemicals |
| D009570 | Nitriles |
| D001572 | Benzofurans |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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