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Detecting Depression and Bipolar Disorder in Adolescents Using a Biomarker Panel

Detecting Depression and Bipolar Disorder in Adolescents Using a Biomarker Panel

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01957501
Enrollment
75
Registered
2013-10-08
Start date
2013-07-31
Completion date
2016-03-31
Last updated
2017-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder, Major Depressive Disorder, Serum Biomarkers

Keywords

Major Depressive Disorder, Bipolar Disorder, Adolescents, Biomarker

Brief summary

Depression and bipolar disorder are major public health concerns for adolescents today. Teenage depression and bipolar disorder are associated with social isolation, family stress, school failure, substance abuse and suicide. Screening for depression and bipolar disorder so that treatment can be started early in the course of illness is an urgent public health priority. Many teens with bipolar disorder are incorrectly diagnosed as having unipolar depression. It is critical that adolescents receive proper screening and assessment that leads to an accurate diagnosis and treatment. An efficient, cost-effective, blood-based screening program could be performed on an annual or semi-annual basis to potentially detect depression and then differentiate between unipolar and bipolar depression. If this type of screening were able to detect a significant percentage of teens with depression or bipolar disorder, the positive impact on U.S. public health would be substantial. The purpose of this study is to conduct a pilot study to assess the probability of detecting adolescent unipolar and bipolar depression through blood samples.

Interventions

OTHERMDDScoreTM

The child will receive a single blood draw (about 10 mL).

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
13 Years to 21 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion of Major Depressive Disorder Participants: 1. Male and female patients between the ages of 13 and 17 years 2. Participants must be able to give informed assent, and parent(s)/guardian(s) must be able to give informed permission for study participation 3. Diagnosis of MDD or depression not otherwise specified, as defined by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition-TR criteria (DSM-IV-TR) 4. Current mood state depressed for \> 2 weeks Inclusion of Bipolar Disorder Participants: 1. Male and female patients between the ages of 13 and 17 years 2. Participants must be able to give informed assent, and parent (s)/guardian (s) must be able to give informed permission for study participation 3. Diagnosis of Bipolar I Disorder, Bipolar II Disorder, or not otherwise specified, as defined by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition-TR criteria 4. Current mood state depressed for \> 2 weeks Inclusion of Healthy Control Participants: 1. Males and females between the ages of 13 and 17 years 2. Participants must not meet DSM-IV-TR diagnostic criteria for a psychiatric or substance abuse disorder 3. Participants must be able to give informed assent and parent (s)/guardian (s) must be able to give informed permission for study participation

Exclusion criteria

Exclusion of Major Depressive Disorder and Bipolar Disorder Participants: 1. Meet the DSM-IV criteria for substance abuse or dependence in the last month 2. History of fainting or other significant adverse event during blood draws in the past 3. Dysthymia 4. Daily use of oral or inhaled steroids 5. High risk of suicidal behaviors, homicidal behaviors, or self-harm 6. A medical condition, such as Addison's Disease, which is highly likely to influence the inflammatory or HPA responses Exclusion of Healthy Control Participants: 1. Clinically significant psychiatric or substance abuse disorder 2. Unstable medical or neurological illness 3. History of fainting or other significant adverse event during blood draws in the past 4. Daily use of oral or inhaled steroids 5. A medical condition, such as Addison's Disease, which is highly likely to influence the inflammatory or HPA responses

Design outcomes

Primary

MeasureTime frameDescription
Biomarker for Major Depressive Disorder (MDD) and Bipolar Disorder in Adolescents4 yearsThe MDDScore™ will determine the biomarker of Major Depressive Disorder (MDD) and Bipolar Disorder. The MDDScore™ is determined using nine blood based biomarkers (inflammatory markers \[4\], stress related hormones \[2\], neuroendocrine \[1\] and metabolic proteins \[2\]) on physiological pathways related to MDD. The test results for the MDDScore™ range from 1 to 10. If the patient's score is 1, the patient has a less than 10% likelihood of having MDD. If the patient's MDDScore™ is 10, the patient has a greater than 90% likelihood of having MDD. An MDDScore™ of 5 or less is considered normal or negative and a score of 6 or more is considered diseased or positive. This same scoring system would hold true for classifying the likelihood of having bipolar disorder, as well. Test characteristics, such as sensitivity and specificity, are calculated based on this determination.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026