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Clinical Trials/NCT06081426
NCT06081426
Recruiting
Not Applicable

Elucidating Neurobiological Mechanisms Underlying the Therapeutic Effect of the Ketogenic Diet in Bipolar Disorder (BD): a Multidisciplinary Mechanistic Study

University of Pittsburgh1 site in 1 country107 target enrollmentJanuary 12, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bipolar Disorder
Sponsor
University of Pittsburgh
Enrollment
107
Locations
1
Primary Endpoint
Fasting hepatic function panel at Baseline: bilirubin
Status
Recruiting
Last Updated
4 months ago

Overview

Brief Summary

The investigators aim to examine the effect of the ketogenic diet on brain activity, metabolism, and emotions in adults with Bipolar Disorder (BD).

Detailed Description

The investigators hypothesize that a ketogenic diet will enhance levels of the ketone body β-Hydroxybutyrate (beta OHB), resulting in reduced mania/hypomania severity and predisposition to mania/hypomania in individuals with BD. To test this hypothesis in depth, the investigators will use a novel, multidisciplinary mechanistic study using multimodal neuroimaging, peripheral markers of mitochondrial metabolism, and participant-derived induced pluripotent stem cell (iPSC)-derived organoids.

Registry
clinicaltrials.gov
Start Date
January 12, 2024
End Date
January 1, 2027
Last Updated
4 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mary Phillips, MD MD (Cantab)

Professor

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • All participants:
  • 18-40 years of age
  • Not following a ketogenic diet
  • BD hypomanic group (n=30):
  • Meeting sex proportion: 50% female
  • Meeting diagnosis proportion: 50:50% Bipolar I: Bipolar II (BDI:II) (Diagnostic and Statistical Manual of Mental Disorders 5; DSM-5)
  • Score greater than 10 on the Young Mania Rating Scale score(YMRS)
  • BD medications will be allowed as in our previous studies: any combination of atypical antipsychotics, lithium, antidepressants, anxiolytics (common in BD)
  • BD euthymic group (n=30):
  • Meeting sex proportion: 50% female

Exclusion Criteria

  • All participants:
  • Not between 18-40 years of age
  • History of head injury, neurological, pervasive developmental disorder (e.g. autism), systemic medical disease and treatment (medical records, participant report)
  • Mini-Mental State Examination score (cognitive state) \<24
  • Premorbid National Adult Reading Test Intelligent Quotient (NAART IQ) estimate\<85
  • Visual disturbance: \<20/40 Snellen visual acuity
  • History of alcohol/substance use disorder (SUD; all substances, including nicotine), and/or illicit substance use (except cannabis) over the last 6 months (SCID-5). Note: lifetime/present cannabis use (at non-abuse (\<3 times in the past month) and non SUD levels) will be allowed, given its common usage in BD and young adults. Cannabis SUD over the last 6 months will not be allowed. Urine tests on scan days will exclude current illicit substance use (except cannabis). Salivary alcohol tests on scan days will exclude intoxicated individuals
  • MRI exclusion: metallic objects, e.g., surgical implants; claustrophobia; positive pregnancy test for females or self-report pregnancy
  • Unable to understand English
  • Conditions related to the pancreas, liver, thyroid or gallbladder.

Outcomes

Primary Outcomes

Fasting hepatic function panel at Baseline: bilirubin

Time Frame: Baseline (all participants)

Fasting levels of bilirubin in the blood

Blood oxygen level-dependent (BOLD) signal at Scan 3

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

The blood oxygen level-dependent (BOLD) signal indicates brain activity and connectivity

Manic symptoms at Scan 1

Time Frame: Baseline Scan 1 (all participants)

The Young Mania Rating Scale (YMRS) indicates the level of manic symptoms with a total score that varies between zero (better outcome) and 60 (worse outcome)

Manic symptoms at Scan 3

Time Frame: Scan 3 at end of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

The Young Mania Rating Scale (YMRS) indicates the level of manic symptoms with a total score that varies between zero (better outcome) and 60 (worse outcome)

Fasting lipids at Baseline

Time Frame: Baseline (all participants)

Fasting lipid blood levels

Fasting Glucose at end of second dietary phase

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting glucose blood levels

Fasting Glucose at Baseline

Time Frame: Baseline (all participants)

Fasting glucose blood levels

Blood oxygen level-dependent (BOLD) signal at Scan 1

Time Frame: Baseline Scan 1 (all participants)

The blood oxygen level-dependent (BOLD) signal indicates brain activity and connectivity

Fasting hepatic function panel at Baseline: total protein

Time Frame: Baseline (all participants)

Fasting levels of total protein in the blood

Fasting hepatic function panel at Baseline: albumin

Time Frame: Baseline (all participants)

Fasting levels of albumin in the blood

Fasting Glucose at halfway point through first dietary phase

Time Frame: Halfway point through first dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting glucose blood levels

Fasting hepatic function at end of first dietary phase: total protein

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of total protein in the blood

Fasting hepatic function panel at Baseline: liver enzyme

Time Frame: Baseline (all participants)

Fasting levels of liver enzyme in the blood

Fasting lipids at halfway point through first dietary phase

Time Frame: Halfway point through first dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting lipid blood levels

Fasting hepatic function at halfway point through first dietary phase: liver enzyme

Time Frame: Halfway point through first dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of liver enzyme in the blood

Fasting lipids at end of first dietary phase

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting lipid blood levels

Fasting hepatic function at end of first dietary phase: liver enzyme

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of liver enzyme in the blood

Fasting Glucose at halfway point through second dietary phase

Time Frame: Halfway point through second dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting glucose blood levels

Fasting hepatic function at halfway point through second dietary phase: albumin

Time Frame: Halfway point through second dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of albumin in the blood

Blood oxygen level-dependent (BOLD) signal at Scan 2

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

The blood oxygen level-dependent (BOLD) signal indicates brain activity and connectivity

Manic symptoms at Scan 2

Time Frame: Scan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

The Young Mania Rating Scale (YMRS) indicates the level of manic symptoms with a total score that varies between zero (better outcome) and 60 (worse outcome)

Fasting hepatic function at halfway point through first dietary phase: total protein

Time Frame: Halfway point through first dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of total protein in the blood

Fasting Glucose at end of first dietary phase

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting glucose blood levels

Fasting hepatic function at end of first dietary phase: bilirubin

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of bilirubin in the blood

Fasting lipids at halfway point through second dietary phase

Time Frame: Halfway point through second dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting lipid blood levels

Fasting hepatic function at halfway point through second dietary phase: total protein

Time Frame: Halfway point through second dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of total protein in the blood

Fasting hepatic function at halfway point through first dietary phase: albumin

Time Frame: Halfway point through first dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of albumin in the blood

Fasting hepatic function at halfway point through first dietary phase: bilirubin

Time Frame: Halfway point through first dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of bilirubin in the blood

Fasting hepatic function at halfway point through second dietary phase: liver enzyme

Time Frame: Halfway point through second dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of liver enzyme in the blood

Fasting hepatic function at end of second dietary phase: total protein

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of total protein in the blood

Fasting hepatic function at end of second dietary phase: albumin

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of albumin in the blood

Fasting hepatic function at end of second dietary phase: liver enzyme

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of liver enzyme in the blood

Fasting hepatic function at end of first dietary phase: albumin

Time Frame: End of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of albumin in the blood

Lactate at Baseline

Time Frame: Baseline Scan 1 (all participants)

Lactate concentrations in the brain

Lactate at end of first dietary phase

Time Frame: Scan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Lactate concentrations in the brain

Glutamate at end of first dietary phase

Time Frame: Scan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Glutamate concentrations in the brain

Fasting hepatic function at halfway point through second dietary phase: bilirubin

Time Frame: Halfway point through second dietary phase (4-5 weeks) (participants with Bipolar Disorder)

Fasting levels of bilirubin in the blood

Fasting hepatic function at end of second dietary phase: bilirubin

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of bilirubin in the blood

Gamma-aminobutyric acid (GABA) at Baseline

Time Frame: Baseline Scan 1 (all participants)

Gamma-aminobutyric acid (GABA) concentrations in the brain

Glutamate at end of second dietary phase

Time Frame: Scan 3 at end of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Glutamate concentrations in the brain

Lactate at end of second dietary phase

Time Frame: Scan 3 at end of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Lactate concentrations in the brain

Fasting lipids at end of second dietary phase

Time Frame: End of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting lipids blood levels

Gamma-aminobutyric acid (GABA) at end of first dietary phase

Time Frame: Scan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Gamma-aminobutyric acid (GABA) concentrations in the brain

Glutamate at Baseline

Time Frame: Baseline Scan 1 (all participants)

Glutamate concentrations in the brain

Gamma-aminobutyric acid (GABA) at end of second dietary phase

Time Frame: Scan 3 at end of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Gamma-aminobutyric acid (GABA) concentrations in the brain

Secondary Outcomes

  • Average total sleep time during Ketogenic vs Normal diet(Wrist actigraphy will be collected throughout the 8-10wk ketogenic diet and normal diet study intervals)
  • Ecological momentary assessments (EMA) during the second dietary phase: Suicidality monitoring(The second dietary phase (8-10 weeks) (participants with Bipolar Disorder))
  • Average rest-activity rhythm interdaily stability during Ketogenic vs Normal diet(Wrist actigraphy will be collected throughout the 8-10 wk ketogenic diet and normal diet study intervals.)
  • Ecological momentary assessments (EMA) during the first dietary phase: Mood monitoring(The first dietary phase (8-10 weeks) (participants with Bipolar Disorder))
  • Ecological momentary assessments (EMA) during the second dietary phase: Mood monitoring(The second dietary phase (8-10 weeks) (participants with Bipolar Disorder))
  • Ecological momentary assessments (EMA) during the second dietary phase: Energy monitoring(The second dietary phase (8-10 weeks) (participants with Bipolar Disorder))
  • Ecological momentary assessments (EMA) during the first dietary phase: Suicidality monitoring(The first dietary phase (8-10 weeks) (participants with Bipolar Disorder))
  • Ecological momentary assessments (EMA) during the first dietary phase: Energy monitoring(The first dietary phase (8-10 weeks) (participants with Bipolar Disorder))

Study Sites (1)

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