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Examining Neurobiological Mechanisms Underlying the Therapeutic Effect of the Ketogenic Diet in Bipolar Disorder (BD)

Not Applicable
Recruiting
Conditions
Bipolar Disorder
Interventions
Other: Non-ketogenic Diet
Other: No diet
Other: Ketogenic Diet
Registration Number
NCT06081426
Lead Sponsor
University of Pittsburgh
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
107
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
  • Meeting diagnosis proportion: 50:50% BDI:II (DSM-5)
  • Score less than or equal to 10 on YMRS
  • BD medications will be allowed as in our previous studies: any combination of atypical antipsychotics, lithium, antidepressants, anxiolytics (common in BD)

Healthy Control (HC) Group (n=30):

  • Sex matched with BD groups
  • No psychiatric history
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.
  • Taking anticoagulants and/or those with blood dyscrasias (illnesses) who have coagulation disorders (eg, hemophilia) because of the ketomojo finger stick blood tests
  • Scoring 3 or higher on positive symptom factor questions on the Positive and Negative Syndrome Scale (PANSS) questionnaire (indicative of psychotic symptoms)
  • Currently following a ketogenic diet
  • Head circumference larger than 24 inches (62cm) and/or chest circumference larger than 55 inches (139 cm)

BD hypomanic group:

  • Must be meeting sex proportions: not 50% female
  • Must be meeting diagnosis proportions: not 50:50% BDI:II (DSM-5)
  • Diagnosis of BD in a manic or euthymic episode
  • Score 10 or lower on the Young Mania Rating Scale score(YMRS)
  • Using psychotropic medications other than those allowed in inclusion criteria
  • Does not have a smartphone with a) iOS version 12.0 or above, or b) Android version 8 and later to use with the Keto-Mojo app

BD euthymic group:

  • Not meeting sex proportion: not 50% female
  • Not meeting diagnosis proportion: not 50:50% BDI:II
  • Diagnosis of BD in a depressive, hypomanic, or manic episode
  • Score greater than 10 on YMRS
  • Using psychotropic medications other than those allowed in inclusion criteria
  • Does not have a smartphone with a) iOS version 12.0 or above, or b) Android version 8 and later to use with the Keto-Mojo app

Healthy Control (HC) Group

  • Not sex-matched with BD groups
  • Has psychiatric history

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
1st phase Non-ketogenic Diet / 2nd phase Ketogenic DietNon-ketogenic DietParticipants with Bipolar Disorder will consume a non-ketogenic diet for the first phase of the study and then a ketogenic diet for the second phase of the study
1st phase Ketogenic Diet / 2nd phase Non-ketogenic DietNon-ketogenic DietParticipants with Bipolar Disorder will consume a ketogenic diet for the first phase of the study and then a non-ketogenic diet for the second phase of the study
No dietNo dietParticipants without Bipolar Disorder will not participate in the diet phases of the study
1st phase Non-ketogenic Diet / 2nd phase Ketogenic DietKetogenic DietParticipants with Bipolar Disorder will consume a non-ketogenic diet for the first phase of the study and then a ketogenic diet for the second phase of the study
1st phase Ketogenic Diet / 2nd phase Non-ketogenic DietKetogenic DietParticipants with Bipolar Disorder will consume a ketogenic diet for the first phase of the study and then a non-ketogenic diet for the second phase of the study
Primary Outcome Measures
NameTimeMethod
Fasting hepatic function panel at Baseline: bilirubinBaseline (all participants)

Fasting levels of bilirubin in the blood

Blood oxygen level-dependent (BOLD) signal at Scan 3End 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 1Baseline 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 3Scan 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 BaselineBaseline (all participants)

Fasting lipid blood levels

Fasting Glucose at end of second dietary phaseEnd of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting glucose blood levels

Fasting Glucose at BaselineBaseline (all participants)

Fasting glucose blood levels

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

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

Fasting hepatic function panel at Baseline: total proteinBaseline (all participants)

Fasting levels of total protein in the blood

Fasting hepatic function panel at Baseline: albuminBaseline (all participants)

Fasting levels of albumin in the blood

Fasting Glucose at halfway point through first dietary phaseHalfway 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 proteinEnd 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 enzymeBaseline (all participants)

Fasting levels of liver enzyme in the blood

Fasting lipids at halfway point through first dietary phaseHalfway 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 enzymeHalfway 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 phaseEnd 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 enzymeEnd 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 phaseHalfway 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: albuminHalfway 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 2End 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 2Scan 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 proteinHalfway 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 phaseEnd of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting glucose blood levels

Fasting hepatic function at end of first dietary phase: bilirubinEnd 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 phaseHalfway 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 proteinHalfway 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: albuminHalfway 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: bilirubinHalfway 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 enzymeHalfway 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 proteinEnd 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: albuminEnd 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 enzymeEnd 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: albuminEnd of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of albumin in the blood

Lactate at BaselineBaseline Scan 1 (all participants)

Lactate concentrations in the brain

Lactate at end of first dietary phaseScan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Lactate concentrations in the brain

Fasting hepatic function at halfway point through second dietary phase: bilirubinHalfway 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: bilirubinEnd of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting levels of bilirubin in the blood

Gamma-aminobutyric acid (GABA) at BaselineBaseline Scan 1 (all participants)

Gamma-aminobutyric acid (GABA) concentrations in the brain

Glutamate at end of first dietary phaseScan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Glutamate concentrations in the brain

Glutamate at end of second dietary phaseScan 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 phaseScan 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 phaseEnd of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Fasting lipids blood levels

Gamma-aminobutyric acid (GABA) at end of first dietary phaseScan 2 at end of first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Gamma-aminobutyric acid (GABA) concentrations in the brain

Glutamate at BaselineBaseline Scan 1 (all participants)

Glutamate concentrations in the brain

Gamma-aminobutyric acid (GABA) at end of second dietary phaseScan 3 at end of second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Gamma-aminobutyric acid (GABA) concentrations in the brain

Secondary Outcome Measures
NameTimeMethod
Average total sleep time during Ketogenic vs Normal dietWrist actigraphy will be collected throughout the 8-10wk ketogenic diet and normal diet study intervals

Total sleep time will be assessed using wrist actigraphy. Wrist actigraphy will be collected continuously, at-home.

Ecological momentary assessments (EMA) during the second dietary phase: Suicidality monitoringThe second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Suicidality monitoring in real time in participants with Bipolar Disorder: answer yes or no to having self-harm/suicide thoughts and plans

Average rest-activity rhythm interdaily stability during Ketogenic vs Normal dietWrist actigraphy will be collected throughout the 8-10 wk ketogenic diet and normal diet study intervals.

Rest-activity rhythm interdaily stability will be assessed using wrist actigraphy. Wrist actigraphy will be collected continuously, at-home

Ecological momentary assessments (EMA) during the first dietary phase: Mood monitoringThe first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Mood monitoring in real time in participants with Bipolar Disorder: rate mood on a scale of 1-7 with 1 being very low mood and 7 being very high mood

Ecological momentary assessments (EMA) during the second dietary phase: Mood monitoringThe second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Mood monitoring in real time in participants with Bipolar Disorder: rate mood on a scale of 1-7 with 1 being very low mood and 7 being very high mood

Ecological momentary assessments (EMA) during the first dietary phase: Suicidality monitoringThe first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Suicidality monitoring in real time in participants with Bipolar Disorder: answer yes or no to having self-harm/suicide thoughts and plans

Ecological momentary assessments (EMA) during the first dietary phase: Energy monitoringThe first dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Energy monitoring in real time in participants with Bipolar Disorder: rate energy on a scale of 1-7 with 1 being very low energy and 7 being very high energy

Ecological momentary assessments (EMA) during the second dietary phase: Energy monitoringThe second dietary phase (8-10 weeks) (participants with Bipolar Disorder)

Energy monitoring in real time in participants with Bipolar Disorder: rate energy on a scale of 1-7 with 1 being very low energy and 7 being very high energy

Trial Locations

Locations (1)

University of Pittsburgh Medical Center

🇺🇸

Pittsburgh, Pennsylvania, United States

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