MedPath

Neuroimmune Mechanisms in Obesity

Phase 1
Withdrawn
Conditions
Obesity
Interventions
Registration Number
NCT05553405
Lead Sponsor
Yale University
Brief Summary

Aim 1: To measure levels of microglia using the radiotracer \[11C\]PBR28 and PET brain imaging in obese (n=50) vs. lean individuals (n=50). The investigators will recruit 100 subjects who will participate in a single \[11C\]PBR28 scan to measure levels of TSPO, a marker of microglia.

Aim 2: To determine differences in brain functional connectivity at rest and in response to a decision- making task in obese (n=50) vs. lean individuals (n=50) using fMRI imaging. The same subjects from Aim 1 will participate in a resting state functional magnetic resonance imaging (fMRI) followed by a decision making task during fMRI acquisition.

Aim 3: To assess whether acute elevation of lipid levels through intralipid infusion in lean, healthy individuals (n=20) will induce microglial activation. 20 lean individuals will be recruited to participate in a paradigm that includes a baseline \[11C\]PBR28 scan, an infusion of intralipid, and a second \[11C\]PBR28 scan approximately 4 hours post intralipid infusion. The investigators will attempt to utilize subjects from aim 1 in order to use their baseline scans for this paradigm.

Aim 4: To determine whether there are differences in levels of microglia between individuals with and without type 1 diabetes (n=20). 20 patients with diabetes (type 1 diabetes or type 2 diabetes)will be recruited to participate in a single \[11C\]PBR28 scan to compare to Aim 1 participants.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Age 18-55 years
  • Able to read and write English and provide voluntary informed consent
  • Physically and psychiatrically healthy by medical history, physical, psychiatric, neurological, EKG and laboratory examinations
  • For Aims 1-3: HbA1C < 5.7%
  • For Aim 4: HbA1C >6.5% and known diagnosis of T1DM or T2DM
Exclusion Criteria
  • Abnormal labs including Creatinine>1.5mg/dL, Hematocrit < 35% for females and < 39% for males, ALT/AST >2.5X upper limit of normal, abnormal TSH
  • Known significant thyroid, hepatic, neurologic, psychiatric, cerebrovascular, or cardiovascular disease
  • >5% body weight change in last 6 months
  • Current or recent regular steroid use in last 6 months, illicit drug use that is deemed to interfere with results including problematic alcohol use as defined by NIAAA
  • Current regular use of psychotropic and/or potentially psychoactive prescription medications
  • Regular use of any vitamins/supplements that could affect lipids
  • Current regular use of non-steroidal anti-inflammatory medications, statins, or lipid lowering agents
  • Vaccination in the last month
  • Individuals who are classified as "low binders" for the rs6971 polymorphism (<10% of the population)
  • For females, physical or laboratory (-HCG) evidence of pregnancy, seeking pregnancy, or lactating. A urine drug screen and pregnancy test will be performed at screening and prior to the imaging session. Subjects who screen positive will be excluded.

Note: If a subject tests positive for an illicit substance, the PI will determine if the substance would interfere with the results and may terminate participation if applicable. Results of the test would only be noted in the subjects de-identified chart to document the occurrence.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Post-Intralipid Infusion [11C]PBR28 PET ScanIntralipid InfusionSubjects will complete a second 120-minute \[11C\]PBR28 PET scan 4 hours after Intralipid Infusion
Primary Outcome Measures
NameTimeMethod
Baseline [11C]PBR28 VT valuesAt baseline

\[11C\]PBR28 VT values in our primary regions of interest (PFC and hippocampus) from PET Scan. Linear mixed-effect models will be conducted to evaluate differences in \[11C\]PBR28 VT values between lean, healthy controls (n=40) and individuals with obesity (n=40), controlling for rs6971 genotype, age, and sex.

Post-Intralipid [11C]PBR28 VT valuesApproximately 3 Hours After Intralipid Infusion

\[11C\]PBR28 VT values in our primary regions of interest (PFC and hippocampus) from PET Scan. Linear mixed-effect models will be conducted to evaluate differences in \[11C\]PBR28 VT values between lean, healthy controls (n=40) and individuals with obesity (n=40), controlling for rs6971 genotype, age, and sex.

Baseline Functional ConnectivityAt baseline

ICD values will be obtained from primary a priori regions of interest (vmPFC and hippocampus) with PET Scan. Independent t-tests will be used to compare the ICD data between the study groups.

Post-Intralipid Functional ConnectivityApproximately 3 Hours After Intralipid Infusion

ICD values will be obtained from primary a priori regions of interest (vmPFC and hippocampus) with PET Scan. Independent t-tests will be used to compare the ICD data between the study groups.

Baseline Microglial ActivationAt baseline

Regional \[11C\]PBR28 VT values from pre-lipid infusion PET Scan

Post-Intralipid Microglial ActivationApproximately 3 Hours After Intralipid Infusion

Percent change in regional \[11C\]PBR28 VT values from pre-lipid infusion PET Scan to post-lipid infusion PET Scan will be calculated across brain regions. Increased microglial activation will be measured as a 20% or more increase in TSPO levels from scan 1 to scan 2

Secondary Outcome Measures
NameTimeMethod
Baseline Visual AttentionAt baseline

Visual attention: response latency to identify card color (log10(ms); higher \~ worse attention).

Post-Intralipid Infusion Visual AttentionApproximately 1 Hour After Intralipid Infusion

Visual attention: response latency to identify card color (log10(ms); higher \~ worse attention).

Baseline Visual LearningAt baseline

Visual learning: % of correctly identified repeat cards (arcsine(% correct); higher values \~ better learning).

Post-Intralipid Infusion Visual LearningApproximately 1 Hour After Intralipid Infusion

Visual learning: % of correctly identified repeat cards (arcsine(% correct); higher values \~ better learning).

Baseline Verbal MemoryAt baseline

Verbal memory: # of correctly recalled items from a grocery list (3 trials). Verbal recall: # of correctly recalled items from a grocery list after a delay (1 trial; higher \~ better memory/recall).

Post-Intralipid Verbal MemoryApproximately 1 Hour After Intralipid Infusion

Verbal memory: # of correctly recalled items from a grocery list (3 trials). Verbal recall: # of correctly recalled items from a grocery list after a delay (1 trial; higher \~ better memory/recall).

Baseline Executive FunctionAt baseline

Executive function: number of errors navigating a 'hidden' maze (5 trials; higher \~ worse executive function).

Post-Intralipid Executive FunctionApproximately 1 Hour After Intralipid Infusion

Executive function: number of errors navigating a 'hidden' maze (5 trials; higher \~ worse executive function).

Baseline Visual-Motor Processing SpeedAt baseline

Visual-motor processing speed: response latency to detect a card flipped over (log10(ms); higher \~ worse processing speed).

Post-Intralipid Visual-Motor Processing SpeedApproximately 1 Hour After Intralipid Infusion

Visual-motor processing speed: response latency to detect a card flipped over (log10(ms); higher \~ worse processing speed).

Baseline Working MemoryAt baseline

Working memory: % of correctly identified cards that matched the card presented either one- or two-cards previously (arcsine(% correct); higher \~ better working memory).

Post-Intralipid Working MemoryApproximately 1 Hour After Intralipid Infusion

Working memory: % of correctly identified cards that matched the card presented either one- or two-cards previously (arcsine(% correct); higher \~ better working memory).

Baseline Social CognitionAt baseline

Social cognition: response latency to identify the mismatched facial expression based on its emotional content (ms; log10; higher \~ worse social cognition).

Post-Intralipid Social CognitionApproximately 1 Hour After Intralipid Infusion

Social cognition: response latency to identify the mismatched facial expression based on its emotional content (ms; log10; higher \~ worse social cognition).

Baseline Reward ResponsivenessAt baseline

Reward responsiveness will be quantified via computerized Probabilistic Reward Task

Post-Intralipid Reward ResponsivenessApproximately 1 Hour After Intralipid Infusion

Reward responsiveness will be quantified via computerized Probabilistic Reward Task

Trial Locations

Locations (1)

Yale University

🇺🇸

New Haven, Connecticut, United States

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