RecruitingPhase 4NCT07087106

Glucose Consumption in MS Using [F-18]FDG-PET

Novel Assessment of Glucose Consumption in Multiple Sclerosis Utilizing [F-18]FDG-PET


Sponsor

Brigham and Women's Hospital

Enrollment

50 participants

Start Date

May 31, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Given the need for better diagnostic imaging techniques in multiple sclerosis (MS), the study aims to investigate the utility of \[F-18\]FDG positron emission tomography (PET) in MS. The study will be assessing glucose consumption patterns in subjects with progressive MS (PMS) and relapsing-remitting MS (RRMS), as well as healthy controls. PET will be compared to magnetic resonance imaging (MRI) lesion load and brain atrophy, and serum and blood biomarkers, as well as clinical measures of physical disability, cognitive impairment, fatigue, and depression. This study's findings may pave a path for integrating \[F-18\]FDG-PET in routine clinical practice for MS, improving patient experiences and outcomes. The specific aims of the study are: Aim 1: To compare glucose consumption in the brain in subjects with PMS, relapsing-remitting MS (RRMS), and healthy controls, using the radiolabeled glucose analogue 18-fluorodeoxyglucose, also known as \[F-18\]FDG. Aim 2: To compare the relationship between FDG-PET and standard 3T MRI measures including global and regional brain atrophy and lesion load, and to compare FDG-PET with MRI in terms of their relationship with clinical measures of physical disability, cognitive impairment, fatigue and depression in MS subjects. Aim 3: To assess the relationship of FDG-PET with serum and blood biomarkers, including but not limited to sNfL, GFAP, IL-6, and TNFα in MS.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study uses brain imaging (PET and MRI scans) to measure how the brain uses glucose (sugar) in people with multiple sclerosis (MS). Researchers hope this will help them better understand MS and track how the disease progresses over time. **You may be eligible if...** - You are 18–70 years old - You have been diagnosed with any form of MS (relapsing-remitting, secondary progressive, or primary progressive) - You are willing to undergo PET and MRI scans - You can give informed consent **You may NOT be eligible if...** - You have another neurological disorder, prior serious head injury, or substance abuse history - You have a psychiatric condition such as bipolar disorder or schizophrenia - You are pregnant, nursing, or trying to become pregnant - You have claustrophobia or a non-MRI-compatible implanted device - You have taken corticosteroids in the past four weeks Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUG[F-18]FDG

PET radiopharmaceutical


Locations(1)

Brigham & Women's Hospital

Boston, Massachusetts, United States

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NCT07087106


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