Simultaneous FMRI and NIRS to Estimate Brain Cerebral Metabolism

Mass General Brigham

Status: Completed

Conditions: Healthy

Study type: Observational

Funder types: Other

Identifiers

NCT01825096

2012p00622

Details and patient eligibility

About

The principal advantages of functional magnetic resonance imaging (fMRI) with blood-oxygenation- level-dependent (BOLD) contrast for studying brain function are: non-invasiveness, ubiquitous availability, relatively high spatiotemporal resolution, and the ability to map function over the entire brain. Thus, BOLD fMRI is the most widely applied technology to study healthy brain function and pathophysiology associated with disease. In studies of drug abuse and psychiatric illness though, normal assumptions mapping BOLD signals to neurometabolism may be violated. Generally, these effects are ignored, resulting in large study-to-study variability.

Quantitative fMRI (qfMRI) measures metabolism directly and is more suitable for studies of drug abuse and psychiatric illness. However, qfMRI is too complex for routine use. Cerebral metabolism during brain activation during visual stimulation measured with a new fMRI approach that is simple enough for clinical applications will be compared to CMRO2 activation measured using standard qfMRI.

Full description

Healthy subjects will undergo a single imaging session. During the imaging session, fMRI and simultaneous near-infrared spectroscopy measurements will be made during visual stimulation (e.g., viewing a flashing checkerboard). This is a methods development study focused on comparing a new method for estimating CMRO2 associated with brain activation with the standard fMRI approach for estimating CMRO2.

Enrollment: 1 patient

Sex: Male

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male
• 18 to 40 years old
• Physically healthy by self-report

Exclusion criteria

Diagnosis of current drug abuse/dependence, including nicotine, as assessed by DSM-IV criteria

• Current diagnosis of Axis I disorder using DSM-IV criteria, or any Axis I disorder within past 5 years
• Current daily use of antipsychotic, antidepressant, or other psychoactive prescription drug, as well as daily use of non-prescription drugs
• Life threatening or unstable medical illness, or one that can create marked change in mental state
• Heavy caffeine use (greater than 300 mg on a regular, daily basis)
• History of seizure disorder
• Subjects that report any history or current major medical illness (cardiovascular, pulmonary, psychiatric, or neurological disorders)
• Subjects who have metal in their body or suffer from claustrophobia cannot participate in this research study.
• Additional MR exclusion criteria may include people with:
• Cardiac pacemakers
• Metal clips on blood vessels (also called stents)
• Artificial heart valves
• Artificial arms, hands, legs, etc.
• Brain stimulator devices
• Implanted drug pumps
• Ear implants
• Eye implants or known metal fragments in eyes
• Exposure to shrapnel or metal filings (wounded in military combat, sheet metal workers, welders, and others)
• Other metallic surgical hardware in vital areas
• Certain tattoos with metallic ink (subjects are asked to inform research staff if they have a tattoo)
• Metal Containing Intrauterine Devices (IUDs).
• Certain transdermal (skin) patches such as Transderm Scop (scopolamine for motion sickness).

Trial design

1 participants in 1 patient group

baseline

Description:

No intervention. Participants are scanned at baseline.