FUNCTIONAL MRI in MOTOR IMAGERY JEFFREY S. ROSS, M.D. NEURORADIOLOGY CLEVELAND CLINIC FOUNDATION ROSSJ1@CCF.ORG FUNCTIONAL MRI • BRAIN IS UNIQUE – Strong relation between location and function • MULTIPLE TECHNIQUES TO EVALUATE FUNCTION – Clinical cases (strokes, tumors, epilepsy, etc.) – Animal lesion studies – EEG, MEG, etc. – Direct intraoperative electrical stimulation – Functional imaging (PET, FMRI) BASICS Change in local brain activity Change in local brain metabolism Change in local hemodynamics BASICS • IMAGE DURING 2 BEHAVIORAL STATES – Control state – Activation state • “DIFFERENCE” IMAGE SHOWS “ACTIVATED” BRAIN – Brain activated depends critically on design of task – Tasks carefully designed to isolate function of interest • BLOOD FLOW USED AS ENDOGENOUS CONTRAST BOLD FMRI basics • BOLD: Blood Oxygenation Level Dependent • Signal changes based on blood O2 level – Oxyhemoglobin (HbO2) diamagnetic – Deoxyhemoglobin (Hb) weakly paramagnetic • Paramagnetic substance – Causes local magnetic field heterogeneity – Shortens T2, T2* relaxation times – Lowers signal in tissue BOLD effect 100% O2 Room air Rat brain at 9 tesla (Ogawa et al MRM 14:68, 1990) BOLD EFFECT • BLOOD O2 LEVEL – Blood flow – Tissue metabolism • NEURAL ACTIVATION – Increase in local blood flow greater than – Increase in local O2 extraction – Increased capillary, venous HbO2 – More HbO2 causes increased signal • SMALL • DELAYED WITH RESPECT TO STIMULUS ONSET • LASTS A FEW SECONDS • FIELD STRENGTH DEPENDENT BOLD EFFECT RESTING ARTERY CAP ACTIVATED VEIN CBF CBV O2 SAT fMRI signal • SIGNAL CHANGES OF 2-5% • STRONGLY FIELD DEPENDENT • LAG TIME FOR RESPONSE, AT LEAST 300 msec UP TO 4s off 0 on off on off PROBLEMS • IMAGE NOISE • MOTION SENSITIVE – Head motion under 0.5 mm can ruin data • SILENT REGIONS – MAKE NOTHING OF WHAT YOU DON’T SEE • ACTIVATED REGIONS – ACTUAL CONTRIBUTION TO COGNITIVE TASK? • ANATOMICAL ACCURACY – LOCALIZATION OF EXTENT OF ACTIVATION – ASSUME ACTIVATION TAKES FORM OF DISCRETE LOCAL INCREASE IN FLOW PROBLEMS • PARADIGM DESIGN – ASSUME BRAIN IN STABLE COGNITIVE STATE DURING MEASUREMENT – HOW OFTEN REPEATED – HOW EASY/HARD TO PERFORM – NATURAL OR TIGHTLY CONTROLLED – COGNITIVE DEMANDS – EMOTIONS • MACROSCOPIC LANDMARKS – SEVERAL “SPACES” – TALAIRACH • PRECISE TEMPORAL RELATIONSHIP Mapping the Sensori-motor Homunculus TONGUE LIP HAND ELBOW SHOULDER HIP KNEE ANKLE WORD GENERATION MOTOR IMAGERY Introduction • Mental imagery involves rehearsing or practicing a task in the mind with no physical movement • The technique is commonly utilized, and widely advocated • Physical foundation of imagery not well characterized for fast, complex, automatic motor movements such as the golf swing LEADBETTER’S IMAGES GOLF DIGEST, MARCH 2001 It's a great image for any golfer faced with a pressure shot. Replay an old "tape" from your memory bank, thinking of a past success rather than calling up a negative memory. You'll then have an excellent chance of duplicating the successful shot. Introduction • This study evaluated motor imagery of the golf swing, of golfers of various handicaps, using fMRI to: • 1) Assess whether areas of brain activation could be defined by this technique and; • 2) To define any association between activated brain areas and golf skill. Materials and Methods • Six golfers of various handicap levels (0,5,7,10,11,13) with evaluated with functional MRI during a control condition and during mental imagery of their golf swing. • Five of the six subjects were right handed, and play golf right handed. • The subject with a 5 handicap (hcp) was left handed, but plays golf right handed. • 6 males, 24-50 years of age, average age 39 years. Materials and Methods • 1st person perspective, as they would on a practice tee, with each swing mentally occurring every 1.5-2 seconds. No preshot routine. • Two control conditions were evaluated, “rest” and “wall” PARADIGMS • REST – subjects were told to project themselves into a restful state, such as sitting quietly on a beach, taking care not to move mentally (or physically) during the study • WALL – were told to imagine leaning against a wall with their hands outstretched and pushing against it Materials and Methods • Functional studies were performed on either a 1.5T whole body (Symphony, Siemens, Erlangen) or 3T head only (Allegra, Siemens, Erlangen) MRI systems. • On the 1.5T system, the body coil was used to transmit, with a receive-only head coil collecting the data. • A transmit/receive head coil was used to acquire the 3T functional studies. • Functional images : 2D multi-slice gradient echo EPI acquisition. Sixteen slice locations were collected every 3-4 sec with fat saturation. RESULTS • Vermis, SMA, cerebellum and motor regions generally showed the greatest activation • Little activation seen in cingulate gyrus, right temporal lobe, deep gray matter, and brainstem • Wall vs. golf paradigm showed generally diminished activation across all regions compared to the Rest vs. golf • Decreased activation most extensively with the better players RESULTS • Assuming a limit of 2% activation, 95% confidence intervals were generated. This showed with a 95% confidence that the following areas were activated greater than 2% – 13 handicap: Brainstem, Left motor, Left sensory, Left SMA, Left temporal, Right cerebellum, Right SMA, Vermis – 7 handicap: Left SMA – 5 handicap: no areas – 0 handicap: no areas rm R is SM L A S R L MA ce m o L reb tor ce ell re um be ll R um m L oto r f L ron se ta n l L sor pa y R rie oc ta l br cip i ai ta n l R ste s m L ens de o e ry L pg te re m y L po oc ra cip l R ita fr l R on t R par al de ie e ta R pg l te re m L po y ci ra n R gu l ci lat ng e ul at e Ve Percent area activation, 13 handicap averaged five series of “rest vs. golf” 14 12 10 8 Series1 6 4 2 0 R cingulate L cingulate R temporal R deep grey R frontal R parietal L occipital L deep grey L temporal R sensory R occipital brainstem total Vermis R SMA L SMA L motor R cerebellum L cerebellum R motor L sensory L frontal L parietal 25 20 15 10 5 0 0 rest 5 rest 7 rest 10 rest 11 rest 13 rest 13 rest 11 rest 10 rest 7 rest 5 rest 0 rest Vermis R SMA L SMA L motor R cerebellum L cerebellum R motor L sensory L frontal L parietal R occipital brainstem total R sensory L temporal L deep grey L occipital R parietal R frontal R deep grey R temporal L cingulate R cingulate 14 12 10 8 6 4 2 0 0 wall 5 wall 7 wall 11 wall 13 wall 13 wall 11 wall 7 wall 5 wall 0 wall Vermis R SMA L SMA L motor R cerebellum L cerebellum R motor L frontal L sensory L parietal R occipital Brainstem R sensory L deep gray L temporal L occipital R frontal R parietal R deep gray R temporal L cingulate R cingulate 14 12 10 8 6 4 2 0 0 wall 5 wall 7 wall 11 wall 13 wall 13 wall 11 wall 7 wall 5 wall 0 wall REST VS GOLF 13 HANDICAP CONCLUSIONS • Demonstrated the feasibility of defining areas of brain activation during imagery of a complex, coordinated motor task • Suggests increased activation with increasing handicap CONCLUSIONS • Generally good agreement of golf swing imagery with brain activation areas defined in the literature including: – Primary motor control (motor cortex) – Imagery (parietal cortex) – Execution areas (premotor cortex of frontal lobe, lateral cerebellum, basal ganglia, vermis and medial cerebellar hemispheres) – Action planning areas (frontal and parietal cortex, SMA, lateral cerebellum) – Error detection (cingulate, cerebellum) CONCLUSIONS • Increased activation with high handicap players could potentially relate to two effects: – 1) that increased activation reflects a failure to learn and become highly automatic or – 2) that increased activation is essentially pathologic, and related to a loss of automaticity with compensatory increased brain activity. • Development of automaticity is relative and can be dynamic and reversible • Classic example of this pathology is writer’s cramp (focal dystonia) where the severe functional disturbances can be explained in terms of a loss of automaticity and an increased need for controlled processing • Ross JS et al. The Minds Eye: Functional imaging of golf motor imagery. American Journal of Neuroradiology, 24:1036-1044, June/July 2003. QUESTIONS? rossj1@ccf.org