Wednesday, December 2 | 10:20 a.m.-10:30 a.m. | VN41-08 | Room N228
Ever wonder how caffeine kick-starts the brain after that morning coffee? Japanese researchers may have an answer, as they used 3-tesla arterial spin-labeled MRI (ASL-MRI) to show how caffeine intake induces global and regional perfusion changes in the brain.Caffeine is known to produce an increase in neurotransmitters, such as glutamate and dopamine, to wake cerebral vessels. However, caffeine's effect on global and regional cerebral blood flow is not fully understood.
"We carried out arterial spin labeling with the advantage of long T1-weighted relaxation times and high signal-to-noise ratio due to 3T. As arterial spin-labeling perfusion does not involve ionizing radiation or exogenous contrast media injection, it is suitable for performing volunteer studies," said co-author Dr. Toshinori Hirai in the department of diagnostic radiology at Kumamoto University.
The study took nine healthy volunteers ranging from 23 to 38 years of age and performed volumetric T1-weighted and arterial spin labeling 30 minutes after the delivery of 200 mg of caffeine. The subjects were prohibited from ingesting caffeine during the seven hours preceding the experiment.
After caffeine intake, the mean standard deviation in the global cerebral blood flow for gray matter and white matter was 15.8 ± 12.9% and 16.6 ± 16.1%, respectively. The regions of the brain exhibited a significant global cerebral blood flow reduction (p < 0.05) and significant regional cerebral blood flow hypoperfusion in the bilateral medial occipital lobes (p < 0.005).
As for potential future research, Hirai suggested that the response and change of brain perfusion with antipsychotic drugs could be evaluated by using arterial spin labeling.











![Overview of the study design. (A) The fully automated deep learning framework was developed to estimate body composition (BC) (defined as subcutaneous adipose tissue [SAT] in liters; visceral adipose tissue [VAT] in liters; skeletal muscle [SM] in liters; SM fat fraction [SMFF] as a percentage; and intramuscular adipose tissue [IMAT] in deciliters) from MRI. The fully automated framework comprised one model (model 1) to quantify different BC measures (SAT, VAT, SM, SMFF, and IMAT) as three-dimensional (3D) measures from whole-body MRI scans. The second model (model 2) was trained to identify standardized anatomic landmarks along the craniocaudal body axis (z coordinate field), which allowed for subdividing the whole-body measures into different subregions typically examined on clinical routine MRI scans (chest, abdomen, and pelvis). (B) BC was quantified from whole-body MRI in over 66,000 individuals from two large population-based cohort studies, the UK Biobank (UKB) (36,317 individuals) and the German National Cohort (NAKO) (30,291 individuals). Bar graphs show age distribution by sex and cohort. BMI = body mass index. (C) After the performance assessment of the fully automated framework, the change in BC measures, distributions, and profiles across age decades were investigated. Age-, sex-, and height-adjusted body composition reference curves were calculated and made publicly available in a web-based z-score calculator (https://circ-ml.github.io).](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/05/body-comp.XgAjTfPj1W.jpg?auto=format%2Ccompress&fit=crop&h=112&q=70&w=112)



