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Abstract Details

Optical Properties and Oximetry Parameters of Cerebral Atrophic and Normal Regions in Healthy Volunteers
Aging, Dementia, and Behavioral Neurology
P5 - Poster Session 5 (5:30 PM-6:30 PM)
9-018
It is not known if brain atrophy can affect optical properties and cerebral oximetry results as measured by Time-Domain Near Infrared Spectroscopy (TD-NIRS).
Cerebral Time-Domain Near Infrared Spectroscopy (TD-NIRS) provides reproducible absolute absorption and scattering coefficients, haemoglobin species’ concentration and tissue oxygen saturation (StO2) in the cerebral outer layers. 
TD-NIRS measurements were performed on healthy volunteers on multiple head regions. We measured absorption and scattering coefficients (μa, μs'), hemoglobin species concentration and oxygen saturation (StO2). According to neuroimaging investigations with fiducial markers, we classified the brain area underlying each TD-NIRS probe as “atrophic” or “normal” region. Regional cerebral atrophy was defined according to Global Cortical Atrophy (GCA) rating scale.
We analyzed 50 healthy volunteers (age 64.0±14.9). The mean values of absorption coefficients, hemoglobin species and StO2 were comparable between atrophic and normal cerebral regions. We observed significantly lower mean values of μs’ at 690 nm wavelength in atrophic areas compared to normal regions (7.374 (±1.232) vs. 8.279 (±0.974) cm-1, p=0.008]. In binomial logistic regression analysis together with age, μs’(690) was independently associated with atrophy (beta=0.45, CI 95% 0.24-0.86, p=0.015). A cut-off of μs’(690) <7.5 cm-1 had a sensitivity of 86% and specificity of 58% in correctly predicting atrophic areas (AUC 71.2%, CI 95% 54.2%-88.2%).
In our cohort, atrophic and normal regions displayed comparable values of absorption coefficients, haemoglobin species and StO2, but significantly lower scattering coefficient at 690 nm wavelength. These results might be consistent with the presence in atrophic region of a ticker layer of cerebrospinal fluid, which has a lower density compared to brain tissue, while the concentration of haemoglobin species in the microcirculation is not affected. This finding might suggest that reduced scattering coefficient might be explored as a surrogate marker of cerebral atrophy.
Authors/Disclosures

PRESENTER
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