Diffuse optical assessment of cerebral-autoregulation in older adults stratified by cerebrovascular risk

被引:14
作者
Bahrani, Ahmed A. [1 ,2 ,3 ]
Kong, Weikai [1 ]
Shang, Yu [4 ]
Huang, Chong [1 ]
Smith, Charles D. [2 ,5 ,6 ]
Powell, David K. [5 ,7 ]
Jiang, Yang [2 ,5 ,8 ]
Rayapati, Abner O. [9 ]
Jicha, Gregory A. [2 ,5 ,6 ]
Yu, Guoqiang [1 ]
机构
[1] Univ Kentucky, Dept Biomed Engn, Lexington, KY 40506 USA
[2] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40506 USA
[3] Univ Baghdad, Al Khwarizmi Coll Engn, Biomed Engn Dept, Baghdad, Iraq
[4] North Univ China, Shanxi Prov Key Lab Biomed Imaging & Big Data, Taiyuan, Shanxi, Peoples R China
[5] Univ Kentucky, Magnet Resonance Imaging & Spect Ctr MRISC, Lexington, KY 40506 USA
[6] Univ Kentucky, Dept Neurol, Lexington, KY 40506 USA
[7] Univ Kentucky, Dept Neurosci, Lexington, KY 40506 USA
[8] Univ Kentucky, Dept Behav Sci, Lexington, KY 40506 USA
[9] Univ Kentucky, Dept Psychiat, Lexington, KY 40506 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
cerebral blood flow; cerebral blood oxygenation; cerebral-autoregulation; cerebrovascular disease; diffuse correlation spectroscopy; head-up-tilting; low-frequency oscillation; near-infrared spectroscopy; LOW-FREQUENCY OSCILLATIONS; ARTERIAL-BLOOD PRESSURE; TISSUE ARCHITECTURE; PERFUSION SIGNAL; FLOW; HEMODYNAMICS; DISEASE; BRAIN; OXYGENATION; METABOLISM;
D O I
10.1002/jbio.202000073
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Diagnosis of cerebrovascular disease (CVD) at early stages is essential for preventing sequential complications. CVD is often associated with abnormal cerebral microvasculature, which may impact cerebral-autoregulation (CA). A novel hybrid near-infrared diffuse optical instrument and a finger plethysmograph were used to simultaneously detect low-frequency oscillations (LFOs) of cerebral blood flow (CBF), oxy-hemoglobin concentration ([HbO(2)]), deoxy-hemoglobin concentration ([Hb]) and mean arterial pressure (MAP) in older adults before, during and after 70 degrees head-up-tilting (HUT). The participants with valid data were divided based on Framingham risk score (FRS, 1-30 points) into low-risk (FRS <= 15, n = 13) and high-risk (FRS >15, n = 11) groups for developing CVD. The LFO gains were determined by transfer function analyses with MAP as the input, and CBF, [HbO(2)] and [Hb] as the outputs (CA proportional to 1/Gain). At resting-baseline, LFO gains in the high-risk group were relatively lower compared to the low-risk group. The lower baseline gains in the high-risk group may attribute to compensatory mechanisms to maintain stronger steady-state CAs. However, HUT resulted in smaller gain reductions in the high-risk group compared to the low-risk group, suggesting weaker dynamic CAs. LFO gains are potentially valuable biomarkers for early detection of CVD based on associations with CAs.
引用
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页数:13
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