APOE4 carriers display loss of anticipatory cerebrovascular regulation across the Alzheimer's disease continuum

被引:0
作者
Palmer, Jacqueline A. [1 ,2 ,3 ]
Kaufman, Carolyn S. [4 ,5 ]
Whitaker-Hilbig, Alicen A. [6 ,7 ]
Billinger, Sandra A. [2 ,3 ]
机构
[1] Univ Minnesota, Med Sch, Div Phys Therapy & Rehabil Sci, Minneapolis, MN 55455 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS USA
[3] Univ Kansas, Alzheimers Dis Res Ctr, Fairway, KS USA
[4] Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS USA
[5] Stanford Univ, Dept Internal Med, Stanford Hlth Care, Palo Alto, CA USA
[6] Med Coll Wisconsin, Dept Phys Med & Rehabil, Milwaukee, WI USA
[7] Med Coll Wisconsin, Cardiovasc Ctr, Milwaukee, WI USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; apolipoprotein E epsilon 4; dynamic cerebral autoregulation; mild cognitive impairment; transcranial Doppler ultrasound; DYNAMIC CEREBRAL AUTOREGULATION; BLOOD-FLOW-VELOCITY; APOLIPOPROTEIN-E; ORTHOSTATIC HYPOTENSION; GENETIC RISK; EXERCISE; ADULTS; HYPOPERFUSION; HYPERTENSION; VARIABILITY;
D O I
10.1002/alz.70229
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND Maintenance of cerebral blood flow during orthostasis is impaired with aging and associated with cognitive decline, but the effect of the apolipoprotein epsilon 4 allele (APOE4) is unknown. METHODS Older adults (n = 108) (APOE4 carriers, n = 47; non-carriers, n = 61) diagnosed as having normal cognition (NC), mild cognitive impairment (MCI), or Alzheimer's disease (AD) underwent transcranial Doppler ultrasound assessment of middle cerebral artery blood velocity (MCAv) and beat-to-beat mean arterial blood pressure (MAP) during a sit-to-stand transition. Anticipatory and orthostasis-induced MCAv and MAP responses were compared between genotypes and diagnostic classifications. RESULTS Cognitively normal APOE4 carriers showed greater anticipatory MCAv increase, greater MCAv decrease with orthostasis, and shorter latency of peripheral MAP responses to orthostasis compared to non-carriers. MCAv and MAP responses were delayed and attenuated across the APOE4 disease continuum, with no differences between genotypes in MCI and AD. DISCUSSION Unique cerebral and peripheral vascular compensation observed in APOE4 carriers may be neuroprotective for AD development.
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页数:12
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