TY - JOUR
T1 - Hemoglobin, hematocrit, and changes in cerebral blood flow
T2 - The Second Manifestations of ARTerial disease-Magnetic Resonance study
AU - van der Veen, Pieternella H.
AU - Muller, Majon
AU - Vincken, Koen L.
AU - Westerink, Jan
AU - Mali, Willem P. T. M.
AU - van der Graaf, Yolanda
AU - Geerlings, Mirjam I.
AU - Doevendans, PAFM
PY - 2015/3
Y1 - 2015/3
N2 - Hemoglobin and hematocrit are important determinants of blood viscosity and arterial oxygen content and may therefore influence cerebral blood flow (CBF). We examined cross-sectional and prospective associations of hemoglobin and hematocrit with CBF in 569 patients with manifest arterial disease (mean age 57 +/- 10 years) with available data on magnetic resonance angiography to measure parenchymal CBF. Mean (SD) parenchymal CBF at baseline was 52.3 (9.8) mL/min/100 mL and decreased with 1.5 (11.0) mL/min/100 mL after on average 3.9 years of follow-up. Linear regression analyses showed that greater hemoglobin and hematocrit values were associated with lower baseline parenchymal CBF and more decline in parenchymal CBF over time, independent of cardiovascular risk factors, use of antiplatelet drugs, anticoagulants, or diuretics, and brain measures: adjusted mean differences (95% confidence interval [CI]) in decline in parenchymal CBF between patients in the lower and upper quartiles of hemoglobin and hematocrit were -2.48 (95% CI -3.70 to -1.25) and = 3.69 (95% CI -5.45 to -1.94) mL/min/100 mL. Higher hemoglobin and hematocrit were associated with lower baseline parenchymal CBF and a greater decline in parenchymal CBF over time, possibly as a result of physiological compensating mechanisms. (C) 2015 Elsevier Inc. All rights reserved.
AB - Hemoglobin and hematocrit are important determinants of blood viscosity and arterial oxygen content and may therefore influence cerebral blood flow (CBF). We examined cross-sectional and prospective associations of hemoglobin and hematocrit with CBF in 569 patients with manifest arterial disease (mean age 57 +/- 10 years) with available data on magnetic resonance angiography to measure parenchymal CBF. Mean (SD) parenchymal CBF at baseline was 52.3 (9.8) mL/min/100 mL and decreased with 1.5 (11.0) mL/min/100 mL after on average 3.9 years of follow-up. Linear regression analyses showed that greater hemoglobin and hematocrit values were associated with lower baseline parenchymal CBF and more decline in parenchymal CBF over time, independent of cardiovascular risk factors, use of antiplatelet drugs, anticoagulants, or diuretics, and brain measures: adjusted mean differences (95% confidence interval [CI]) in decline in parenchymal CBF between patients in the lower and upper quartiles of hemoglobin and hematocrit were -2.48 (95% CI -3.70 to -1.25) and = 3.69 (95% CI -5.45 to -1.94) mL/min/100 mL. Higher hemoglobin and hematocrit were associated with lower baseline parenchymal CBF and a greater decline in parenchymal CBF over time, possibly as a result of physiological compensating mechanisms. (C) 2015 Elsevier Inc. All rights reserved.
KW - Atherosclerosis
KW - Brain imaging
KW - Cerebral blood flow
KW - Hemorheology
KW - Magnetic resonance imaging
KW - INTIMA-MEDIA THICKNESS
KW - CARDIOVASCULAR-DISEASE
KW - SMART-MR
KW - POLYCYTHEMIA-VERA
KW - OLDER-ADULTS
KW - BRAIN
KW - VISCOSITY
KW - ANEMIA
KW - OXYGEN
KW - RISK
UR - http://www.scopus.com/inward/record.url?scp=84923544645&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2014.12.019
DO - 10.1016/j.neurobiolaging.2014.12.019
M3 - Article
C2 - 25618615
AN - SCOPUS:84923544645
SN - 0197-4580
VL - 36
SP - 1417
EP - 1423
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 3
ER -