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February 03, 2015; 84 (5) Article

Arterial stiffness and progression of structural brain changes

The SMART-MR study

Hadassa M. Jochemsen, Majon Muller, Michiel L. Bots, Philip Scheltens, Koen L. Vincken, Willem P.T.M. Mali, Yolanda van der Graaf, Mirjam I. Geerlings
First published December 31, 2014, DOI: https://doi.org/10.1212/WNL.0000000000001201
Hadassa M. Jochemsen
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Majon Muller
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Michiel L. Bots
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Philip Scheltens
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Koen L. Vincken
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Willem P.T.M. Mali
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Yolanda van der Graaf
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Mirjam I. Geerlings
From the Julius Center for Health Sciences and Primary Care (H.M.J., M.M., M.L.B., Y.v.d.G., M.I.G.), Image Sciences Institute (K.L.V.), and Department of Radiology (W.P.T.M.M.), University Medical Center Utrecht; the Alzheimer Center & Department of Neurology (H.M.J., P.S.), Neuroscience Campus Amsterdam, VU University Medical Center; and the Department of Geriatrics/Internal Medicine (M.M.), Leids University Medical Center, Leiden, the Netherlands.
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Citation
Arterial stiffness and progression of structural brain changes
The SMART-MR study
Hadassa M. Jochemsen, Majon Muller, Michiel L. Bots, Philip Scheltens, Koen L. Vincken, Willem P.T.M. Mali, Yolanda van der Graaf, Mirjam I. Geerlings
Neurology Feb 2015, 84 (5) 448-455; DOI: 10.1212/WNL.0000000000001201

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Abstract

Objective: To examine the cross-sectional and prospective associations between arterial stiffness and structural brain changes within the Second Manifestations of Arterial Disease–Magnetic Resonance (SMART-MR) study, a prospective cohort study among patients with manifest arterial disease.

Methods: Distension measurements of the common carotid arteries and a brain MRI were performed in 526 patients (mean age 59 ± 10 years). After a mean follow-up of 4.1 years (range 3.6–5.8), brain MRI was repeated in 308 patients. Brain segmentation was used to quantify total brain volume, cortical gray matter volume, ventricular volume, and white matter lesion (WML) volume (relative to intracranial volume). Infarcts were rated visually.

Results: Cross-sectional multivariable regression analyses showed that 1 SD decrease in carotid distension, indicating increased arterial stiffness, was associated with smaller relative total brain and cortical gray matter volumes (B = −0.24%, 95% confidence interval [CI] −0.44 to −0.04%, and B = −0.47%, 95% CI −0.75 to −0.19%), with larger WML volume (B = 0.09%, 95% CI −0.01 to 0.19%), and with higher risk of having nonlacunar (cortical or large subcortical) brain infarcts (relative risk = 1.44, 95% CI 1.14 to 1.81). However, our prospective findings showed that carotid distension was not significantly associated with progression of brain atrophy, WML volume, or brain infarcts.

Conclusion: In this population of patients with manifest arterial disease, stiffening of the carotid arteries was cross-sectionally associated with more brain atrophy, WML volume, and nonlacunar infarcts, but did not lead to changes in brain volumes or infarcts after 4 years.

GLOSSARY

ACE=
angiotensin-converting enzyme;
ANCOVA=
analysis of covariance;
BA=
basilar artery;
BMI=
body mass index;
BP=
blood pressure;
CC=
compliance coefficient;
CI=
confidence interval;
CIMT=
carotid intima media thickness;
DC=
distensibility coefficient;
FLAIR=
fluid-attenuated inversion recovery;
ICA=
internal carotid artery;
ICV=
intracranial volume;
IR=
inversion recovery;
OR=
odds ratio;
pCBF=
parenchymal cerebral blood flow;
RR=
relative risk;
SMART-MR=
Second Manifestations of Arterial Disease–Magnetic Resonance;
TE=
echo time;
TI=
inversion time;
TR=
repetition time;
WML=
white matter lesion;
YEM=
Young's elastic modulus

Footnotes

  • Coinvestigators are listed on the Neurology® Web site at Neurology.org.

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Editorial, page 440

  • Supplemental data at Neurology.org

  • Received December 20, 2013.
  • Accepted in final form September 15, 2014.
  • © 2014 American Academy of Neurology
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