4.2 Article

Observation of Reduced Homeostatic Metabolic Activity and/or Coupling in White Matter Aging

Journal

JOURNAL OF NEUROIMAGING
Volume 30, Issue 5, Pages 658-665

Publisher

WILEY
DOI: 10.1111/jon.12744

Keywords

Aging; blood brain barrier; DCE-MRI; water cycling; white matter

Funding

  1. National Institutes of Health [AG033638, NS40801, EB007258, AG008017, NS089260]
  2. Oregon Partnership for Alzheimer's Research
  3. Conrad N. Hilton Foundation
  4. National MS Society [RG3168A1]
  5. Oregon Opportunity

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BACKGROUND AND PURPOSE Transvascular water exchange plays a key role in the functional integrity of the blood-brain barrier (BBB). In white matter (WM), a variety of imaging modalities have demonstrated age-related changes in structure and metabolism, but the extent to which water exchange is altered remains unclear. Here, we investigated the cumulative effects of healthy aging on WM capillary water exchange. METHODS A total of 38 healthy adults (aged 36-80 years) were studied using 7T dynamic contrast enhanced MRI. Blood volume fraction (v(b)) and capillary water efflux rate constant (k(po)) were determined by fitting changes in the(1)H(2)O longitudinal relaxation rate constant (R-1) during contrast agent bolus passage to a two-compartment exchange model. WM volume was determined by morphometric analysis of structural images. RESULTS R(1)values and WM volume showed similar trajectories of age-related decline. Among all subjects,v(b)andk(po)averaged 1.7 (+/- 0.5) mL/100 g of tissue and 2.1 (+/- 1.1) s(-1), respectively. Whilev(b)showed minimal changes over the 40-year-age span of participants,k(po)declined 0.06 s(-1)(ca. 3%) per year (r= -.66;P < .0005), from near 4 s(-1)at age 30 to ca. 2 s(-1)at age 70. The association remained significant after controlling for WM volume. CONCLUSIONS Previous studies have shown thatk(po)tracks Na+, K+-ATPase activity-dependent water exchange at the BBB and likely reflects neurogliovascular unit (NGVU) coupled metabolic activity. The age-related decline ink(po)observed here is consistent with compromised NGVU metabolism in older individuals and the dysregulated cellular bioenergetics that accompany normal brain aging.

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