4.7 Article

Coupled Changes in Brain White Matter Microstructure and Fluid Intelligence in Later Life

期刊

JOURNAL OF NEUROSCIENCE
卷 35, 期 22, 页码 8672-8682

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0862-15.2015

关键词

cognitive aging; diffusion tensor imaging; fluid intelligence; fractional anisotropy; processing speed; white matter microstructure

资金

  1. Disconnected Mind project
  2. Age UK
  3. UK Medical Research Council (MRC)
  4. Scottish Funding Council as part of the SINAPSE Collaboration
  5. Biotechnology and Biological Sciences Research Council (BBSRC)
  6. MRC
  7. MRC [G0701120, G1001245, G0700704, MR/M013111/1] Funding Source: UKRI
  8. Medical Research Council [MR/K026992/1, MR/M013111/1, G0701120, G1001245, G0700704] Funding Source: researchfish

向作者/读者索取更多资源

Understanding aging-related cognitive decline is of growing importance in aging societies, but relatively little is known about its neural substrates. Measures of white matter microstructure are known to correlate cross-sectionally with cognitive ability measures, but only a few small studies have tested for longitudinal relations among these variables. We tested whether there were coupled changes in brain white matter microstructure indexed by fractional anisotropy (FA) and three broad cognitive domains (fluid intelligence, processing speed, and memory) in a large cohort of human participants with longitudinal diffusion tensor MRI and detailed cognitive data taken at ages 73 years (n = 731) and 76 years (n = 488). Longitudinal changes in white matter microstructure were coupled with changes in fluid intelligence, but not with processing speed or memory. Individuals with higher baseline white matter FA showed less subsequent decline in processing speed. Our results provide evidence for a longitudinal link between changes in white matter microstructure and aging-related cognitive decline during the eighth decade of life. They are consistent with theoretical perspectives positing that a corticocortical disconnection partly explains cognitive aging.

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