4.6 Article

Diffusion Tensor Imaging of the Olfactory System in Older Adults With and Without Hyposmia

Journal

FRONTIERS IN AGING NEUROSCIENCE
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2021.648598

Keywords

hyposmia; gray matter; olfaction; older adults; orbitofrontal cortex; MRI

Funding

  1. National Institute on Aging (NIA) [N01-AG-6-2101, N01-AG-6-2103, N01-AG-6-2106]
  2. NIA [R01-AG028050]
  3. NINR [R01-NR012459]
  4. Intramural Research Program of the NIH, National Institute on Aging

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This study compared the gray matter microstructural characteristics of olfactory regions in older adults with and without hyposmia. The results showed that older adults with higher mean diffusivity in regions important for olfaction are more likely to have hyposmia up to ten years prior. The findings suggest that hyposmia could potentially serve as an early biomarker for brain microstructural abnormalities in older adults with varying cognitive functions.
Objectives: To compare gray matter microstructural characteristics of higher-order olfactory regions among older adults with and without hyposmia. Methods: Data from the Brief Smell Identification Test (BSIT) were obtained in 1998-99 for 265 dementia-free adults from the Health, Aging, and Body Composition study (age at BSIT: 74.9 +/- 2.7; 62% White; 43% male) who received 3T diffusion tensor imaging in 2006-08 [Interval of time: mean (SD): 8.01 years (0.50)], Apolipoprotein (ApoE epsilon 4) genotypes, and repeated 3MS assessments until 2011-12. Cognitive status (mild cognitive impairment, dementia, normal cognition) was adjudicated in 2011-12. Hyposmia was defined as BSIT <= 8. Microstructural integrity was quantified by mean diffusivity (MD) in regions of the primary olfactory cortex amygdala, orbitofrontal cortex (including olfactory cortex, gyrus rectus, the orbital parts of the superior, middle, and inferior frontal gyri, medial orbital part of the superior frontal gyrus), and hippocampus. Multivariable regression models were adjusted for total brain atrophy, demographics, cognitive status, and ApoE epsilon 4 genotype. Results: Hyposmia in 1998-99 (n = 57, 21.59%) was significantly associated with greater MD in 2006-08, specifically in the orbital part of the middle frontal gyrus, and amygdala, on the right [adjusted beta (p value): 0.414 (0.01); 0.527 (0.01); respectively]. Conclusion: Older adults with higher mean diffusivity in regions important for olfaction are more likely to have hyposmia up to ten years prior. Future studies should address whether hyposmia can serve as an early biomarker of brain microstructural abnormalities for older adults with a range of cognitive functions, including those with normal cognition.

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