Neuroimaging, clinical and life course correlates of normal-appearing white matter integrity in 70-year-olds

Author:

James Sarah-Naomi12ORCID,Manning Emily N2ORCID,Storey Mathew2,Nicholas Jennifer M23,Coath William2ORCID,Keuss Sarah E2,Cash David M2ORCID,Lane Christopher A2,Parker Thomas2,Keshavan Ashvini2,Buchanan Sarah M2,Wagen Aaron24,Harris Mathew2ORCID,Malone Ian2ORCID,Lu Kirsty2ORCID,Needham Louisa P1,Street Rebecca2,Thomas David5,Dickson John6,Murray-Smith Heidi2,Wong Andrew1,Freiberger Tamar2,Crutch Sebastian J2,Fox Nick C2,Richards Marcus1ORCID,Barkhof Frederik47,Sudre Carole H148,Barnes Josephine2,Schott Jonathan M12ORCID

Affiliation:

1. MRC Unit for Lifelong Health and Ageing at UCL, Institute of Cardiovascular Science, University College London , London , UK

2. Dementia Research Centre, UCL Queen Square Institute of Neurology, University College London , London , UK

3. Department of Medical Statistics, London School of Hygiene and Tropical Medicine , London , UK

4. Centre for Medical Image Computing, University College London , London , UK

5. Neuroradiological Academic Unit, Department of Brain Repair and Rehabilitation, UCL Queen Square Institute of Neurology , London , UK

6. Institute of Nuclear Medicine, University College London Hospitals Foundation Trust , London , UK

7. Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit , Amsterdam, The   Netherlands

8. School of Biomedical Engineering, King’s College , London , UK

Abstract

Abstract We investigate associations between normal-appearing white matter microstructural integrity in cognitively normal ∼70-year-olds and concurrently measured brain health and cognition, demographics, genetics and life course cardiovascular health. Participants born in the same week in March 1946 (British 1946 birth cohort) underwent PET-MRI around age 70. Mean standardized normal-appearing white matter integrity metrics (fractional anisotropy, mean diffusivity, neurite density index and orientation dispersion index) were derived from diffusion MRI. Linear regression was used to test associations between normal-appearing white matter metrics and (i) concurrent measures, including whole brain volume, white matter hyperintensity volume, PET amyloid and cognition; (ii) the influence of demographic and genetic predictors, including sex, childhood cognition, education, socio-economic position and genetic risk for Alzheimer’s disease (APOE-ɛ4); (iii) systolic and diastolic blood pressure and cardiovascular health (Framingham Heart Study Cardiovascular Risk Score) across adulthood. Sex interactions were tested. Statistical significance included false discovery rate correction (5%). Three hundred and sixty-two participants met inclusion criteria (mean age 70, 49% female). Higher white matter hyperintensity volume was associated with lower fractional anisotropy [b = −0.09 (95% confidence interval: −0.11, −0.06), P < 0.01], neurite density index [b = −0.17 (−0.22, −0.12), P < 0.01] and higher mean diffusivity [b = 0.14 (−0.10, −0.17), P < 0.01]; amyloid (in men) was associated with lower fractional anisotropy [b = −0.04 (−0.08, −0.01), P = 0.03)] and higher mean diffusivity [b = 0.06 (0.01, 0.11), P = 0.02]. Framingham Heart Study Cardiovascular Risk Score in later-life (age 69) was associated with normal-appearing white matter {lower fractional anisotropy [b = −0.06 (−0.09, −0.02) P < 0.01], neurite density index [b = −0.10 (−0.17, −0.03), P < 0.01] and higher mean diffusivity [b = 0.09 (0.04, 0.14), P < 0.01]}. Significant sex interactions (P < 0.05) emerged for midlife cardiovascular health (age 53) and normal-appearing white matter at 70: marginal effect plots demonstrated, in women only, normal-appearing white matter was associated with higher midlife Framingham Heart Study Cardiovascular Risk Score (lower fractional anisotropy and neurite density index), midlife systolic (lower fractional anisotropy, neurite density index and higher mean diffusivity) and diastolic (lower fractional anisotropy and neurite density index) blood pressure and greater blood pressure change between 43 and 53 years (lower fractional anisotropy and neurite density index), independently of white matter hyperintensity volume. In summary, poorer normal-appearing white matter microstructural integrity in ∼70-year-olds was associated with measures of cerebral small vessel disease, amyloid (in males) and later-life cardiovascular health, demonstrating how normal-appearing white matter can provide additional information to overt white matter disease. Our findings further show that greater ‘midlife’ cardiovascular risk and higher blood pressure were associated with poorer normal-appearing white matter microstructural integrity in females only, suggesting that women’s brains may be more susceptible to the effects of midlife blood pressure and cardiovascular health.

Funder

Alzheimer’s Research UK

Medical Research Council Dementias Platform UK

Wolfson Foundation

Alzheimer’s Association

AVID Radiopharmaceuticals

Medical Research Council

National Institute for Health and Care Research

University College London

Leonard Wolfson Experimental Neurology Centre

Weston Brain Institute

Selfridges Foundation

Alzheimer’s Research UK Senior Fellowship

Alzheimer’s Society Junior Fellowship

University College London Hospital National Institute for Health and Care Research Biomedical Research Centre

UK Dementia Research Institute

Publisher

Oxford University Press (OUP)

Subject

Neurology,Cellular and Molecular Neuroscience,Biological Psychiatry,Psychiatry and Mental health

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