Cardiorespiratory fitness alters the influence of a polygenic risk score on biomarkers of AD.

Neurology

From the Geriatric Research Education and Clinical Center (S.A.S., E.A.B., C.M.C., C.L.G., B.B.B., S.A., S.C.J., O.C.O.) and Research Service (D.B.C.), William S. Middleton Memorial VA Hospital, Madison, WI; Wisconsin Alzheimer's Disease Research Center (S.A.S., E.A.B., D.F.E., R.L.K., C.M.C., B.B.B., S.A., M.A.S., B.P.H., S.C.J., C.D.E., O.C.O.), Madison; Departments of Population Health Sciences (B.F.D., C.D.E.), Kinesiology (D.F.E., D.B.C.), Neurology (C.L.G.), and Anesthesiology (K.J.H.), University of Wisconsin School of Medicine and Public Health, Madison; Clinical Neurochemistry Laboratory (H.Z., K.B.), Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Sweden; Department of Molecular Neuroscience (H.Z.), UCL Institute of Neurology, Queen Square, London, UK; and Wisconsin Alzheimer's Institute (D.F.E., C.M.C., C.L.G., B.B.B., S.A., M.A.S., K.J.H., B.P.H., S.C.J., C.D.E., O.C.O.), Madison.

Published: April 2017

Objective: To examine whether a polygenic risk score (PRS) derived from and is associated with CSF biomarkers of Alzheimer disease (AD) pathology and whether higher cardiorespiratory fitness (CRF) modifies the association between the PRS and CSF biomarkers.

Methods: Ninety-five individuals from the Wisconsin Registry for Alzheimer's Prevention were included in these cross-sectional analyses. They were genotyped for , , and , from which a PRS was calculated for each participant. The participants underwent lumbar puncture for CSF collection. β-Amyloid 42 (Aβ), Aβ, total tau (t-tau), and phosphorylated tau (p-tau) were quantified by immunoassays, and Aβ/Aβ and tau/Aβ ratios were computed. CRF was estimated from a validated equation incorporating sex, age, body mass index, resting heart rate, and self-reported physical activity. Covariate-adjusted regression analyses were used to test for associations between the PRS and CSF biomarkers. In addition, by including a PRS×CRF term in the models, we examined whether these associations were modified by CRF.

Results: A higher PRS was associated with lower Aβ/Aβ ( < 0.001), higher t-tau/Aβ ( = 0.012), and higher p-tau/Aβ ( = 0.040). Furthermore, we observed PRS × CRF interactions for Aβ/Aβ ( = 0.003), t-tau/Aβ ( = 0.003), and p-tau/Aβ ( = 0.001). Specifically, the association between the PRS and these CSF biomarkers was diminished in those with higher CRF.

Conclusions: In a late-middle-aged cohort, CRF attenuates the adverse influence of genetic vulnerability on CSF biomarkers. These findings support the notion that increased cardiorespiratory fitness may be beneficial to those at increased genetic risk for AD.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405766PMC
http://dx.doi.org/10.1212/WNL.0000000000003862DOI Listing

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