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Article type: Research Article
Authors: Gaitán, Julian M.a | Asthana, Sanjaya; b; c | Carlsson, Cynthia M.a; b; c | Engelman, Corinne D.a; b; d | Johnson, Sterling C.a; b; c | Sager, Mark A.a; b | Wang, Dane | Dubal, Dena B.e; 1; * | Okonkwo, Ozioma C.a; b; c; 1; *
Affiliations: [a] Wisconsin Alzheimer’s Disease Research Center, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA | [b] Wisconsin Alzheimer’s Institute, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA | [c] Geriatric Research Education and Clinical Center, William S. Middleton Memorial Veterans Hospital, Madison, WI, USA | [d] Department of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA | [e] Department of Neurology and Weill Institute for Neurosciences, University of California, San Francisco, SanFrancisco, CA, USA
Correspondence: [*] Correspondence to:Dena B. Dubal, MD, PhD, University of California –San Francisco Weill Institute for Neurosciences, 675 Nelson Rising Lane, San Francisco, CA 94158, USA. Tel.: +1 415 502 7237; E-mail: dena.dubal@ucsf.edu and Ozioma C. Okonkwo, PhD, University of Wisconsin— Madison, J5/156M, Clinical Science Center, 600 Highland Avenue, Madison, WI 53792, USA. Tel.: +1 608 265 4479; E-mail: ozioma@medicine.wisc.edu.
Note: [1] Denotes co-senior authorship.
Abstract: Background:Klotho is a longevity and neuroprotective hormone encoded by the KLOTHO gene, and heterozygosity for the KL-VS variant confers a protective effect against neurodegenerative disease. Objective:Test whether klotho concentrations in serum or cerebrospinal fluid (CSF) vary as a function of KLOTHO KL-VS genotype, determine whether circulating klotho concentrations from serum and CSF differ from one another, and evaluate whether klotho levels are associated with Alzheimer’s disease risk factors. Methods:Circulating klotho was measured in serum (n = 1,116) and CSF (n = 183) of cognitively intact participants (aged 62.4 ± 6.5 years; 69.5% female). KLOTHO KL-VS zygosity (non-carrier; heterozygote; homozygote) was also determined. Linear regression was used to test whether klotho hormone concentration varied as a function of KL-VS genotype, specimen source, and demographic and clinical characteristics. Results:Serum and CSF klotho were higher in KL-VS carriers than non-carriers. Klotho concentration was higher in CSF than in serum. Females had higher serum and CSF klotho, while younger age was associated with higher klotho in CSF. Conclusion:In a cohort enriched for risk for Alzheimer’s disease, heterozygotic and homozygotic carriers of the KL-VS allele, females, and younger individuals have higher circulating klotho. Fluid source, KL-VS genotype, age, and sex should be considered in analyses of circulating klotho on brain health.
Keywords: Alzheimer’s disease, cerebrospinal fluid, KL-VS, Klotho, serum
DOI: 10.3233/JAD-220571
Journal: Journal of Alzheimer's Disease, vol. 90, no. 4, pp. 1557-1569, 2022
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