KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer's disease.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 34158479.
- Also identified by DOI 10.1038/s41467-021-23755-z and PMC identifier 8219708.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Klotho-VS heterozygosity (KL-VS<sup>het</sup>) is associated with reduced risk of Alzheimer's disease (AD). However, whether KL-VS<sup>het</sup> is associated with lower levels of pathologic tau, i.e., the key AD pathology driving neurodegeneration and cognitive decline, is unknown. Here, we assessed the interaction between KL-VS<sup>het</sup> and levels of beta-amyloid, a key driver of tau pathology, on the levels of PET-assessed neurofibrillary tau in 551 controls and patients across the AD continuum. KL-VS<sup>het</sup> showed lower cross-sectional and longitudinal increase in tau-PET per unit increase in amyloid-PET when compared to that of non-carriers. This association of KL-VS<sup>het</sup> on tau-PET was stronger in Klotho mRNA-expressing brain regions mapped onto a gene expression atlas. KL-VS<sup>het</sup> was related to better memory functions in amyloid-positive participants and this association was mediated by lower tau-PET. Amyloid-PET levels did not differ between KL-VS<sup>het</sup> carriers versus non-carriers. Together, our findings provide evidence to suggest a protective role of KL-VS<sup>het</sup> against amyloid-related tau pathology and tau-related memory impairments in elderly humans at risk of AD dementia.
Medical subject headings
- Alzheimer Disease
- Amyloid beta-Peptides
- Glucuronidase
- Memory Disorders
- tau Proteins