KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer's disease.
Julia NeitzelNicolai FranzmeierAnna RubinskiMartin DichgansMatthias Brendelnull nullRainer MalikMichael EwersPublished in: Nature communications (2021)
Klotho-VS heterozygosity (KL-VShet) is associated with reduced risk of Alzheimer's disease (AD). However, whether KL-VShet 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-VShet 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-VShet 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-VShet on tau-PET was stronger in Klotho mRNA-expressing brain regions mapped onto a gene expression atlas. KL-VShet 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-VShet carriers versus non-carriers. Together, our findings provide evidence to suggest a protective role of KL-VShet against amyloid-related tau pathology and tau-related memory impairments in elderly humans at risk of AD dementia.
Keyphrases
- cerebrospinal fluid
- cognitive decline
- positron emission tomography
- pet ct
- computed tomography
- gene expression
- mild cognitive impairment
- pet imaging
- working memory
- dna methylation
- newly diagnosed
- multiple sclerosis
- prognostic factors
- radiation therapy
- neoadjuvant chemotherapy
- subarachnoid hemorrhage
- binding protein
- resting state