Klotho Gene Expression Is Decreased in Peripheral Blood Mononuclear Cells in Patients with Alzheimer's Disease and Frontotemporal Dementia.


Journal

Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863

Informations de publication

Date de publication:
2023
Historique:
medline: 8 8 2023
pubmed: 2 7 2023
entrez: 2 7 2023
Statut: ppublish

Résumé

The longevity gene Klotho (KL) was recently associated with neurodegenerative diseases including Alzheimer's disease (AD). Its role in the brain has not been completely elucidated, although evidence suggests that KL-VS heterozygosity is associated with a reduced risk of AD in Apolipoprotein E ɛ4 carriers. Conversely, no data about genetic association with frontotemporal dementia (FTD) are available so far. To investigate the involvement of KL in AD and FTD by the determination of the genetic frequency of KL-VS variant and the expression analysis of KL gene. A population consisting of 438 patients and 240 age-matched controls was enrolled for the study. KL-VS and APOE genotypes were assessed by allelic discrimination through a QuantStudio 12K system. KL gene expression analysis was performed in a restricted cohort of patients consisting of 43 AD patients, 41 FTD patients and 19 controls. KL gene expression was assessed in peripheral blood mononuclear cells with specific TaqMan assay. Statistical analysis was performed using GraphPad 9 Prims software. KL-VS frequency was comparable to the ones found in literature and no differences were found in both allelic and genotypic frequencies between patients and controls were found. Conversely, KL expression levels were significantly lower in AD and FTD patients compared with controls (mean fold regulation - 4.286 and - 6.561 versus controls in AD and FTD, respectively, p = 0.0037). This is the first study investigating KL in FTD. We showed a decreased expression of the gene in AD and FTD, independent of the genotype, suggesting a role of Klotho in common steps during neurodegeneration.

Sections du résumé

BACKGROUND
The longevity gene Klotho (KL) was recently associated with neurodegenerative diseases including Alzheimer's disease (AD). Its role in the brain has not been completely elucidated, although evidence suggests that KL-VS heterozygosity is associated with a reduced risk of AD in Apolipoprotein E ɛ4 carriers. Conversely, no data about genetic association with frontotemporal dementia (FTD) are available so far.
OBJECTIVE
To investigate the involvement of KL in AD and FTD by the determination of the genetic frequency of KL-VS variant and the expression analysis of KL gene.
METHODS
A population consisting of 438 patients and 240 age-matched controls was enrolled for the study. KL-VS and APOE genotypes were assessed by allelic discrimination through a QuantStudio 12K system. KL gene expression analysis was performed in a restricted cohort of patients consisting of 43 AD patients, 41 FTD patients and 19 controls. KL gene expression was assessed in peripheral blood mononuclear cells with specific TaqMan assay. Statistical analysis was performed using GraphPad 9 Prims software.
RESULTS
KL-VS frequency was comparable to the ones found in literature and no differences were found in both allelic and genotypic frequencies between patients and controls were found. Conversely, KL expression levels were significantly lower in AD and FTD patients compared with controls (mean fold regulation - 4.286 and - 6.561 versus controls in AD and FTD, respectively, p = 0.0037).
CONCLUSION
This is the first study investigating KL in FTD. We showed a decreased expression of the gene in AD and FTD, independent of the genotype, suggesting a role of Klotho in common steps during neurodegeneration.

Identifiants

pubmed: 37393504
pii: JAD230322
doi: 10.3233/JAD-230322
doi:

Substances chimiques

KL protein, human EC 3.2.1.31

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1225-1231

Auteurs

Federica Sorrentino (F)

University of Milan, Milan, Italy.

Chiara Fenoglio (C)

University of Milan, Milan, Italy.
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Luca Sacchi (L)

University of Milan, Milan, Italy.

Maria Serpente (M)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Andrea Arighi (A)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Tiziana Carandini (T)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Beatrice Arosio (B)

University of Milan, Milan, Italy.

Evelyn Ferri (E)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Marina Arcaro (M)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Caterina Visconte (C)

University of Milan, Milan, Italy.

Emanuela Rotondo (E)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Elio Scarpini (E)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Daniela Galimberti (D)

University of Milan, Milan, Italy.
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

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