# Associations Between Klotho Levels, KL-VS Heterozygosity and Cognition in Schizophrenia

**Authors:** Vijaya Majumdar, Prosenjeet Chakroborty, Rashmi Arasappa, K Murugesh, Shanthala Hegde, Amrutha Jose, N K Manjunath, Arpitha Dharmappa

PMC · DOI: 10.1093/schizbullopen/sgae030 · Schizophrenia Bulletin Open · 2024-12-25

## TL;DR

The study explores how Klotho levels and a genetic variant affect cognitive function in schizophrenia patients and healthy controls.

## Contribution

It identifies distinct interaction patterns between Klotho and disease status across different cognitive domains in schizophrenia.

## Key findings

- The CD cluster showed a strong negative interaction between disease status and Klotho for executive function.
- Positive interactions for response inhibition were observed in the CD cluster, with stronger effects at protein levels.
- Results suggest caution in generalizing Klotho's effects on cognition in schizophrenia.

## Abstract

The relationship between Klotho and cognitive dysfunction in schizophrenia has been scarcely explored, with a few paradoxical findings. Hence, we aimed to enhance our understanding by testing associations between the functional KL-VS gene variant and circulating protein levels.

This case-control study included 239 healthy controls and 241 patients with schizophrenia, who were comprehensively characterized by neurocognitive tests and further subtyped into cognitive clusters; cognitively deficient (CD) and cognitively spared (CS), using K-means cluster analysis. Linear regression models were run to assess the main and iinteraction effects of the KL-VS heterozygosity (KL-VSHet+)/KL levels with confounding variables (disease status and age) on cognitive scores.

There was no main effect of KL-VSHet+ on the cognitive domains, but the CD cluster exhibited strong negative interactions between disease status and Klotho for executive function at the gene level, KL-VSHet+ × disease status, β = −.61, P = .043, with comparatively higher effect observed for KL levels, KL levels × disease status, β = −.91, P = .028. There was an opposing positive interaction for response inhibition, KL-VSHet+ × disease status, limited again to the CD cluster, β = .35, P = .046, with a higher effect at protein levels, KL levels × disease status, β = .72, <.004, though without CD cluster effect.

Overall, these dissociable patterns of association across cognitive domains indicate the need to exert caution over accepting any generalised direction of effect of Klotho at gene or protein level on cognition in schizophrenia.

## Linked entities

- **Proteins:** CG9701 (uncharacterized protein)
- **Diseases:** schizophrenia (MONDO:0005090)

## Full-text entities

- **Genes:** KL (klotho) [NCBI Gene 9365] {aka HFTC3, KLA}
- **Diseases:** Schizophrenia (MESH:D012559), CD (MESH:D003072)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC11904889/full.md

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Source: https://tomesphere.com/paper/PMC11904889