Literature DB >> 29274997

Electroconvulsive therapy enhances the anti-ageing hormone Klotho in the cerebrospinal fluid of geriatric patients with major depression.

Carolin Hoyer1, Alexander Sartorius2, Suna Su Aksay2, Jan Malte Bumb3, Christoph Janke4, Manfred Thiel4, Dieter Haffner5, Maren Leifheit-Nestler5, Laura Kranaster6.   

Abstract

Klotho is a humoral factor with pleiotropic effects. Most notably, Klotho deficiency is associated with a phenotype comprising organ manifestations accompanying aging including atherosclerosis and cognitive impairment. Research on the role of Klotho in affective disorder is scarce, which is surprising in light of the fact that depression is associated with accelerated cellular aging as well as aging-related phenotypes and comorbidity observed in Klotho deficiency. On these grounds we investigated Klotho levels in the cerebrospinal fluid (CSF) and serum of eight geriatric patients undergoing electroconvulsive therapy (ECT) for severe depression. We hypothesize that ECT as a highly effective antidepressant treatment leads enhances Klotho levels. We found a significant difference between pre- and post-ECT CSF Klotho (792.5pg/ml vs. 991.3pg/ml, p=0.0020), but no difference in serum Klotho (602.5 vs. 594.3, p=0.32). Moreover, CSF Klotho increase positively correlated with the number of single ECT sessions that were performed in each patient (F1, 6)=7.84, p=0.031). Conjointly, the results of our exploratory study with a small sample size suggest a central nervous system-specific impact of ECT on Klotho, which may in turn partake in mediating the antidepressant effect of ECT. We suggest the modulation of neuroinflammatory processes, which have been ascribed pathophysiological relevance within the conceptual framework of the neuroinflammation hypothesis of depression, through ECT as a potential mechanism by which Klotho is enhanced in response to treatment. Further preclinical and clinical investigation should aim for a precise identification of the role of Klotho in depressive disorder.
Copyright © 2017 Elsevier B.V. and ECNP. All rights reserved.

Entities:  

Keywords:  Cerebrospinal fluid; Depression; ECT; Electroconvulsive therapy; Klotho

Mesh:

Substances:

Year:  2017        PMID: 29274997     DOI: 10.1016/j.euroneuro.2017.12.012

Source DB:  PubMed          Journal:  Eur Neuropsychopharmacol        ISSN: 0924-977X            Impact factor:   4.600


  3 in total

1.  Life extension factor klotho regulates behavioral responses to stress via modulation of GluN2B function in the nucleus accumbens.

Authors:  Han-Jun Wu; Wen-Ning Wu; Hua Fan; Liu-Er Liu; Jin-Qiong Zhan; Yi-Heng Li; Chun-Nuan Chen; Shu-Zhen Jiang; Jian-Wen Xiong; Zhi-Min Yu; Bo Wei; Wei Wang; Yuan-Jian Yang
Journal:  Neuropsychopharmacology       Date:  2022-04-21       Impact factor: 8.294

2.  Peripheral levels of the anti-aging hormone Klotho in patients with depression.

Authors:  Alexander Sartorius; Maria Gilles; Anna-Maria Pfeifer; Michael Deuschle; Carolin Hoyer; Dieter Haffner; Maren Leifheit-Nestler; Laura Kranaster
Journal:  J Neural Transm (Vienna)       Date:  2019-05-04       Impact factor: 3.575

3.  Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy.

Authors:  Jerome C Foo; Fabian Streit; Josef Frank; Stephanie H Witt; Jens Treutlein; Bernhard T Baune; Susanne Moebus; Karl-Heinz Jöckel; Andreas J Forstner; Markus M Nöthen; Marcella Rietschel; Alexander Sartorius; Laura Kranaster
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2018-12-02       Impact factor: 3.568

  3 in total

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