Experimentally induced subclinical hypothyroidism causes decreased functional connectivity of the cuneus: A resting state fMRI study.


Journal

Psychoneuroendocrinology
ISSN: 1873-3360
Titre abrégé: Psychoneuroendocrinology
Pays: England
ID NLM: 7612148

Informations de publication

Date de publication:
04 2019
Historique:
received: 31 08 2018
revised: 10 12 2018
accepted: 11 12 2018
pubmed: 18 12 2018
medline: 18 3 2020
entrez: 18 12 2018
Statut: ppublish

Résumé

The aim of this study was to experimentally evaluate the effects of subclinical mild hypothyroidism on brain network connectivity as determined by resting state fMRI (rsfMRI) which serves as a proxy for global changes in brain function. Fifteen otherwise healthy patients with complete hypothyroidism under stable, long term levothyroxine substitution volunteered for the study. They reduced their pretest levothyroxine dosage by 30% for 52-56 days. Basally and after partial levothyroxine withdrawal, rsfMRI along with a neuropsychological analysis was performed. RsfMRI was subjected to graph-theory-based analysis to investigate whole-brain intrinsic functional connectivity. The desired subclinical hypothyroidism was achieved in all subjects. This was associated with a significant decrease in resting-state functional connectivity specifically in the cuneus (0.05 FWE corrected at cluster level) which was mainly caused by a weaker functional connectivity to the cerebellum and regions of the default mode network, i.e. the medial prefrontal cortex, the precuneus and the bilateral angular gyri. The decrease in cuneus connectivity was correlated to the increase in TSH serum levels. A working memory task showed a slightly longer reaction time and less accuracy after partial levothyroxine withdrawal. Even short-term partial levothyroxine partial withdrawal leads to deficits in working memory tasks and to a weaker integration of the cuneus within the default mode network.

Identifiants

pubmed: 30557763
pii: S0306-4530(18)30906-5
doi: 10.1016/j.psyneuen.2018.12.012
pii:
doi:

Substances chimiques

Thyroxine Q51BO43MG4

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

158-163

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Anna Göbel (A)

Department of Neurology, University of Lübeck, Lübeck, Germany. Electronic address: anna.goebel@neuro.uni-luebeck.de.

Martin Göttlich (M)

Department of Neurology, University of Lübeck, Lübeck, Germany.

Marcus Heldmann (M)

Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Psychology II, University of Lübeck, Lübeck, Germany.

René Georges (R)

Department of Internal Medicine I, University of Lübeck, Lübeck, Germany.

Relana Nieberding (R)

Department of Internal Medicine I, University of Lübeck, Lübeck, Germany.

Berenike Rogge (B)

Department of Neurology, University of Lübeck, Lübeck, Germany.

Alexander Sartorius (A)

Central Institute of Mental Health, Mannheim, Germany.

Georg Brabant (G)

Department of Internal Medicine I, University of Lübeck, Lübeck, Germany.

Thomas F Münte (TF)

Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Psychology II, University of Lübeck, Lübeck, Germany.

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