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DOI 10.1093/cercor/bhad358

Медицинская библиотека · Cerebral cortex (New York, N.Y. : 1991) · 2023

Reduced gray matter volume in the default-mode network associated with insulin resistance.

Asano Saki, Ogawa Akitoshi, Osada Takahiro, Oka Satoshi, Nakajima Koji, Oshima Yasushi, Tanaka Sakae, Kaga Hideyoshi, Tamura Yoshifumi, Watada Hirotaka, Kawamori Ryuzo, Konishi Seiki

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Insulin resistance may lead to structural and functional abnormalities of the human brain. However, the mechanism by which insulin resistance impairs the brain remains elusive. In this study, we used two large neuroimaging databases to investigate the brain regions where insulin resistance was associated with the gray matter volume and to examine the resting-state functional connectivity between these brain regions and each hypothalamic nucleus. Insulin resistance was associated with reduced gray matter volume in the regions of the default-mode and limbic networks in the cerebral cortex in older adults. Resting-state functional connectivity was prominent between these networks and the paraventricular nucleus of the hypothalamus, a hypothalamic interface connecting functionally with the cerebral cortex. Furthermore, we found a significant correlation in these networks between insulin resistance-related gray matter volume reduction and network paraventricular nucleus of the hypothalamus resting-state functional connectivity. These results suggest that insulin resistance-related gray matter volume reduction in the default-mode and limbic networks emerged through metabolic homeostasis mechanisms in the hypothalamus.

Для цитирования: Asano Saki, Ogawa Akitoshi, Osada Takahiro, Oka Satoshi, Nakajima Koji, Oshima Yasushi, Tanaka Sakae, Kaga Hideyoshi, Tamura Yoshifumi, Watada Hirotaka, Kawamori Ryuzo, Konishi Seiki. Reduced gray matter volume in the default-mode network associated with insulin resistance.. Cerebral cortex (New York, N.Y. : 1991). 2023. DOI: 10.1093/cercor/bhad358.

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