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. 2026 Feb:235:111748.
doi: 10.1016/j.brainresbull.2026.111748. Epub 2026 Jan 24.

Brain functional connectivity initiates structured reorganization at a critical oxygen threshold during hypoxia

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Free article

Brain functional connectivity initiates structured reorganization at a critical oxygen threshold during hypoxia

Daehun Kang et al. Brain Res Bull. 2026 Feb.
Free article

Abstract

The human brain, one of the most energy-demanding organs, continuously adapts to internal and external challenges. Hypoxia, a reduction in oxygen availability, poses a substantial threat to brain function. Despite its importance, the nature of the brain's adaptive response to hypoxia remains poorly understood. In this study, we investigated dynamic functional connectivity (FC) under acute hypoxic conditions (FiO2 = 7.7 % and 11.8 %) in healthy adults using blood-oxygenation-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) and concurrent advanced physiological monitoring, including partial pressures of end-tidal oxygen (PetO2) and carbon dioxide (PetCO2) and peripheral oxygen saturation (SpO2), and a Go/No-Go cognitive task to assess behavioral performance. Principal component analysis identified a hypoxia-responsive component in dynamic FCs across 400 cerebral parcels. This component captured hypoxia-specific FC changes that coincided with a critical drop in PetO2 (∼53 mmHg), preceding subsequent changes in SpO2, bulk BOLD signals, and behavioral performance. These FC changes were network-specific, with a marked increase primarily centered on the default mode network (DMN), which selectively synchronized with other high-level cognitive networks. In contrast, hypoxia-responsive connectivity showed limited involvement of visual networks, including connectivity with the DMN. These findings suggest that the brain engages in proactive and structured FC adaptations in anticipation of oxygen decline, rather than in response to it. FC-based metrics offer new insights into the temporal dynamics of brain resilience and may hold translational value for the early detection of vulnerability in neurological or neurodegenerative disorders.

Keywords: Arterial oxygen pressure; End-tidal oxygen; Functional connectivity; Hypoxia; Proactive organization.

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Conflict of interest statement

Declaration of Competing Interest Yunhong Shu, Joshua D. Trzasko and Matt A. Bernstein acknowledge the following financial interest: Mayo Clinic has licensed intellectual property related to the compact 3 T to GE Healthcare, and Matt A. Bernstein is a former employee of GE Medical Systems and receives pension payments Other authors, including Daehun Kang, Koji Uchida, Clifton R. Haider, Norbert G. Campeau, Myung-Ho In, Erin M. Gray, Kirk M. Welker, Max R. Trenerry, David R. Holmes III, Michael J. Joyner, Timothy B. Curry, John Huston III, have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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