ReviewMetabolic brain disease2026
Vitamin D and hypoxia-inducible factors signaling interplay: A hypothesis-driven review of therapeutic strategies for acute cerebral infarction.
Review in Metabolic brain disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
Acute cerebral infarction (ACI) is a severe cerebrovascular disease characterized by a steadily rising global incidence rate, emerging as a leading cause of disability and mortality worldwide. Hypoxia-inducible factors (HIFs) play a pivotal role in the pathophysiological process of ACI. In recent years, mounting evidence has suggested a potential interplay between vitamin D (Vit D) and HIFs. Preclinical studies (e.g., rat cerebral ischemia models) have demonstrated that Vit D can stabilize HIF-1α, a key member of the HIFs family, which in turn reduces cerebral infarct volume by up to 50%. Clinical studies (patient cohort follow-ups) further reveal that ACI patients with Vit D-deficiency face a 30% higher risk of poor outcomes. Based on these findings, this review proposes a core hypothesis: Vit D exerts a neuroprotective effect in ACI by modulating HIFs’-related mechanisms, providing a novel direction for disease treatment. We speculate that for Vit D-deficient ACI patients, initiating supplementation therapy (e.g., 6000 IU/day) within 72 h ofn onset can reduce infarct volume by ≥ 40% by enhancing the protective effects of HIFs. In summary, the Vit D-HIFs axis is a highly promising therapeutic target for ACI, and future research should focus on validating this mechanism and promoting its clinical translation.
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