Research Progress in Sunlight Therapy for Chronic Kidney Disease

Chronic kidney disease (CKD) is a globally prevalent progressive disease characterized by complex interorgan signaling dysregulation. Fibroblast growth factor 23 (FGF23) and active vitamin D3 (VD3 and 1,25(OH) 2 D 3 ) play critical roles in calcium–phosphate homeostasis. FGF23 reduces intestinal phosphate absorption by inhibiting 1,25(OH) 2 D 3 synthesis, whereas 1,25(OH) 2 D 3 negatively regulates FGF23 expression. In patients with CKD, this balance is disrupted, leading to elevated FGF23 levels, reduced 1,25(OH) 2 D 3 levels, and exacerbated kidney dysfunction and complications. Since the primary source of VD3 is cutaneous synthesis via ultraviolet B radiation, sunlight exposure can markedly increase VD3 production, subsequently increasing 1,25(OH) 2 D 3 levels. This suggests that sunlight therapy may serve as a potential intervention for modulating FGF23 and improving calcium–phosphate metabolism in patients with CKD. This review systematically summarizes the regulatory mechanisms of sunlight on VD3 synthesis, the role of FGF23 in CKD progression, and the potential applications of sunlight therapy in CKD management. Additionally, we discuss the applicability of sunlight therapy across different individuals, its limitations, and potential optimization strategies, providing insights for future research.

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Publication Details

Journal
Journal of Bio-X Research
Published
2025-01-01
DOI
https://doi.org/10.34133/jbioxresearch.0051
Primary Topic
Parathyroid Disorders and Treatments
Type
article
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0.00
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article

Research Progress in Sunlight Therapy for Chronic Kidney Disease

Jiaxin Deng, Long Zhou, Yinghong Li, Jun Zhu et al.
Journal of Bio-X Research
Parathyroid Disorders and Treatments
article

Research Progress in Sunlight Therapy for Chronic Kidney Disease

Jiaxin Deng, Long Zhou, Yinghong Li, Jun Zhu, Honghui Wang, Wenyue Ma
article en

Abstract

Chronic kidney disease (CKD) is a globally prevalent progressive disease characterized by complex interorgan signaling dysregulation. Fibroblast growth factor 23 (FGF23) and active vitamin D3 (VD3 and 1,25(OH) 2 D 3 ) play critical roles in calcium–phosphate homeostasis. FGF23 reduces intestinal phosphate absorption by inhibiting 1,25(OH) 2 D 3 synthesis, whereas 1,25(OH) 2 D 3 negatively regulates FGF23 expression. In patients with CKD, this balance is disrupted, leading to elevated FGF23 levels, reduced 1,25(OH) 2 D 3 levels, and exacerbated kidney dysfunction and complications. Since the primary source of VD3 is cutaneous synthesis via ultraviolet B radiation, sunlight exposure can markedly increase VD3 production, subsequently increasing 1,25(OH) 2 D 3 levels. This suggests that sunlight therapy may serve as a potential intervention for modulating FGF23 and improving calcium–phosphate metabolism in patients with CKD. This review systematically summarizes the regulatory mechanisms of sunlight on VD3 synthesis, the role of FGF23 in CKD progression, and the potential applications of sunlight therapy in CKD management. Additionally, we discuss the applicability of sunlight therapy across different individuals, its limitations, and potential optimization strategies, providing insights for future research.

Journal of Bio-X ResearchVol. 8
Hunan University (CN)
Zero hunger
Openalex Percentile: Top 86%
Parathyroid Disorders and Treatments
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