Aug 2026· Reviews in Endocrine & Metabolic Disorders· 0 citations· 116 references
Medicine
TL;DR
A review of recent findings regarding FGF23 focuses on its classical role as a hormone and its broader effects as a humoral factor on other organs, focusing on the exact mechanisms underlying these pleiotropic actions.
Excessive mineralocorticoid receptor (MR) activation in the heart and vasculature leads to pathological effects such as extracellular matrix accumulation, oxidative stress, and sustained inflammation. While MR’s role in cardiovascular and renal systems is well understood, MR signaling has also been implicated as a key...
Husam Bensreti, Joseph C. Shaver, Christopher L. Yearwood et al.· Journal of Endocrinology· 0 citations
The progression of chronic kidney disease (CKD) entails the development of complications, such as anemia and disturbances in mineral homeostasis, among others, and both of them have been shown to be closely related. In fact, high phosphorus (P) and excessive production of fibroblast growth factor 23 (FGF23) are hallmar...
K. Valdés-Díaz, R. García-Sáez, Casimiro Valle et al.· International Journal of Mol...· 0 citations
Fibroblast growth factor 23 (FGF23) is involved in the regulation of phosphate metabolism and has been linked to vascular calcification. However, the genetic association between FGF23 and abdominal aortic calcification (AAC) remains unclear. We conducted a bidirectional two-sample Mendelian randomization (MR) study to...
Lei Song, Juan Chen, Cheng Xue et al.· Medicine· 0 citations
An overview of FGF/FGFR signaling is provided and its cellular and physiological functions are summarized and the relationship between aberrant (including hyperactivated or inactivated) FGF/FGFR signaling and diverse diseases is explored.
Miao-Yu Song, Xi Liu, Yang Xiao et al.· MedComm· 0 citations
Osteoporosis is increasingly recognized as a heterogeneous syndrome rather than a single disease, driven by diverse pathophysiological mechanisms. Subtypes-including postmenopausal estrogen deficiency, age-related bone loss, anorexia nervosa, and GLP-1 receptor agonist-associated weight loss-exhibit distinct bone turno...
Bo-Lun Li, Lin-Yi Liu, E. Luo et al.· Baillière's Best Practice &...· 0 citations
Background/Objectives: X-linked hypophosphatemia (XLH), the most frequent heritable cause of hypophosphatemic rickets, is characterized by impaired linear growth and skeletal deformities, that can lead to disproportionate short stature. Linear growth depends on the coordinated regulation of systemic endocrine signals a...
Michela Ferrarese, V. Camozzi, L. Guazzarotti· Endocrines· 0 citations
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