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Article Synopsis
  • Vascular calcification (VC) is a serious issue in patients with chronic kidney disease (CKD) that can lead to increased cardiovascular mortality, mainly due to the transformation of vascular smooth muscle cells (VSMCs) into osteoblast-like cells influenced by exosomes and microRNAs.
  • The study explored the effects of the Bushen Huoxue (BSHX) formula on VC using both in vitro models with high phosphate and an in vivo CKD-VC rat model, examining various biochemical and cellular markers related to calcification.
  • Results showed that exosomal miRNA-32 plays a significant role in VC development and that the PI3K/AKT signaling pathway is involved, suggesting a potential therapeutic mechanism of
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Article Synopsis
  • Gastrointestinal severe adverse events like ulceration and perforation have been linked to polystyrene sulfonate and sevelamer, especially in patients with chronic kidney disease, but the exact cause is unclear.* -
  • A meta-analysis of existing research found that polystyrene sulfonate is significantly more likely to cause severe issues such as necrosis or perforation compared to sevelamer (p < 0.001).* -
  • The findings indicate that while sevelamer may cause inflammation or ulceration, polystyrene sulfonate is more strongly associated with severe outcomes, including a higher risk of death (p < 0.001).*
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Tumoral calcinosis is an extremely rare genetic disease caused by mutations in three genes, GALNT3, FGF23, and KL, which disrupt phosphorus metabolism. The hallmark of this condition is the formation of tumors in the soft tissues around the joints. Other phenotypic features of tumoral calcinosis are dental involvement and brain and vascular calcifications.

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Introduction: Case reports have suggested a causative role between sevelamer use and subsequent gastrointestinal bleeding (GIB), but no large observational studies have evaluated this association.

Methods: Using the United States Renal Data System database from 2015 to 2019, we examined the association between initiation of sevelamer (vs. non-sevelamer containing phosphate binders) and GIB hospitalization as well as all-cause mortality among individuals on hemodialysis.

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Data suggest that non-calcium-based binders, and specifically sevelamer, may lead to lower rates of death when compared with calcium-based binders in end-stage renal disease (ESRD) patients. However, the association between sevelamer use and mortality for those with non-dialysis-dependent chronic kidney disease (NDD-CKD) patients has been uncertain. Our research is presented in a prospective cohort study.

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