Join nephrologist Dr. Vivek Bhalla (@BhallaResearch)
& Science Communicator Rebecca Handler (@rmh199) in the lab as he shares a story that began with a single patient’s case of early-onset kidney disease and led to a genetic discovery: https://t.co/khb914xwqE
#Nephrology
Hypertension (high blood pressure) is one of the most common complications of PKD. When hypertension is left untreated, it can further damage the kidneys and increase the risk of heart disease and stroke.
Learn more about managing this symptom of PKD: https://t.co/M8853CJOlU
Study identifies excessive, unregulated aldosterone as a modifiable driver of obesity-related CV risk, highlighting need for trials targeting aldosterone or mineralocorticoid receptors to mitigate early cardiometabolic injury. https://t.co/MfyVGACaQZ
@rmohty@spjuraschek Nor about the sufficiency of MRA therapy with respect to raising renin…(that I’m aware of)….quite plausible that someone has done this work but has not made it to guidelines
Anecdotally, MRAs work very well for BP control including monotherapy in this population. 3/n
TRPC6 inhibition for the treatment of focal segmental glomerulosclerosis: a randomised, placebo-controlled, phase 2 trial of BI 764198 - The Lancet https://t.co/QN5K71wUwZ @TheLancet
This month marks 10 years of JCI Insight!
A special shoutout to authors, editors, reviewers, readers, and all those dedicated to biomedical research, ranging from preclinical to clinical studies. This video highlights selected covers through the years.
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Music: Bensound; License code: LDOZSSOUYFKAOLR8; Artist: Theatre Of Delays
@Eickelberg_MD
Please help us bring hope and light into this Holiday Season.
One of our @StanfordNeph@StanfordAbdTxp faculty families is working to save their child’s life from a rare genetic condition.
Please read, share and support.
https://t.co/naGsRMZb2u
Please help us bring hope and light into this Holiday Season.
One of our @StanfordNeph@StanfordAbdTxp faculty families is working to save their child’s life from a rare genetic condition.
Please read, share and support.
https://t.co/naGsRMZb2u
who sought to sift through these factors to demonstrate that this could indeed work. There is lots to still do, both in lab and in clinic, and there are risks/benefits to calculate, but for those families suffering with a rare disease, this may be possible @StanfordNeph 4/x.
Dissecting through renal physiology in the context of patient care is difficult but eminently valuable. Inspired by the landmark work of Hoorn et al., https://t.co/Rv1fbQQO9P showing the effect of tacrolimus on phosphorylated NCC, we sought to understand if the use of CNIs 1/x.
Gitelman syndrome (GS) is a rare, autosomal-recessive salt-losing tubulopathy often requiring lifelong electrolyte supplementation. A new case report describes a patient with GS who initiated tacrolimus, a calcineurin phosphatase inhibitor, after orthotopic heart transplantation. The patient achieved normokalemia and improved blood pressure without needing potassium supplements. Read the full text for free: https://t.co/Xa6YtIxj9g @AHAScience #AHAJournals
but there are only historical controls and multiple confounding factors in patients who receive tacrolimus (diuretics, PJP prophylaxis, PPIs, RAASi, etc). I'm thankful to Ms. Halee Yue @UCLAHealth and Dr. Martina Cacciapuoti @MartiCacciaNeph 3/x