KatalinSusztak University of PennsylvaniaUnited States

KatalinSusztak
Dr. Susztak has made fundamental discoveries, paving the way for the development of targeted therapies that could improve the lives of over 30 million Americans with kidney disease. She delineated the genetic underpinning of kidney function heritability, and pioneered human kidney tissue banking as well as genomics and epigenetics profiling at single cell resolution. Susztak has identified more than a dozen new risk genes for kidney disease and revealed the previously unsuspected role of proximal tubule cells in regulating kidney function. She was the first to demonstrate the causal role of APOL1 gene variants that are only found in individuals with African ancestry in kidney disease, thereby explaining the increased risk of renal disease in Black patients. Her work also demonstrated that APOL1 gene variants affect the risk and prognosis of sepsis and COVID-19 infection. Beyond her unique contributions to the genetics of kidney disease, Dr. Susztak defined the cellular pathways of APOL1 toxicity, including NLRP3 and STING, which has enabled the development of targeted therapeutics in a dramatic example of precision/personalized medicine which also addresses health disparities. She is also the founder of the PENN/CHOP Kidney Innovation Center and the Transformative Researches In Diabetic Nephropathy study, an innovative academic-industry partnership that is. developing and testing novel therapies to improve the lives of those with kidney disease.
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First Name
Katalin
Last Name
Susztak
Institution
Country.
United States

Saturday, February 8, 2025

Time Session
9:45 a.m.
11:15 a.m.
ArvindConjeevaram Chair canchi8@gmail.comHead - Nephrology Dept, Trustwell Hospitals, Bangalore India
DebasishBanerjee Chair dbanerje@sgul.ac.ukSt George's University Hospital NHS Foundation TrUnited Kingdom
LIGUISEN Chair guisenli@163.comUESTC, CSN, ChinaChina
  • How Do I Treat Renal Complications in Patients With Sickle Cell Disease?
    ClaireSharpe Speaker claire.sharpe@nottingham.ac.ukUniversity of Nottingham and King's College Hospital, LondonUnited Kingdom
  • iPSCs to Model Rare Kidney Diseases for Drug Discovery: The Examples of FSGS and ADPKD
    ArielaBenigni Speaker ariela.benigni@marionegri.itMario Negri Institute for Pharmacological Research, ItalyItaly
  • Kidney Multiome-based Genetic Scorecard Reveals Convergent Coding and Regulatory Variants
    KatalinSusztak Speaker ksusztak@pennmedicine.upenn.eduUniversity of PennsylvaniaUnited States
  • Primary Hyperoxaluria: A Hope for Gene Therapy?
    YaacovFrishberg Speaker yaacovf@ekmd.huji.ac.ilIsrael
  • Q&A
Neelkamal Hall 305