TY - JOUR
T1 - Therapeutic trials in adult FSGS
T2 - lessons learned and the road forward
AU - De Vriese, An S.
AU - Wetzels, Jack F.
AU - Glassock, Richard J.
AU - Sethi, Sanjeev
AU - Fervenza, Fernando C.
N1 - Publisher Copyright:
© 2021, Springer Nature Limited.
PY - 2021/9
Y1 - 2021/9
N2 - Focal segmental glomerulosclerosis (FSGS) is not a specific disease entity but a lesion that primarily targets the podocyte. In a broad sense, the causes of the lesion can be divided into those triggered by a presumed circulating permeability factor, those that occur secondary to a process that might originate outside the kidneys, those caused by a genetic mutation in a podocyte or glomerular basement membrane protein, and those that arise through an as yet unidentifiable process, seemingly unrelated to a circulating permeability factor. A careful attempt to correctly stratify patients with FSGS based on their clinical presentation and pathological findings on kidney biopsy is essential for sound treatment decisions in individual patients. However, it is also essential for the rational design of therapeutic trials in FSGS. Greater recognition of the pathophysiology underlying podocyte stress and damage in FSGS will increase the likelihood that the cause of an FSGS lesion is properly identified and enable stratification of patients in future interventional trials. Such efforts will facilitate the identification of effective therapeutic agents.
AB - Focal segmental glomerulosclerosis (FSGS) is not a specific disease entity but a lesion that primarily targets the podocyte. In a broad sense, the causes of the lesion can be divided into those triggered by a presumed circulating permeability factor, those that occur secondary to a process that might originate outside the kidneys, those caused by a genetic mutation in a podocyte or glomerular basement membrane protein, and those that arise through an as yet unidentifiable process, seemingly unrelated to a circulating permeability factor. A careful attempt to correctly stratify patients with FSGS based on their clinical presentation and pathological findings on kidney biopsy is essential for sound treatment decisions in individual patients. However, it is also essential for the rational design of therapeutic trials in FSGS. Greater recognition of the pathophysiology underlying podocyte stress and damage in FSGS will increase the likelihood that the cause of an FSGS lesion is properly identified and enable stratification of patients in future interventional trials. Such efforts will facilitate the identification of effective therapeutic agents.
UR - http://www.scopus.com/inward/record.url?scp=85106041330&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85106041330&partnerID=8YFLogxK
U2 - 10.1038/s41581-021-00427-1
DO - 10.1038/s41581-021-00427-1
M3 - Review article
C2 - 34017116
AN - SCOPUS:85106041330
SN - 1759-5061
VL - 17
SP - 619
EP - 630
JO - Nature Reviews Nephrology
JF - Nature Reviews Nephrology
IS - 9
ER -