» Articles » PMID: 30287750

Fetal Renal Echogenicity Associated with Maternal Focal Segmental Glomerulosclerosis: The Effect of Transplacental Transmission of Permeability Factor SuPAR

Overview
Journal J Clin Med
Specialty General Medicine
Date 2018 Oct 6
PMID 30287750
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

We report a case of a pregnant woman with nephrotic syndrome due to biopsy-proven focal segmental glomerulosclerosis (FSGS) whose fetus developed echogenic kidneys and severe oligohydramnios by 27 weeks of gestation. Maternal treatment with prednisone resulted in normalization of the amniotic fluid indices and resolution of fetal renal echogenicity. The newborn was noted to have transient renal dysfunction and proteinuria, resolving by 6 weeks postpartum. The transplacental passage of permeability factors is postulated to have caused both the fetal and newborn renal presentation, with significantly elevated levels of soluble urokinase-type plasminogen activator receptor (suPAR) noted in the cord blood. This case documents the transplacental maternal-fetal transmission of suPAR, demonstrating the potential for maternal-fetal transmission of deleterious, disease-causing entities, and adds to the differential diagnosis of fetal echogenic kidneys. Further, this is the first documentation of a fetal response to maternal systemic therapy.

Citing Articles

Kidney Biopsy in a Pregnant Patient with Suspected Glomerular Disease: Commentary.

Hladunewich M Kidney360. 2023; 4(10):1359-1361.

PMID: 37578503 PMC: 10617797. DOI: 10.34067/KID.0000000000000244.


Efficacy of Rituximab in Treatment-Resistant Focal Segmental Glomerulosclerosis With Elevated Soluble Urokinase-Type Plasminogen Activator Receptor and Activation of Podocyte β3 Integrin.

Hladunewich M, Cattran D, Sethi S, Hayek S, Li J, Wei C Kidney Int Rep. 2022; 7(1):68-77.

PMID: 35005315 PMC: 8720804. DOI: 10.1016/j.ekir.2021.10.017.


Rituximab or plasmapheresis for prevention of recurrent focal segmental glomerulosclerosis after kidney transplantation: A systematic review and meta-analysis.

Boonpheng B, Hansrivijit P, Thongprayoon C, Mao S, Vaitla P, Bathini T World J Transplant. 2021; 11(7):303-319.

PMID: 34316454 PMC: 8291000. DOI: 10.5500/wjt.v11.i7.303.


The Search for Biomarkers to Aid in Diagnosis, Differentiation, and Prognosis of Childhood Idiopathic Nephrotic Syndrome.

Stone H, Magella B, Bennett M Front Pediatr. 2019; 7:404.

PMID: 31681707 PMC: 6805718. DOI: 10.3389/fped.2019.00404.

References
1.
Suthar K, Vanikar A, Trivedi H . Renal transplantation in primary focal segmental glomerulosclerosis using a tolerance induction protocol. Transplant Proc. 2008; 40(4):1108-10. DOI: 10.1016/j.transproceed.2008.03.076. View

2.
Sharma M, Sharma R, McCarthy E, Savin V . The focal segmental glomerulosclerosis permeability factor: biochemical characteristics and biological effects. Exp Biol Med (Maywood). 2004; 229(1):85-98. DOI: 10.1177/153537020422900111. View

3.
Gohh R, Yango A, Morrissey P, Monaco A, Gautam A, Sharma M . Preemptive plasmapheresis and recurrence of FSGS in high-risk renal transplant recipients. Am J Transplant. 2005; 5(12):2907-12. DOI: 10.1111/j.1600-6143.2005.01112.x. View

4.
Avni F, Garel C, Cassart M, DHaene N, Hall M, Riccabona M . Imaging and classification of congenital cystic renal diseases. AJR Am J Roentgenol. 2012; 198(5):1004-13. DOI: 10.2214/AJR.11.8083. View

5.
Sharif B, Barua M . Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis. Curr Opin Nephrol Hypertens. 2018; 27(3):194-200. DOI: 10.1097/MNH.0000000000000408. View