A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability

• Published in: Pediatric nephrology (Berlin, West) Vol. 37; no. 8; pp. 1855 - 1866
• Main Authors: Yılmaz, Esra Karabağ, Saygili, Seha, Gulhan, Bora, Canpolat, Nur, Bayazıt, Aysun Karabay, Kilic, Beltinge Demircioglu, Akıncı, Nurver, Benzer, Meryem, Goknar, Nilufer, Tufan, Asli Kavaz, Kalyoncu, Mukaddes, Nalcacioglu, Hulya, Tekcan, Demet, Yıldız, Gizem, Agbas, Ayse, Nayır, Ahmet, Topaloglu, Rezan, Caliskan, Salim, Ozaltin, Fatih
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.08.2022; Springer Nature B.V
• Subjects: Angiotensin; Angiotensin-converting enzyme inhibitors; Biopsy; Calcineurin; Calcineurin inhibitors; Genetic diversity; Genetic screening; Genotypes; Immunosuppressive agents; Kidney diseases; Medical prognosis; Medicine; Medicine & Public Health; Nephrology; Nephrotic syndrome; Original Article; Patients; Pediatrics; Peptidyl-dipeptidase A; Phenotypes; Proteinuria; Sclerosis; Steroid hormones; Survival; Urology; Prognosis; Treatment; Children; Diffuse mesangial sclerosis; Focal segmental glomerulosclerosis; Intrafamilial variability; PLCε1
• ISSN: 0931-041X; 1432-198X
• DOI: 10.1007/s00467-021-05371-7

Background The phenotypic and genotypic spectrum and kidney outcome of PLCε1- related kidney disease are not well known. We attempted to study 25 genetically confirmed cases of PLCε1- related kidney disease from 11 centers to expand the clinical spectrum and to determine the relationship between phenotypic and genotypic features, kidney outcome, and the impact of treatment on outcome. Methods Data regarding demographics, clinical and laboratory characteristics, histopathological and genetic test results, and treatments were evaluated retrospectively. Results Of 25 patients, 36% presented with isolated proteinuria, 28% with nephrotic syndrome, and 36% with chronic kidney disease stage 5. Twenty patients underwent kidney biopsy, 13 (65%) showed focal segmental glomerulosclerosis (FSGS), and 7 (35%) showed diffuse mesangial sclerosis (DMS). Of the mutations identified, 80% had non-missense, and 20% had missense; ten were novel. No clear genotype–phenotype correlation was observed; however, significant intrafamilial variations were observed in three families. Patients with isolated proteinuria had significantly better kidney survival than patients with nephrotic syndrome at onset ( p  = 0.0004). Patients with FSGS had significantly better kidney survival than patients with DMS ( p  = 0.007). Patients who presented with nephrotic syndrome did not respond to any immunosuppressive therapy; however, 4/9 children who presented with isolated proteinuria showed a decrease in proteinuria with steroids and/or calcineurin inhibitors. Conclusion PLCε1 -related kidney disease may occur in a wide clinical spectrum, and genetic variations are not associated with clinical presentation or disease course. However, clinical presentation and histopathology appear to be important determinants for prognosis. Immunosuppressive medications in addition to angiotensin-converting enzyme inhibitors may be beneficial for selected patients. Graphical abstract “A higher resolution version of the Graphical abstract is available as Supplementary information”.