Litcius/Paper detail

Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease

Ryota Suzuki, Nana Sakakibara, Yuta Ichikawa, Hideaki Kitakado, Chika Ueda, Yu Tanaka, Eri Okada, Atsushi Kondo, Shinya Ishiko, Shingo Ishimori, China Nagano, Tomohiko Yamamura, Tomoko Horinouchi, Takayuki Okamoto, Kandai Nozu

2023Kidney International Reports10 citationsDOIOpen Access PDF

Abstract

Laminin subunit beta-2 (LAMB2)-associated disease, termed Pierson syndrome, presents with congenital nephrotic syndrome and ocular and neuromuscular symptoms. In recent years, however, the widespread use of next-generation sequencing has helped us discover a variety of phenotypes associated with this disease. Therefore, we conducted this systematic review. A literature search of patients with LAMB2 variants was conducted, and 110 patients were investigated, including 12 of our patients. For genotype-phenotype correlation analyses, the extracted data were investigated for pathogenic variant types, the severity of nephropathy, and extrarenal symptoms. Survival analyses were also performed for the onset age of end-stage kidney disease (ESKD). Among all patients, 81 (78%) presented with congenital nephrotic syndrome, and 52 (55%) developed ESKD within 12 months. The median age at ESKD onset was 6.0 months. Kidney survival analysis showed that patients with biallelic truncating variants had a significantly earlier progression to ESKD than those with other variants (median age 1.2 months vs. 60.0 months, p < 0.05). Although the laminin N-terminal domain is functionally important in laminin proteins, and variants in the laminin N-terminal domain are said to result in a severe kidney phenotype such as earlier onset age and worse prognosis, there were no significant differences in onset age of nephropathy and progression to ESKD between patients with non-truncating variants located in the laminin N-terminal domain and those with variants located outside this domain. This study revealed a diversity of LAMB2-associated diseases, characteristics of LAMB2 nephropathy, and genotype-phenotype correlations.

Topics & Concepts

MedicineNephrotic syndromeCongenital nephrotic syndromeGenotypeKidney diseaseFocal segmental glomerulosclerosisPhenotypeDiseaseInternal medicineNephropathyGenotype-phenotype distinctionKidneyPediatricsProteinuriaBioinformaticsPathologyGastroenterologyGeneticsEndocrinologyGeneDiabetes mellitusBiologyCell Adhesion Molecules ResearchWnt/β-catenin signaling in development and cancerCellular transport and secretion