Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4

Am J Ophthalmol. 2023 Aug:252:188-204. doi: 10.1016/j.ajo.2023.03.025. Epub 2023 Mar 27.

Abstract

Purpose: Senior-Loken syndrome (SLSN) is an autosomal recessive disorder characterized by retinopathy and nephronophthisis. This study aimed to evaluate whether different phenotypes are associated with different variants or subsets of 10 SLSN-associated genes based on an in-house data set and a literature review.

Design: Retrospective case series.

Methods: Patients with biallelic variants in SLSN-associated genes, including NPHP1, INVS, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8, WDR19, CEP164, and TRAF3IP1, were recruited. Ocular phenotypes and nephrology medical records were collected for comprehensive analysis.

Results: Variants in 5 genes were identified in 74 patients from 70 unrelated families, including CEP290 (61.4%), IQCB1 (28.6%), NPHP1 (4.2%), NPHP4 (2.9%), and WDR19 (2.9%). The median age at the onset of retinopathy was approximately 1 month (since birth). Nystagmus was the most common initial sign in patients with CEP290 (28 of 44, 63.6%) or IQCB1 (19 of 22, 86.4%) variants. Cone and rod responses were extinguished in 53 of 55 patients (96.4%). Characteristic fundus changes were observed in CEP290- and IQCB1-associated patients. During follow-up, 70 of the 74 patients were referred to nephrology, among whom nephronophthisis was not detected in 62 patients (88.6%) at a median age of 6 years but presented in 8 patients (11.4%) aged approximately 9 years.

Conclusions: Patients with pathogenic variants in CEP290 or IQCB1 presented early with retinopathy, whereas other patients with INVS, NPHP3, or NPHP4 variants first developed nephropathy. Therefore, awareness of the genetic and clinical features may facilitate the clinical management of SLSN, especially early intervention of kidney problems for patients with eyes affected first.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calmodulin-Binding Proteins / genetics
  • Humans
  • Kidney Diseases, Cystic* / diagnosis
  • Kidney Diseases, Cystic* / genetics
  • Kidney Diseases, Cystic* / pathology
  • Mutation
  • Proteins / genetics
  • Retinal Diseases*
  • Retrospective Studies
  • Transcription Factors / genetics

Substances

  • Calmodulin-Binding Proteins
  • INVS protein, human
  • IQCB1 protein, human
  • NPHP4 protein, human
  • Proteins
  • Transcription Factors

Supplementary concepts

  • Nephronophthisis 3
  • Nephronophthisis 4
  • Nephronophthisis, familial juvenile
  • Senior Loken Syndrome