4.4 Article

Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population

Journal

JOURNAL OF HUMAN GENETICS
Volume 67, Issue 7, Pages 427-440

Publisher

SPRINGERNATURE
DOI: 10.1038/s10038-022-01020-5

Keywords

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Funding

  1. Health Labor Sciences Research Grant for the Research on Measures for Intractable Diseases [H24-nanchi-ippan-041, H29-nanchi-ippan-039]
  2. Japan Society for the Promotion of Science (KAKENHI) [JP15K09261, 18K08243]
  3. Grants-in-Aid for Scientific Research [18K08243] Funding Source: KAKEN

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Nephronophthisis is a common kidney disease related to abnormalities in primary cilia. This study identified multiple causative genes for NPHP-RCs using genetic analysis, and found that most patients showed extrarenal manifestations. Comprehensive genetic analysis using NGS is useful for diagnosing patients with NPHP-RCs.
Nephronophthisis is an autosomal-recessive kidney disease that is caused by abnormalities in primary cilia. Nephronophthisis-related ciliopathies (NPHP-RCs) are a common cause of end-stage kidney disease (ESKD) in children and adolescents. NPHP-RCs are often accompanied by extrarenal manifestations, including intellectual disability, retinitis pigmentosa, or polydactyly. Although more than 100 causative genes have been identified, its diagnosis is difficult because the clinical features of each mutation often overlap. From September 2010 to August 2021, we performed genetic analysis, including next-generation sequencing (NGS), in 574 probands with kidney dysfunction and retrospectively studied cases genetically diagnosed with NPHP-RCs. Results We detected mutations related to NPHP-RCs in 93 patients from 83 families. Members of 60 families were diagnosed using NGS, and the mutations and the corresponding number of families are as follows: NPHP1 (24), NPHP3 (10), OFD1 (7), WDR35 (5), SDCCAG8 (4), BBS10 (3), TMEM67 (3), WDR19 (3), BBS1 (2), BBS2 (2), IFT122 (2), IFT140 (2), IQCB1 (2), MKKS (2), SCLT1 (2), TTC21B (2), ALMS1 (1), ANKS6 (1), BBS4 (1), BBS12 (1), CC2D2A (1), DYNC2H1 (1), IFT172 (1), and MAPKBP1 (1). A total of 39 cases (41.9%) progressed to ESKD at the time of genetic analysis, whereas 58 cases (62.3%) showed extrarenal manifestations, the most common being developmental delay, intellectual disability, and autism spectrum disorder in 44 patients. Comprehensive genetic analysis using NGS is useful for diagnosing patients with NPHP-RCs.

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