Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
Monoallelic mutations of DNAJB11 were recently described in seven pedigrees with atypical clinical presentations of autosomal dominant polycystic kidney disease. DNAJB11 encodes one of the main cofactors of the endoplasmic reticulum chaperon BiP, a heat-shock protein required for efficient protein folding and trafficking. Here we conducted an international collaborative study to better characterize the DNAJB11-associated phenotype. Thirteen different loss-of-function variants were identified in 20 new pedigrees (54 affected individuals) by targeted next-generation sequencing, whole-exome sequencing or whole-genome sequencing. Amongst the 77 patients (27 pedigrees) now in total reported, 32 reached end stage kidney disease (range, 55-89 years, median age 75); without a significant difference between males and females. While a majority of patients presented with non-enlarged polycystic kidneys, renal cysts were inconsistently identified in patients under age 45. Vascular phenotypes, including intracranial aneurysms, dilatation of the thoracic aorta and dissection of a carotid artery were present in four pedigrees. We accessed Genomics England 100,000 genomes project data, and identified pathogenic variants of DNAJB11 in nine of 3934 probands with various kidney and urinary tract disorders. The clinical diagnosis was cystic kidney disease for eight probands and nephrocalcinosis for one proband. No additional pathogenic variants likely explaining the kidney disease were identified. Using the publicly available GnomAD database, DNAJB11 genetic prevalence was calculated at 0.85/10.000 individuals. Thus, establishing a precise diagnosis in atypical cystic or interstitial kidney disease is crucial, with important implications in terms of follow-up, genetic counseling, prognostic evaluation, therapeutic management, and for selection of living kidney donors.
|ISBN||1523-1755 (Electronic) 0085-2538 (Linking)|
|Authors||Huynh, V. T.; Audrezet, M. P.; Sayer, J. A.; Ong, A. C.; Lefevre, S.; Le Brun, V.; Despres, A.; Senum, S. R.; Chebib, F. T.; Barroso-Gil, M.; Patel, C.; Mallett, A. J.; Goel, H.; Mallawaarachchi, A. C.; Van Eerde, A. M.; Ponlot, E.; Kribs, M.; Genkyst Study Group, Genomics England Research Consortium; Le Meur, Y.; Harris, P. C.; Cornec-Le Gall, E.|
|Responsible Garvan Author|
|Publisher Name||KIDNEY INTERNATIONAL|
|URL link to publisher's version||https://www.ncbi.nlm.nih.gov/pubmed/32631624|