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AuthorVoskarides K.
AuthorPapagregoriou G.
AuthorHadjipanagi D.
AuthorPetrou I.
AuthorSavva I.
AuthorElia A.
AuthorAthanasiou Y.
AuthorPastelli A.
AuthorKkolou M.
AuthorHadjigavriel M.
AuthorStavrou C.
AuthorPierides A.
AuthorDeltas C.
Available date2019-10-06T09:38:33Z
Publication Date2018
Publication NameBMC Nephrology
ISSN1471-2369
URIhttp://dx.doi.org//10.1186/s12882-018-0906-5
URIhttp://hdl.handle.net/10576/12066
AbstractBackground: About 40-50% of patients with familial microscopic hematuria (FMH) caused by thin basement membrane nephropathy (TBMN) inherit heterozygous mutations in collagen IV genes (COL4A3, COL4A4). On long follow-up, the full phenotypic spectrum of these patients varies a lot, ranging from isolated MH or MH plus low-grade proteinuria to chronic renal failure of variable degree, including end-stage renal disease (ESRD). Methods: Here, we performed Whole Exome Sequencing (WES) in patients of six families, presenting with autosomal dominant FMH, with or without progression to proteinuria and loss of renal function, all previously found negative for severe collagen IV mutations. Hierarchical filtering of the WES data was performed, followed by mutation prediction analysis, Sanger sequencing and genetic segregation analysis. Results: In one family with four patients, we found evidence for the contribution of two co-inherited variants in two crucial genes expressed in the glomerular basement membrane (GBM); LAMA5-p.Pro1243Leu and COL4A5-p.Asp654Tyr. Mutations in COL4A5 cause classical X-linked Alport Syndrome, while rare mutations in the LAMA5 have been reported in patients with focal segmental glomerulosclerosis. The phenotypic spectrum of the patients includes hematuria, proteinuria, focal segmental glomerulosclerosis, loss of kidney function and renal cortical cysts. Conclusions: A modifier role of LAMA5 on the background of a hypomorphic Alport syndrome causing mutation is a possible explanation of our findings. Digenic inheritance is another scenario, following the concept that mutations at both loci more accurately explain the spectrum of symptoms, but further investigation is needed under this concept. This is the third report linking a LAMA5 variant with human renal disease and expanding the spectrum of genes involved in glomerular pathologies accompanied by familial hematurias. The cystic phenotype overlaps with that of a mouse model, which carried a Lama5 hypomorphic mutation that caused severely reduced Lama5 protein levels and produced kidney cysts. 2018 The Author(s).
SponsorThe work was supported from the Cyprus Research Promotion Foundation through the grant NEW INFRASTRUCTURE/STRATEGIC/0308/24 to CD (co-funded by the European Regional Development Fund and the Republic of Cyprus). The funding body did not contribute to the design of study, collection, analysis and interpretation of data, or in manuscript writing.
LanguageEnglish
PublisherBioMed Central Ltd.
dc.source Scopus
SubjectAlport syndrome
SubjectCollagen IV
SubjectDigenic inheritance
SubjectFamilial hematuria
SubjectFSGS
SubjectKidney disease
SubjectLaminin alpha 5
SubjectMetalloproteinase
SubjectModifier gene
SubjectRenal cysts
SubjectSynaptopodin
SubjectThin Basement Membrane Nephropathy (TBMN)
TitleCOL4A5 and LAMA5 variants co-inherited in familial hematuria: Digenic inheritance or genetic modifier effect?
TypeArticle
Issue Number1
Volume Number19


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