liu.seSearch for publications in DiVA
Change search
ReferencesLink to record
Permanent link

Direct link
Evidence against ZNF469 being causative for keratoconus in Polish patients
Poznan University of Medical Science, Poland; Polish Academic Science, Poland.
Warsaw University of Technology, Poland; Baylor Coll Med, TX 77030 USA.
Medical University of Warsaw, Poland.
Medical University of Warsaw, Poland.
Show others and affiliations
2016 (English)In: Acta Ophthalmologica, ISSN 1755-375X, E-ISSN 1755-3768, Vol. 94, no 3, 289-294 p.Article in journal (Refereed) PublishedText
Abstract [en]

PurposeKeratoconus (KTCN) is a degenerative disorder characterized by stromal thinning and protrusion of the cornea, resulting in severe impairment of visual function. A recent study proposed that rare heterozygous mutations in ZNF469 determine KTCN aetiology. MethodsTo investigate the contribution of ZNF469 to KTCN, we Sanger sequenced ZNF469 in 42 unrelated Polish patients with KTCN and 49 Polish individuals with high myopia (HM) and compared the results with whole-exome sequencing (WES) data performed in 268 Polish individuals without ocular abnormalities. ResultsThe average number of ZNF469 non-synonymous variants was 16.31 and 16.0 for individuals with KTCN and HM, respectively (p=0.3724). All identified variants were previously reported. Alternative allele frequency (AAF) was determined based on the WES results. Among missense variants, only one (rs528085780) has AAF0.001 and was identified in one patient with sporadic KTCN. However, the resulting Arg1864Lys substitution was not predicted to be deleterious. ConclusionIn summary, we have not found a significant enrichment of sequence variants in ZNF469 in Polish patients with KTCN. High prevalence of ZNF469 variants identified in our KTCN group is typical for a common genetic variation observed in general population. Our findings indicate that variation in ZNF469 is not responsible for KTCN and other genetic variants are involved in the development and progression of this disease in Polish patients.

Place, publisher, year, edition, pages
WILEY-BLACKWELL , 2016. Vol. 94, no 3, 289-294 p.
Keyword [en]
keratoconus; keratoconus genetics; Sanger sequencing; whole-exome sequencing; ZNF469
National Category
Neurology
Identifiers
URN: urn:nbn:se:liu:diva-128138DOI: 10.1111/aos.12968ISI: 000374693000030PubMedID: 26806788OAI: oai:DiVA.org:liu-128138DiVA: diva2:929608
Note

Funding Agencies|National Science Centre in Poland [2012/05/E/NZ5/02127, 2013/10/M/NZ2/00283]; Poznan University of Medical Sciences [2013/08/T/NZ5/00754, 502-14-03301402-10201]

Available from: 2016-05-19 Created: 2016-05-19 Last updated: 2016-06-03

Open Access in DiVA

No full text

Other links

Publisher's full textPubMed

Search in DiVA

By author/editor
Frajdenberg, Agata
By organisation
Department of Ophthalmology in Linköping
In the same journal
Acta Ophthalmologica
Neurology

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 56 hits
ReferencesLink to record
Permanent link

Direct link