(Vienna, Graz, 16-10-2025) A research team from the Medical University of Vienna and the Medical University of Graz has discovered a previously unknown genetic cause of hereditary optic atrophy, a degenerative disease of the optic nerve associated with gradual loss of vision. The results, currently published in the journal Genetics in Medicine, open up new possibilities for the genetic diagnosis of this disease and provide important approaches for future research into the underlying disease mechanisms.
The starting point for the research was the genetic examination of a large Austrian family in which seven individuals across three generations suffered from optic atrophy. Genome-wide sequencing revealed a previously undescribed variant in the PPIB gene (peptidylprolyl isomerase B). This gene contains the blueprint for an enzyme that helps proteins in the body to adopt their correct structure and breaks down proteins with faulty structures.
In cultured cells from affected individuals, the research team showed that this gene variant impairs the function of mitochondria – the "power plants" of cells. Impaired mitochondrial function is detectable in most known forms of hereditary optic atrophy. By analysing archived genome data, a total of twelve additional affected individuals carrying the same genetic mutation were identified in eight other families. "We have thus succeeded in describing the PPIB gene as a new optic atrophy gene," says study leader Wolfgang M. Schmidt from the Center for Anatomy and Cell Biology at MedUni Vienna, summarising the results of the research. "The identification of this genetic variant creates the possibility of a genetic diagnosis, which has been lacking in many cases," adds co-study leader Thomas P. Georgi from the Department of Ophthalmology at Med Uni Graz. This is important in order to be able to provide targeted advice to affected families and tailor medical care to the individual needs of those affected.
60 percent of those affected without a genetic diagnosis
Optic atrophy is a degenerative disease of the optic nerve that leads to gradual damage to the retinal ganglion cells – the nerve cells that transmit visual signals from the retina to the brain. The first symptoms are usually reduced visual acuity, impaired colour perception or central visual field defects. The disease can be inherited; around 20 forms of optic atrophy are currently known. Most variants involve a disturbance of mitochondrial function. Despite advances in genetic diagnostics, the exact genetic cause remains unclear in around 60 percent of those affected.
This study – a collaboration between the Center for Anatomy and Cell Biology at MedUni Vienna, the Department of Ophthalmology and Optometry at MedUni Vienna, the Center for Cancer Research at MedUni Vienna and the University Eye Clinic at MedUni Graz – has now filled this gap with regard to the PPIB gene. Future studies will clarify how exactly the PPIB variant influences cell metabolism and whether further genetic changes in this gene are associated with optic atrophy.
Publication: Genetics in Medicine
A recurrent missense variant in the PPIB gene encoding peptidylprolyl isomerase B underlies adult-onset autosomal dominant optic atrophy.
Katharina Valentin, Monika Kustermann, Mona R. Schneider, Haleh Aminfar, Kathrin Vollnhofer, Andreas Wedrich, Christoph Stapf, Martin Bertich, Markus Ritter, Theresa Mendrina, Daniel Valcanover, Walter Berger, Margret Eckhard, Andy Sombke, Stephanie V. Lilja, Amina Paquay, Bernhard Rosensteiner, Iris Schmidt, Reginald E. Bittner, Thomas P. Georgi, Berthold Pemp, Wolfgang M. Schmidt.
https://doi.org/10.1016/j.gim.2025.101595
The article is published in "Genetics in Medicine, an official journal of the American College of Medical Genetics and Genomics (ACMG)".