© Eurac Research/Annelie Bortolotti

An international research consortium led by Eurac Research has identified 147 gene regions, that affect Kidney function. The study has just been published in Nature Genetics.

In the most comprehensive and detailed study of kidney genetics so far, an international research consortium led by Eurac Research and the University of Freiburg, analysed the genetic makeup of over one million people. The scientists identified 147 gene regions which influence kidney function and for many of these regions they have isolated the specific gene involved. This study has helped to elucidate the mechanisms that control renal function enabling the assessment of risk factors that result in hereditary chronic renal failure. The study involved more than 300 researchers from 25 countries and the results were published last Friday in the renowned journal Nature Genetics.

Chronic renal failure affects more than 5 per cent of the population. The deterioration of renal function is irreversible: a specific treatment does not yet exist as scientist do not know which genes to target in order to develop an effective drug. What genetic factors influence the kidney function and in what ways are, therefore, fundamental research questions. The scientists from the CKDGen (Chronic Kidney Disease Genetics) Consortium thus set out to explore the relationship between genetic material and two important parameters for assessing kidney function: the glomerular filtration rate – a measure of the speed with which kidney filters metabolic products from the bloodstream – and the blood urea. Data from over one million people made it possible to identify 147 gene regions which control the function and development of the kidney.

With this result the research can now take the next step: build a gene registry to assess the risks of hereditary renal failure. Eurac Research’s Cristian Pattaro, an Epidemiologist and the study coordinator, explains, “There is still a long way to go, but with these indicators it will be possible to predict at birth a person’s genetic predisposition to chronic renal failure”. He notes that “when someone knows their genetic risk they can adjust their lifestyle accordingly and make sure to have regular medical checkups.”
In a closer analysis of the 147 gene regions identified, the researchers have isolated 27 genes with a particular influence on renal function. Pattaro explains, “these genes are potential targets for the development of effective medical therapies.”

The study is a collaboration of over 120 epidemiological studies from around the world. These studies are similar to Eurac Research’s CHRIS study in which over 13,000 people from Vinschgau, an area in South Tyrol, Northern Italy, participated. The scientists, for example, analysed data from studies such as the US ‘Million Veteran Program (300,000 participants) and large biobanks in Japan, Great Britain and Iceland. In the future, the researchers want to not only investigate the function of individual genes in more detail, but also to expand the reach of the population studies beyond Europe and Asia, in order to draw a truly global genetic map of the kidney.

Related Articles

Article
Dallo studio del colpo di fuoco una speranza per la cura dell’aspergillosi

Un progetto finanziato dall’Euregio nei prossimi tre anni investigherà il meccanismo di trasmissione e crescita degli agenti patogeni responsabili della malattia delle piante da frutto e del fungo che causa l’aspergillosi.

Article
Persönlichkeitsschutz und medizinische Forschung

Gesundheitsdaten sind sensible Informationen, doch sie zu teilen, bringt die Wissenschaft voran. Wie kann man die Freiheit der Forschung garantieren ohne die Rechte des Einzelnen zu verletzen?

Article
Eurac Research sviluppa modelli di cellule 3D per studiare meglio il Parkinson

Per capire come si comportano le cellule neuronali dei malati di Parkinson, i biologi e genetisti di Eurac Research utilizzano modelli sempre più sofisticati. Il nuovo sistema che stanno testando permette di trasformare le cellule staminali pluripotenti indotte in neuroni tridimensionali, anziché bidimensionali. In questo modo, i ricercatori hanno a disposizione un modello più simile alla realtà e possono confrontare con maggiore precisione le cellule di persone sane con quelle dei malati di Parkinson.

Article
Nanotecnologie. Individuata pellicola biocompatibile che evita il rigetto dei bioelettrodi

Le possibili applicazioni future? Nello studio di patologie e sindromi come l’epilessia e per restaurare la vista in pazienti con il nervo ottico compromesso.