Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice

Giglio, Sabrina
Member of the Collaboration Group
;
2022-01-01

Abstract

The overall diagnostic yield of massively parallel sequencing (MPS) based-tests in patients with chronic kidney disease (CKD) is around 30% for pediatric cases and 6-30% for adult cases. These figures should encourage nephrologists to frequently use genetic testing as a diagnostic means for their patients, but in reality several barriers appear to hinder the implementation of NGS diagnostics in routine clinical practice. In this paper, we aim to support the nephrologist to overcome these barriers. After a detailed discussion on the general items that are important to genetic testing in nephrology, namely (1) genetic testing modalities and their indications, (2) clinical information needed for high-quality interpretation of the genetic test, (3) clinical benefit of genetic testing and (4) genetic counselling, we will describe each of these items more specifically for the different groups of genetic kidney diseases and for CKD of unknown origin.
2022
2021
Inglese
37
2
239
254
16
Esperti anonimi
internazionale
scientifica
Chronic kidney disease; Clinical benefit; Genetic counselling; Genetic testing; Massively parallel sequencing; Monogenic diseases
Knoers, Nine; Antignac, Corinne; Bergmann, Carsten; Dahan, Karin; Giglio, Sabrina; Heidet, Laurence; Lipska-Ziętkiewicz, Beata S; Noris, Marina; Remuzzi, Giuseppe; Vargas-Poussou, Rosa; Schaefer, Franz
1.1 Articolo in rivista
info:eu-repo/semantics/article
1 Contributo su Rivista::1.1 Articolo in rivista
262
11
open
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