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Published in: Diabetologia 2/2019

Open Access 01-02-2019 | Article

A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

Authors: Tarunveer S. Ahluwalia, Christina-Alexandra Schulz, Johannes Waage, Tea Skaaby, Niina Sandholm, Natalie van Zuydam, Romain Charmet, Jette Bork-Jensen, Peter Almgren, Betina H. Thuesen, Mathilda Bedin, Ivan Brandslund, Cramer K. Christensen, Allan Linneberg, Emma Ahlqvist, Per-Henrik Groop, Samy Hadjadj, David-Alexandre Tregouet, Marit E. Jørgensen, Niels Grarup, Oluf Pedersen, Matias Simons, Leif Groop, Marju Orho-Melander, Mark I. McCarthy, Olle Melander, Peter Rossing, Tuomas O. Kilpeläinen, Torben Hansen

Published in: Diabetologia | Issue 2/2019

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Abstract

Aims/hypothesis

Identifying rare coding variants associated with albuminuria may open new avenues for preventing chronic kidney disease and end-stage renal disease, which are highly prevalent in individuals with diabetes. Efforts to identify genetic susceptibility variants for albuminuria have so far been limited, with the majority of studies focusing on common variants.

Methods

We performed an exome-wide association study to identify coding variants in a two-stage (discovery and replication) approach. Data from 33,985 individuals of European ancestry (15,872 with and 18,113 without diabetes) and 2605 Greenlanders were included.

Results

We identified a rare (minor allele frequency [MAF]: 0.8%) missense (A1690V) variant in CUBN (rs141640975, β = 0.27, p = 1.3 × 10−11) associated with albuminuria as a continuous measure in the combined European meta-analysis. The presence of each rare allele of the variant was associated with a 6.4% increase in albuminuria. The rare CUBN variant had an effect that was three times stronger in individuals with type 2 diabetes compared with those without (pinteraction = 7.0 × 10−4, β with diabetes = 0.69, β without diabetes = 0.20) in the discovery meta-analysis. Gene-aggregate tests based on rare and common variants identified three additional genes associated with albuminuria (HES1, CDC73 and GRM5) after multiple testing correction (pBonferroni < 2.7 × 10−6).

Conclusions/interpretation

The current study identifies a rare coding variant in the CUBN locus and other potential genes associated with albuminuria in individuals with and without diabetes. These genes have been implicated in renal and cardiovascular dysfunction. The findings provide new insights into the genetic architecture of albuminuria and highlight target genes and pathways for the prevention of diabetes-related kidney disease.
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Metadata
Title
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria
Authors
Tarunveer S. Ahluwalia
Christina-Alexandra Schulz
Johannes Waage
Tea Skaaby
Niina Sandholm
Natalie van Zuydam
Romain Charmet
Jette Bork-Jensen
Peter Almgren
Betina H. Thuesen
Mathilda Bedin
Ivan Brandslund
Cramer K. Christensen
Allan Linneberg
Emma Ahlqvist
Per-Henrik Groop
Samy Hadjadj
David-Alexandre Tregouet
Marit E. Jørgensen
Niels Grarup
Oluf Pedersen
Matias Simons
Leif Groop
Marju Orho-Melander
Mark I. McCarthy
Olle Melander
Peter Rossing
Tuomas O. Kilpeläinen
Torben Hansen
Publication date
01-02-2019
Publisher
Springer Berlin Heidelberg
Published in
Diabetologia / Issue 2/2019
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-018-4783-z

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