The frameshifted VNTR length determines the kidney survival in ADTKD-MUC1

Introduction: Autosomal dominant tubulointerstitial kidney disease due to MUC1 variants (ADTKD-MUC1) is caused by pathogenic variants leading to a frameshift in the MUC1 gene, most often because of the duplication of a cytosine in a 7-cytosine stretch within the coding variable number tandem repeat (VNTR). It has been regarded as genotypically uniform despite marked clinical heterogeneity. However, as the duplication can arise in any repeat unit, the length of the toxic MUC1-frameshift protein (MUC1-fs) may differ substantially between patients. We thus hypothesised that MUC1-fs length may determine disease severity. Methods: In this retrospective cohort study, we evaluated 49 patients with genetically confirmed ADTKD-MUC1. Mutant VNTR alleles were reconstructed by Oxford Nanopore long-read sequencing. The correlation between total and MUC1-fs length and age at kidney failure (KF) was assessed using statistical models accounting for familial clustering. Results: Median KF-free survival was 43 years (95% CI 37-55) for MUC1-fs above the median (>780 amino acids) versus 65 years (95% CI 54-not reached) below it (log-rank p = 0.0039). MUC1-fs length was associated with KF (HR 1.19 per 100 amino acids, 95% CI 1.03-1.37, p = 0.015). The estimate was stable across five handlings of familial clustering, including leave-one-family-out and random one-per-family sampling. Longer MUC1-fs was also correlated with faster eGFR decline. By contrast, the total length of the mutant protein showed a weaker association with KF, and no association when both measures were modelled together, suggesting that the signal lies in the frameshifted portion rather than in overall allele size. Conclusions: In this exploratory cohort, MUC1-fs length, determined by the position of the duplication within the VNTR, was associated in a graded manner with age at KF, independently of familial clustering. These findings suggest that ADTKD-MUC1 is not genotypically uniform and that reporting the frameshift position could refine prognosis.

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Journal
medRxiv
Published
2026-10-30
DOI
https://doi.org/10.64898/2026.10.28.26365901
Primary Topic
Genetic and Kidney Cyst Diseases
Type
preprint

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preprint

The frameshifted VNTR length determines the kidney survival in ADTKD-MUC1

Jessica Kachmar, Hassan Saei, Guillaume Dorval, Bertrand Knebelmann et al.
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medRxiv
Genetic and Kidney Cyst Diseases
preprint

The frameshifted VNTR length determines the kidney survival in ADTKD-MUC1

Jessica Kachmar, Hassan Saei, Guillaume Dorval, Bertrand Knebelmann, Olivier Gribouval, Corinne Antignac, Laurence Heidet, Zaina Ait Arkoub, Manon Mautret‐Godefroy, Mouad Ouahmane, Aurélien Caux, Vincent Morinere, Maxime Fercocq
preprint en

Abstract

Introduction: Autosomal dominant tubulointerstitial kidney disease due to MUC1 variants (ADTKD-MUC1) is caused by pathogenic variants leading to a frameshift in the MUC1 gene, most often because of the duplication of a cytosine in a 7-cytosine stretch within the coding variable number tandem repeat (VNTR). It has been regarded as genotypically uniform despite marked clinical heterogeneity. However, as the duplication can arise in any repeat unit, the length of the toxic MUC1-frameshift protein (MUC1-fs) may differ substantially between patients. We thus hypothesised that MUC1-fs length may determine disease severity. Methods: In this retrospective cohort study, we evaluated 49 patients with genetically confirmed ADTKD-MUC1. Mutant VNTR alleles were reconstructed by Oxford Nanopore long-read sequencing. The correlation between total and MUC1-fs length and age at kidney failure (KF) was assessed using statistical models accounting for familial clustering. Results: Median KF-free survival was 43 years (95% CI 37-55) for MUC1-fs above the median (>780 amino acids) versus 65 years (95% CI 54-not reached) below it (log-rank p = 0.0039). MUC1-fs length was associated with KF (HR 1.19 per 100 amino acids, 95% CI 1.03-1.37, p = 0.015). The estimate was stable across five handlings of familial clustering, including leave-one-family-out and random one-per-family sampling. Longer MUC1-fs was also correlated with faster eGFR decline. By contrast, the total length of the mutant protein showed a weaker association with KF, and no association when both measures were modelled together, suggesting that the signal lies in the frameshifted portion rather than in overall allele size. Conclusions: In this exploratory cohort, MUC1-fs length, determined by the position of the duplication within the VNTR, was associated in a graded manner with age at KF, independently of familial clustering. These findings suggest that ADTKD-MUC1 is not genotypically uniform and that reporting the frameshift position could refine prognosis.

medRxiv
Assistance Publique – Hôpitaux de Paris (FR), Centre Hospitalier de l’Université de Montréal (CA), Institut des Maladies Génétiques Imagine (FR)
Agence Nationale de la Recherche
Good health and well-being
Genetic and Kidney Cyst Diseases
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