Comprehensive proteomics reveals stage-specific signatures in blood that precede diabetic kidney disease onset and progression

Diabetic kidney disease is the leading cause of kidney failure worldwide, yet the molecular events underlying disease initiation and progression remain unclear. We measured 5,420 circulating proteins in 830 adults with type 1 diabetes and examined their longitudinal associations with onset and progression of kidney disease over 10 years of follow-up. We identified 130 proteins associated with at least one outcome independent of established clinical risk factors, of which 59 replicated in an independent cohort. HAVCR1/KIM-1, GFRA1, CD14 and GDF15 predicted albuminuria onset up to a decade before detectable disease. Albuminuria progression pointed to the kidney—liver axis (ASGR1, RBP4), whereas rapid kidney function decline and incident kidney failure pointed to immune and tumor necrosis factor receptor signaling. Mendelian randomization prioritized UMOD, SORT1, CLSPN, MAST4 and EGF as potential targets. These findings reveal molecular perturbations preceding clinical manifestations of diabetic kidney disease and identify distinct pathways associated with disease progression.

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Journal
medRxiv
Published
2026-11-11
DOI
https://doi.org/10.64898/2026.11.10.26367534
Primary Topic
Chronic Kidney Disease and Diabetes
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preprint
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preprint

Comprehensive proteomics reveals stage-specific signatures in blood that precede diabetic kidney disease onset and progression

Heather Jackson, FinnDiane Study Group, Viji Nair, Andrew Parton et al.
medRxiv
Chronic Kidney Disease and Diabetes
preprint

Comprehensive proteomics reveals stage-specific signatures in blood that precede diabetic kidney disease onset and progression

Heather Jackson, FinnDiane Study Group, Viji Nair, Andrew Parton, Xiaoqi Luo, Laura Jane Smyth, Per‐Henrik Groop, Erkka Valo, Anna Syreeni, Emma H. Dahlström, Zeinab Abdelrahman, Niina Sandholm, Valma Harjutsalo, Gareth J. McKay, Katalin Suszták, Amy Jayne McKnight, Matthias Kretzler, Claire Hill, Wenjun Ju, Stefan Mutter, Alexander Peter Maxwell, Joanna M. Kouki
preprint en

Abstract

Diabetic kidney disease is the leading cause of kidney failure worldwide, yet the molecular events underlying disease initiation and progression remain unclear. We measured 5,420 circulating proteins in 830 adults with type 1 diabetes and examined their longitudinal associations with onset and progression of kidney disease over 10 years of follow-up. We identified 130 proteins associated with at least one outcome independent of established clinical risk factors, of which 59 replicated in an independent cohort. HAVCR1/KIM-1, GFRA1, CD14 and GDF15 predicted albuminuria onset up to a decade before detectable disease. Albuminuria progression pointed to the kidney—liver axis (ASGR1, RBP4), whereas rapid kidney function decline and incident kidney failure pointed to immune and tumor necrosis factor receptor signaling. Mendelian randomization prioritized UMOD, SORT1, CLSPN, MAST4 and EGF as potential targets. These findings reveal molecular perturbations preceding clinical manifestations of diabetic kidney disease and identify distinct pathways associated with disease progression.

medRxiv
Queen's University Belfast (GB), University of Helsinki (FI), University of Michigan (US), Folkhälsans Forskningscentrum (FI), University of Pennsylvania (US)
Chronic Kidney Disease and Diabetes
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