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Review
. 2025 Feb;42(2):e15431.
doi: 10.1111/dme.15431. Epub 2024 Sep 5.

Lessons learned from the FinnDiane Study: Epidemiology and metabolic risk factors for diabetic kidney disease in type 1 diabetes

Affiliations
Review

Lessons learned from the FinnDiane Study: Epidemiology and metabolic risk factors for diabetic kidney disease in type 1 diabetes

Fanny Jansson Sigfrids et al. Diabet Med. 2025 Feb.

Abstract

Aims: Across its operational span of more than 25 years, the observational, nationwide, multicentre Finnish Diabetic Nephropathy (FinnDiane) Study has aimed to unravel mechanisms underlying diabetic kidney disease, with a special focus on its metabolic risk factors. We sought to compile key findings relating to this topic and to offer a current perspective on the natural course of diabetic kidney disease among individuals with type 1 diabetes.

Methods: In this narrative review, articles relevant to the subject published by the FinnDiane Study were identified and summarized together with work published by others, when relevant.

Results: The FinnDiane Study has underscored the significance of dysglycaemia and insulin resistance, increased visceral fat mass, hypertension and dyslipidaemia-particularly high triglycerides and remnant cholesterol-as risk factors for diabetic kidney disease. Factors like abdominal obesity seem to influence the early stages of the disease, while the presence of the metabolic syndrome becomes implicated at later stages. Epidemiological reports have revealed that after an initial decline, the cumulative incidence of albuminuria plateaued post-1980s, with the progression rate to kidney failure remaining high. Fortunately, 23% of the FinnDiane cohort regressed to less advanced stages of albuminuria, improving their overall prognosis.

Conclusion: A substantial burden of albuminuria associated with type 1 diabetes persists, and therefore, novel kidney-protecting therapies are highly awaited. In addition, given that metabolic factors influence the progression of diabetic kidney disease both in its early and advanced stages, emphasis should be placed on ensuring that their treatment targets are met.

Keywords: albuminuria; diabetic kidney disease; dyslipidaemia; hypertension; insulin resistance; metabolic syndrome; type 1 diabetes.

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Conflict of interest statement

F.J.S. reports receiving lecture fees from AstraZeneca and Boehringer Ingelheim. P‐H.G. reports receiving lecture fees from Astellas Pharma, AstraZeneca, Boehringer Ingelheim, Eli Lilly, Elo Water, Genzyme, Medscape, Merck, Sharp & Dohme, Mundipharma, Novartis, Novo Nordisk, PeerVoice, Sanofi and Sciarc. P‐H.G. reports being an advisory board member for AbbVie, Astellas Pharma, AstraZeneca, Bayer, Boehringer Ingelheim, Eli Lilly, Janssen Pharmaceuticals, Medscape, Merck, Sharp& Dohme, Mundipharma, Nestlé, Novartis, Novo Nordisk and Sanofi. No other potential conflicts of interest relevant to this article were reported.

Figures

FIGURE 1
FIGURE 1
A visual summary of the Finnish Diabetic Nephropathy (FinnDiane) Study, its main baseline characteristics, as well as participant characterization. DXA, dual‐energy X‐ray absorptiometry; IMT, intima‐media thickness; MRI, magnetic resonance imaging.
FIGURE 2
FIGURE 2
The updated natural history of diabetic kidney disease in type 1 diabetes, according to findings from a Finnish, population‐based study as presented by researchers from the Finnish Diabetic Nephropathy (FinnDiane) Study. The 15‐year cumulative progression rates are derived from the 1980–99 calendar year diagnosis cohort in Jansson Sigfrids et al., whereas the regression rates stem from Jansson et al.
FIGURE 3
FIGURE 3
The various phenotypes of chronic kidney disease and their relative prevalences in type 1 diabetes, according to findings from the Finnish Diabetic Nephropathy (FinnDiane) Study. Figure adapted from Thorn et al. A1 denotes normal to mildly increased albuminuria (albumin‐creatinine ratio <3 mg/mmol, or albumin excretion rate <20 μg/min or <30 mg/24 h), A2–3 moderately to severely increased albuminuria (albumin‐creatinine ratio ≥3 mg/mmol, or albumin excretion rate ≥20 μg/min or ≥30 mg/24 h), G1–2 normal to mildly decreased kidney function (eGFR ≥60 mL/min/1.73 m2) and G3–5 impaired kidney function (eGFR <60 mL/min/1.73 m2).
FIGURE 4
FIGURE 4
Metabolic risk factors associated with increased risk of diabetic kidney disease onset or progression in the Finnish Diabetic Nephropathy (FinnDiane) Study. Created with BioRender.com.

References

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