Evidence map›Paper›PMID 42455227›Full record

ReviewDiabetes therapy : research, treatment and education of diabetes and related disorders2026

Trajectory of Kidney Function in T1D over Time: A Scoping Review.

Favian Co, Reid Whitlock, Arvind Katta, Carolina Aldworth, Jon Mares, Zihe Zheng, Mauricio Ferri, Nicole Askin, Navdeep Tangri

Abstract readReview
In one paragraph

Review in Diabetes therapy : research, treatment and education of diabetes and related disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Favian CoSeven Oaks General Hospital Chronic Disease Innovation Centre, 2LB19-2300 McPhillips St, Winnipeg, MB, R2V 3M3, Canada.
Reid WhitlockSeven Oaks General Hospital Chronic Disease Innovation Centre, 2LB19-2300 McPhillips St, Winnipeg, MB, R2V 3M3, Canada. rwhitlock@sogh.mb.ca.ORCID http://orcid.org/0000-0002-7046-0358
Arvind KattaMedical Affairs, Bayer US, LLC, Whippany, NJ, USA.
Carolina AldworthMedical Affairs, Bayer US, LLC, Whippany, NJ, USA.
Jon MaresMedical Affairs, Bayer US, LLC, Whippany, NJ, USA.
Zihe ZhengMedical Affairs, Bayer US, LLC, Whippany, NJ, USA.
Mauricio FerriMedical Affairs, Bayer US, LLC, Whippany, NJ, USA.
Nicole AskinWRHA Virtual Library, University of Manitoba, Winnipeg, MB, Canada.
Navdeep TangriSeven Oaks General Hospital Chronic Disease Innovation Centre, 2LB19-2300 McPhillips St, Winnipeg, MB, R2V 3M3, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionType 1 diabetes (T1D) is associated with chronic kidney disease (CKD) and major adverse cardiovascular events (MACE). Contemporary data on the natural history of kidney function decline and the effect of therapies on slowing disease progression in T1D-related CKD are limited. We conducted a scoping review to describe the natural trajectory of kidney function and its effects in individuals with T1D in the USA.

methodsIn our scoping review of observational studies and grey literature, we searched EMBASE (Ovid), Cumulative Index to Nursing and Allied Health Literature [CINAHL; Elton B. Stephens Company (EBSCO)], MEDLINE (Ovid), Scopus (Elsevier), Global Health (Ovid), and the Food and Drug Administration from inception to 25 April 2025. The study population included adults (age ≥ 18 years) with T1D in the USA. Our outcomes were change in estimated glomerular filtration rate (eGFR), urine albumin-to-creatinine ratio (UACR), MACE (myocardial infarction, ischemic stroke, cardiovascular death, unstable angina, or heart failure hospitalization), and healthcare resource use (HCRU). We screened 6437 abstracts and selected 22 texts that matched our criteria.

resultsIn one cohort, more than 50.0% of individuals with T1D developed moderately increased albuminuria (UACR > 30-299 mg/g) after 20 years and two cohort studies in T1D observed a progressive annual eGFR decline of 3 mL/min/1.73 m

conclusionsT1D is associated with a high burden of CKD, MACE, and healthcare costs. A clearer understanding of the trajectory of kidney function decline in T1D would help providers and policymakers understand the impact potential therapies to treat T1D-related CKD may have on reducing the risk of kidney failure, MACE, and HCRU.

Indexed as

eGFRMACENatural historyPharmacotherapiesType 1 diabetesUACR

Identifiers

PMID42455227
PMCPMC13546246

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.