Cited by 47Diabetes Treatment and ManagementChronic Kidney Disease and DiabetesAcute Kidney Injury Research

Renal hemodynamic effects of sodium-glucose cotransporter 2 inhibitors in hyperfiltering people with type 1 diabetes and people with type 2 diabetes and normal kidney function

Open access
van Bommel, Erik J.M., Lytvyn, Yuliya, Perkins, Bruce A., Soleymanlou, Nima, Fagan, Nora M., Koitka-Weber, Audrey, Joles, Jaap A., Cherney, David Z.I. +1 more·2020·Kidney International

Integrity signals

Registry

Crossref · 10.1016/j.kint.2019.12.021

Cites

19 of 19 references verified0 citation errors · 0 not checkable

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Recomputing p-values needs the paper’s full text.

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  • Differences in renal hemodynamic effects of SGLT2 inhibitors between type 1 and type 2 diabetes are probably explained by patient characteristics such as baseline vascular resistance, age, diabetes duration, and concomitant ACE inhibitor/ARB or insulin use.

    “The differential effects of SGLT2 inhibitors on renal hemodynamic physiology between patients with T1D and T2D are probably explained by differences in patient characteristics, including differences in baseline renal hemodynamic status, such as the degree of vascular resistance, age, diabetes duration, and concomitant medication use; in particular, ACE inhibitors or ARBs and insulin (van Bommel et”
  • In a randomized double-blind trial in type 2 diabetes, dapagliflozin caused an acute GFR fall accompanied by reduced renal blood flow and renovascular resistance.

    “In a randomized, double-blinded trial with dapagliflozin in patients with T2D, van Bommel et al. demonstrated that dapagliflozin causes an acute fall in GFR that was accompanied by a reduction in renal blood flow and renovascular resistance (van Bommel et al., 2020).”

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Authors
van Bommel, E. J. M., Lytvyn, Y., Perkins, B. A., Soleymanlou, N., Fagan, N. M., Koitka-Weber, A., Joles, J. A., Cherney, D. Z. I., & van Raalte, D. H.
Affiliations
  • University of Toronto (CA)
  • Mount Sinai Hospital (CA)
  • Boehringer Ingelheim (Canada) (CA)
  • Boehringer Ingelheim (United States) (US)
  • University Medical Center Utrecht (NL)
Venue
Kidney International
Publisher
Elsevier BV
Published
2020-04
Volume
97
Issue
4
Pages
631-635
ISSN
0085-2538 (ISSN-L)
OpenAlex
W3011798818
Cited by
47
References
19
Citations by year
2026: 4 · 2025: 7 · 2024: 7 · 2023: 9 · 2022: 8 · 2021: 7 · 2020: 5
Type
journal article
Language
en
Open access
Locations
  • Kidney International (publishedVersion)
  • PubMed (publishedVersion)
  • Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
  • Pure Amsterdam UMC (submittedVersion, other-oa)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
  • Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
Funders
  • AstraZeneca (BI 10773, NCT01392560)
  • Boehringer Ingelheim
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
  • Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
Keywords
SGLT2 inhibitors, renal hemodynamics, type 1 diabetes, type 2 diabetes, hyperfiltration, diabetic nephropathy, proximal tubule, glycosuria, plasma glucose, blood pressure, uric acid, body weight
MeSH terms
Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Glucose, Hemodynamics, Humans, Kidney, Sodium

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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

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