Evidence map›Paper›PMID 38752266›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2024

Ketonuria as an Indicator of Improvement of Renal Function in Patients with Type 2 Diabetes Receiving SGLT2 Inhibitor Treatment.

Hyun Ah Kim, Han Na Jang, Sung Hye Kong, Young Lee, Sung Hee Choi, Young Min Cho, Hak Chul Jang, Tae Jung Oh

Abstract read
In one paragraph

Article in Endocrinology and metabolism (Seoul, Korea), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

  1. Observational
  2. Review
  3. Article
  4. Review
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

8 authors.

Hyun Ah KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Han Na JangDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Sung Hye KongDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Young LeeVeterans Medical Research Institute, Veterans Health Service Medical Center, Seoul, Korea.
Sung Hee ChoiDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Young Min ChoDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Hak Chul JangDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Tae Jung OhDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Funding

Seoul National University Bundang Hospital 14-2016-0022
6 · The paper itself

Abstract

We investigated the potential association between ketonuria during treatment with sodium-glucose cotransporter-2 (SGLT2) inhibitors and its renoprotective effect in patients with type 2 diabetes. We included 192 patients who had received SGLT2 inhibitors for more than 6 months. After propensity score matching, 52 patients each were allocated into groups with or without ketonuria, respectively. The estimated glomerular filtration rate exhibited a significant improvement only in subjects with ketonuria (without ketonuria: mean difference, -0.02 mL/min/1.73 m2 [95% confidence interval (CI), -3.87 to 3.83 mL/min/1.73 m2] vs. with ketonuria: mean difference, 6.81 mL/min/1.73 m2 [95% CI, 3.16 to 10.46 mL/min/1.73 m2]; P<0.001). Improvement in estimated glomerular filtration rate at 6 months was associated with female sex and lower baseline body weight, blood pressure, and triglyceride levels in patients with ketonuria. In conclusion, the presence of ketonuria was associated with the renoprotective effect of SGLT2 inhibitors, and female sex and the absence of metabolic syndrome components may serve as additional indicators of these medications' substantial renoprotective effects in individuals with ketonuria.

Indexed as

Diabetes Mellitus, Type 2Glomerular Filtration RateSodium-Glucose Transporter 2 InhibitorsAgedDiabetic NephropathiesFemaleHumansKetosisKidneyMaleMiddle AgedRetrospective StudiesSodium-Glucose Transporter 2 InhibitorsDiabetes mellitus, type 2KetosisRenal protectionSodium-glucose transporter 2 inhibitors

Identifiers

PMID38752266
PMCPMC11375305

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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 OpenQuestion graph.