Evidence map›Paper›PMID 28292877›Full record

ArticlePhysiological reports2017

The effects of dual PPAR

Anette Ericsson, Pernilla Tonelius, Mark Lal, Alan Sabirsh, Gerhard Böttcher, Lena William-Olsson, Maria Strömstedt, Camilla Johansson, Gina Hyberg, Sofia Tapani and 2 more

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Revisiting Experimental Models of Diabetic Nephropathy.International journal of molecular sciences · 2020
    Review
  9. The effects of dual PPARPhysiological reports · 2017
    Article
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

12 authors at 1 institution in 1 country.

Anette EricssonCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden anette.e.ericsson@astrazeneca.com.
Pernilla ToneliusCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Mark LalCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Alan SabirshCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Gerhard BöttcherDrug, Safety & Metabolism, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Lena William-OlssonCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Maria StrömstedtCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Camilla JohanssonDrug, Safety & Metabolism, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Gina HybergDrug, Safety & Metabolism, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Sofia TapaniDiscovery Sciences Innovative Medicines Research Unit, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Ann-Cathrine Jönsson-RylanderCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
Robert UnwinCardiovascular & Metabolic Disease Innovative Medicines, AstraZeneca R&D Gothenburg, Mölndal, Sweden.
AstraZeneca (Sweden) · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The leptin-deficient BTBRob/ob mouse develops progressive albuminuria and morphological lesions similar to human diabetic nephropathy (DN), although whether glomerular hyperfiltration, a recognized feature of early DN that may contribute to renal injury, also occurs in this model is not known. Leptin replacement has been shown to reverse the signs of renal injury in this model, but in contrast, the expected renoprotection by angiotensin-converting enzyme (ACE) inhibition in BTBRob/ob mice seems to be limited. Therefore, to investigate the potential renal benefits of improved metabolic control in this model, we studied the effect of treatment with the dual peroxisome proliferator-activated receptor (PPAR)

Indexed as

Angiotensin-Converting Enzyme InhibitorsAnimalsBlood GlucoseBlood PressureDiabetes MellitusDiabetic NephropathiesDisease Models, AnimalEnalaprilKidneyMembrane ProteinsMicePPAR alphaPPAR gammaRenin-Angiotensin SystemRepressor ProteinsTriglyceridesAngiotensin-Converting Enzyme InhibitorsBlood GlucoseEnalaprilMembrane ProteinsnephrinPPAR alphaPPAR gammaRepressor ProteinsTriglyceridesWT1 protein, mouseWT1 Proteinsangiotensin‐converting enzymeBTBRob/ob mousediabetic kidney diseaseperoxisome proliferator‐activated receptor

Identifiers

PMID28292877
PMCPMC5350186
OpenAlexW2595201862

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.