Evidence map›Paper›PMID 24166068›Full record

ArticleInternational journal of obesity (2005)2014

Weight loss surgery improves the metabolic status in an obese rat model but does not affect bladder fibrosis associated with high fat diet feeding.

A Oberbach, N Schlichting, M Heinrich, S Lehmann, H Till, F W Mohr, F Mannello, J-U Stolzenburg, J Neuhaus

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Article in International journal of obesity (2005), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

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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 at 5 institutions in 3 countries.

A Oberbach1] Department of Cardiac Surgery, University Leipzig, Heart Center Leipzig, Leipzig, Germany [2] Integrated Research and Treatment Center (IFB) Adiposity Diseases, University of Leipzig, Leipzig, Germany.
N Schlichting1] Integrated Research and Treatment Center (IFB) Adiposity Diseases, University of Leipzig, Leipzig, Germany [2] Department of Pediatric Surgery, University of Leipzig, Leipzig, Germany.
M Heinrich1] Department of Cardiac Surgery, University Leipzig, Heart Center Leipzig, Leipzig, Germany [2] Integrated Research and Treatment Center (IFB) Adiposity Diseases, University of Leipzig, Leipzig, Germany.
S LehmannIntegrated Research and Treatment Center (IFB) Adiposity Diseases, University of Leipzig, Leipzig, Germany.
H TillDepartment of Pediatric Surgery, Medical University of Graz, Medical School, Graz, Austria.
F W MohrDepartment of Cardiac Surgery, University Leipzig, Heart Center Leipzig, Leipzig, Germany.
F MannelloDepartment of Biomolecular Sciences, Section of Clinical Biochemistry and Cell Biology, University 'Carlo Bo', Urbino (PU), Italy.
J-U StolzenburgDepartment of Urology, University of Leipzig, Leipzig, Germany.
J NeuhausDepartment of Urology, University of Leipzig, Leipzig, Germany.ORCID 0000000324846994
Leipzig Heart Institute · DEIFB Adiposity Diseases · DELeipzig University · DEMedical University of Graz · ATUniversity of Urbino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBladder dysfunction has one of the highest prevalences as a comorbidity of obesity in industrialized countries. The aetiopathogenesis of obesity-associated bladder dysfunction is still obscure, but there is growing evidence that general metabolic changes in obese patients may be in part responsible. As demonstrated recently, high fat diet (HFD) significantly alters the protein expression in the urinary bladder, activates multiple signalling pathways associated with cell survival and inflammation and ultimately provokes bladder fibrosis in an obese rat model. The study aimed to elucidate the role of matrix metalloproteases (MMPs) and their specific tissue inhibitors of metalloproteases (TIMPs) in obesity-related bladder extracellular matrix (ECM) remodelling and the effect of weight loss surgery via sleeve gastrectomy (SG) on phenotype and molecular parameters.

methodsTwenty-four male Sprague-Dawley rats were used for (i) characterization of the HFD phenotype and (ii) evaluation of alterations following SG. Metabolic status, the degree of bladder fibrosis and tissue expression and activity of MMP2, MMP9, MMP14, TIMP1 and TIMP2 were analysed by immunohistochemistry, enzyme-linked immunosorbent assay and activity assays. Statistical differences were calculated by analysis of variance or independent Student's t-test. A P-value <0.05 was considered statistically significant.

resultsIn HFD rats, we found significant alterations in lipid metabolism, fat mass, free fatty acid profile, insulin resistance and inflammatory markers. Voided volume was significantly decreased, and bladder showed marked fibrosis. MMPs and TIMPs were differentially regulated depending on animal status (controls, chow diet, HFD, and SG- and sham-operated animals) in both urothelium and detrusor smooth muscle. Although animal weight and most metabolic parameters were positively affected by SG, bladder fibrosis persisted. The limitations of this study were 1 month follow-up and lack of direct measurement of bladder function.

conclusionsEarly diagnosis of the bladder dysfunction associated with obesity is essential to allow targeted early intervention, that is, before manifestation of potentially irreversible ECM fibrotic alterations.

Indexed as

Weight LossAnimalsBariatric SurgeryCells, CulturedDiet, High-FatDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFibrosisLipid MetabolismMaleMatrix MetalloproteinasesObesityRatsRats, Sprague-DawleyUrinary BladderUrinary Bladder DiseasesMatrix Metalloproteinases

Identifiers

PMID24166068
OpenAlexW2076657550

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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.