Urinary TIMP-2 and MMP-2 are significantly associated with poor bladder compliance in adult patients with spina bifida.


Journal

Neurourology and urodynamics
ISSN: 1520-6777
Titre abrégé: Neurourol Urodyn
Pays: United States
ID NLM: 8303326

Informations de publication

Date de publication:
11 2019
Historique:
received: 06 07 2019
accepted: 25 08 2019
pubmed: 6 9 2019
medline: 21 5 2020
entrez: 6 9 2019
Statut: ppublish

Résumé

To assess the predictive values of six urinary markers (nerve growth factor [NGF], brain-derived neurotrophic factor [BDNF], matrix metalloproteinase 2 [MMP-2], tissue inhibitor metalloproteinase 2 [TIMP-2], transformation growth factor β-1 [TGF-B1], and prostaglandin 2 [PGE2]) for adverse urodynamic features and for upper urinary tract damage in adult patients with spina bifida. A single-center prospective trial was conducted from March 2015 to March 2017 including all consecutive adult patients with spina bifida seen for urodynamic testing. The urine was collected and stored at -80°C. A urodynamic and an upper urinary tract were systematically performed. At the end of the inclusion period, urines were defrosted and urinary nerve growth factor, BDNF, TIMP-2, and TGF-B1 were assessed using validated ELISA kits. The urinary markers levels were adjusted on the urinary creatinine level. Urinary MMP-2 levels were assessed by zymography. Fourty patients were included. Only TIMP-2 and MMP-2 were significantly associated with poor bladder compliance (P = .043 and P = .039, respectively). TIMP-2 was also the only urinary marker significantly associated with upper urinary tract damage on imaging (OR = 19.81; P = .02). Of all urodynamic parameters, bladder compliance and maximum detrusor pressure were the only ones associated with upper urinary tract damage on imaging (P = .01 and P = .02), The diagnostic performances of urinary TIMP-2 for upper urinary tract damage were slightly superior to PdetMax and bladder compliance with an area under the curve of 0.72. Urinary TIMP-2 and MMP-2 were significantly associated with poor bladder compliance and urinary TIMP-2 was significantly associated with upper urinary tract damage. These findings support a pathophysiological role of extracellular matrix remodeling in poor bladder compliance of adult patients with spina bifida.

Identifiants

pubmed: 31486131
doi: 10.1002/nau.24163
doi:

Substances chimiques

Biomarkers 0
Brain-Derived Neurotrophic Factor 0
NGF protein, human 0
TGFB1 protein, human 0
TIMP2 protein, human 0
Transforming Growth Factor beta1 0
Tissue Inhibitor of Metalloproteinase-2 127497-59-0
BDNF protein, human 7171WSG8A2
Nerve Growth Factor 9061-61-4
MMP2 protein, human EC 3.4.24.24
Matrix Metalloproteinase 2 EC 3.4.24.24
Dinoprostone K7Q1JQR04M

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2151-2158

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Benoit Peyronnet (B)

Service d'urologie, CHU Rennes, Rennes, France.
Centre de référence spina bifida, CHU Rennes, Rennes, France.
Equipe thématique INPHY CIC 1414 et INSERM UMR 991, CHU Rennes, Rennes, France.

Claire Richard (C)

Service d'urologie, CHU Rennes, Rennes, France.
Centre de référence spina bifida, CHU Rennes, Rennes, France.

Claude Bendavid (C)

Service de Biochimie, CHU Rennes, Rennes, France.

Florian Naudet (F)

Service de pharmaco-épidémiologie, CHU Rennes, Rennes, France.

Juliette Hascoet (J)

Service d'urologie, CHU Rennes, Rennes, France.
Centre de référence spina bifida, CHU Rennes, Rennes, France.
Equipe thématique INPHY CIC 1414 et INSERM UMR 991, CHU Rennes, Rennes, France.

Charlène Brochard (C)

Centre de référence spina bifida, CHU Rennes, Rennes, France.
Equipe thématique INPHY CIC 1414 et INSERM UMR 991, CHU Rennes, Rennes, France.
Service de Gastro-Entérologie, CHU Rennes, Rennes, France.

Nelly Senal (N)

Centre de référence spina bifida, CHU Rennes, Rennes, France.
Service de médecine physique et réadaptation, Fondation Calvé, Berck-sur-mer, France.

Magali Jezequel (M)

Centre de référence spina bifida, CHU Rennes, Rennes, France.

Quentin Alimi (Q)

Service d'urologie, CHU Rennes, Rennes, France.
Centre de référence spina bifida, CHU Rennes, Rennes, France.

Zine-Eddine Khene (ZE)

Service d'urologie, CHU Rennes, Rennes, France.

Anne Corlu (A)

Unité INSERM UMR 1241, Rennes, France.

Bruno Clément (B)

Unité INSERM UMR 1241, Rennes, France.

Laurent Siproudhis (L)

Centre de référence spina bifida, CHU Rennes, Rennes, France.
Equipe thématique INPHY CIC 1414 et INSERM UMR 991, CHU Rennes, Rennes, France.
Service de pharmaco-épidémiologie, CHU Rennes, Rennes, France.

Guillaume Bouguen (G)

Equipe thématique INPHY CIC 1414 et INSERM UMR 991, CHU Rennes, Rennes, France.
Service de Gastro-Entérologie, CHU Rennes, Rennes, France.

Jacques Kerdraon (J)

Centre de référence spina bifida, CHU Rennes, Rennes, France.
Service des blessés médullaires, Centre de rééducation de Kerpape, Ploemeur, France.

Andrea Manunta (A)

Service d'urologie, CHU Rennes, Rennes, France.
Centre de référence spina bifida, CHU Rennes, Rennes, France.

Xavier Gamé (X)

Département d'Urologie, Transplantation Rénale et Andrologie, CHU Rangueil, Toulouse, France.

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Classifications MeSH