Angiopoietin-Like Protein 2 Promotes the Progression of Diabetic Kidney Disease.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 01 2019
Historique:
received: 13 12 2017
accepted: 14 08 2018
pubmed: 24 8 2018
medline: 4 12 2019
entrez: 24 8 2018
Statut: ppublish

Résumé

Angiopoietin-like protein 2 (ANGPTL2) is a circulating, proinflammatory protein. To examine the role of ANGPTL2 in the pathogenesis of diabetic kidney disease (DKD), we studied the epigenetic regulation of angptl2 expression in patients with diabetes. We determined the relationship between serum ANGPTL2 levels and the progression of DKD in cross-sectional (220 patients) and cohort (145 patients, 7-year follow-up) studies. Furthermore, we investigated the direct effect of ANGPTL2 on podocyte function. The main outcome was progression of DKD. We found that the expression of angptl2 was decreased by the methylation of its promoter region. Multivariate logistic regression analyses revealed that the baseline level of serum ANGPTL2 was an independent risk factor for the progression of DKD during follow-up periods. In cultured podocytes, ANGPTL2 directly increased albumin permeability through the translocation of zonula occludens-1 from the membrane to the cytosol via activation of focal adhesion kinase. ANGPTL2 might be directly involved in podocyte dysfunction and independently associated with the progression of DKD stages.

Identifiants

pubmed: 30137449
pii: 5075163
doi: 10.1210/jc.2017-02705
doi:

Substances chimiques

ANGPTL2 protein, human 0
Angiopoietin-Like Protein 2 0
Angiopoietin-like Proteins 0
Zonula Occludens-1 Protein 0
Focal Adhesion Kinase 1 EC 2.7.10.2

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

172-180

Auteurs

Toshihisa Ishii (T)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

Fumihiko Furuya (F)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

Kazuya Takahashi (K)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

Miho Shikata (M)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

Takeyuki Takamura (T)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

Hidetoshi Kobayashi (H)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

Asako Miyazaki (A)

Kua-hause Isawa, Isawa Onsen Hospital, Fuefuki, Yamanashi, Japan.

Jun Morinaga (J)

Department of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Kazutoyo Terada (K)

Department of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Yuichi Oike (Y)

Department of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Eiichiro Kanda (E)

Department of Nephrology and Hypertension, Kawasaki Medical School, Okayama, Japan.

Kenichiro Kitamura (K)

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

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Classifications MeSH