Placental and serum levels of human Klotho in severe preeclampsia: A potential sensitive biomarker.


Journal

Placenta
ISSN: 1532-3102
Titre abrégé: Placenta
Pays: Netherlands
ID NLM: 8006349

Informations de publication

Date de publication:
15 09 2019
Historique:
received: 13 03 2019
revised: 26 07 2019
accepted: 19 08 2019
pubmed: 26 8 2019
medline: 10 7 2020
entrez: 26 8 2019
Statut: ppublish

Résumé

The Klotho (KL) gene, initially defined as an anti-aging gene in mice, shares 86% of the amino acid sequence withthe human KL protein. The KL gene plays roles in endothelial nitric oxide production, angiogenesis, antioxidant enzyme production and protecting against endothelial dysfunction, all of which may be associated with preeclampsia (PE). Human KL is the precursor of the gene products: α-KL and β-KL. In this study, we evaluated the gene expression, serum and placental levels of human KL in women with severe PE, pregnant women with chronic hypertension and healthy pregnant controls. Also, the gene expression, serum and placental levels of human decorin (DCN) were evaluated. A total of 36 patients with severe PE, 10 with chronic hypertension, and 28 with healthy controls were enrolled. Placental and serum levels together with of KL and DCN were measured by ELISA and alsogene expression of these were evaluated. Placental and serum KL levels were significantly higher in the PE than in the controls and in women with chronic hypertension. Serum DCN levels were significantly higher in the PE women compared to controls and pregnant women with chronic hypertension. Placental DCN was similar in PE and healthy controls. There was no significant difference in the gene expression of KL and DCN in the groups. The best cut-off level for human KL to identify the presence of PE was calculated as 12.48 pg/ml with a sensitivity of 100% and and specificity of 96%, whereas for DCN 62.33 ng/ml to assess the presence of PE with a sensitivity of 86.1% and a specificity of 88%. Human KL may be a valuable marker for PE, with high sensitivity and specificity. It also appears to be more sensitive and specific than human DCN.

Identifiants

pubmed: 31446221
pii: S0143-4004(19)30637-X
doi: 10.1016/j.placenta.2019.08.084
pii:
doi:

Substances chimiques

Biomarkers 0
DCN protein, human 0
Decorin 0
Glucuronidase EC 3.2.1.31
Klotho Proteins EC 3.2.1.31

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

49-55

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Isil Uzun Cilingir (I)

Trakya University, Faculty of Medicine, Department of Obsterics & Gynecology, Division of Perinatology, Edirne, Turkey. Electronic address: isiluzuncilingir@gmail.com.

Fusun Varol (F)

Trakya University, Faculty of Medicine, Department of Obsterics & Gynecology, Division of Perinatology, Edirne, Turkey.

Hakan Gurkan (H)

Trakya University, Faculty of Medicine,Department of Medical Genetics, Edirne, Turkey.

Havva Sutcu (H)

Trakya University, Faculty of Medicine, Department of Obsterics & Gynecology, Division of Perinatology, Edirne, Turkey.

Engin Atli (E)

Trakya University, Faculty of Medicine,Department of Medical Genetics, Edirne, Turkey.

Damla Eker (D)

Trakya University, Faculty of Medicine,Department of Medical Genetics, Edirne, Turkey.

Cihan Inan (C)

Trakya University, Faculty of Medicine, Department of Obsterics & Gynecology, Division of Perinatology, Edirne, Turkey.

Selen Erzincan (S)

Trakya University, Faculty of Medicine, Department of Obsterics & Gynecology, Division of Perinatology, Edirne, Turkey.

Cenk Sayin (C)

Trakya University, Faculty of Medicine, Department of Obsterics & Gynecology, Division of Perinatology, Edirne, Turkey.

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Classifications MeSH