Sklerostin des Osteozyten-von der Expression zur klinischen Anwendung

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Sklerostin des Osteozyten-von der Expression zur klinischen Anwendung. / Wölfel, Eva Maria; Busse, Björn; Jähn, Katharina.

In: OSTEOLOGIE, Vol. 29, No. 1, 01.02.2020, p. 14-20.

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@article{e006295390cb46b1aa616c876c3ad6b9,
title = "Sklerostin des Osteozyten-von der Expression zur klinischen Anwendung",
abstract = "Sclerostin is a secreted glycoprotein and a product of the SOST gene, which is primarily expressed in osteocytes. Expression of sclerostin leads to inhibition of osteoblast-induced bone formation and therefore to reduced bone mass. In contrast, the loss-of-function deletion of the SOST gene induces a high bone mass bone phenotype. Furthermore, sclerostin may act on the osteocyte itself which leads to an increased osteoclast-induced bone resorption and supports osteocytic osteolysis. Sclerostin expression can be influenced by different mechanisms and represents a potential treatment option based on the anabolic action in bone formation. The sclerostin antibody Romosozumab is available since the beginning of 2019 in Japan and the US and first studies have shown positive effects on fracture risk and BMD in postmenopausal women. Other studies present data on sclerostin serum values in correlation with fractures and diseases such as diabetes mellitus type 2 which leave the unanswered question whether sclerostin is a possible biomarker for fracture risk diagnostics.",
keywords = "mechanosensation, osteocyte, Sclerostin, Wnt-signalling pathway",
author = "W{\"o}lfel, {Eva Maria} and Bj{\"o}rn Busse and Katharina J{\"a}hn",
note = "Publisher Copyright: {\textcopyright} 2020 Georg Thieme Verlag KG Stuttgart • New York. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
year = "2020",
month = feb,
day = "1",
doi = "10.1055/a-1026-8852",
language = "Deutsch",
volume = "29",
pages = "14--20",
journal = "OSTEOLOGIE",
issn = "1019-1291",
publisher = "Schattauer",
number = "1",

}

RIS

TY - JOUR

T1 - Sklerostin des Osteozyten-von der Expression zur klinischen Anwendung

AU - Wölfel, Eva Maria

AU - Busse, Björn

AU - Jähn, Katharina

N1 - Publisher Copyright: © 2020 Georg Thieme Verlag KG Stuttgart • New York. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.

PY - 2020/2/1

Y1 - 2020/2/1

N2 - Sclerostin is a secreted glycoprotein and a product of the SOST gene, which is primarily expressed in osteocytes. Expression of sclerostin leads to inhibition of osteoblast-induced bone formation and therefore to reduced bone mass. In contrast, the loss-of-function deletion of the SOST gene induces a high bone mass bone phenotype. Furthermore, sclerostin may act on the osteocyte itself which leads to an increased osteoclast-induced bone resorption and supports osteocytic osteolysis. Sclerostin expression can be influenced by different mechanisms and represents a potential treatment option based on the anabolic action in bone formation. The sclerostin antibody Romosozumab is available since the beginning of 2019 in Japan and the US and first studies have shown positive effects on fracture risk and BMD in postmenopausal women. Other studies present data on sclerostin serum values in correlation with fractures and diseases such as diabetes mellitus type 2 which leave the unanswered question whether sclerostin is a possible biomarker for fracture risk diagnostics.

AB - Sclerostin is a secreted glycoprotein and a product of the SOST gene, which is primarily expressed in osteocytes. Expression of sclerostin leads to inhibition of osteoblast-induced bone formation and therefore to reduced bone mass. In contrast, the loss-of-function deletion of the SOST gene induces a high bone mass bone phenotype. Furthermore, sclerostin may act on the osteocyte itself which leads to an increased osteoclast-induced bone resorption and supports osteocytic osteolysis. Sclerostin expression can be influenced by different mechanisms and represents a potential treatment option based on the anabolic action in bone formation. The sclerostin antibody Romosozumab is available since the beginning of 2019 in Japan and the US and first studies have shown positive effects on fracture risk and BMD in postmenopausal women. Other studies present data on sclerostin serum values in correlation with fractures and diseases such as diabetes mellitus type 2 which leave the unanswered question whether sclerostin is a possible biomarker for fracture risk diagnostics.

KW - mechanosensation

KW - osteocyte

KW - Sclerostin

KW - Wnt-signalling pathway

UR - http://www.scopus.com/inward/record.url?scp=85080922120&partnerID=8YFLogxK

U2 - 10.1055/a-1026-8852

DO - 10.1055/a-1026-8852

M3 - SCORING: Zeitschriftenaufsatz

AN - SCOPUS:85080922120

VL - 29

SP - 14

EP - 20

JO - OSTEOLOGIE

JF - OSTEOLOGIE

SN - 1019-1291

IS - 1

ER -