Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.

Osteonecrosis is a common dose-limiting toxicity of glucocorticoids. Data from clinical trials suggest that other medications can increase the risk of glucocorticoid-induced osteonecrosis. Here we utilized a mouse model to study the effect of asparaginase treatment on dexamethasone-induced osteonecr...

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Main Authors: Chengcheng Liu, Laura J Janke, Jitesh D Kawedia, Laura B Ramsey, Xiangjun Cai, Leonard A Mattano, Kelli L Boyd, Amy J Funk, Mary V Relling
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4788417?pdf=render
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spelling doaj-99df12c3602f4a46b214c282a3d3223f2020-11-24T21:37:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01113e015143310.1371/journal.pone.0151433Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.Chengcheng LiuLaura J JankeJitesh D KawediaLaura B RamseyXiangjun CaiLeonard A MattanoKelli L BoydAmy J FunkMary V RellingOsteonecrosis is a common dose-limiting toxicity of glucocorticoids. Data from clinical trials suggest that other medications can increase the risk of glucocorticoid-induced osteonecrosis. Here we utilized a mouse model to study the effect of asparaginase treatment on dexamethasone-induced osteonecrosis. Mice receiving asparaginase along with dexamethasone had a higher rate of osteonecrosis than those receiving only dexamethasone after 6 weeks of treatment (44% vs. 10%, P = 0.006). Similarly, epiphyseal arteriopathy, which we have shown to be an initiating event for osteonecrosis, was observed in 58% of mice receiving asparaginase and dexamethasone compared to 17% of mice receiving dexamethasone only (P = 0.007). As in the clinic, greater exposure to asparaginase was associated with greater plasma exposure to dexamethasone (P = 0.0001). This model also recapitulated other clinical risk factors for osteonecrosis, including age at start of treatment, and association with the systemic exposure to dexamethasone (P = 0.027) and asparaginase (P = 0.036). We conclude that asparaginase can potentiate the osteonecrotic effect of glucocorticoids.http://europepmc.org/articles/PMC4788417?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Chengcheng Liu
Laura J Janke
Jitesh D Kawedia
Laura B Ramsey
Xiangjun Cai
Leonard A Mattano
Kelli L Boyd
Amy J Funk
Mary V Relling
spellingShingle Chengcheng Liu
Laura J Janke
Jitesh D Kawedia
Laura B Ramsey
Xiangjun Cai
Leonard A Mattano
Kelli L Boyd
Amy J Funk
Mary V Relling
Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.
PLoS ONE
author_facet Chengcheng Liu
Laura J Janke
Jitesh D Kawedia
Laura B Ramsey
Xiangjun Cai
Leonard A Mattano
Kelli L Boyd
Amy J Funk
Mary V Relling
author_sort Chengcheng Liu
title Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.
title_short Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.
title_full Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.
title_fullStr Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.
title_full_unstemmed Asparaginase Potentiates Glucocorticoid-Induced Osteonecrosis in a Mouse Model.
title_sort asparaginase potentiates glucocorticoid-induced osteonecrosis in a mouse model.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Osteonecrosis is a common dose-limiting toxicity of glucocorticoids. Data from clinical trials suggest that other medications can increase the risk of glucocorticoid-induced osteonecrosis. Here we utilized a mouse model to study the effect of asparaginase treatment on dexamethasone-induced osteonecrosis. Mice receiving asparaginase along with dexamethasone had a higher rate of osteonecrosis than those receiving only dexamethasone after 6 weeks of treatment (44% vs. 10%, P = 0.006). Similarly, epiphyseal arteriopathy, which we have shown to be an initiating event for osteonecrosis, was observed in 58% of mice receiving asparaginase and dexamethasone compared to 17% of mice receiving dexamethasone only (P = 0.007). As in the clinic, greater exposure to asparaginase was associated with greater plasma exposure to dexamethasone (P = 0.0001). This model also recapitulated other clinical risk factors for osteonecrosis, including age at start of treatment, and association with the systemic exposure to dexamethasone (P = 0.027) and asparaginase (P = 0.036). We conclude that asparaginase can potentiate the osteonecrotic effect of glucocorticoids.
url http://europepmc.org/articles/PMC4788417?pdf=render
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