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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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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