Literature DB >> 22215042

High risk of osteonecrosis of the femoral head in autoimmune disease patients showing no immediate increase in hepatic enzyme under steroid therapy.

Shunichiro Okazaki1, Satoshi Nagoya, Motohisa Yamamoto, Kenji Tateda, Hiroki Takahashi, Toshihiko Yamashita, Hiroshi Matsumoto.   

Abstract

Aim of the study is to determine the relationship between liver function and the incidence of ONF after steroid therapy in AID patients. The present study investigated 58 AID patients who had received high-dose systemic steroid therapy to determine whether a correlation exists between parameters of hepatic function and steroid-induced ONF at the precise time-point when steroid-induced ONF develops. The patients were divided into two groups on the basis of MRI findings: ONF (n = 31) and non-ONF (n = 27). The ONF group showed no increase in AST, ALT, or LDH within 4 weeks after the commencement of steroid therapy. By contrast, the non-ONF group showed an immediate and significant increase in all of these parameters. In the ONF group, hepatic steatosis and elevated triglyceride levels were also observed. Following 4 weeks of steroid therapy, there were no significant differences in biochemical data between two groups. Patients showing no immediate increase in ALT and AST in response to steroid therapy were at high risk of ONF. These findings provide important insights into the pathogenesis of steroid-induced ONF and may facilitate the development of prevention strategies in patients with AID.

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Year:  2012        PMID: 22215042     DOI: 10.1007/s00296-011-2295-y

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  16 in total

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5.  Osteonecrosis development in a novel rat model characterized by a single application of oxidative stress.

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Review 6.  Nontraumatic osteonecrosis of the femoral head: ten years later.

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Authors:  S Okazaki; Y Nishitani; S Nagoya; M Kaya; T Yamashita; H Matsumoto
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10.  Immunosuppression by glucocorticoids: inhibition of NF-kappa B activity through induction of I kappa B synthesis.

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3.  Experimental rat model for alcohol-induced osteonecrosis of the femoral head.

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5.  Association of common comorbidities with osteonecrosis: a nationwide population-based case-control study in Denmark.

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6.  Development of non-traumatic osteonecrosis of the femoral head requires toll-like receptor 7 and 9 stimulations and is boosted by repression on nuclear factor kappa B in rats.

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7.  The proton pump inhibitor, lansoprazole, prevents the development of non-traumatic osteonecrosis of the femoral head: an experimental and prospective clinical trial.

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  7 in total

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