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DOI 10.3109/08820139.2014.892510

Медицинская библиотека · Immunological investigations · 2014

Cytokines and insulin resistance after zoledronic acid-induced acute phase response.

Kassi Georgia, Papamichael Konstantinos, Papaioannou Garyfallia, Giagourta Irene, Thanou Stavroula, Triantaphyllopoulou Maria, Zapanti Evagelia, Papandroulaki Fotini, Ktena Vasiliki, Karga Helen

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Аннотация

Zoledronic acid is known to induce a transient acute phase response (APR). The aim of the study was to investigate whether an APR caused by zoledronic acid administration can induce insulin resistance in post-menopausal osteoporotic women and the potential involvement of different inflammatory markers, cytokines and adipokines to this response. Insulin resistance was calculated by the homeostasis model assessment (HOMA-IR). APR symptoms appeared in 30 post-menopausal osteoporotic women within 24 h and attenuated on day 3 after zoledronic acid infusion. Twenty-eight age- and body mass index-matched, patients without an APR following zoledronic acid administration, served as a control group. In patients with APR, concurrently with a significant increase in serum high sensitive C-reactive protein (hsCRP), interleukin-6 (hsIL-6), tumour necrosis factor-alpha (hsTNF-α) and cortisol levels on days one and two, serum insulin was also significantly elevated, resulting in an increased HOMA-IR. Leptin and resistin significantly increased on day two in contrast to adiponectin which declined, though not statistically significant. The alterations in HOMA-IR were mainly associated to the increase of hsCRP and leptin. In conclusion, zoledronic acid induces an acute, short term insulin resistance, due to an APR, by altering the levels of various adipokines and cytokines.

Для цитирования: Kassi Georgia, Papamichael Konstantinos, Papaioannou Garyfallia, Giagourta Irene, Thanou Stavroula, Triantaphyllopoulou Maria, Zapanti Evagelia, Papandroulaki Fotini, Ktena Vasiliki, Karga Helen. Cytokines and insulin resistance after zoledronic acid-induced acute phase response.. Immunological investigations. 2014. DOI: 10.3109/08820139.2014.892510.

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