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Patients with Endogenous Cushing's Syndrome. 21. Chapter 7. A Clinical Case of Pregnancy in a Patient. Treated with Ibandronic Acid 3.0 Intravenously. 23.
ENDOCRINOLOGY RESEARCH AND CLINICAL DEVELOPMENTS

GLUCOCORTICOID-INDUCED OSTEOPOROSIS FRACTURES AND BONE REMODELING IN PATIENTS WITH ENDOGENOUS CUSHING'S SYNDROME

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ENDOCRINOLOGY RESEARCH AND CLINICAL DEVELOPMENTS

GLUCOCORTICOID-INDUCED OSTEOPOROSIS FRACTURES AND BONE REMODELING IN PATIENTS WITH ENDOGENOUS CUSHING'S SYNDROME ZHANNA E. BELAYA LIUDMILA Y. ROZHINSKAYA ALEXANDER G. SOLODOVNIKOV NATALIA V. DRAGUNOVA AND GALINA A. MELNICHENKO

New York

Copyright © 2013 by Nova Science Publishers, Inc. All rights reserved. No part of this book may be reproduced, stored in a retrieval system or transmitted in any form or by any means: electronic, electrostatic, magnetic, tape, mechanical photocopying, recording or otherwise without the written permission of the Publisher. For permission to use material from this book please contact us: Telephone 631-231-7269; Fax 631-231-8175 Web Site: http://www.novapublishers.com

NOTICE TO THE READER The Publisher has taken reasonable care in the preparation of this book, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. No liability is assumed for incidental or consequential damages in connection with or arising out of information contained in this book. The Publisher shall not be liable for any special, consequential, or exemplary damages resulting, in whole or in part, from the readers’ use of, or reliance upon, this material. Any parts of this book based on government reports are so indicated and copyright is claimed for those parts to the extent applicable to compilations of such works. Independent verification should be sought for any data, advice or recommendations contained in this book. In addition, no responsibility is assumed by the publisher for any injury and/or damage to persons or property arising from any methods, products, instructions, ideas or otherwise contained in this publication. This publication is designed to provide accurate and authoritative information with regard to the subject matter covered herein. It is sold with the clear understanding that the Publisher is not engaged in rendering legal or any other professional services. If legal or any other expert assistance is required, the services of a competent person should be sought. FROM A DECLARATION OF PARTICIPANTS JOINTLY ADOPTED BY A COMMITTEE OF THE AMERICAN BAR ASSOCIATION AND A COMMITTEE OF PUBLISHERS. Additional color graphics may be available in the e-book version of this book.

Library of Congress Cataloging-in-Publication Data ISBN: 978-1-62948-341-2

Published by Nova Science Publishers, Inc. † New York

Contents vii 

Preface Chapter 1

Introduction



Chapter 2

The Prevalence of Low Traumatic Fractures among Patients with Endogenous Cushing’s Syndrome



Chapter 3

Chapter 4 Chapter 5 Chapter 6

Chapter 7

The Influence of a Mild Disruption of the Cortisol Level on Bone in Patients with Adrenal Incidentaloma

11 

Pathogenesis of Glucocorticoid-Induced Osteoporosis

13 

The Restoration of Bone after the Remission of Cushing’s Syndrome

19 

The Possibility of Pharmacotherapy of Glucocorticoid-Induced Osteoporosis in Patients with Endogenous Cushing’s Syndrome

21 

A Clinical Case of Pregnancy in a Patient Treated with Ibandronic Acid 3.0 Intravenously

23 

Conclusion

27 

Acknowledgments

29 

References

31 

Index

43

Preface This work is primarily focused on data related to the characteristics, pathogenesis and treatment of bone complications in patients with endogenous Cushing’s syndrome (CS) of various etiologies. The chapter is based on the retrospective and prospective data of patients with active CS as well as on literature review. We paid special attention to discussing pregnancy and bisphosphonate (BP) use, outlining the clinical case of a successful pregnancy in a patient treated with ibandronic acid (Bonviva). Materials and methods: Two hundred and twenty three patients with proven CS were interviewed on their recent low traumatic fractures. A thoracic and lumbar X-ray was performed to reveal vertebral fractures. Bone mineral density (BMD) was measured by DXA (Lunar). The level of free urinary cortisol (24h UFC) was measured by an immunochemiluminescence assay (extraction with diethyl ether) on a Vitros ECi. Late-night serum cortisol and markers of bone remodeling were assayed by electrochemiluminescence (ECLIA) Cobas e601 Roche. The other parameters were measured using commercially available assays. Results: among 223 patients with active CS, low traumatic fractures were confirmed in 43%; in most cases there were multiple fractures of the vertebras. BMD loss was mild. Patients with fractures statistically significantly differed in terms of sex (men fractured more frequently than women), had lower osteocalcin (OC) and higher 24hUFC as well as latenight serum cortisol. After regression analysis, the main predictors of low-traumatic fracture occurrence was 24h UFC (p