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Radiology of Osteoporosis PDF

248 Pages·2008·9.218 MB·English
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GG MEDICAL rr aa RADIOLOGY mm pp Diagnostic pp Imaging (( EE dd A. L. Baert .. Radiology )) M. Knauth K. Sartor of Osteoporosis 11 R a 2nd Revised Edition d i o l o g y Rank o CTR f TRAP O Int˜evgʼri3ns Carboanhydrase II s H2O + CO2 H2CO3 H++ HCO3– HCO3– t Sealing zone Lysosomes Cl– Cl– e o S. Grampp p o r Editor H+ ATPase o s Cathepsin K i Metalloproteinases H+ Cl– s Mineralized Matrix 1 3 I Contents MEDICAL RADIOLOGY Diagnostic Imaging Editors: A. L. Baert, Leuven M. Knauth, Göttingen K. Sartor, Heidelberg III Contents S. Grampp (Ed.) Radiology of Osteoporosis 2nd Revised Edition With Contributions by J. E. Adams · R. Barkmann · P. M. Bernecker · D. Diacinti · K. Engelke · H. K. Genant S. Grampp · R. Gruber · G. Guglielmi · G. Holzer · H. Imhof · M. Jergas · C. Krestan T. M. Link · M. Peterlik · P. Pietschmann · S. Prevrhal · H. Resch · C. van Kuijk R. R. van Rijn Foreword by A. L. Baert With 169 Figures in 225 Separate Illustrations, 15 in Color and 17 Tables 123 IV Contents Stephan Grampp, MD Univ. Dozent Dr. Grampp & Dr. Henk OEG Röntgenordination Lenaustrasse 23 2000 Stockerau Austria Medical Radiology · Diagnostic Imaging and Radiation Oncology Series Editors: A. L. Baert · L. W. Brady · H.-P. Heilmann · M. Knauth · M. Molls · C. Nieder · K. Sartor Continuation of Handbuch der medizinischen Radiologie Encyclopedia of Medical Radiology ISBN 978-3-540-25888-9 e-ISBN 978-3-540-68604-0 DOI 10.007 / b 136255 Medical Radiology · Diagnostic Imaging and Radiation Oncology ISSN 0942-5373 Library of Congress Control Number: 2005934451 (cid:164) 2008 Springer-Verlag Berlin Heidelberg This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specif- ically the rights of translation, reprinting, reuse of illustrations, recitations, broadcasting, reproduction on microfi lm or in any other way, and storage in data banks. Duplication of this publication or parts thereof is permitted only under the provisions of the German Copyright Law of September 9, 1965, in its current version, and permission for use must always be obtained from Springer-Verlag. Violations are liable for prosecution under the German Copyright Law. The use of general descriptive names, trademarks, etc. in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. Product liability: The publishers cannot guarantee the accuracy of any information about dosage and application contained in this book. In every individual case the user must check such information by consulting the relevant literature. Cover design and Typesetting: Verlagsservice Teichmann, Mauer Printed on acid-free paper 9 8 7 6 5 4 3 2 1 springer.com V Contents Foreword It is a great pleasure to introduce this second fully revised and updated edition of Radiology of Osteoporosis. The need for the publication of this second edition, only 4 years following the fi rst edition, indicates the great interest among radiologists, and several other medical disciplines, in the diagnosis and management of this very common condition and its possible complications. One of the great merits of this book is that it deals with all aspects of osteoporosis, including morphology and function. The outstanding qualifi cations and high level of expertise of the editor, Prof. S. Grampp, and of the contributing authors are a guarantee for the up-to-date and com- prehensive contents of this outstanding volume. I am confi dent that this volume will again meet with great interest among radiolo- gists and all other clinicians involved in the care of patients with osteoporosis and that it will enjoy the same success as the fi rst edition. Leuven Albert L. Baert VII Contents Preface There is almost universal agreement among the clinical community that the measure- ment of bone mineral density in potentially healthy individuals is the only means of assessing fracture risk and skeletal status. In patients with risk factors, measurement of BMD adds substantially to the assessment of fracture risk. For each of the methods and related skeletal sites, there is a wealth of scientifi c data emphasising the relationship between decreasing bone density and mass on the one hand and increasing fracture risk on the other. Indeed, all measurement techniques presented here are able to provide valuable information in most clinical circumstances, as well as information that cannot be obtained by other means. Selection of any of the available methods for clinical practice can be governed by practical considerations such as availability, cost and reimbursement, time and effort involved, as well as patient acceptance. We wrote this book to guide the clinical practitioner through this minefi eld of scien- tifi c knowledge and it is our sincere hope that it will assist in daily practice. Due to the success of the fi rst edition, we decided to update and upgrade this volume to the very latest clinical and scientifi c knowledge. (Since the fi rst edition sold so rap- idly, we are confi dent of continued success. We do not expect the same sort of popu- lar movement to the bookstores as historically seen in the Nika insurrection of 532 [B yzantium], the Harry Potter craze [Europe, beginning of the millennium], or the Cavalli Fashion Massacre [Central Europe 2007 – if you do not know about this and are not female, ask someone who is]. But still an editor can hope.) I am especially grateful to the authors who are amongst the most prominent and knowledgeable in this particular scientifi c fi eld for their effort and dedication. Stockerau Stephan Grampp IX Contents Contents 1 Introduction to Bone Development, Remodelling and Repair Reinhard Gruber, Peter Pietschmann, and Meinrad Peterlik . . . . . . 1 2 Pathophysiology and Aging of Bone Peter Pietschmann, Reinhard Gruber, and Meinrad Peterlik . . . . . . 25 3 Pathophysiology of Rheumatoid Arthritis and Other Disorders Heinrich Resch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43 4 Therapeutic Approaches and Mechanisms of Drug Action Peter M. Bernecker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53 5 Orthopedic Surgery Gerold Holzer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69 6 Radiology of Osteoporosis Michael Jergas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77 7 Dual Energy X-Ray Absorptiometry Judith E. Adams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105 8 Vertebral Morphometry Giuseppe Guglielmi and Daniele Diacinti . . . . . . . . . . . . . . . . . . . 125 9 Spinal Quantitative Computed Tomography Rick R. van Rijn and Cornelis van Kuijk . . . . . . . . . . . . . . . . . . . . 137 10 pQCT: Peripheral Quantitative Computed Tomography Sven Prevrhal, Klaus Engelke, and Harry K. Genant. . . . . . . . . . . . 143 11 Quantitative Ultrasound Reinhard Barkmann. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 163 12 Magnetic Resonance Imaging Thomas M. Link . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175 X Contents 13 Structure Analysis Using High-Resolution Imaging Techniques Thomas M. Link . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187 14 Densitometry in Clinical Practice Stephan Grampp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 197 15 Practical Cases Christian Krestan and Herwig Imhof . . . . . . . . . . . . . . . . . . . . . 205 Subject Index. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237 List of Contributors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 243 1 Introduction to Bone Development, Remodelling and Repair 1 Introduction to Bone Development, Remodelling and Repair Reinhard Gruber, Peter Pietschmann, and Meinrad Peterlik CONTENTS 1.1 Introduction 1.1 Introduction 1 Bone is a specialized form of mineralized connective 1.2 Structure, Cells and Matrix 2 tissue that is build by various types of metabolically 1.2.1 Structural Organization and Parameters of active cells during embryonic and postnatal develop- Bone Strength 2 ment. In the adult, the same cells contribute to the 1.2.2 The Bone Cells 3 maintenance of structural and functional integrity, 1.2.3 The Organic Matrix 4 and accomplish the healing process following injury. 1.3 Bone Development, Remodelling and Bone not only shows a marked rigidity and mechani- Regeneration 5 cal stability while still maintaining some degree of 1.3.1 Bone Development 5 elasticity, but also constitutes the most important 1.3.2 Bone Remodelling 5 storage site for calcium and inorganic phosphate 1.3.3 Bone Regeneration 7 (Baron 1993). Osteoporosis is a systemic disease 1.4 Regulatory Mechanisms of Development where rigidity and mechanical stability of bone and Function 8 declines, until bone loses the ability to withstand 1.4.1 Regulatory Mechanisms in functional loading or weak traumata. A transient Chondrocytes 9 1.4.2 Regulatory Mechanisms in Osteoblasts 10 but disproportional bone loss of 20%–30% trabecu- 1.4.3 Regulatory Mechanisms in Osteoclast lar and 5%–10% cortical bone is most apparent in Development and Function 11 women during the fi rst postmenopausal decade. The following slow phase accounts for 20%–30% of tra- 1.5 Local and Systemic Regulation of becular and cortical bone loss in both sexes. Epide- Bone Remodelling 13 1.5.1 Local Regulation of Bone Mass by miologic data show that the lifetime risk to acquire Growth F actors, Cytokines and hip fractures is 17% for white women and 6% for Prostaglandins 14 white men (Cummings and Melton 2002; Melton 1.5.2 Systemic Factors that 1995). Progress in medical care and education has Regulate Bone Mass 14 contributed to an increased average life span, which 1.5.2.1 Parathyroid Hormone 14 1.5.2.2 1,25-Dihydroxyvitamin D 15 3 1.5.2.3 Calcitonin 15 1.5.2.4 Oestradiol 15 1.5.3 Sympathic Nervous System 16 R. Gruber, PhD Associate Professor, Department of Oral Surgery, Vienna 1.6 Discussion of Current Status and University Clinic of Dentistry, Medical University of Vienna, Perspectives 17 Waehringer Strasse 25a, 1090 Vienna, Austria P. Pietschmann, MD References 18 Associate Professor of Pathophysiology and Internal Medicine, Department of Pathophysiology, Medical University of Vienna, Waehringer Guertel 18–20, 1090 Vienna, Austria and Ludwig Boltzmann-Institute of Aging Research, Langobarden- strasse 122, 1220 Vienna, Austria M. Peterlik, MD, PhD Professor and Head of the Department of P athophysiology, Medical University of Vienna, Waehringer Guertel 18–20, 1090 Vienna, Austria 2 R. Gruber, P. Pietschmann, and M. Peterlik is, however, associated with a higher risk of acquir- The outer bone surface is in contact with the sur- ing age-related diseases such as osteoporosis. On the rounding soft tissue via the periosteum. The inner other hand, progress has been made on diagnosing bone surface faces the medullary cavity and is cov- osteoporosis and monitoring disease progression. ered by the endosteum. Both periosteum and end- Potent drugs are available that help reduce the risk osteum are connective tissues organized in layers. of fracture and new pharmacologic substances are The cambium layer is in intimate contact with the already in the pipeline (Delmas 2002; Rodan and mineralized structure and provides a pool of mesen- Martin 2000). Improvement in patient care is possi- chymal cells with the potential to differentiate into ble because of a substantial increase in the functional the chondrogenic and the osteogenic lineage. understanding of the genetic and molecular mecha- Trabecular bone and cortical bone are composed nism on bone development, remodelling and repair, of the same microstructural elements: cells, organic and as a result, the pathophysiology of osteoporosis. matrix, crystalline inorganic matrix and soluble fac- The aim of this chapter is to give an update on the tors. The calcifi ed matrix of adult bone is built up fundamental aspects of bone biology with regard to in multiple layers of oriented collagen fi bers, giving the coordinated action of bone cells during devel- rise to the typical structure of lamellar bone. The opment, remodelling and repair. We briefl y review lamellae are arranged parallel to each other, as on the structural and cellular composition of the bone the surface of fl at bones and trabecular structures, matrix and focus on genetic and molecular mecha- or in concentric layers around blood vessels and nisms that control cell differentiation and activity. nerves, forming the haversian system synonymic for This information is considered a scientifi c basis for osteons in the corticalis. The haversian canals are the following chapters on the pathophysiology of connected to the periosteum and the endosteum by age-related bone loss (see Chap. 2), bone loss associ- Volkmann’s canals. Blood fl ow in bone totals 200– ated with chronic infl ammation (see Chap. 3), as well 400 ml/min in adult humans, indicating that bone is as the chapter dealing with the current approaches a highly vascularized tissue. in osteoporosis therapy (see Chap. 4). Under conditions in which rapid formation of new bone is required, e.g. during skeletal growth in early childhood and in periods of bone regeneration, or in particular metabolic bone disorders, instead of lamellar bone, immature “woven” bone is formed, 1.2 in which the collagen fi bers are randomly oriented Structure, Cells and Matrix and the degree of mineralization is relatively low. Woven bone is later remodelled into lamellar bone, 1.2.1 which has better mechanical properties. Formation, Structural Organization and Parameters of remodelling, and repair of the structural elements Bone Strength require the coordinated action of the bone cells: osteoblasts, osteocytes, lining cells, and osteoclasts At the structural level, two different forms of bone (Baron 1993; Marks 2002; Schenk and Hunziker can be distinguished: cortical or compact bone, 1994). which, for example, forms the diaphysis of long Bone strength is defi ned by the parameters mass, bones, thus providing protection for the medul- geometry, material properties, and microstruc- lary cavity. Trabecular, cancellous, or spongy bone, ture. The bone mass accounts for about half of the which in long bones is found at their ends, at the decrease in bone strength in the elderly. The diame- epiphyses, makes up the greater part of vertebral ter of the corticalis is a parameter of bone geometry. bodies. The total skeleton comprises around 20% Material properties are modulated by the mineral trabecular bone. Trabecular bone has a porosity crystals and the correct synthesis of the single com- of 50%–90%, cortical bone of approximately 10% ponents of the bone matrix. The diameter of the tra- (Sikavitsas et al. 2001). The high surface-to-volume beculae as well their horizontal and vertical inter- ratio of trabecular bone involves its metabolic func- connectivity are further determinants that together tion, whereas cortical bone has mainly a structural defi ne bone strength (Paris et al. 2000; Riggs and and protective role. Parfi tt 2005).

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