Der Nuklearmediziner 2006; 29(4): 249-254
DOI: 10.1055/s-2006-942253
Skelettszintigraphie - Update 2006

© Georg Thieme Verlag Stuttgart · New York

Quantifizierung des Knochenstoffwechsels in der konventionellen Skelettszintigraphie

Quantification of Skeletal Uptake in Conventional Bone ScanningW. U. Kampen1 , E. Oltmanns1 , N. Czech1 , U. Lützen1 , W. Brenner2
  • 1Klinik für Nuklearmedizin, Universitätsklinikum Schleswig-Holstein, Campus Kiel
  • 2Klinik und Poliklinik für Nuklearmedizin, Universitätsklinikum Hamburg-Eppendorf
Further Information

Publication History

Publication Date:
30 November 2006 (online)

Zusammenfassung

Die vorliegende Arbeit beschreibt eine einfache Methode der Analyse des Ganzkörper-Knochenstoffwechsels und fasst mögliche Anwendungen bei Patienten mit systemischen Skeletterkrankungen zusammen. Die Bestimmung der prozentualen Aufnahme des diagnostischen Radiopharmakons 99mTc-HDP sowie der therapeutisch genutzten Bisphosphonate 186Re-HEDP und 153Sm-EDTMP in den Knochen, die Kinetik ihrer Urinausscheidung und der in den Weichteilen retinierten Aktivität erfolgt mittels einfacher Region-of-Interest-Analyse konventioneller Skelettszintigramme. Die so erhaltenen Daten erlauben den Vergleich verschiedener osteotroper Radiopharmaka und ermöglichen eine genauere Dosimetrie im Vergleich mit der herkömmlichen Messung der Ganzkörperretention über die Aktivitätsbestimmung im Sammelurin. Darüber hinaus kann eine Abschätzung des systemischen Knochenstoffwechsels auch bei der Diagnostik von Erkrankungen hilfreich sein, bei denen die Skelettszintigraphie keine fokalen pathognomonischen Befunde liefert. Die Methode ist in der klinischen Routine problemlos einsetzbar und ihre Ergebnisse stimmen mit Literaturdaten anderer Methoden gut überein.

Abstract

This paper describes a simple method for the analysis of whole-body bone metabolism and summarizes possible applications in patients suffering from metabolic bone diseases. Quantification of bone uptake, soft-tissue retention and urinary excretion of radiopharmaceuticals both for diagnostics such as 99mTc-HDP and 186Re-HEDP and 153Sm-EDTMP for radionuclide therapy is achieved by regions-of-interest analysis of conventional bone scans. The data obtained allow a comparison between different osteotropic radiopharmaceuticals as well as an improved and reliable dosimetry compared to the most frequently applied method of whole-body retention measurement by simple analysis of urinary excretion. Moreover, estimation of whole-body bone uptake using the described technique can be helpful for the diagnosis of systemic bone disease in which bone scanning does not reveal focal pathologies. The method described here is routinely applicable in daily clinical routine and the data are well in line with those obtained by other methods.

Literatur

  • 1 Scillitani A, Dicembrino F, Chiodini I. et al . Global skeletal uptake of 99mTc-Methylene Diphosphonate (GSU) in patients affected by endocrine diseases: Comparison with biochemical markers of bone turnover.  Osteoporos Int. 2002;  13 829-834
  • 2 Fogelman I, Bessent R G, Turner J G, Citrin D L, Boyle I T, Greig W R. The use of whole-body retention of Tc-99m diphosphonate in the diagnosis of metabolic bone disease.  J Nucl Med. 1978;  19 270-275
  • 3 Holmes R A. Quantification of skeletal Tc-99m labelled phosphates to detect metabolic bone disease.  J Nucl Med. 1978;  19 330-331
  • 4 Hyldstrup L, Mogensen N, Jensen G F, McNair P, Transbol I. Urinary Tc-99m-diphosphonate excretion as a simple method to quantify bone metabolism.  Scand J Clin Lab Invest. 1984;  44 105-109
  • 5 Smith M L, Martin W, Fogelman I, Bessent R G. Relative distribution of diphosphonate between bone and soft tissue at 4 and 24 hours: concise communication.  J Nucl Med. 1983;  24 208-211
  • 6 Nisbet A P, Edwards S, Lazarus C R. et al . Chromium 51 EDTA/Technetium 99m MDP plasma ratio to measure skeletal function.  Br J Rheumatol. 1984;  57 677-680
  • 7 Martin W, Fogelman I, Bessent R G. Measurement of 24-hour whole-body retention of Tc-99m HEDP by a gamma camera.  J Nucl Med. 1981;  22 542-545
  • 8 D'Addabbo A, Rubini G, Mele M, Lauriero F. A new method for assessing Tc-99m-MDP bone uptake from a bone scan image: quantitative measurements of radioactivity in global skeletal region of interest.  Nucl Med Commun. 1992;  13 55-60
  • 9 Carnevale V, Frusciante V, Scillitani A. et al . Age-related changes in the global skeletal uptake of technetium-99m methylene diphosphonate in healthy women.  Eur J Nucl Med. 1996;  23 1473-1477
  • 10 Frusciante V, Carnevale V, Scillitani A. et al . Global skeletal uptake of technetium-99m methylene diphosphonate in female patients receiving suppressive doses of L-thyroxine for differenziated thyroid cancer.  Eur J Nucl Med. 1998;  25 139-143
  • 11 Carnevale V, Dicembrino F, Frusciante V, Chiodini I, Minisola S, Scillitani A. Different patterns of global and regional skeletal uptake of 99mTc-Methylene Diphosphonate with age: relevance to the pathogenesis of bone loss.  J Nucl Med. 2000;  41 1478-1483
  • 12 Brenner W, Bohuslavizki K H, Sieweke N, Tinnemeyer S, Clausen M, Henze E. Quantification of diphosphonate uptake based on conventional bone scanning.  Eur J Nucl Med. 1997;  24 1284-1290
  • 13 Brenner W, Sieweke N, Bohuslavizki K H, Kampen W U, Zuhayra M, Clausen M, Henze E. Age- and sex-related bone uptake of Tc-99m-HDP measured by whole-body bone scanning.  Nuklearmedizin. 2000;  39 127-132
  • 14 Fogelman I, Pearson D W, Bessent R G, Tofe A J, Francis M D. A comparison of skeletal uptake of three diphosphonates by whole-body retention.  J Nucl Med. 1981;  22 880-883
  • 15 Rubini G, Lauriero F, Rubini D, D'Addabbo A. Tc-99m-MDP global skeletal uptake and markers of bone metabolism in patients with bone disease.  Nucl Med Commun. 1993;  14 567-572
  • 16 Jaworski A FG. Pathophysiology, diagnosis and treatment of osteomalacia.  Orthop Clin North Am. 1972;  3 623-652
  • 17 Resnick D. The “rugger jersey” vertebral body.  Arthr Rheum. 1981;  24 1191-1192
  • 18 Serafini A N, Houston S J, Resche I. et al . Palliation of pain associated with metastatic bone cancer using Sm-153 lexidronam: a double-blind, placebo-controlled clinical trial.  J Clin Oncol. 1998;  16 1574-1581
  • 19 Maxon H R, Schroder L E, Hertzberg V S. et al . Rhenium-186(Sn)HEDP for treatment of painful osseous metastases: results of a double-blind crossover comparison with placebo.  J Nucl Med. 1991;  32 1877-1881
  • 20 Bayouth J E, Macey D J, Kasi L P, Fossella F V. Dosimetry and toxicity of 153Sm-EDTMP administered for bone pain due to skeletal metastases.  J Nucl Med. 1994;  35 63-69
  • 21 Brenner W, Kampen W U, Kampen A M, Henze E. Skeletal uptake and soft-tissue retention of 186-Re-HEDP and 153-Sm-EDTMP in patients with metastatic bone disease.  J Nucl Med. 2001;  42 230-236
  • 22 De Klerk J MH, van Dijk A, van het Ship A D, Zonnenberg B A, van Rijk P P. Pharmacokinetics of rhenium-186 after administration of rhenium-186-HEDP to patients with bone metastases.  J Nucl Med. 1992;  33 646-651
  • 23 Eary J F, Collins C, Stabin M. et al . Samarium-153-EDTMP biodistribution and dosimetry estimation.  J Nucl Med. 1993;  34 1031-1036
  • 24 Rensburg A J, Alberts A S, Louw W KA. Quantifying the radiation dosage to individual skeletal lesions treated with samarium-153-EDTMP.  J Nucl Med. 1998;  39 2110-2115
  • 25 Lange U, Teichmann J, Stracke H. Correlation between plasma TNF-α, IGF-1, biochemical markers of bone metabolism, markers of inflammation/disease activity and clinical manifestations in ankylosing spondylitis.  Eur J Med Res. 2000;  29 507-511
  • 26 Yilmaz N, Ozaslan J. Biochemical bone turnover markers in patients with ankylosing spondylitis.  Clin Rheumatol. 2000;  19 92-98
  • 27 Bronson W D, Walker S E, Hillman L S, Keisler D, Hoyt T, Allen S H. Bone mineral density and biochemical markers of bone metabolism in ankylosing spondylitis.  J Rheumatol. 1998;  25 929-935
  • 28 Mitra D, Elvins D M, Collins A J. Biochemical markers of bone metabolism in mild ankylosing spondylitis and their relationship with bone mineral density and vertebral fractures.  J Rheumatol. 1999;  26 2201-2204
  • 29 Kampen W U, Oltmanns E, Brenner W, Czech N, Soti Z, Zuhayra M, Henze E. Szintigraphische Analyse des Knochenstoffwechsels bei Patienten mit Spondylitis ankylosans.  Nuklearmedizin. 2006;  45 A66

PD Dr. med. Dipl. Biol. W. U. Kampen , Leitender Oberarzt

Klinik für Nuklearmedizin · Universitätsklinikum Schleswig-Holstein, Campus Kiel

Arnold-Heller-Str. 9

24105 Kiel

Phone: 04 31/5 97 30 63

Fax: 04 31/5 97 30 65

Email: ukampen@nuc-med.uni-kiel.de

    >