Assessment of Porcine Bone Metabolism by Dynamic [18F]Fluoride Ion PET: Correlation with Bone Histomorphometry

UNLABELLED The aim of this study was to quantify regional bone blood flow and [(18)F]fluoride ion influx with [(18)F]fluoride ion PET and correlate the results with specific static and dynamic indices of bone metabolism in healthy pigs. METHODS During continuous ventilation (fractional concentration of oxygen in inspired gas = 0.3), dynamic PET scans 120 min in duration were obtained for 9 mini pigs after intravenous injection of 10.0 +/- 1.2 MBq (mean +/- SD) of [(18)F]fluoride ion per kilogram of body weight. Iliac crest bone biopsies were performed immediately before the PET scan to determine static and dynamic indices of bone metabolism (i.e., the mineral apposition rate) by bone histomorphometry. Kinetic rate constants describing influx (K(1)) and efflux (k(2)) of [(18)F]fluoride as well as chemisorption and incorporation of [(18)F]fluoride (k(3)) and reverse transport (k(4)) were determined for 6 vertebral bodies in each animal. Blood flow estimates (f) were derived from K(1) values corrected for the permeability-surface area product using a previously derived correction algorithm. A rate constant describing the net forward transport rate of fluoride (K(i)) and the fluoride volume flux (K(flux)) derived from a 2-tissue-compartment model was calculated and compared with the results of Patlak graphic analysis (K(pat)). RESULTS A significant correlation was found between mineral apposition rate and K(i) (P < 0.005), K(flux) (P < 0.01), K(pat), K(1), and f (P < 0.05). The values of f, K(i), K(flux), and K(pat) did not correlate significantly with other static or dynamic histomorphometric indices or with age, serum alkaline phosphatase, or parathyroid hormone levels. The values of f and K(i) correlated linearly (y = 0.023 + 0.32x; r(2) = 0.74; P < 0.001). CONCLUSION PET bone studies using [(18)F]fluoride ion provide quantitative estimates of bone blood flow and metabolic activity that correlate with histomorphometric indices of bone formation in the normal bone tissue of the mini pig. Therefore, it seem reasonable to assume that [(18)F]fluoride ion PET can reduce the number of invasive bone biopsies, thus facilitating follow-up of patients with metabolic bone diseases.

[1]  E Y Chao,et al.  A comparison of the effect of open intramedullary nailing and compression-plate fixation on fracture-site blood flow and fracture union. , 1981, The Journal of bone and joint surgery. American volume.

[2]  B. Vernon‐roberts,et al.  Variation in histomorphometric estimates across different sites of the iliac crest. , 1989, Journal of clinical pathology.

[3]  M. Blau,et al.  Fluorine-18: a new isotope for bone scanning. , 1962, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[4]  T G Turkington,et al.  Performance characteristics of a whole-body PET scanner. , 1994, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[5]  M. Piert,et al.  Blood Flow Measurements with [15O]H2O and [18F]Fluoride Ion PET in Porcine Vertebrae , 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[6]  Z. Schwartz,et al.  Uptake and biodistribution of technetium-99m-MD32P during rat tibial bone repair. , 1993, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[7]  I. Fogelman,et al.  Skeletal Nuclear Medicine , 1996 .

[8]  E. Hoffman Positron emission tomography : principles and quantitation , 1986 .

[9]  J. Achard,et al.  Invasive versus non‐invasive diagnosis of renal bone disease , 1997, Current opinion in nephrology and hypertension.

[10]  M. Grynpas,et al.  Fluoride effects on bone crystals , 1990, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[11]  P. Kelly,et al.  Inhibition of transport of 47Ca and 85Sr by lanthanum in canine cortical bone. , 1974, Journal of applied physiology.

[12]  J. Nuyts,et al.  Fluoride kinetics of the axial skeleton measured in vivo with fluorine-18-fluoride PET. , 1997, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[13]  C. Crone,et al.  THE PERMEABILITY OF CAPILLARIES IN VARIOUS ORGANS AS DETERMINED BY USE OF THE 'INDICATOR DIFFUSION' METHOD. , 1963, Acta physiologica Scandinavica.

[14]  E. M. Renkin Transport of potassium-42 from blood to tissue in isolated mammalian skeletal muscles. , 1959, The American journal of physiology.

[15]  R. Wootton,et al.  The single-passage extraction of 18F in rabbit bone. , 1974, Clinical physics and physiological measurement : an official journal of the Hospital Physicists' Association, Deutsche Gesellschaft fur Medizinische Physik and the European Federation of Organisations for Medical Physics.

[16]  C. Patlak,et al.  Graphical Evaluation of Blood-to-Brain Transfer Constants from Multiple-Time Uptake Data. Generalizations , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[17]  S. Silverton,et al.  Technetium-99m-pyrophosphate: studies in vivo and in vitro. , 1975, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[18]  L. Mosekilde,et al.  Calcium-restricted ovariectomized Sinclair S-1 minipigs: an animal model of osteopenia and trabecular plate perforation. , 1992, Bone.

[19]  M. Phelps,et al.  Bone metabolic activity measured with positron emission tomography and [18F]fluoride ion in renal osteodystrophy: correlation with bone histomorphometry. , 1993, The Journal of clinical endocrinology and metabolism.

[20]  J. Bergh,et al.  Skeletal metastases from breast cancer: uptake of 18F-fluoride measured with positron emission tomography in correlation with CT , 1998, Skeletal Radiology.

[21]  J. Wark,et al.  The potential of sheep for the study of osteopenia: current status and comparison with other animal models. , 1995, Bone.

[22]  J Kotzerke,et al.  Sensitivity in detecting osseous lesions depends on anatomic localization: planar bone scintigraphy versus 18F PET. , 1999, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[23]  C S Patlak,et al.  Graphical Evaluation of Blood-to-Brain Transfer Constants from Multiple-Time Uptake Data , 1983, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[24]  R. Wootton,et al.  Skeletal blood flow, iliac histomorphometry, and strontium kinetics in osteoporosis: a relationship between blood flow and corrected apposition rate. , 1988, The Journal of clinical endocrinology and metabolism.

[25]  M. Drezner,et al.  Bone histomorphometry: Standardization of nomenclature, symbols, and units: Report of the asbmr histomorphometry nomenclature committee , 1987, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[26]  P. Kelly,et al.  The relationship of increased capillary filtration and bone formation. , 1993, Clinical orthopaedics and related research.

[27]  R. Wootton The single-passage extraction of 18F in rabbit bone. , 1986, Clinical science and molecular medicine.

[28]  J. Barrio,et al.  Evaluation of the skeletal kinetics of fluorine-18-fluoride ion with PET. , 1992, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[29]  G. Bormans,et al.  Measurement of skeletal flow with positron emission tomography and 18F-fluoride in femoral head osteonecrosis , 1998, Archives of Orthopaedic and Trauma Surgery.

[30]  M. Rohlin,et al.  Bone histomorphometry using interactive image analysis. A methodological study with application on the human temporomandibular joint. , 1997, European journal of oral sciences.