دورية أكاديمية

Detection of early metaphyseal changes in a piglet model of Legg-Calvé-Perthes disease using quantitative mapping of MRI relaxation times.

التفاصيل البيبلوغرافية
العنوان: Detection of early metaphyseal changes in a piglet model of Legg-Calvé-Perthes disease using quantitative mapping of MRI relaxation times.
المؤلفون: Buko EO; Department of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota, USA.; Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, Minnesota, USA., Armstrong AR; Department of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota, USA., Laine JC; Gillette Children's Specialty Healthcare, St. Paul, Minnesota, USA.; Department of Orthopedic Surgery, University of Minnesota, Minneapolis, Minnesota, USA., Tóth F; Department of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota, USA., Johnson CP; Department of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota, USA.; Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, Minnesota, USA.
المصدر: Journal of orthopaedic research : official publication of the Orthopaedic Research Society [J Orthop Res] 2024 May 26. Date of Electronic Publication: 2024 May 26.
Publication Model: Ahead of Print
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8404726 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1554-527X (Electronic) Linking ISSN: 07360266 NLM ISO Abbreviation: J Orthop Res Subsets: MEDLINE
أسماء مطبوعة: Publication: 2006- : Hoboken, NJ : Wiley
Original Publication: New York, N.Y. : Raven Press, [c1983-
مستخلص: Legg-Calvé-Perthes disease (LCPD) is a childhood hip disorder characterized by ischemic injury to the epiphysis of the femoral head, but changes to the metaphysis have also been implicated in its pathogenesis. Quantitative magnetic resonance imaging (MRI) relaxation time mapping techniques are potentially useful to detect injury in LCPD, but studies to date have focused on the epiphysis. The purpose of this study was to assess whether T2, T1ρ, adiabatic T1ρ, and adiabatic T2ρ relaxation times can detect early metaphyseal changes in an LCPD piglet model. Complete epiphyseal ischemia of one femoral head was surgically induced and confirmed using contrast-enhanced MRI in n = 10 6-week-old piglets; the contralateral side was unoperated. The bilateral hips were imaged 1 week after surgery in vivo at 3T MRI using relaxation time mapping and contrast-enhanced MRI. Relaxation times and thicknesses of the metaphyseal primary and secondary spongiosa were measured and compared between the ischemic and contralateral-control femoral heads using paired t-tests. In the ischemic femoral heads, T2 relaxation times were significantly increased in the primary spongiosa (6.7 ± 9.8 ms, p = 0.029), and T2, T1ρ, adiabatic T1ρ, and adiabatic T2ρ relaxation times were significantly decreased in the secondary spongiosa (respectively: -13.3 ± 9.3 ms, p = 0.013; -32 ± 23 ms, p < 0.001; -43 ± 41 ms, p = 0.009; and -39 ± 13 ms, p < 0.001). The secondary spongiosa thickness was also significantly decreased in the ischemic femoral heads (p < 0.001). In conclusion, T2, T1ρ, adiabatic T1ρ, and adiabatic T2ρ relaxation time mapping techniques can detect early changes in the metaphysis following ischemic injury to the epiphysis of the femoral head in a piglet model of LCPD.
(© 2024 The Author(s). Journal of Orthopaedic Research® published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society.)
References: Kim HKW, Herring JA. Pathophysiology, classifications, and natural history of Perthes disease. Orthop Clin North Am. 2011;42:285‐295.
Catterall A, Pringle J, Byers P, et al. A review of the morphology of Perthes' disease. J Bone Joint Surg Br. 1982;64:269‐275.
Mindell ER, Sherman MS. Late results in Legg‐Perthes disease. J Bone Joint Surg Am. 1951;33 A:1‐23.
Katz JF, Siffert RS. Capital necrosis, metaphyseal cyst and subluxation in coxa plana. Clin Orthop Relat Res. 1975;106:75‐85.
Smith SR, Ions GK, Gregg PJ. The radiological features of the metaphysis in Perthes disease. J Pediatr Orthop. 1982;2:401‐404.
Hoffinger SA, Henderson RC, Renner JB, Dales MC, Rab GT. Magnetic resonance evaluation of “metaphyseal” changes in Legg‐Calvé‐Perthes disease. J Pediatr Orthop. 1993;13:602‐606.
Jaramillo D, Kasser JR, Villegas‐Medina OL, Gaary E, Zurakowski D. Cartilaginous abnormalities and growth disturbances in Legg‐Calvé‐Perthes disease: evaluation with MR imaging. Radiology. 1995;197:767‐773.
Song HR, Dhar S, Na JB, et al. Classification of metaphyseal change with magnetic resonance imaging in Legg‐Calvé‐Perthes disease. J Pediatr Orthop. 2000;20:557‐561.
Merlini L, Combescure C, De Rosa V, Anooshiravani M, Hanquinet S. Diffusion‐weighted imaging findings in Perthes disease with dynamic gadolinium‐enhanced subtracted (DGS) MR correlation: a preliminary study. Pediatr Radiol. 2010;40:318‐325.
Yoo WJ, Kim YJ, Menezes NM, Cheon JE, Jaramillo D. Diffusion‐weighted MRI reveals epiphyseal and metaphyseal abnormalities in Legg‐Calvé‐Perthes disease: a pilot study. Clin Orthop Relat Res. 2011;469:2881‐2888.
Boutault JR, Baunin C, Bérard E, et al. Diffusion MRI of the neck of the femur in Legg‐Calve‐Perthes disease: a preliminary study. Diagn Interv Imaging. 2013;94:78‐83.
Baunin C, Sanmartin‐Viron D, Accadbled F, et al. Prognosis value of early diffusion MRI in Legg Perthes Calvé disease. Orthop Traumatol Surg Res. 2014;100:317‐321.
Yoo WJ, Choi IH, Cho TJ, et al. Risk factors for femoral head deformity in the early stage of Legg‐Calvé‐Perthes disease: MR contrast enhancement and diffusion indexes. Radiology. 2016;279:562‐570.
Gracia G, Baunin C, Vial J, Accadbled F, Sales de Gauzy J. Diffusion‐weighted MRI for outcome prediction in early Legg‐Calvé‐Perthes disease: medium‐term radiographic correlations. Orthop Traumatol Surg Res. 2019;105:547‐550.
Conway JJ. A scintigraphic classification of Legg‐Calvé‐Perthes disease. Semin Nucl Med. 1993;23:274‐295.
Tsao AK, Dias LS, Conway JJ, Straka P. The prognostic value and significance of serial bone scintigraphy in Legg‐Calvé‐Perthes disease. J Pediatr Orthop. 1997;17:230‐239.
Lamer S, Dorgeret S, Khairouni A, et al. Femoral head vascularisation in Legg‐Calvé‐Perthes disease: comparison of dynamic gadolinium‐enhanced subtraction MRI with bone scintigraphy. Pediatr Radiol. 2002;32:580‐585.
Armstrong AR, Tóth F, Carlson CS, Kim HKW, Johnson CP. Effects of acute femoral head ischemia on the growth plate and metaphysis in a piglet model of Legg‐Calvé‐Perthes disease. Osteoarthritis Cartilage. 2023;31:766‐774.
Iannotti JP. Growth plate physiology and pathology. Orthop Clin North Am. 1990;21:1‐17.
Mackie EJ, Ahmed YA, Tatarczuch L, Chen KS, Mirams M. Endochondral ossification: how cartilage is converted into bone in the developing skeleton. Int J Biochem Cell Biol. 2008;40:46‐62.
Kim HKW, Skelton DN, Quigley EJ. Pathogenesis of metaphyseal radiolucent changes following ischemic necrosis of the capital femoral epiphysis in immature pigs. A preliminary report. J Bone Joint Surg Am. 2004;86:129‐135.
Johnson CP, Wang L, Tóth F, et al. Quantitative MRI helps to detect hip ischemia: preclinical model of Legg‐Calvé‐Perthes disease. Radiology. 2018;289:386‐395.
Johnson CP, Tóth F, Carlson CS, et al. T1ρ and T2 mapping detect acute ischemic injury in a piglet model of Legg–Calvé–Perthes disease. J Orthop Res. 2022;40:484‐494.
Johnson CP, Toth F, Armstrong AR, et al. Quantitative T2, T1ρ, and diffusion mapping of early‐stage ischemic osteonecrosis of the femoral head: an in vivo piglet model study at 3T MRI. Proceedings of the 29th Annual Meeting of ISMRM. Virtual. 2020:1145.
Johnson CP, Bhave S, Armstrong AR, Toth F. Utility of adiabatic T1ρ and T2ρ mapping to detect ischemic injury to the femoral head: an in vivo piglet model study at 3T MRI. Proceedings of the 30th Annual Meeting of ISMRM. Virtual. 2021:0154.
Kim HK, Su PH, Qiu YS. Histopathologic changes in growth‐plate cartilage following ischemic necrosis of the capital femoral epiphysis. J Bone Joint Surg Am. 2001;83:688‐697.
Kim HKW, Su PH. Development of flattening and apparent fragmentation following ischemic necrosis of the capital femoral epiphysis in a piglet model. J Bone Joint Surg Am. 2002;84:1329‐1334.
Jaramillo D, Connolly SA, Mulkern RV, Shapiro F. Developing epiphysis: MR imaging characteristics and histologic correlation in the newborn lamb. Radiology. 1998;207:637‐645.
Laor T, Jaramillo D. MR imaging insights into skeletal maturation: what is normal? Radiology. 2009;250:28‐38.
Jaimes C, Chauvin NA, Delgado J, Jaramillo D. MR imaging of normal epiphyseal development and common epiphyseal disorders. Radiographics. 2014;34:449‐471.
Wongdee K, Krishnamra N, Charoenphandhu N. Endochondral bone growth, bone calcium accretion, and bone mineral density: how are they related? J Physiol Sci. 2012;62:299‐307.
Bojorquez JZ, Bricq S, Acquitter C, Brunotte F, Walker PM, Lalande A. What are normal relaxation times of tissues at 3 T? Magn Reson Imaging. 2017;35:69‐80.
Mathur‐De vré R. Biomedical implications of the relaxation behaviour of water related to NMR imaging. Br J Radiol. 1984;57:955‐976.
معلومات مُعتمدة: R56AR078315 United States AR NIAMS NIH HHS; P41EB027061 United States EB NIBIB NIH HHS; UL1TR002494 United States TR NCATS NIH HHS; L40 AR079814 United States AR NIAMS NIH HHS; K01AR070894 United States AR NIAMS NIH HHS; K01 OD034070 United States OD NIH HHS
فهرسة مساهمة: Keywords: Legg‐Calvé‐Perthes disease (LCPD); growth plate; magnetic resonance imaging; metaphysis; spongiosa
تواريخ الأحداث: Date Created: 20240526 Latest Revision: 20240626
رمز التحديث: 20240626
DOI: 10.1002/jor.25904
PMID: 38796746
قاعدة البيانات: MEDLINE
الوصف
تدمد:1554-527X
DOI:10.1002/jor.25904