TY - JOUR
T1 - Effects of sclerotic changes on stress concentration in early-stage osteonecrosis
T2 - A patient-specific, 3D finite element analysis
AU - Utsunomiya, Takeshi
AU - Motomura, Goro
AU - Ikemura, Satoshi
AU - Kubo, Yusuke
AU - Sonoda, Kazuhiko
AU - Hatanaka, Hiroyuki
AU - Baba, Shoji
AU - Kawano, Koichiro
AU - Yamamoto, Takuaki
AU - Nakashima, Yasuharu
N1 - Funding Information:
Conflicts of interest: None. Grant sponsor: Grants-in-Aid in Scientific Research; Grant numbers: 16K10906, 16H07057. Correspondence to: Goro Motomura, (T: +81-92-642-5487; F: +81-92-642-5507; E-mail: goromoto@ortho.med.kyushu-u.ac.jp)
Funding Information:
This work was partially supported by Grants-in-Aid in Scientific Research (grant numbers 16K10906, 16H07057) from Japan Society for the Promotion of Science. The authors thank Mr. Junji Kishimoto, a statistician from the Digital Medicine Initiative Kyushu University, for his advice on the statistical analysis.
PY - 2018/12
Y1 - 2018/12
N2 - Stress distribution remains unclear in early-stage osteonecrosis of the femoral head (ONFH). To clarify this issue, we generated patient-specific finite element models (FEMs) from 51 patients with ONFH. Patients’ hips were classified into three groups: ONFH without a sclerotic boundary (Stage 1, n = 6), ONFH with a sclerotic boundary (Stage 2, n = 10), and ONFH with both a sclerotic boundary and <2 mm collapse (Stage 3, n = 35). Four hips without ONFH were used as controls. Stress distribution in each FEM was compared with magnetic resonance imaging (MRI) and computed tomography (CT) results. Fifteen wholly resected femoral heads in Stage 3 hips were assessed by micro-CT. Furthermore, we histologically examined three Stage 2 femoral heads that subsequently developed subchondral fractures after FEM analyses. In all FEMs of both control and Stage 1 hip, stress was equally distributed on the femoral head surface. However, in all FEMs of both Stages 2 and 3 hips, stress was concentrated at the lateral boundary of the femoral head surface, corresponding to both a low-intensity band on T1-weighted MRI images and sclerotic changes on CT. On micro-CT, subchondral fractures consistently began at the lateral boundary with sclerotic changes, in which bone volume fraction was increased. Histology showed breakage of subchondral plates at the junction between necrotic and reparative zones. In early-stage ONFH, sclerotic changes caused stress concentration, which can trigger subchondral fractures at the lateral boundary. Clinical Significance: Our results will clarify the pathogenic mechanism of collapse in ONFH.
AB - Stress distribution remains unclear in early-stage osteonecrosis of the femoral head (ONFH). To clarify this issue, we generated patient-specific finite element models (FEMs) from 51 patients with ONFH. Patients’ hips were classified into three groups: ONFH without a sclerotic boundary (Stage 1, n = 6), ONFH with a sclerotic boundary (Stage 2, n = 10), and ONFH with both a sclerotic boundary and <2 mm collapse (Stage 3, n = 35). Four hips without ONFH were used as controls. Stress distribution in each FEM was compared with magnetic resonance imaging (MRI) and computed tomography (CT) results. Fifteen wholly resected femoral heads in Stage 3 hips were assessed by micro-CT. Furthermore, we histologically examined three Stage 2 femoral heads that subsequently developed subchondral fractures after FEM analyses. In all FEMs of both control and Stage 1 hip, stress was equally distributed on the femoral head surface. However, in all FEMs of both Stages 2 and 3 hips, stress was concentrated at the lateral boundary of the femoral head surface, corresponding to both a low-intensity band on T1-weighted MRI images and sclerotic changes on CT. On micro-CT, subchondral fractures consistently began at the lateral boundary with sclerotic changes, in which bone volume fraction was increased. Histology showed breakage of subchondral plates at the junction between necrotic and reparative zones. In early-stage ONFH, sclerotic changes caused stress concentration, which can trigger subchondral fractures at the lateral boundary. Clinical Significance: Our results will clarify the pathogenic mechanism of collapse in ONFH.
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U2 - 10.1002/jor.24124
DO - 10.1002/jor.24124
M3 - Article
C2 - 30098226
AN - SCOPUS:85052379644
SN - 0736-0266
VL - 36
SP - 3169
EP - 3177
JO - Journal of Orthopaedic Research
JF - Journal of Orthopaedic Research
IS - 12
ER -