矢状面
医学
股骨头
骨关节炎
髋关节发育不良
髋臼
显著性差异
骨盆
口腔正畸科
核医学
外科
解剖
射线照相术
内科学
病理
替代医学
作者
Makoto Iwasa,Wataru Ando,Keisuke Uemura,Hirofumi Hamada,Masaki Takao,Nobuhiko Sugano
出处
期刊:The bone & joint journal
[British Editorial Society of Bone and Joint Surgery]
日期:2021-11-01
卷期号:103-B (11): 1656-1661
被引量:7
标识
DOI:10.1302/0301-620x.103b11.bjj-2021-0472.r1
摘要
Aims Pelvic incidence (PI) is considered an important anatomical parameter for determining the sagittal balance of the spine. The contribution of an abnormal PI to hip osteoarthritis (OA) remains controversial. In this study, we aimed to investigate the relationship between PI and hip OA, and the difference in PI between hip OA without anatomical abnormalities (primary OA) and hip OA with developmental dysplasia of the hip (DDH-OA). Methods In this study, 100 patients each of primary OA, DDH-OA, and control subjects with no history of hip disease were included. CT images were used to measure PI, sagittal femoral head coverage, α angle, and acetabular anteversion. PI was also subdivided into three categories: high PI (larger than 64.0°), medium PI (42.0° to 64.0°), and low PI (less than 42.0°). The anterior centre edge angles, posterior centre edge angles, and total sagittal femoral head coverage were measured. The correlations between PI and sagittal femoral head coverage, α angle, and acetabular anteversion were examined. Results No significant difference in PI was observed between the three groups. There was no significant difference between the groups in terms of the category distribution of PI. The DDH-OA group had lower mean sagittal femoral head coverage than the other groups. There were no significant correlations between PI and other anatomical factors, including sagittal femoral head coverage, α angle, and acetabular anteversion. Conclusion No associations were found between mean PI values or PI categories and hip OA. Furthermore, there was no difference in PI between patients with primary OA and DDH-OA. From our evaluation, we found no evidence of PI being an independent factor associated with the development of hip OA. Cite this article: Bone Joint J 2021;103-B(11):1656–1661.
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