Teraguchi Masatoshi, Yoshimura Noriko, Hashizume Hiroshi, Muraki Shigeyuki, Yamada Hiroshi, Oka Hiroyuki, Minamide Akihito, Ishimoto Yuyu, Nagata Keiji, Kagotani Ryohei, Tanaka Sakae, Kawaguchi Hiroshi, Nakamura Kozo, Akune Toru, Yoshida Munehito
Department of Orthopaedic surgery, Wakayama Medical University, 811-1 Kimiidera, Wakayama, 641-8509, Japan.
Department of Joint Disease Research, 22nd Century Medical & Research Center, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
PLoS One. 2016 Feb 3;11(2):e0147565. doi: 10.1371/journal.pone.0147565. eCollection 2016.
The objective of the present study was to examine the associations between metabolic syndrome (MS) components, such as overweight (OW), hypertension (HT), dyslipidemia (DL), and impaired glucose tolerance (IGT), and intervertebral disc degeneration (DD).
The present study included 928 participants (308 men, 620 women) of the 1,011 participants in the Wakayama Spine Study. DD on magnetic resonance imaging was classified according to the Pfirrmann system. OW, HT, DL, and IGT were assessed using the criteria of the Examination Committee of Criteria for MS in Japan.
Multivariable logistic regression analysis revealed that OW was significantly associated with cervical, thoracic, and lumbar DD (cervical: odds ratio [OR], 1.28; 95% confidence interval [CI], 0.92-1.78; thoracic: OR, 1.75; 95% CI, 1.24-2.51; lumbar: OR, 1.87; 95% CI, 1.06-3.48). HT and IGT were significantly associated with thoracic DD (HT: OR, 1.54; 95% CI, 1.09-2.18; IGT: OR, 1.65; 95% CI, 1.12-2.48). Furthermore, subjects with 1 or more MS components had a higher OR for thoracic DD compared with those without MS components (vs. no component; 1 component: OR, 1.58; 95% CI, 1.03-2.42; 2 components: OR, 2.60; 95% CI, 1.62-4.20; ≥3 components: OR, 2.62; 95% CI, 1.42-5.00).
MS components were significantly associated with thoracic DD. Furthermore, accumulation of MS components significantly increased the OR for thoracic DD. These findings support the need for further studies of the effects of metabolic abnormality on DD.
本研究的目的是探讨代谢综合征(MS)的组成部分,如超重(OW)、高血压(HT)、血脂异常(DL)和糖耐量受损(IGT)与椎间盘退变(DD)之间的关联。
本研究纳入了和歌山脊柱研究中1011名参与者中的928名(308名男性,620名女性)。磁共振成像上的DD根据Pfirrmann系统进行分类。OW、HT、DL和IGT使用日本MS诊断标准审查委员会的标准进行评估。
多变量逻辑回归分析显示,OW与颈椎、胸椎和腰椎DD显著相关(颈椎:比值比[OR],1.28;95%置信区间[CI],0.92 - 1.78;胸椎:OR,1.75;95% CI,1.24 - 2.51;腰椎:OR,1.87;95% CI,1.06 - 3.48)。HT和IGT与胸椎DD显著相关(HT:OR,1.54;95% CI,1.09 - 2.18;IGT:OR,1.65;95% CI,1.12 - 2.48)。此外,与没有MS组分的受试者相比,有1种或更多MS组分的受试者发生胸椎DD的OR更高(与无组分相比;1种组分:OR,1.58;95% CI,1.03 - 2.42;2种组分:OR,2.60;95% CI,1.62 - 4.20;≥3种组分:OR,2.62;95% CI,1.42 - 5.00)。
MS组分与胸椎DD显著相关。此外,MS组分的积累显著增加了胸椎DD的OR。这些发现支持进一步研究代谢异常对DD影响的必要性。