Association between serum and urine biomarkers and lumbar spine individual radiographic features: the Johnston County Osteoarthritis Project

被引:41
作者
Goode, A. P. [1 ]
Marshall, S. W. [2 ]
Kraus, V. B. [3 ]
Renner, J. B. [4 ]
Stuermer, T. [5 ]
Carey, T. S. [6 ]
Irwin, D. E. [5 ]
Jordan, J. M. [7 ]
机构
[1] Duke Univ, Med Ctr, Dept Community & Family Med, Durham, NC 27708 USA
[2] Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC 27515 USA
[3] Duke Univ, Med Ctr, Dept Rheumatol, Durham, NC 27708 USA
[4] Univ N Carolina, Dept Radiol, Chapel Hill, NC 27515 USA
[5] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[6] Univ N Carolina, Director Cecil G Sheps Ctr, Chapel Hill, NC 27515 USA
[7] Univ N Carolina, Dept Med Orthoped & Epidemiol, Div Rheumatol Allergy & Immunol, Chapel Hill, NC 27515 USA
基金
美国医疗保健研究与质量局; 美国国家卫生研究院;
关键词
Biomarkers; Lumbar spine; Hip osteoarthritis; Knee osteoarthritis; Hand osteoarthritis; OLIGOMERIC MATRIX PROTEIN; LOW-BACK-PAIN; KNEE OSTEOARTHRITIS; DISC DEGENERATION; HIP-OSTEOARTHRITIS; CARTILAGE; PROGRESSION; COLLAGEN; SYMPTOMS; WOMEN;
D O I
10.1016/j.joca.2012.08.003
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Objective: (1) To determine associations between radiographic features of lumbosacral (LS) spine disc space narrowing (DSN) and osteophytes (OST) and joint metabolism biomarkers (serum cartilage oligomeric matrix protein (COMP), hyaluronic acid (HA), collagen neoepitope (C2C). C-propeptide of type II procollagen (CP-II), urine C-terminal cross-linking telopeptide (CTX-II) and N-terminal telopeptide (NTX-I)). (2) To explore interactions with race, gender and low back symptoms. Design: Cross-sectional analysis of 547 participants enrolled in the Johnston County (JoCo) Osteoarthritis Project from 2003 to 2004. Mean biomarker levels were estimated with linear regression. Proportional and partial-proportional odds models were used to estimate associations. Interactions were tested with likelihood ratio tests at a P-value < 0.10. Biomarkers were natural log (In) transformed. Results: Significant differences in mean biomarker levels were found across severity of DSN for InHA and InC2C and InCTX-II across severity of both DSN and OST. Moderate-to-strong associations were found between biomarkers of type II collagen and DSN, whereas associations with OST were weak. An association between InHA and DSN was seen in women (adjusted odds ratio [aOR] = 1.34 (95% confidence intervals (CI) 1.08, 1.65)) but no association among men (aOR = 0.90 (95% CI 0.63, 1.26)). In Caucasians there was a decreased association with NTX-I and OST (aOR = 0.67 (95% CI 0.49, 0.91)) and no association in African Americans (AAs) (aOR = 1.06 (95% CI 0.76, 1.47)). There was a positive association of InCOMP with DSN among those with low back symptoms (aOR = 1.82 (95% CI 1.02, 3.27)), but no association in those without low back symptoms (aOR = 0.65 (95% CI 0.35, 1.20)). Conclusion: Joint metabolism biomarkers suggest biological differences in the pathologic process involved in DSN and OST that may be gender (HA) and ethnicity (NTX-I) specific. (C) 2012 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1286 / 1293
页数:8
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