Biomarkers reflect differences in osteoarthritis phenotypes of the lumbar spine: the Johnston County Osteoarthritis Project

被引:26
作者
Goode, A. P. [1 ]
Nelson, A. E. [2 ]
Kraus, V. B. [3 ,4 ]
Renner, J. B. [5 ]
Jordan, J. M. [2 ]
机构
[1] Duke Univ, Sch Med, Duke Clin Res Inst, Dept Orthoped Surg, Durham, NC 27706 USA
[2] Univ N Carolina, Thurston Arthrit Res Ctr, Dept Med, Chapel Hill, NC USA
[3] Duke Univ, Sch Med, Duke Mol Physiol Inst, Durham, NC USA
[4] Duke Univ, Sch Med, Div Rheumatol, Durham, NC USA
[5] Univ N Carolina, Thurston Arthrit Res Ctr, Dept Radiol, Chapel Hill, NC USA
关键词
Lumbar spine; Biomarkers; Phenotypes; Osteoarthritis; LOW-BACK-PAIN; INDIVIDUAL RADIOGRAPHIC FEATURES; FACET JOINT OSTEOARTHRITIS; KNEE OSTEOARTHRITIS; AFRICAN-AMERICANS; DISC DEGENERATION; BIOCHEMICAL MARKERS; HIP OSTEOARTHRITIS; ASSOCIATION; SERUM;
D O I
10.1016/j.joca.2017.07.007
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
摘要
Objective: To determine differences in biomarker levels between radiographic phenotypes of facet joint osteoarthritis (FOA) only, spine OA only ((disc space narrowing (DSN) and vertebral osteophytes (OST)) or the combination of FOA and spine OA. Design: A cross-sectional analysis of data from 555 participants in the Johnston County Osteoarthritis Project was performed. Lumbar spine levels were graded by severity (OST and DSN) and presence (FOA) of degeneration. Biomarkers included hyaluronan (HA) and type II collagen (CTX-II). Adjusted risk ratios (aRRR) were estimated using multinomial regression, with adjustment for age, race, sex, body mass index (BMI), and radiographic OA (knee, hip, hand). Interactions were tested between sex, race and low back symptoms. Results: FOA only was present in 22.4%, 14.5% had spine OA only, and 34.6% had the combination of FOA and spine OA. Compared to the reference group of neither FOA or spine OA, a one unit higher ln HA level was associated with 31% higher relative risk ratio (RRR = 1.31 (95% 1.03, 1.67)) of having FOA only, while, a one unit higher lnuCTX-II level was associated with 84% higher relative risk ratio (RRR = 1.84 (95% CI 1.19, 2.84)) of having spine OA only. No significant interactions were identified. Conclusion: Interestingly, OA affecting the synovial facet joint was associated with a marker of inflammation (HA). Spine OA, affecting intervertebral discs that contain collagen type II, was associated with a marker reflecting collagen type II degradation (CTX-II). These findings suggest that biomarkers may reflect the different pathophysiologic processes of lumbar spine OA phenotypes. (C) 2017 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1672 / 1679
页数:8
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